Category: 3. Business

  • Alizadeh A, Dyck SM, Karimi-Abdolrezaee S. Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Front Neurol. 2019;10:282.

    PubMed 
    PubMed Central 

    Google Scholar 

  • National Spinal Cord Injury Statistical Center. Traumatic spinal cord injury facts and figures at a glance. Birmingham, AL: University of Alabama at Birmingham [Internet]. 2024; Available from: https://msktc.org/sites/default/files/Facts-and-Figures-2024-Eng-508.pdf

  • Anderson KD. Targeting recovery: priorities of the spinal cord-injured population. J Neurotrauma. 2004;21(10):1371–83.

    PubMed 

    Google Scholar 

  • Brown-Triolo DL, Roach MJ, Nelson K, Triolo R. Consumer perspectives on mobility: implications for neuroprosthesis design. Journal of Rehabilitation Research & Development. 2002;39(6).

  • Harkema S, Gerasimenko Y, Hodes J, Burdick J, Angeli C, Chen Y, et al. Effect of epidural stimulation of the lumbosacral spinal cord on voluntary movement, standing, and assisted stepping after motor complete paraplegia: a case study. Lancet. 2011;377(9781):1938–47.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Rowald A, Komi S, Demesmaeker R, Baaklini E, Hernandez-Charpak SD, Paoles E, et al. Activity-dependent spinal cord neuromodulation rapidly restores trunk and leg motor functions after complete paralysis. Nat Med. 2022;28(2):260–71.

    CAS 
    PubMed 

    Google Scholar 

  • Gill ML, Grahn PJ, Calvert JS, Linde MB, Lavrov IA, Strommen JA, et al. Neuromodulation of lumbosacral spinal networks enables independent stepping after complete paraplegia. Nat Med. 2018;24(11):1677–82.

    CAS 
    PubMed 

    Google Scholar 

  • Angeli CA, Boakye M, Morton RA, Vogt J, Benton K, Chen Y, et al. Recovery of over-ground walking after chronic motor complete spinal cord injury. N Engl J Med. 2018;379(13):1244–50.

    PubMed 

    Google Scholar 

  • Hofstoetter US, Perret I, Bayart A, Lackner P, Binder H, Freundl B, et al. Spinal motor mapping by epidural stimulation of lumbosacral posterior roots in humans. iScience. 2021. https://doi.org/10.1016/j.isci.2020.101930.

    Article 
    PubMed 

    Google Scholar 

  • Gorgey AS, Trainer R, Sutor TW, Goldsmith JA, Alazzam A, Goetz LL, et al. A case study of percutaneous epidural stimulation to enable motor control in two men after spinal cord injury. Nat Commun. 2023;14(1):2064.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Mesbah S, Herrity A, Ugiliweneza B, Angeli C, Gerasimenko Y, Boakye M, et al. Neuroanatomical mapping of the lumbosacral spinal cord in individuals with chronic spinal cord injury. Brain Commun. 2023;5(1):fcac330.

    PubMed 

    Google Scholar 

  • Mong ER, Kethireddy S, Staudt MD. Spinal cord stimulator paddle lead revision and replacement for misplaced or displaced electrodes. World Neurosurg. 2024. https://doi.org/10.1016/j.wneu.2024.03.154.

    Article 
    PubMed 

    Google Scholar 

  • Dombovy-Johnson ML, D’Souza RS, Ha CT, Hagedorn JM. Incidence and risk factors for spinal cord stimulator lead migration with or without loss of efficacy: a retrospective review of 91 consecutive thoracic lead implants. Neuromodulation Technol Neural Interface. 2022;25(5):731–7.

    Google Scholar 

  • Alazzam AM, Ballance WB, Smith AC, Rejc E, Weber KA, Trainer R, et al. Peak slope ratio of the recruitment curves compared to muscle evoked potentials to optimize standing configurations with percutaneous epidural stimulation after spinal cord injury. J Clin Med. 2024;13(5):1344.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Boakye M, Ball T, Dietz N, Sharma M, Angeli C, Rejc E, et al. Spinal cord epidural stimulation for motor and autonomic function recovery after chronic spinal cord injury: a case series and technical note. Surg Neurol Int. 2023. https://doi.org/10.25259/SNI_1074_2022.

    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Rejc E, Angeli CA, Bryant N, Harkema SJ. Effects of stand and step training with epidural stimulation on motor function for standing in chronic complete paraplegics. J Neurotrauma. 2017;34(9):1787–802.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Capogrosso M, Wenger N, Raspopovic S, Musienko P, Beauparlant J, Luciani LB, et al. A computational model for epidural electrical stimulation of spinal sensorimotor circuits. J Neurosci. 2013;33(49):19326–40.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Greiner N, Barra B, Schiavone G, Lorach H, James N, Conti S, et al. Recruitment of upper-limb motoneurons with epidural electrical stimulation of the cervical spinal cord. Nat Commun. 2021;12(1):435.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Choi EH, Gattas S, Brown NJ, Hong JD, Limbo JN, Chan AY, et al. Epidural electrical stimulation for spinal cord injury. Neural Regen Res. 2021;16(12):2367–75.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Saigal R, Renzi C, Mushahwar VK. Intraspinal microstimulation generates functional movements after spinal-cord injury. IEEE Trans Neural Syst Rehabil Eng. 2004;12(4):430–40.

    PubMed 

    Google Scholar 

  • Mushahwar VK, Gillard DM, Gauthier MJ, Prochazka A. Intraspinal micro stimulation generates locomotor-like and feedback-controlled movements. IEEE Trans Neural Syst Rehabil Eng. 2002;10(1):68–81.

    PubMed 

    Google Scholar 

  • Sunshine MD, Cho FS, Lockwood DR, Fechko AS, Kasten MR, Moritz CT. Cervical intraspinal microstimulation evokes robust forelimb movements before and after injury. J Neural Eng. 2013;10(3):036001.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Zimmermann JB, Seki K, Jackson A. Reanimating the arm and hand with intraspinal microstimulation. J Neural Eng. 2011;8(5):054001.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Gaunt RA, Prochazka A, Mushahwar VK, Guevremont L, Ellaway PH. Intraspinal microstimulation excites multisegmental sensory afferents at lower stimulus levels than local α-motoneuron responses. J Neurophysiol. 2006;96(6):2995–3005.

    CAS 
    PubMed 

    Google Scholar 

  • Zimmermann JB, Jackson A. Closed-loop control of spinal cord stimulation to restore hand function after paralysis. Front Neurosci. 2014;8:87.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Bizzi E, Giszter SF, Loeb E, Mussa-Ivaldi FA, Saltiel P. Modular organization of motor behavior in the frog’s spinal cord. Trends Neurosci. 1995;18(10):442–6.

    CAS 
    PubMed 

    Google Scholar 

  • Giszter SF. Spinal primitives and intra-spinal micro-stimulation (ISMS) based prostheses: a neurobiological perspective on the “known unknowns” in ISMS and future prospects. Front Neurosci. 2015;9:72.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Moritz CT, Lucas TH, Perlmutter SI, Fetz EE. Forelimb movements and muscle responses evoked by microstimulation of cervical spinal cord in sedated monkeys. J Neurophysiol. 2007;97(1):110–20.

    PubMed 

    Google Scholar 

  • Hachmann JT, Jeong JH, Grahn PJ, Mallory GW, Evertz LQ, Bieber AJ, et al. Large animal model for development of functional restoration paradigms using epidural and intraspinal stimulation. PLoS ONE. 2013;8(12):e81443.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Sharpe AN, Jackson A. Upper-limb muscle responses to epidural, subdural and intraspinal stimulation of the cervical spinal cord. J Neural Eng. 2014;11(1):016005.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Mushahwar VK, Collins DF, Prochazka A. Spinal cord microstimulation generates functional limb movements in chronically implanted cats. Exp Neurol. 2000;163(2):422–9.

    CAS 
    PubMed 

    Google Scholar 

  • Tawakol O, Herman MD, Foxley S, Mushahwar VK, Towle VL, Troyk PR. In-vivo testing of a novel wireless intraspinal microstimulation interface for restoration of motor function following spinal cord injury. Artif Organs. 2024;48(3):263–73.

    CAS 
    PubMed 

    Google Scholar 

  • Nashold B, Friedman H, Grimes J. Electrical stimulation of the conus medullaris to control bladder emptying in paraplegia: a ten-year review. Stereotact Funct Neurosurg. 1982;45(1–2):40–3.

    CAS 

    Google Scholar 

  • Nashold BS, Friedman H, Glenn JF, Grimes JH, Barry WF, Avery R. Electromicturition in paraplegia: implantation of a spinal neuroprosthesis. Arch Surg. 1972;104(2):195–202.

    PubMed 

    Google Scholar 

  • Boergens KM, Tadić A, Hopper MS, McNamara I, Fell D, Sahasrabuddhe K, et al. Laser ablation of the pia mater for insertion of high-density microelectrode arrays in a translational sheep model. J Neural Eng. 2021;18(4):045008.

    Google Scholar 

  • Rocca A, Lehner C, Wafula-Wekesa E, Luna E, Fernández-Cornejo V, Abarca-Olivas J, et al. Robot-assisted implantation of a microelectrode array in the occipital lobe as a visual prosthesis. J Neurosurg. 2023;140(4):1169–76.

    PubMed 

    Google Scholar 

  • Roser F, Tatagiba M, Maier G. Spinal robotics: current applications and future perspectives. Neurosurgery. 2013;72:A12–8.

    Google Scholar 

  • Zeng B, Meng F, Ding H, Wang G. A surgical robot with augmented reality visualization for stereoelectroencephalography electrode implantation. Int J Comput Assist Radiol Surg. 2017;12:1355–68.

    PubMed 

    Google Scholar 

  • Prochazka A, Mushahwar V, Yakovenko S. Activation and coordination of spinal motoneuron pools after spinal cord injury. Prog Brain Res. 2002;137:109–24.

    PubMed 

    Google Scholar 

  • Guevremont L, Renzi CG, Norton JA, Kowalczewski J, Saigal R, Mushahwar VK. Locomotor-related networks in the lumbosacral enlargement of the adult spinal cat: activation through intraspinal microstimulation. IEEE Trans Neural Syst Rehabil Eng. 2006;14(3):266–72.

    PubMed 

    Google Scholar 

  • Toossi A, Bergin B, Marefatallah M, Parhizi B, Tyreman N, Everaert DG, et al. Comparative neuroanatomy of the lumbosacral spinal cord of the rat, cat, pig, monkey, and human. Sci Rep. 2021;11(1):1955.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Lee JH, Jones CF, Okon EB, Anderson L, Tigchelaar S, Kooner P, et al. A novel porcine model of traumatic thoracic spinal cord injury. J Neurotrauma. 2013;30(3):142–59.

    PubMed 

    Google Scholar 

  • Leonard AV, Menendez JY, Pat BM, Hadley MN, Floyd CL. Localization of the corticospinal tract within the porcine spinal cord: implications for experimental modeling of traumatic spinal cord injury. Neurosci Lett. 2017;648:1–7.

    CAS 
    PubMed 

    Google Scholar 

  • Smith AC, Ahmed RU, Weber KA, Negahdar M, Gibson D, Boakye M, et al. Spinal cord lesion MRI and behavioral outcomes in a miniature pig model of spinal cord injury: exploring preclinical potential through an ad hoc comparison with human SCI. Spinal Cord Ser Cases. 2024;10(1):44.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Ahmed RU, Knibbe CA, Wilkins F, Sherwood LC, Howland DR, Boakye M. Porcine spinal cord injury model for translational research across multiple functional systems. Exp Neurol. 2023;359:114267.

    PubMed 

    Google Scholar 

  • Mirkiani S, Roszko DA, O’Sullivan CL, Faridi P, Hu DS, Fang D, et al. Overground gait kinematics and muscle activation patterns in the Yucatan mini pig. J Neural Eng. 2022;19(2):026009.

    Google Scholar 

  • Boakye M, Morehouse J, Ethridge J, Burke DA, Khattar NK, Kumar C, et al. Treadmill-based gait kinematics in the Yucatan mini pig. J Neurotrauma. 2020;37(21):2277–91.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Schiavone G, Wagner F, Fallegger F, Kang X, Vachicouras N, Barra B, et al. Long-term functionality of a soft electrode array for epidural spinal cord stimulation in a minipig model. In IEEE; 2018. p. 1432–5.

  • Hogan MK, Barber SM, Rao Z, Kondiles BR, Huang M, Steele WJ, et al. A wireless spinal stimulation system for ventral activation of the rat cervical spinal cord. Sci Rep. 2021;11(1):14900.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Afridi AK, Steele AG, Martin C, Sayenko DG, Barber SM. Ventral epidural stimulation for motor recovery after spinal cord injury: illustrative case. Journal of Neurosurgery: Case Lessons. 2024;8(12).

  • Lin D, Lee JM, Wang C, Park HG, Lieber CM. Injectable ventral spinal stimulator evokes programmable and biomimetic hindlimb motion. Nano Lett. 2023;23(13):6184–92.

    CAS 
    PubMed 

    Google Scholar 

  • Harland B, Kow CY, Svirskis D. Spinal intradural electrodes: opportunities, challenges and translation to the clinic. Neural Regen Res. 2023. https://doi.org/10.4103/1673-5374.380895.

    Article 
    PubMed Central 

    Google Scholar 

  • Olmsted ZT, Wu PB, Katouzian A, Dorsi MJ. Intrathecal placement of percutaneous spinal cord stimulation leads: illustrative cases. Journal of Neurosurgery: Case Lessons. 2024;8(13).

  • Chapman KB, Sayed D, Lamer T, Hunter C, Weisbein J, Patel KV, et al. Best practices for dorsal root ganglion stimulation for chronic pain: guidelines from the American Society of Pain and Neuroscience. J Pain Res. 2023;839–79.

  • King KW, Cusack WF, Nanivadekar AC, Ayers CA, Urbin M, Gaunt RA, et al. DRG microstimulation evokes postural responses in awake, standing felines. J Neural Eng. 2019;17(1):016014.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Ayers CA, Fisher LE, Gaunt RA, Weber DJ. Microstimulation of the lumbar DRG recruits primary afferent neurons in localized regions of lower limb. J Neurophysiol. 2016;116(1):51–60.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Dalrymple AN, Ting JE, Bose R, Trevathan JK, Nieuwoudt S, Lempka SF, et al. Stimulation of the dorsal root ganglion using an Injectrode®. J Neural Eng. 2021;18(5):056068.

    Google Scholar 

  • Toossi A, Everaert DG, Perlmutter SI, Mushahwar VK. Functional organization of motor networks in the lumbosacral spinal cord of non-human primates. Sci Rep. 2019;9(1):13539.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Toossi A, Everaert DG, Seres P, Jaremko JL, Robinson K, Kao CC, et al. Ultrasound-guided spinal stereotactic system for intraspinal implants. J Neurosurg Spine. 2018;29(3):292–305.

    PubMed 

    Google Scholar 

  • Mirkiani S, O’Sullivan CL, Roszko DA, Faridi P, Hu DS, Everaert DG, et al. Safety of mapping the motor networks in the spinal cord using penetrating microelectrodes in Yucatan minipigs. Journal of Neurosurgery: Spine. 2024;1(aop):1–13.

  • Borrell JA, Frost SB, Peterson J, Nudo RJ. A 3d map of the hindlimb motor representation in the lumbar spinal cord in Sprague Dawley rats. J Neural Eng. 2016;14(1):016007.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Mushahwar VK, Horch KW. Selective activation of muscle groups in the feline hindlimb through electrical microstimulation of the ventral lumbo-sacral spinal cord. IEEE Trans Rehabil Eng. 2000;8(1):11–21.

    CAS 
    PubMed 

    Google Scholar 

  • Bamford JA, Todd KG, Mushahwar VK. The effects of intraspinal microstimulation on spinal cord tissue in the rat. Biomaterials. 2010;31(21):5552–63.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Roszko DA, Mirkiani S, Tyreman N, Wilson D, Toossi A, Mushahwar VK. Laser-microfabricated polymer multielectrodes for intraspinal microstimulation. IEEE Trans Biomed Eng. 2022;70(1):354–65.

    PubMed 

    Google Scholar 

  • Toossi A, Everaert DG, Uwiera RR, Hu DS, Robinson K, Gragasin FS, et al. Effect of anesthesia on motor responses evoked by spinal neural prostheses during intraoperative procedures. J Neural Eng. 2019;16(3):036003.

    PubMed 

    Google Scholar 

  • Vanderhorst VG, Holstege G. Organization of lumbosacral motoneuronal cell groups innervating hindlimb, pelvic floor, and axial muscles in the cat. J Comp Neurol. 1997;382(1):46–76.

    CAS 
    PubMed 

    Google Scholar 

  • Tresch MC, Bizzi E. Responses to spinal microstimulation in the chronically spinalized rat and their relationship to spinal systems activated by low threshold cutaneous stimulation. Exp Brain Res. 1999;129:401–16.

    CAS 
    PubMed 

    Google Scholar 

  • Capogrosso M, Milekovic T, Borton D, Wagner F, Moraud EM, Mignardot JB, et al. A brain–spine interface alleviating gait deficits after spinal cord injury in primates. Nature. 2016;539(7628):284–8.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Sharrard W. The segmental innervation of the lower limb muscles in man: Arris and Gale lecture delivered at the Royal College of Surgeons of England on 2nd January 1964. Ann R Coll Surg Engl. 1964;35(2):106.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Sharrard W. The distribution of the permanent paralysis in the lower limb in poliomyelitis: a clinical and pathological study. J Bone Joint Surgery British. 1955;37(4):540–58.

    Google Scholar 

  • Yakovenko S, Mushahwar V, VanderHorst V, Holstege G, Prochazka A. Spatiotemporal activation of lumbosacral motoneurons in the locomotor step cycle. J Neurophysiol. 2002;87(3):1542–53.

    PubMed 

    Google Scholar 

  • Bamford J, Putman C, Mushahwar V. Intraspinal microstimulation preferentially recruits fatigue-resistant muscle fibres and generates gradual force in rat. J Physiol. 2005;569(3):873–84.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Holinski B, Mazurek K, Everaert D, Toossi A, Lucas-Osma A, Troyk P, et al. Intraspinal microstimulation produces over-ground walking in anesthetized cats. J Neural Eng. 2016;13(5):056016.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Snow S, Horch KW, Mushahwar VK. Intraspinal microstimulation using cylindrical multielectrodes. IEEE Trans Biomed Eng. 2006;53(2):311–9.

    PubMed 

    Google Scholar 

  • Lau B, Guevremont L, Mushahwar VK. Strategies for generating prolonged functional standing using intramuscular stimulation or intraspinal microstimulation. IEEE Trans Neural Syst Rehabil Eng. 2007;15(2):273–85.

    PubMed 

    Google Scholar 

  • Vogelstein RJ, Tenore FV, Guevremont L, Etienne-Cummings R, Mushahwar VK. A silicon central pattern generator controls locomotion in vivo. IEEE Trans Biomed Circuits Syst. 2008;2(3):212–22.

    CAS 
    PubMed 

    Google Scholar 

  • Dalrymple AN, Roszko DA, Sutton RS, Mushahwar VK. Pavlovian control of intraspinal microstimulation to produce over-ground walking. J Neural Eng. 2020;17(3):036002.

    PubMed 

    Google Scholar 

  • Dalrymple AN, Everaert DG, Hu DS, Mushahwar VK. A speed-adaptive intraspinal microstimulation controller to restore weight-bearing stepping in a spinal cord hemisection model. J Neural Eng. 2018;15(5):056023.

    PubMed 

    Google Scholar 

  • Fiori L, Castiglia SF, Chini G, Draicchio F, Sacco F, Serrao M, et al. The lower limb muscle co-activation map during human locomotion: from slow walking to running. Bioengineering. 2024;11(3):288.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Cheng R, Sui Y, Sayenko D, Burdick JW. Motor control after human SCI through activation of muscle synergies under spinal cord stimulation. IEEE Trans Neural Syst Rehabil Eng. 2019;27(6):1331–40.

    PubMed 

    Google Scholar 

  • Rasmussen S, Chan A, Goslow G Jr. The cat step cycle: electromyographic patterns for hindlimb muscles during posture and unrestrained locomotion. J Morphol. 1978;155(3):253–69.

    CAS 
    PubMed 

    Google Scholar 

  • Aagaard P, Simonsen E, Andersen J, Magnusson S, Bojsen-Møller F, Dyhre-Poulsen P. Antagonist muscle coactivation during isokinetic knee extension. Scand J Med Sci Sports. 2000;10(2):58–67.

    CAS 
    PubMed 

    Google Scholar 

  • Latash ML. Muscle coactivation: definitions, mechanisms, and functions. J Neurophysiol. 2018;120(1):88–104.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Baratta R, Solomonow M, Zhou B, Letson D, Chuinard R, D’ambrosia R. Muscular coactivation: the role of the antagonist musculature in maintaining knee stability. Am J Sports Med. 1988;16(2):113–22.

    CAS 
    PubMed 

    Google Scholar 

  • Tsuchida T, Ensini M, Morton S, Baldassare M, Edlund T, Jessell T, et al. Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes. Cell. 1994;79(6):957–70.

    CAS 
    PubMed 

    Google Scholar 

  • Tripodi M, Stepien AE, Arber S. Motor antagonism exposed by spatial segregation and timing of neurogenesis. Nature. 2011;479(7371):61–6.

    CAS 
    PubMed 

    Google Scholar 

  • Takeoka A, Arber S. Functional local proprioceptive feedback circuits initiate and maintain locomotor recovery after spinal cord injury. Cell Rep. 2019;27(1):71–85.

    CAS 
    PubMed 

    Google Scholar 

  • Ronzano R, Skarlatou S, Barriga BK, Bannatyne BA, Bhumbra GS, Foster JD, et al. Spinal premotor interneurons controlling antagonistic muscles are spatially intermingled. Elife. 2022;11:e81976.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Levine AJ, Hinckley CA, Hilde KL, Driscoll SP, Poon TH, Montgomery JM, et al. Identification of a cellular node for motor control pathways. Nat Neurosci. 2014;17(4):586–93.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Hanson TL, Diaz-Botia CA, Kharazia V, Maharbiz MM, Sabes PN. The “sewing machine” for minimally invasive neural recording. BioRxiv. 2019;578542.

  • Vomero M, Ciarpella F, Zucchini E, Kirsch M, Fadiga L, Stieglitz T, et al. On the longevity of flexible neural interfaces: establishing biostability of polyimide-based intracortical implants. Biomaterials. 2022;281:121372.

    CAS 
    PubMed 

    Google Scholar 

  • Luan L, Wei X, Zhao Z, Siegel JJ, Potnis O, Tuppen CA, et al. Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration. Sci Adv. 2017;3(2):e1601966.

    PubMed 
    PubMed Central 

    Google Scholar 

  • Lee Y, Shin H, Lee D, Choi S, Cho I, Seo J. A lubricated nonimmunogenic neural probe for acute insertion trauma minimization and long-term signal recording. Adv Sci. 2021;8(15):2100231.

    CAS 

    Google Scholar 

  • Sridar S, Churchward MA, Mushahwar VK, Todd KG, Elias AL. Peptide modification of polyimide-insulated microwires: towards improved biocompatibility through reduced glial scarring. Acta Biomater. 2017;60:154–66.

    CAS 
    PubMed 

    Google Scholar 

  • Toossi A, Everaert DG, Azar A, Dennison CR, Mushahwar VK. Mechanically stable intraspinal microstimulation implants for human translation. Ann Biomed Eng. 2017;45:681–94.

    PubMed 

    Google Scholar 

  • Soloukey S, de Rooij JD, Osterthun R, Drenthen J, De Zeeuw CI, Huygen FJ, et al. The dorsal root ganglion as a novel neuromodulatory target to evoke strong and reproducible motor responses in chronic motor complete spinal cord injury: a case series of five patients. Neuromodul Technol Neural Interface. 2021;24(4):779–93.

  • Holinski BJ, Mazurek KA, Everaert DG, Stein RB, Mushahwar VK. Restoring stepping after spinal cord injury using intraspinal microstimulation and novel control strategies. In IEEE; 2011. p. 5798–801.

  • Kramer J, Liem L, Russo M, Smet I, Van Buyten JP, Huygen F. Lack of body positional effects on paresthesias when stimulating the dorsal root ganglion (DRG) in the treatment of chronic pain. Neuromodul Technol Neural Interface. 2015;18(1):50–7.

  • Holinski B, Everaert D, Mushahwar V, Stein R. Real-time control of walking using recordings from dorsal root ganglia. J Neural Eng. 2013;10(5):056008.

    CAS 
    PubMed 
    PubMed Central 

    Google Scholar 

  • Mushahwar V, Aoyagi Y, Stein R, Prochazka A. Movements generated by intraspinal microstimulation in the intermediate gray matter of the anesthetized, decerebrate, and spinal cat. Can J Physiol Pharmacol. 2004;82(8–9):702–14.

    CAS 
    PubMed 

    Google Scholar 

Continue Reading

  • Disruption of low-frequency narrowband EEG microstate networks in Parkinson’s disease with mild cognitive impairment | Journal of NeuroEngineering and Rehabilitation

    Participants and study design

    This investigation enrolled a total of 67 individuals, comprising 47 individuals diagnosed with primary PD who were undergoing treatment at Beijing Rehabilitation Hospital, affiliated with Capital Medical University (25 males and 22 females), along with 20 individuals without any neurological conditions (healthy controls, HC) sourced from the local population, ensuring parity in gender and age. These controls had no past records of neurological impairments. Motor function was primarily appraised via the Movement Disorder Society Unified Parkinson’s Disease Rating Scale part III (MDS-UPDRS III). Concurrently, cognitive abilities were assessed through the Mini-Mental State Examination (MMSE) as well as the Montreal Cognitive Assessment (MoCA) scales [22]. The MoCA is the most frequently used standard screening tool for PD-MCI, with a specificity of 82%, a sensitivity of 41%, and a diagnostic accuracy of 68% while maintaining clinical relevance [23]. From the MoCA results, two groups emerged among the 47 participants with PD: those with normal cognition (PD-NC, score > 25) and those with mild cognitive impairment (PD-MCI, score ≤ 25). With the approval of the Ethics Committee of Beijing Rehabilitation Hospital, Capital Medical University, we collected the data for this study (Approval Number: 2023bkky044). The data acquisition adhered rigorously to the ethical principles outlined in the Declaration of Helsinki. Before participating, all participants gave written informed consent.

    EEG data acquisition and preprocessing

    EEG data were recorded using a 30-channel electrode system (actiCAP snap, Brain Products GmbH, Gilching, Germany). The electrode positions included frontal electrodes (Fp1, Fz, F3, F4, F7, F8), fronto-central electrodes (FT9, FT10, FC5, FC6, FC1, FC2), central electrodes (C3, Cz, C4), parietal electrodes (CP5, CP6, CP1, CP2, Pz, P3, P4, P7, P8), and occipital electrodes (O1, Oz, O2). Participants sat relaxed with eyes closed in dimly lit rooms, maintaining wakefulness. The impedance of all electrodes was kept under 5 kΩ. The EEG signals were sampled at 1000 Hz for 15 min per individual. A rigorous, multi-stage preprocessing pipeline was applied to the raw EEG data to ensure high data quality and mitigate the constraints of the acquisition setup. Data were originally recorded using an actiCAP system with TP9 as the online reference. The data were first filtered using a zero-phase bandpass filter (0.5–45 Hz; Hamming-windowed Finite Impulse Response filter in EEGLAB) to attenuate low-frequency drifts and high-frequency noise. As the online reference (TP9) is suboptimal for Independent Component Analysis (ICA), the data were offline-referenced to the average of the bilateral mastoids (TP9 and TP10). This approach established a pragmatic and stable non-cephalic reference point for ICA, consistent with established practices in the field [24]. Subsequently, the data were decomposed into 30 independent components using the Infomax ICA algorithm. To ensure the validity of the decomposition and the accuracy of artifact rejection, a robust, semi-automated component classification strategy was employed. An initial, data-driven labeling was performed using ICLabel [25], followed by a rigorous manual review conducted by two experienced researchers. Components unambiguously identified as ocular (blinks, saccades), cardiac, or muscle artifacts (along with other categories) were rejected. A 5-minute continuous portion of EEG data per participant was selected for the purpose of microstate analysis. Due to the intermittent nature of artifacts, this 5-minute segment was often composed of multiple concatenated artifact-free intervals. The artifact-free EEG data were down-sampled to 125 Hz and then filtered for the broadband range (1–30 Hz). This broadband range was divided into four narrow bands based on their frequency ranges: the 1–4 Hz delta band, the 4–7 Hz theta band, the 7–13 Hz alpha band, and the 13–30 Hz beta band. Each narrow-band signal was further filtered using a zero-phase Finite Impulse Response filter (Hamming window) to ensure precise frequency isolation and temporal fidelity.

    EEG spectral microstate analysis

    The core principle of EEG microstate analysis is to segment the continuous EEG stream into a sequence of quasi-stable topographical maps, achieved by clustering the EEG data at specific time points [26]. The global field potential (GFP) quantifies the aggregate field strength of EEG signals at varying time points, as depicted in formula (1):

    $$ \,GFP\left( t \right) = \sqrt {\frac{1}{N}\sum {\,_{{i = 1}}^{N} } (V_{i}^{{\prime \,}} (t))^{2} } $$

    (1)

    where \(\:{V}_{i}\left(t\right)\) denotes the potential of the \(\:i\)-th electrode at time\(\:\:t\), with \(\:N\) indicating the overall count of electrodes. Since the peak point of GFP typically coincides with the transition between microstates, it allows for the segmentation of microstate time points based on the GFP peak locations. GFP peaks were extracted with a minimum inter-peak distance of 10 ms and a maximum of 1000 peaks per subject. To mitigate noise, peaks with an amplitude exceeding one standard deviation above the mean GFP amplitude were excluded. Microstate templates were derived using a modified k-means clustering algorithm (modkmeans). The number of clusters (k) was fixed at 5, and the clustering procedure was repeated 50 times with random initializations to ensure solution stability. The optimal cluster set was selected based on the lowest cross-validation error, and the resulting maps were sorted by their global explained variance. Clustering iterations were limited to 1000 with a convergence threshold of 1e-6. Following template extraction, a back-fitting procedure was applied to assign a microstate label to each time point of the continuous EEG data for each subject. During this process, the polarity of the EEG signals was ignored to prevent label inversion. Subsequently, temporal smoothing was applied to remove microstate segments shorter than 30 ms, thereby improving the temporal continuity and physiological plausibility of the sequences. The refined, ongoing EEG data from each subject were sorted into their corresponding microstate types A, B, C, D, and E (abbreviated as MS-A, MS-B, MS-C, MS-D, and MS-E) by using the derived microstate type labels as templates. This analysis was performed on both the broadband data and data filtered into four classical frequency bands: delta, theta, alpha, and beta. For each of these five conditions, the preprocessed EEG data were independently matched against the set of microstate templates. From the resulting microstate sequences, several parameters were computed for each microstate class (Fig. 1A): (a) Coverage: The ratio of the duration a microstate is present to the total recording time. (b) Duration: Measures the length of each instance of a microstate. (c) Occurrence: The frequency of microstate occurrences throughout the recording period. (d) Transition Probability (TP): The chance that one microstate in the brain transforms into another.

    Fig. 1
    figure 1

    The scheme of the EEG microstate dynamics and spatiotemporal network analysis. A Steps for frequencyspectral microstate extraction, including bandpass filtering, global field power detection, microstate class identification, and microstate parameter analysis. B Steps for microstate-derived network analysis, including dynamic functional connectivity computation per microstate class by phase lag index, and quantification of temporal variability and spatial variability

    EEG spectral microstate network analysis

    The EEG microstate sequence for each individual was segmented into a series of discrete, non-overlapping intervals based on the assigned microstate labels (A-E). For each resulting microstate window, a functional connectivity network was constructed from 30 EEG electrodes using the Phase Lag Index (PLI). The PLI serves to measure the asymmetry level observed in the phase disparity between two signals [27]. Functional connectivity was estimated independently within each microstate segment, without concatenation or averaging across segments, resulting in a series of state-specific functional connectivity matrices. The segmentation algorithm adaptively defines the duration of each window, thereby avoiding arbitrary temporal partitioning and maintaining physiologically meaningful boundaries. Moreover, microstate segments, typically lasting between 60 and 300 ms, are considered quasi-stationary and have been empirically demonstrated to support reliable phase-based connectivity estimation [21]. Thus, the functional connectivity of paired EEG channels in the interval represented by the \(\:r\)-th microstate window was determined, as illustrated by formula (2),

    $$ F_{r} \left( {i,j} \right) = \left| {~\left\langle {sign~\left[ {~sin\left( {\Delta \phi \left( {t_{l} } \right)} \right)~} \right]} \right\rangle ~} \right|l = 1,2,…,m_{r} ,i \ne j $$

    (2)

    where \(\:{F}_{r}(i,j)\) represents the functional connectivity between electrode channels \(\:i\) and \(\:j\) in the r-th microstate epoch. The notation \(\:\left\langle.\right\rangle\) is employed to denote the average value over that period. \(\:\Delta\varphi\:\left({t}_{l}\right)\) represents the phase differential determined at the \(\:l\)-th time instance, while \(\:{m}_{r}\) stands for the total number of time points within the \(\:r\)-th microstate epoch. By aggregating these PLI values for all pairs of EEG channels, the 30 × 30 adjacency matrix was constructed, which forms the brain network \(\:{F}_{r}\) for the \(\:r\)-th microstate window.

    Subsequently, the functional connection networks corresponding to every distinct microstate category was divided into five different brain network sets (microstate networks A, B, C, D, and E). Utilizing these networks, the temporal and spatial variabilities were computed [21]. Temporal variability, by assessing the correlation between functional connectivity patterns of the same brain region across different time windows, captures the time-dependent changes of the functional architecture in specific brain areas, thereby providing insights into the temporal robustness of the region’s functional connectivity. The specific definition is shown in formula (3):

    $$\:{T}_{i}=1-\frac{1}{v(v-1)}\sum\:_{p,q=1,p\ne\:q}^{v}\text{c}\text{o}\text{r}\text{r}\left({F}_{p}(i,:),{F}_{q}(i,:)\right)$$

    (3)

    where \(\:v\) is the number of microstate windows, \(\:{F}_{p}(i,:)\) indicates the functional arrangement of the \(\:i\)-th channel within the \(\:p\)-th microstate window, while \(\:corr({F}_{p}\left(i,:\right),{F}_{q}\left(i,:\right))\) calculates the correlation coefficient that measures the temporal similarity between two separate functional connectivity patterns. Spatial variability, by evaluating the correlation between the functional connectivity sequences of a particular brain region and those of other regions, reflects both the dynamic changes in local spatial functional connectivity and the spatial consistency of connectivity between regions. The definition is shown in formula (4),

    $$\:{S}_{i}=1-\frac{1}{29\times\:28}\sum\:_{i,h=1,j\ne\:h\ne\:i}^{30}\text{c}\text{o}\text{r}\text{r}\left({F}_{s}(i,j),{F}_{s}(i,h)\right)$$

    (4)

    where \(\:corr({F}_{s}\left(i,j\right),{F}_{s}\left(i,h\right))\) denotes the correlation coefficient that quantifies the relationship between two different spatial functional connectivity patterns, \(\:{F}_{s}\left(i,j\right)\) and \(\:{F}_{s}\left(i,h\right)\). This metric is employed to assess the spatial consistency across all functional connectivity sequences associated with a particular scalp region (channel \(\:i\)) (Fig. 1B).

    Clinical effect prediction

    A feature set for classification was derived from microstate parameters, including coverage, duration, occurrence, and both temporal and spatial variability. These parameters were extracted across multiple frequency bands. To capture the spectral specificity of brain dynamics, these features were organized into distinct sets based on the following frequency bands: delta (1–4 Hz), theta (4–7 Hz), alpha (7–13 Hz), beta (13–30 Hz), and a broadband (1–30 Hz). A Random Forest classifier, implemented using a Bagging ensemble of decision trees, was trained for multi-class classification. To enhance model robustness and generalizability, hyperparameters (i.e., the number of trees, minimum leaf size, and maximum number of splits) were optimized via a Bayesian optimization algorithm. A nested cross-validation (CV) strategy was employed to prevent data leakage and overfitting. In this scheme, an inner 5-fold CV performed hyperparameter tuning, while an outer 5-fold CV provided an unbiased estimate of the model’s performance. To address potential class imbalance, class weights were set to be inversely proportional to class frequencies and applied during model training. The final model performance was determined by averaging the prediction metrics across the five outer folds of the nested CV. Classifier performance was comprehensively assessed using accuracy, sensitivity, and specificity. The results for each metric are reported as the mean ± standard deviation across these folds.

    Statistical analysis

    Data normality was evaluated by applying the Shapiro-Wilk test. The Mann-Whitney U test and independent t-tests were used to examine differences in demographic characteristics and clinical scores among the groups. Repeated measures Analysis of Variance was employed to evaluate group (PD-MCI, PD-NC, and HC) differences across narrowband and broadband microstate network metrics using four model specifications: (1) microstate parameters (3 groups × 3 parameters [coverage, duration, and occurrence] × 5 classes [MS-A, MS-B, MS-C, MS-D, and MS-E]), (2) transition probabilities (3 groups × 20 metrics [A to B/C/D/E, B to A/C/D/E, C to A/B/D/E, D to A/B/C/E, E to A/B/C/D]), (3) microstate network regional temporal or spatial variabilities (3 groups × 5 microstate levels × 30 channels), and (4) microstate network global temporal or spatial variabilities (3 groups × 5 classes [MS-A, MS-B, MS-C, MS-D, and MS-E]). Where significant main and interaction effects emerged (p < 0.05), post hoc analyses was conducted using Bonferroni-corrected paired-samples t-tests. Pearson correlations then quantified relationships between MoCA scores and group-discriminating features in PD subgroups (PD-MCI vs. PD-NC), with independent Bonferroni corrections applied to four metric families per frequency band: microstate parameters, transition probabilities, regional temporal or spatial variabilities, and global temporal or spatial variabilities.

    Continue Reading

  • Re-examining the association between region-specific pain recurrence and muscle force strategies in patients with patellofemoral pain via OpenSim and artificial intelligence: a prospective cohort study toward targeted rehabilitation | Journal of Neur…

    Re-examining the association between region-specific pain recurrence and muscle force strategies in patients with patellofemoral pain via OpenSim and artificial intelligence: a prospective cohort study toward targeted rehabilitation | Journal of Neur…

    In this study, we developed and evaluated an artificial intelligence (machine learning) model to elucidate the muscle force-production characteristics associated with the recurrence of pain in the APP, MBP, and LBP regions. The findings support our hypothesis, indicating that the muscle force–related factors underlying PFP recurrence differ across anatomical regions. Among the three machine learning classifiers employed, the XGBoost model exhibited the highest accuracy, with predictive performance ranging from 95.9% to 98.3% in forecasting pain across these regions. Consequently, SHAP values were computed based on the XGBoost model to visually represent the importance of each feature, thereby delineating the key muscle force patterns that precipitate PFP in distinct regions.

    In addressing overfitting, it is noteworthy that XGBoost incorporates embedded regularization during training, specifically the L1 (lambda) and L2 (alpha) penalties, which effectively constrain model complexity and reduce the likelihood of overfitting to the training set [36]. In addition, we employed five-fold cross-validation within the training data to optimize hyperparameters, thereby avoiding the inappropriate use of the test set for model tuning and further mitigating the risk of overfitting. Nevertheless, given that the AUC achieved by the XGBoost models in this study was relatively high (>0.99), it remains possible that some degree of uncontrollable overfitting occurred. This observation highlights the need for future research to expand both sample size and feature dimensionality, as well as to improve group balance during testing, in order to further safeguard against overfitting.

    Muscle force production patterns associated with APP region pain

    Insufficient strength in the gracilis, tibialis anterior, and internal oblique muscles, combined with excessive strength in the adductor longus and tensor fascia latae, constitutes the principal precipitating factors for pain in the APP region. Although both the gracilis and adductor longus are located on the medial thigh, their distinct insertion sites result in different contributions to joint kinematics [37, 38]. Specifically, the gracilis inserts on the medial aspect of the proximal tibia, facilitating hip internal rotation, whereas the adductor longus terminates at the linea aspera of the femur and functions to externally rotate the hip [37, 38]. Consequently, insufficient strength of the gracilis, combined with excessive strength of the adductor longus, may result in exaggerated hip external rotation during gait. Cadaveric studies have demonstrated that a hip external rotation of 30° can significantly increase patellofemoral joint contact forces [39]. During ambulation, the contact force generated by hip external rotation is continuously loaded onto the anterior aspect of the patella, peaking at knee flexion angles between 30° and 60°. Over time, this repetitive loading may precipitate the recurrence of pain in the APP region [39]. It is noteworthy that recent studies suggest potential differences in neural innervation and functional roles between the proximal and distal regions of the same muscle [40]. For the gracilis, the proximal fibers, originating from the medial aspect of the ischiopubic ramus, may primarily contribute to hip joint motion. In contrast, the distal fibers extend across the knee joint, where they merge with the tendons of the sartorius and semitendinosus to form the pes anserinus, inserting onto the superior medial tibia [41]. This anatomical arrangement suggests that the distal fibers may be more directly involved in knee movement and tibial internal rotation. Considering that current evidence generally supports the association between gracilis insufficiency and the recurrence of PFP, primarily through alterations in hip joint mechanics as previously discussed [37,38,39], clinical practice should place particular emphasis on targeted activation and rehabilitation of the proximal gracilis. Such interventions may help prevent recurrent pain in the APP region.

    Our findings indicate that insufficient tibialis anterior strength is a primary precipitant of pain in the APP region. Notably, previous cohort studies have not clearly delineated the relationship between tibialis anterior strength and PFP. The present study’s ability to capture this association may be attributable to the employment of a machine learning model, which can discern more subtle inter-variable relationships that may be pivotal for PFP prevention. Inadequate tibialis anterior strength disrupts the balance between plantarflexor and dorsiflexor forces at the ankle, thereby impairing sagittal plane stability [42]. As a consequence, the ankle’s capacity for sagittal attenuation is markedly diminished, allowing unbuffered ground reaction forces to be transmitted proximally to the knee and patellofemoral joints, which leads to excessive localized loading on the patellar surface and ultimately precipitates APP pain [43]. Furthermore, the machine learning model revealed that diminished internal oblique strength is associated with APP pain, corroborating findings from previous cross-sectional studies [44]. Insufficient internal oblique strength increases trunk inclination and rotation during ambulation. In particular, when the internal oblique of the contralateral side is weak, the trunk tends to rotate and tilt toward the affected side. Given that the trunk accounts for over 50% of body weight, such a shift in mass distribution results in an increased overall load on the affected limb, thereby elevating patellofemoral joint stress [44]. This heightened joint stress exacerbates anterior patellar wear during knee flexion-extension cycles, ultimately culminating in APP pain [45].

    Excessive strength in the tensor fascia latae is also a major predictor of APP region pain. Previous studies have further reported that such overexertion of the tensor fasciae latae can induce hip flexion [46]. However, during gait, excessive hip flexion results in forward tilting of the trunk, thereby shifting the center of mass anteriorly and increasing the load on the anterior aspect of the knee, ultimately precipitating recurrent APP pain [47]. Moreover, excessive force of the tensor fasciae latae may disrupt the strength balance between the hip flexors and extensors [48], thereby undermining sagittal-plane core stability and consequently amplifying anterior–posterior displacement of the center of mass [49]. In response, the lower limb joints often adopt a “stiff” movement pattern to stabilize the center of mass and prevent falls. Nevertheless, in such a “stiff” gait pattern, energy absorption by tissues distal to the knee may be reduced, thereby increasing the mechanical load on the knee joint. This load may be repeatedly transmitted to the anterior patellar region, ultimately resulting in patellar cartilage damage and the recurrence of APP [47].

    Muscle force production patterns associated with MBP region pain

    The machine learning model identified that excessive strength in the rectus femoris, gracilis, gluteus maximus, and adductor longus muscles, coupled with insufficient strength in the semitendinosus, constitutes the primary mechanism underlying MBP region pain. Notably, the rectus femoris serves as a knee extensor, whereas the semitendinosus—being part of the hamstring group—functions as a knee flexor. Excessive rectus femoris force, combined with insufficient semitendinosus strength, may lead to an increased knee extension moment during gait. Prior investigations have demonstrated that when the knee extension moment reaches 240 Nm, the patellofemoral joint stress escalates by 3.9 MPa [50]. Furthermore, inadequate semitendinosus strength may compromise the dynamic control of the knee’s frontal plane, resulting in augmented lateral displacement of the patella, exacerbation of medial patellar wear, and ultimately the manifestation of MBP region pain in patients with PFP [51]. Recent studies have reported that the proximal and distal compartments of the semitendinosus exhibit distinct discharge rates and differences in the variability of neural drive [40]. It is speculated that the region of the semitendinosus located closer to the knee joint may be more directly involved in knee and patellofemoral joint loading and movement, and thus more strongly associated with the recurrence of MBP. Consequently, targeted stimulation and rehabilitation of this knee-adjacent region of the semitendinosus during clinical training may yield greater therapeutic benefits and improve the effectiveness of preventing MBP recurrence. However, this assumption remains speculative and requires confirmation through future cohort studies.

    During ambulation, excessive force generated by the gracilis and adductor longus muscles is a key precipitant of MBP region pain. In addition to mediating hip internal and external rotation, both muscles are part of the hip adductor group; their combined force production may lead to pronounced hip adduction [52]. Studies by McKenzie et al. [53] and Willson et al. [54] have shown that patients with PFP exhibit significantly greater hip adduction during functional activities—such as running, jump landing, and squatting—compared with healthy controls, thereby further validating these findings. Ultrasonographic data indicate that when hip adduction reaches 20°, lateral displacement of the patella increases by approximately 7.3 mm [55]. Repeated lateral displacement may exacerbate friction at the medial femoral condyle and medial patellar region, ultimately precipitating pain in the MBP region [55].

    Results from the machine learning model indicate that excessive gluteus maximus strength is one of the contributing factors to pain in the MBP region. Previous studies have demonstrated that excessive force production by the gluteus maximus during gait leads to heightened frontal-plane stiffness at the hip joint [56]. Given that the hip and knee joints serve as the primary sites for frontal-plane energy absorption during ground contact—accounting for 59.1% and 38.5% of energy absorption, respectively [57]—excessive hip stiffness markedly reduces its capacity to absorb energy. Consequently, unbuffered ground reaction forces are transferred to the knee joint [57], increasing the frontal-plane load and elevating medial patellar pressure [57]. Moreover, excessive force production by the gluteus maximus during gait may promote an overly upright trunk posture, thereby elevating the center of mass and increasing lateral trunk sway. The lateral forces generated by this trunk movement are repeatedly imposed on the knee joint, which is already burdened by high energy absorption demands [58], ultimately leading to repeated compression of the medial patellar margin and significant pain over time.

    Muscle force production patterns associated with LBP region pain

    Our explainable machine learning model revealed that insufficient strength in the rectus femoris, tensor fascia latae, and gluteus maximus, coupled with excessive force generated by the adductor longus and gracilis, constitutes the primary mechanism underlying pain in the LBP region. Among these, the rectus femoris—an integral component of the quadriceps—primarily generates the knee extension moment during gait [59]. Powers et al. [60] reported that PFP patients exhibit a knee extension moment of 23.6 N·cm/kg, compared to 30.4 N·cm/kg in healthy individuals; the inability of the rectus femoris to produce an adequate extension moment may therefore serve as a precipitating factor for PFP. Moreover, the quadriceps play a critical role in controlling patellar tracking during knee flexion-extension. Weakness in this muscle group can result in aberrant patellar kinematics, including increased frontal plane displacement of the patella and consequent excessive compression of its lateral edge, ultimately leading to pain [59]. It should be noted that previous studies have reported regional heterogeneity in the activation of the rectus femoris under different contraction tasks. Specifically, hip flexion predominantly activates the proximal region of the muscle, whereas knee extension primarily recruits its central and distal regions [61]. This task-dependent distribution is thought to arise from the relatively segregated organization of motor neuron pools within the spinal cord, where neurons innervating the proximal region are mainly located in the rostral part of the motor nucleus, while those serving the distal region are positioned more caudally [61]. Such topographical differentiation provides a mechanistic explanation for the distinct activation patterns of the proximal versus distal regions of the rectus femoris [61]. In the context of the present study, the distal region may be a critical contributor to LBP-related pain, as it is more directly associated with knee and patellofemoral joint function, suggesting that this region should receive particular attention during clinical interventions [61]. However, we did not directly examine the relationship between regional rectus femoris activation and LBP pain in this study. Accordingly, this interpretation remains speculative and requires systematic investigation in future research.

    Based on our findings, insufficient gluteus maximus strength predisposes individuals to LBP region pain. The gluteus maximus not only facilitates hip extension but also functions as a hip external rotator; when its strength is diminished, the hip and femur tend to exhibit excessive internal rotation. Powers et al. [62] demonstrated via magnetic resonance imaging that an 8° increase in femoral internal rotation can induce a 13° patellar external rotation, during which the lateral edge of the patella is repeatedly subjected to friction and compressive forces against the lateral femoral condyle. Moreover, owing to the inherent anatomy of the patellofemoral joint, the lateral force on the patella during gait (0.54 BW) far exceeds that on the medial side (0.15 BW) [63]. Collectively, this loading environment markedly increases the risk of LBP region pain. Furthermore, our machine learning results indicate that insufficient tensor fascia latae strength, combined with excessive force generated by the adductor longus and gracilis, further predisposes to LBP region pain. The tensor fascia latae, a principal component of the hip abductor group [64], contrasts with the adductor longus and gracilis, which are key elements of the hip adductor group. Reduced strength of the tensor fascia latae, combined with excessive force production by the adductor longus and gracilis, leads to pronounced hip adduction during ambulation [52, 65]. Ultrasonographic evidence indicates that, compared with a neutral position, 20° of hip adduction results in a 0.24-cm increase in lateral patellar displacement. Repeated lateral displacement of the patella may exacerbate wear and local compressive loading on its lateral margin, ultimately precipitating LBP region pain [66].

    Implications for preventive training

    Targeted neuromuscular training may alleviate regional PFP by correcting specific deficits in force-generation patterns. For the prevention of APP region pain, it is imperative to enhance the strength of the hip internal rotator group to counteract the excessive force generated by the adductor longus, which predisposes the hip to external rotation. In addition, incorporating resistance exercises for the tibialis anterior, alongside relaxation protocols for the tensor fascia latae to prevent its overcontraction during the stance phase, is recommended. Furthermore, targeted training of the contralateral internal oblique may help correct trunk lean during gait, thereby reducing unilateral knee loading.

    In the context of MBP region pain, emphasis should be placed on augmenting hamstring strength to restore a balanced knee flexion–extension moment and improve knee joint stability. Concurrently, targeted strengthening of the hip abductor group is recommended to counteract the aberrant force production by the gracilis and adductor longus during gait. Furthermore, relaxation training for the gluteus maximus may increase the hip joint’s frontal-plane mobility and its capacity for energy absorption, thereby reducing the overall load on the knee joint.

    For LBP region pain, priority should be given to reinforcing the rectus femoris and gluteus maximus. Concurrently, targeted strengthening of the hip abductor group (e.g., tensor fascia latae) should be implemented, while relaxation training for the hip adductor group (e.g., adductor longus and gracilis) is recommended to correct imbalances between hip adduction and abduction. This integrated approach is expected to enhance proximal joint stability and ultimately reduce lateral displacement and loading of the patellofemoral joint.

    It should be emphasized that although the SHAP dependence plots identified apparent “thresholds” for these risk factors, these values do not represent clinically meaningful cut-off points. Rather, they indicate the points at which the relationship between a given feature and the risk of PFP recurrence begins to change within the model. Accordingly, these thresholds cannot be directly applied in clinical practice and should instead be viewed as preliminary reference values that require further verification and refinement through systematic clinical studies.

    Looking ahead, our model could be integrated into clinical decision-support tools, such as OpenSim-based musculoskeletal modeling platforms or gait analysis systems, to enable direct identification of region-specific risks of PFP recurrence and the muscle strength deficits most in need of improvement. Such integration would not only facilitate the development of individualized intervention strategies but also provide more robust evidence to inform clinical decision making. Furthermore, review studies have indicated that different regions within the same muscle exhibit distinct levels of focal adhesion kinase (FAK) phosphorylation during eccentric and concentric training [67]. For instance, following eccentric training of the vastus lateralis, pY397-FAK levels in the distal region were approximately four times higher than those observed after concentric training, contributing to distal hypertrophy of the quadriceps [67]. Given that different training modalities induce region-specific muscle hypertrophy, future strength interventions for patients with PFP should first identify the specific muscle regions implicated in the condition and then select training strategies that effectively target these regions. This study provides only a preliminary intervention framework by treating the muscle as a single functional unit. Future research should build on these findings to investigate more refined, region-specific approaches.

    Limitations

    Although this study provides preliminary evidence of distinct muscle force strategies associated with PFP across different anatomical regions, several limitations should be acknowledged. First, although SHAP was used to preliminarily identify the points at which the relationship between muscle strength features and the risk of PFP recurrence begins to shift within the machine-learning model, their generalizability may be limited by individual variability and environmental context. To translate these thresholds into clinical practice, further clinical studies are needed for validation and refinement. Furthermore, although a six-month follow-up in a cohort of 299 participants yielded important initial findings, a longer observation window and a larger, more heterogeneous sample would likely offer a more comprehensive understanding of the temporal dynamics and recurrence patterns of PFP. Finally, recent studies have suggested that neural innervation and activation levels may vary across different regions (proximal versus distal) of the same muscle [40]. In the present study, however, the OpenSim modeling approach treated each muscle as a single unit, which made it difficult to examine how region-specific muscle activation might be related to the recurrence of PFP. This limitation underscores the need for future cohort studies to further investigate these region-dependent mechanisms underlying PFP recurrence. Finally, recent studies have demonstrated that neural innervation and activation levels can differ across distinct regions of the same muscle, such as proximal versus distal segments [40, 61]. This phenomenon is likely attributable to the differential spatial organization of motor neurons within the spinal cord that control the proximal and distal portions of the muscle [61]. However, in the present study, the OpenSim modeling approach treated each muscle as a single unit, limiting our ability to investigate the relationship between region-specific muscle activation and PFP recurrence. This limitation underscores the need for future cohort studies to examine the region-dependent mechanisms underlying PFP recurrence. In addition, evidence from training studies indicates that different muscle regions exhibit distinct molecular responses during concentric and eccentric exercises, which can lead to region-specific hypertrophy [67]. Because the present study considered muscles as whole units, it provides limited guidance for interventions targeting specific muscle regions, representing a key limitation of this work.

    Continue Reading

  • International Conference on Medical Radiation Dosimetry

    International Conference on Medical Radiation Dosimetry

    Where Clinical Reality Meets Standards

    As countries around the world expand their clinical use of ionizing radiation, accurate measurement and calculation remain essential for the safe and effective use of radiation-based technologies. Primary and secondary standards laboratories provide reference measurements that allow medical professionals to trace their results directly to the International System of Units — ensuring global consistency. Dosimetry codes of practice reinforce this traceability and enable the optimized application of ionizing radiation in clinical settings. 

    “Recent technological developments — from new diagnostic approaches to cutting-edge computational methodologies that leverage Monte Carlo models and artificial intelligence (AI) — have shaped dosimetry standards, audit practices and quality assurance guidance,” said Mauro Carrara, IAEA Head of Dosimetry and Medical Radiation Physics and one of the symposia’s scientific secretaries. “For medical physicists, radiation metrologists and other scientists and researchers in the field, there is a critical need to comprehensively review innovations while addressing the growing complexity of available tools.” 

    “In building on the legacy of previous symposia since 1987, IDOS2026 will provide an international forum to discuss and disseminate the latest advances across radiation dosimetry, radiation medicine, radiation protection and their associated standards,” said Zakithi Msimang, IAEA medical radiation physicist and the event’s other scientific secretary. “Its proceedings and conclusions promise to provide relevant recommendations for the medical and scientific community.”

    Continue Reading

  • Plastic packaging waste in the EU: 35.3 kg per person – News articles

    Plastic packaging waste in the EU: 35.3 kg per person – News articles

    In 2023, 79.7 million tonnes of packaging waste were generated in the EU, or 177.8 kg per inhabitant. While this marks a reduction of 8.7 kg per capita compared with 2022, the figure remains 21.2 kg higher than in 2013.

    Out of all the packaging waste generated, 40.4% was paper and cardboard, 19.8% was plastic, 18.8% glass, 15.8% wood, 4.9% metal and 0.2% other packaging. 

    An average of 35.3 kg of plastic packaging waste was generated in 2023 for each person living in the EU. Out of this, 14.8 kg were recycled. The amount of generated plastic waste decreased by 1.0 kg compared with 2022, while the amount of recycled plastic waste increased by 0.1 kg. Between 2013 and 2023, the amount of plastic packaging waste generated increased by 6.4 kg per capita, while the amount recycled increased by 3.8 kg.

    Source dataset: env_waspac

    This information comes from data on packaging waste published by Eurostat today. The article presents a handful of findings from the more detailed Statistics Explained article on packaging waste.

    Increase in plastic packaging waste recycling

    In 2023, the EU recycled 42.1% of all the generated plastic packaging waste, indicating an increase in the recycling rate compared with 2013 (38.2%).

    Belgium recorded the highest recycling rate at 59.5%, followed by Latvia (59.2%) and Slovakia (54.1%).

    In contrast, the lowest rates were recorded in Hungary (23.0%), France (25.7%) and Austria (26.9%).

    Recycling rate of plastic packaging waste, 2023 (%). Chart. See link to the full dataset below.

    Source dataset: env_waspac

    Continue Reading

  • Simon Fawell comments on the Credit Suisse v SoftBank judgment in Law360 – Signature Litigation

    1. Simon Fawell comments on the Credit Suisse v SoftBank judgment in Law360  Signature Litigation
    2. The Lawyer and Law 360 quote James Hyne on our involvement in the landmark Greensill trial  Charles Russell Speechlys
    3. ‘A Rare Case’: How Credit Suisse Missed Out In Greensill Trial  Law360
    4. UBS Loses USD 440 Million UK Lawsuit Against SoftBank Over Greensill Collapse  Hubbis
    5. Market Chatter: UBS Loses $440 Million Claim Against SoftBank in London Ruling  富途牛牛

    Continue Reading

  • New China Platform Information Reporting Rules: Deadlines & Compliance

    New China Platform Information Reporting Rules: Deadlines & Compliance

    New China platform information reporting rules require internet companies to submit basic information and the identity and income details of their operators and employees. Before October 31, 2025, these companies must submit employee and operator income data for Q3 2025. Platform companies must immediately prepare to comply with these filing requirements to avoid significant financial penalties and operational suspensions.


    Starting October 1, 2025, internet platform companies (“platform companies”) will be required to formally submit the identity and income information of their operators and employees to the tax authorities for the first time.  

    These obligations arise from the Provisions on the Submission of Tax-Related Information by Internet Platform Enterprises (the “Provisions”), issued by the State Council on June 20, 2025, which set out new tax-related reporting requirements for platform companies. 

    The deadline for the first round of quarterly reporting obligations by platform companies – covering operators’ and employees’ identity and income information – is October 31, 2025.

    Find Business Support

    To support the rollout of the new reporting regime, the State Taxation Administration (STA) released STA Announcement [2025] No. 15, which provides detailed implementation rules. The announcement specifies reporting obligations, technical requirements, and compliance timelines applicable to a wide range of digital platforms.

    According to the General Office of the STA, as of October 15, 6,654 domestic and international platforms had already submitted the required basic information, which was due by July 20, 2025, for companies established before the Provisions’ implementation. In addition, over 4,100 platforms had already submitted tax-related information on their operators and employees, which must be submitted before October 31, covering over 60 percent of affected platforms. This group includes major platforms such as Pinduoduo, Ele.me, and Didi Chuxing. 

    On September 28, 2025, the STA, together with the Ministry of Industry and Information Technology (MIIT) and the Cyberspace Administration of China (CAC), issued a notice providing further guidance on implementing the Provisions. The notice clarified rules on administrative penalties, suspension of operations, and other related matters.

    Explore vital economic, geographic, and regulatory insights for business investors, managers, or expats to navigate China’s business landscape. Our Online Business Guides offer explainer articles, news, useful tools, and videos from on-the-ground advisors who contribute to the Doing Business in China knowledge.
    Start exploring

    Tax-related reporting requirements for platform companies 

    Under the Provisions, internet platform enterprises are required to report certain tax-related information to their competent tax authorities. These obligations apply to e-commerce platform operators under the Electronic Commerce Law of the PRC, as well as other organizations that provide profit-making services such as online transaction venues, transaction matching, or information publication. Individuals providing services on these platforms in a personal capacity are considered “platform employees”. 

    Reporting requirements

    Platform companies must submit information related to the identity and income of platform operators and employees. The types of information and documents that must be provided include at different timeframes, namely:

    1. Within 30 days from the implementation date of the Provisions (June 20, 2025) or within 30 days of commencing internet-based business operations, the following information must be reported:
      1. Platform domain name
      2. Business type
      3. Unified Social Credit Code and name of the relevant operating entity
    2. Within the month following the end of the quarter (October 31 for the third quarter of 2025), the following must be reported:
      1. The identity information of platform operators and employees
      2. The income information of platform operators and employees for the previous quarter 

    Note that companies are not required to submit income information on employees who provide delivery, transport, domestic, or other convenience services through the platforms if they are legally exempt from taxation or enjoy tax incentives. Additionally, companies are not required to resubmit tax-related information when handling withholding declarations, tax returns, and other tax-related matters for platform operators and employees.

    Platforms are not required to report information on operators and employees prior to the implementation of the Provisions. 

    Foreign platform companies (such as Amazon) providing for-profit services in China must report tax-related information in accordance with regulations issued by the State Council tax authorities. 

    Required cooperation with tax authorities 

    When conducting tax inspections or identifying tax risks, tax authorities may request that platform companies and related parties provide supporting information, including: 

    • Contracts and orders of platform operators and employees
    • Transaction details
    • Financial account records
    • Logistics and delivery information

    Companies and related parties must provide this information truthfully and within the timeframe, manner, and scope requested by tax authorities. 

    Waiving of penalties and clarification of “serious circumstances” 

    The September 28 notice states that platform companies that commit certain tax reporting violations outlined in the Provisions will not be penalized if they correct the violations within the time limit set by the tax authorities. 

    These violations are: 

    1. Failure to submit or provide tax-related information within the prescribed time limit;
    2. Concealing, falsely reporting, or omitting tax-related information, or causing the tax-related information to be untrue, inaccurate, or incomplete through the fault of the platform company; and
    3. Refusing to submit or provide tax-related information. 

    Under the Provisions, failure to rectify these violations within the prescribed timeframe may result in fines ranging from RMB 20,000 to RMB 100,000 (US$2,740 to US$13,700), or from RMB 100,000 to RMB 500,000 (US$13,700 to US$68,500 in “serious cases”. In serious cases, companies may also be ordered to suspend operations. 

    What constitutes a “serious case” 

    The September 28 notice also clarifies what constitutes a “serious case” under the Provisions. Specifically, a platform company will be considered to have committed a “serious case” and be subject to the higher penalty bracket if it fails to correct a violation within the timeframe ordered by the tax authorities, and any of the following conditions are met: 

    1. Failing to submit or provide tax-related information, or omitting required tax-related information, for a cumulative total of two or more times within a single year;
    2. Concealing or falsely reporting tax-related information for a cumulative total of two or more times;
    3. Illegally guiding or assisting platform operators or employees to convert the nature of income or split income, through means such as mass registration, changing store unique identifiers, or other methods, resulting in tax-related information being submitted inaccurately, untruthfully, or incompletely;
    4. Forging or tampering with the tax-related information of platform operators or employees, or assisting platform operators or employees in forging or tampering with such information, resulting in tax-related information being submitted inaccurately, untruthfully, or incompletely;
    5. Refusing to submit or provide tax-related information in accordance with regulations through violence, threats, or public boycotts; and
    6. Other serious violations of Article 10 of the Provisions. 

    Suspension of operations

    The notice clarifies that when, as may happen in serious cases, an internet platform is ordered to suspend operations, the competent tax authority is responsible for penalizing the platform for failing to submit tax-related information in accordance with the Provisions. 

    In such cases, the tax authorities may: 

    • Restrict the company’s issuance of invoices;
    • Issue early warnings on the company’s acceptance of invoices; and
    • Report penalties and request that relevant regulatory authorities take legal action.

    If the platform rectifies its violations during the suspension period and actively mitigates any negative impacts, the tax authority that issued the suspension may, upon confirmation, coordinate with regulatory authorities to promptly lift the related punitive measures. 

    Key takeaways for platform companies

    As the October 31 deadline approaches, platform companies should ensure they are fully prepared to submit the required identity and income information for their operators and employees in a timely, accurate, and complete manner. Companies that have not yet reported should immediately coordinate with local tax authorities to avoid delays or errors that could trigger penalties. Attention to the accuracy and completeness of submitted data is critical, as platform companies are responsible for verifying the information they provide, even though errors caused by operators or employees themselves are not penalized if proper verification measures were taken.

    Find Business Support

    Companies should make full use of the guidance and support provided by tax authorities, including training sessions, online tutorials, and secure reporting portals, to streamline submissions and ensure compliance with the Provisions. Understanding the scope of reporting obligations, including exemptions for certain employees who are legally exempt from taxation or enjoy incentives, is essential to avoid unnecessary duplication or misreporting. 

    Platform companies should take particular care to avoid prohibited practices outlined in the September 28 notice. According to the General Office of the STA, some platforms have been found to help employees register en masse as individual businesses in the platform’s location, attempting to convert personal labor income into business income to take advantage of preferential tax treatment and reduce or avoid tax payments. Other platforms or intermediaries have allegedly encouraged operators and employees to split income, register abroad, or change entity identifiers in order to conceal income and evade supervision, impeding normal tax procedures.

    Related Reading

    Overseas internet platforms that provide for-profit services to operators in China should also note that they are also required to report relevant tax information to Chinese tax authorities. Amazon, for example, issued a notice to sellers on October 13, 2025, announcing that it will begin quarterly reporting of Chinese sellers’ identity and income information to China’s tax authorities. The first submission, covering transactions from July to September 2025, is scheduled for completion by October 31. 

    Domestic operators who attempt to evade obligations through offshore registration or other means are subject to the same enforcement measures. The September 28 notice details the penalties for illegal practices by platform enterprises, emphasizing that compliance with these reporting requirements is a legal obligation and that violations will be rigorously enforced.

    About Us

    China Briefing is one of five regional Asia Briefing publications. It is supported by Dezan Shira & Associates, a pan-Asia, multi-disciplinary professional services firm that assists foreign investors throughout Asia, including through offices in Beijing, Tianjin, Dalian, Qingdao, Shanghai, Hangzhou, Ningbo, Suzhou, Guangzhou, Haikou, Zhongshan, Shenzhen, and Hong Kong in China. Dezan Shira & Associates also maintains offices or has alliance partners assisting foreign investors in Vietnam, Indonesia, Singapore, India, Malaysia, Mongolia, Dubai (UAE), Japan, South Korea, Nepal, The Philippines, Sri Lanka, Thailand, Italy, Germany, Bangladesh, Australia, United States, and United Kingdom and Ireland.

    For a complimentary subscription to China Briefing’s content products, please click here. For support with establishing a business in China or for assistance in analyzing and entering markets, please contact the firm at china@dezshira.com or visit our website at www.dezshira.com.

     

    Continue Reading

  • A&O Shearman partners join Berlin Global Dialogue line-up for third consecutive year

    A&O Shearman partners join Berlin Global Dialogue line-up for third consecutive year

    Wolf Bussian, managing partner for Germany at A&O Shearman, added: “In a multipolar world, reliability is everything: power is shifting, responsibility is growing, and technology, trade, and security are inseparable. Those who build smart partnerships will create sustainable prosperity.

    “Multipolarity isn’t a risk in itself, but a mandate to shape outcomes—de-risking, not decoupling; rules, and not bloc-building is how we will secure stability and growth.”

    A&O Shearman leaders on the BGD stage

    A&O Shearman partners will contribute to five high-profile sessions across the program, bringing legal, regulatory and strategic perspectives to discussions at the intersection of markets, policy and technology.

    October 23, 1:30pm–2:45pm

    Shaping a multipolar future: a conversation with the BGD Young Voices

    Hervé Ekué, global managing partner at A&O Shearman will join fellow panelists to discuss ways to strengthen democratic culture, rebuild institutional trust and align economic decision-making with long-term societal goals to address the expectations of emerging generations who are calling for bolder leadership rooted in climate responsibility, democratic values, accountability, and trust.

    October 23, 4:45pm–6:00pm

    War speed: scaling technology under pressure

    Magdalena Nasilowska, partner at A&O Shearman, will moderate a panel examining how Europe can reform procurement, accelerate deployment, and build a defense innovation ecosystem fit for today’s security landscape.

    October 24, 10:30am–11:45am

    The end of predictability? Adapting enterprises to the geopolitical age

    Hervé Ekué, global managing partner at A&O Shearman, will also join a discussion about how companies are rethinking cross-border operating models—from supply chains and legal entity structures to innovation strategies—to build resilience and secure their global footprint, as globalization gives way to fragmentation.

    October 25, 09:30am–10:30am

    The future of the China-Europe relationship

    Xin (Lorna) Chen, partner at A&O Shearman, will moderate a discussion about how China and Europe can rebuild trust, deepen cooperation, and pursue sustainable growth amid global geopolitical change.

    October 25, 09:30am–10:30am

    The pivotal role of middle powers in a multipolar world

    Dirk Arts, partner at A&O Shearman will join a panel debate to discuss how middle powers are reshaping the operating environment for business and investment, and the role they are playing in forging strategic partnerships, shaping regional dynamics, and championing the emergence of competing institutions.

    BGD: bringing decision-makers together to effect change

    BGD brings together established leaders and the next generation of decision-makers to promote dialogue in four key areas shaping the future of the global economy:

    • Geopolitical shifts
    • Climate change
    • Technological advances
    • Global inequality

    With a strong focus on the realities of a multipolar world—from supply chain resilience and defense innovation to digital governance and the evolving role of middle powers—BGD equips enterprises, investors and policymakers with the insights needed to navigate an era defined by uncertainty and reinvention.

    If you plan to attend BGD 2025, please reach out to Ulrich Horstschäfer at ulrich.horstschaefer@allenovery.com to arrange a meeting.

    Continue Reading

  • Toyota Mobility Foundation and Serve the City unite to empower volunteers across Europe

    Toyota Mobility Foundation and Serve the City unite to empower volunteers across Europe

    Toyota Motor Europe NV/SA (TME) oversees the wholesale sales and marketing of Toyota, GR (Gazoo Racing) and Lexus vehicles and parts and accessories, as well as Toyota’s European manufacturing and engineering operations. Toyota directly employs over 26,000 people and has invested over EUR 12 billion in Europe since 1990. Its eight European manufacturing plants are located in Portugal, the UK, France, Poland, Czech Republic and Turkey. Today, there are approximately 14.7 million Toyota and Lexus vehicles on European roads, whose drivers are supported by a network of 28 National Marketing and Sales Companies and around 2,800 retail sales outlets in 53 countries (EU, UK, EFTA countries , Israel, Turkey and other Eastern European countries). In 2024, TME sold 1,217,132 vehicles in Europe for a 7.1% market share. For more information, visit www.toyota-europe.com.

    Toyota believes that when people are free to move, anything is possible. In the pursuit of “Mobility for All”, Toyota aims to create safer, more connected, inclusive and sustainable mobility to achieve its mission of producing “Happiness for All”. In Europe, TME launched the KINTO mobility brand which offers a range of mobility services in 20 countries, and is growing its business-to-business sales of zero-emission fuel cell products and engineering support. Contributing to the UN Sustainable Development Goals, Toyota is working to achieve carbon neutrality in its entire business across Europe. A historic leader in CO2 reduction in Europe, TME aims to achieve 100% CO2 reduction in all new vehicles in Western Europe by 2035 and will continue to offer a full range of electrified powertrains to customers across the region with its hybrid, plug-in hybrid, battery and fuel cell electric vehicles.  

    ';

    Continue Reading

  • Lynk Global and Omnispace to merge in race for direct-to-device satellite spectrum

    Lynk Global and Omnispace to merge in race for direct-to-device satellite spectrum

    TAMPA, Fla. — Lynk Global plans to merge with Omnispace to upgrade its direct-to-device (D2D) services with globally coordinated S-band spectrum, joining SpaceX and AST SpaceMobile in shoring up satellite frequencies after initially relying on cellular partnerships.

    Luxembourg-based multi-orbit operator SES, which has invested in both companies, will become a major strategic shareholder in the combined group, they announced Oct. 22 in a joint news release that offered few details.

    The merged entity would combine Omnispace’s 60 megahertz of S-band spectrum with Lynk’s D2D platform, which is currently providing intermittent messaging and alert services in a handful of island nations with five small satellites in low Earth orbit (LEO).

    Omnispace had planned to use the spectrum for a D2D constellation of more than 600 satellites, after deploying experimental spacecraft in low and medium Earth orbits.

    However, the Washington, D.C.-based venture’s efforts stalled amid its claims of interference from SpaceX’s D2D service.

    The interference issue was specific to the United States, Omnispace vice president of strategy and marketing George Giagtzoglou said via email, where part of the T-Mobile cellular spectrum used by SpaceX overlaps with Omnispace’s S-band frequencies. He said a recent regulatory request from SpaceX to the Federal Communications Commission could help ease the conflict by aligning its frequency use with international S-band allocations.

    “This merger unlocks the full potential of our global S-band spectrum assets and positions us at the forefront of D2D,” Omnispace CEO Ram Viswanathan said in the announcement.

    Ramu Potarazu, CEO of Falls Church, Virginia-based Lynk, said: “We now have the right mix of technology, spectrum and leadership to extend mobile connectivity where and when it’s needed most. 

    “This merger will enable us to accelerate our efforts in delivering seamless, reliable messaging, voice and data services — serving [mobile network operators (MNOs)], as well as consumer, commercial and industrial vehicles, and government and utility sectors worldwide.”

    The deal comes months after Lynk abandoned an attempt to raise capital for its constellation by merging with Slam Corp., a publicly listed shell company led by former MLB star Alex Rodriguez.

    Potarazu outlined plans last month to instead lean on SES and the operator’s network in geostationary and medium Earth orbit to provide a global, continuous D2D service by 2027.

    The company plans to launch a pair of satellites in February to validate new technology, including a multi-orbit relay capability with SES.

    The companies expect to close the merger late this year or early next, pending regulatory approvals. Potarazu would serve as CEO of the combined entity, with Viswanathan as chief strategy officer.

    The spectrum pivot

    Meanwhile, SpaceX is awaiting regulatory approval to acquire S-band spectrum from geostationary broadband operator EchoStar in a deal worth more than $17 billion. 

    SpaceX leverages more than 650 Starlink D2D satellites in LEO to provide services that are currently limited to text messaging, emergency alerts and certain apps in the U.S., New Zealand and Japan.

    In the U.S., the company is using about 10 megahertz of similarly situated terrestrial spectrum from T-Mobile, but plans to boost its D2D capacity twentyfold with a second-generation service that would integrate 50 megahertz of EchoStar’s spectrum.

    AST SpaceMobile only has five BlueBird satellites in LEO, but it aims to deliver continuous coverage in the U.S. and other key markets after ramping up launches over the next 18 months.

    The Texas-based venture has partnered with AT&T and Verizon in the U.S. and is seeking approval to access L-band spectrum in North America from bankrupt satellite operator Ligado Networks. 

    Alongside a deal for global S-band spectrum, subject to country-by-country approval, AST says satellite frequencies are key to its plan to enable broadband speeds of up to 120 megabits per second from space.

    Continue Reading