Category: 8. Health

  • New type of diabetes is officially recognized and linked to nutrition

    New type of diabetes is officially recognized and linked to nutrition

    Type 5 diabetes is no longer a footnote. On April 9, 2025 the International Diabetes Federation confirmed that chronic undernutrition can seed a very different form of blood‑sugar trouble, giving the condition its own place in the global classification system.

    “Malnutrition‑related diabetes has historically been vastly under‑diagnosed and poorly understood,” said Dr. Meredith Hawkins as the vote was announced.


    Hawkins is an endocrinologist at Albert Einstein College of Medicine and founding director of the Global Diabetes Institute (GDI).

    Why a fifth type matters

    Nearly one in nine adults worldwide now lives with some form of diabetes, and more than 250 million people remain unaware of their status, according to the 11th edition of the IDF Diabetes Atlas.

    Most public campaigns focus on type 2 diabetes, yet an estimated 20 to 25 million lean adolescents and young adults in Asia and Africa carry the new diagnosis of type 5, a burden comparable in size to HIV infection in the same regions.

    Unlike type 2, type 5 takes hold where food is scarce, not plentiful. That reality undercuts a long‑standing public narrative that ties diabetes exclusively to over‑nutrition.

    For governments counting every healthcare dollar, a distinct label matters. Budgets follow labels, and without one, entire populations have slipped through screening and treatment programs designed for very different metabolic problems.

    “This is about equity, science, and saving lives,” said Professor Peter Schwarz, president of the IDF, summing up the stakes during the Bangkok congress. 

    Early hunger leaves a lasting mark

    Decades of animal work show that a low‑protein diet during gestation or adolescence stunts pancreatic growth and the formation of beta cells, the tiny factories that make insulin.

    Human epidemiology echoes that biology, linking low birth weight and recurring childhood malnutrition to impaired glucose control later on.

    Researchers now group type 5 under severe insulin‑deficient diabetes, a label that captures the core defect: the pancreas never learned to keep up with sugar loads, even though the rest of the body remains sensitive to insulin.

    In South India, investigators tracked adults whose body‑mass index averaged just 18.3 kg/m² yet whose blood sugar routinely soared; birth‑weight records, where available, pointed to under‑nutrition in the womb.

    Community nutrition programs are therefore viewed not only as anti‑hunger measures but also as long‑range diabetes prevention.

    Public‑health economists note a secondary benefit. Feed a girl properly before and during pregnancy, and her children may avoid the same metabolic trap, breaking an expensive inter‑generational cycle of disease.

    State‑of‑the‑art euglycemic clamp studies, published in 2022, confirmed that type 5 patients secrete dramatically less insulin than matched controls while showing normal or even heightened insulin sensitivity.

    The same work found little visceral fat and modest liver fat, a stark contrast to type 2 profiles. In practical terms, these young adults do not carry the metabolic baggage that fuels insulin resistance in obesity‑driven diabetes.

    Autoantibody screens stay negative, ruling out the immune‑mediated beta‑cell destruction that defines type 1 diabetes.

    The numbers therefore line up: glucose levels look dangerous, C‑peptide looks scant, but inflammatory markers typical of autoimmunity are absent.

    Because the pancreas is small, many experts suspect that oral drugs that nudge the remaining beta cells may help more than high‑dose insulin injections, a strategy that could lower costs and reduce dangerous hypoglycemia in food‑insecure settings.

    Diabetes type causes clinical confusion

    “Doctors are still unsure how to treat these patients, who often don’t live for more than a year after diagnosis,” Dr. Hawkins warned.

    Younger clinicians, trained on the obesity paradigm, may reach for large insulin doses that push already fragile patients into ulcerating hypoglycemia.

    Misclassification also skews surveillance data. When a thin teenager in rural Uganda shows up with elevated glucose but no ketosis, the chart often reads “type 1,” obscuring the true epidemiology and directing precious insulin supplies away from those who need them.

    A 2025 commentary in the Bangladesh Journal of Endocrinology emphasized the threat: standard insulin regimens carry “potentially fatal consequences” for type 5 patients who are mis‑typed as type 1, because even small dosing errors provoke sharp glucose crashes.

    Simple screening cues can help. A BMI below 19 kg/m² in the absence of autoantibodies should prompt consideration of type 5, especially when the history includes prolonged childhood hunger.

    Steps for care of diabetes type 5

    Two weeks after the Bangkok vote, the IDF launched a dedicated working group to write diagnostic criteria, compile treatment algorithms, and build an international patient registry by 2027.

    The panel, co‑chaired by Hawkins and Dr. Nihal Thomas of Christian Medical College in Vellore, India, will test low‑dose insulin, sulfonylureas, and structured nutrition programs in multi‑site trials. Results could reshape essential‑medicine lists in low‑income countries.

    Public‑health agencies are already modeling the economic impact. Analysts predict that shifting even half of misdiagnosed cases from insulin vials to oral drugs could save tens of millions of dollars each year, funds that might be redirected to maternal nutrition.

    Advocates also press for the inclusion of pancreas‑focused imaging in major nutrition cohorts. Measuring organ size early could identify high‑risk children before glucose spirals out of control.

    “We are taking decisive steps to correct this,” said Schwarz, insisting that momentum will continue. Policies built on that momentum will decide whether type 5 becomes another silent killer or a preventable relic of poverty.

    The study is published in Diabetes Care.

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  • Mysterious Leprosy Pathogen Has Lurked in The Americas For 4,000 Years : ScienceAlert

    Mysterious Leprosy Pathogen Has Lurked in The Americas For 4,000 Years : ScienceAlert

    A new study has found that leprosy was circulating in Chile some 4,000 years ago, meaning the disease arrived in the Americas much earlier than previously thought.

    That’s based on an analysis of ancient bones and teeth by researchers from institutions in Germany, Argentina, and Chile, and it challenges the conventional wisdom that leprosy was a disease introduced by European settlers from the 16th century onwards.

    Through a comprehensive study of DNA fragments found in two human skeletons, the researchers were able to match the genetic material to the Mycobacterium lepromatosis pathogen – the less common of two bacteria known to cause leprosy.

    “We were initially suspicious, since leprosy is regarded as a colonial-era disease, but more careful evaluation of the DNA revealed the pathogen to be of the lepromatosis form,” says anthropologist Darío Ramirez, from the National University of Córdoba in Argentina.

    Related: Experts Warn Leprosy Isn’t Ancient History as Cases Surge in The US

    Scientists are still learning about M. lepromatosis, which has only recently been identified. Another bacteria, Mycobacterium leprae, is the dominant strain behind leprosy, and its history and spread has been more clearly mapped to date.

    While there’s a scarcity of samples in the Americas, M. leprae has been tracked back for thousands of years across Eurasia, which is part of the reason why researchers have long thought it traveled from Europe across the Atlantic.

    The researchers found tiny traces of bacteria in human remains. (José Castelleti-Dellepiane/Anna Brizuela)

    Another recent study found traces of M. lepromatosis in remains from Canada and Argentina, stretching back at least a thousand years – again before European settlers showed up. This new find, pushing its arrival back millennia earlier, adds further evidence that we need to rethink the history of leprosy.

    “Ancient DNA has become a great tool that allows us to dig deeper into diseases that have had a long history in the Americas,” says anthropologist Kirsten Bos, from the Max Planck Institute for Evolutionary Anthropology in Germany.

    “The advanced techniques now used to study ancient pathogen DNA allows us to look beyond the suspects and into other diseases that might not be expected from the context.”

    Trying to pick apart this history of disease isn’t easy. Indigenous American peoples would certainly have had afflictions of their own, but they would have also been hit hard by infections imported by colonists – infections their bodies were poorly prepared for.

    The researchers are confident that there’s more to the story, in terms of both modern and ancient forms of the disease – especially in regards to M. lepromatosis. Each archaeological dig and clinical test gives experts more genomes to work with, which then further helps our understanding of disease history, spread, and diversification.

    Part of the skill needed by researchers is knowing what to look for, which is highlighted by this study – previous work in this area may have missed ancient markers of leprosy, simply because no one thought to look for it.

    “This disease was present in Chile as early as 4,000 years ago, and now that we know it was there, we can specifically look for it in other contexts,” says anthropologist Rodrigo Nores, from the National University of Córdoba.

    The research has been published in Nature Ecology & Evolution.

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  • New research confirms that neurons form in the adult brain

    New research confirms that neurons form in the adult brain

    A study in the journal Science presents compelling new evidence that neurons in the brain’s memory centre, the hippocampus, continue to form well into late adulthood. The research from Karolinska Institutet in Sweden provides answers to a fundamental and long-debated question about the human brain’s adaptability.

    The hippocampus is a brain region that is essential for learning and memory and involved in emotion regulation. Back in 2013, Jonas Frisén’s research group at Karolinska Institutet showed in a high-profile study that new neurons can form in the hippocampus of adult humans. The researchers then measured carbon-14 levels in DNA from brain tissue, which made it possible to determine when the cells were formed.

    Identifying cells of origin

    However, the extent and significance of this formation of new neurons (neurogenesis) are still debated. There has been no clear evidence that the cells that precede new neurons, known as neural progenitor cells, actually exist and divide in adult humans.

    “We have now been able to identify these cells of origin, which confirms that there is an ongoing formation of neurons in the hippocampus of the adult brain,” says Jonas Frisén, Professor of Stem Cell Research at the Department of Cell and Molecular Biology, Karolinska Institutet, who led the research.

    From 0 to 78 years of age

    In the new study, the researchers combined several advanced methods to examine brain tissue from people aged 0 to 78 years from several international biobanks. They used a method called single-nucleus RNA sequencing, which analyses gene activity in individual cell nuclei, and flow cytometry to study cell properties. By combining this with machine learning, they were able to identify different stages of neuronal development, from stem cells to immature neurons, many of which were in the division phase.

    To localize these cells, the researchers used two techniques that show where in the tissue different genes are active: RNAscope and Xenium. These methods confirmed that the newly formed cells were located in a specific area of the hippocampus called the dentate gyrus. This area is important for memory formation, learning and cognitive flexibility.

    Hope for new treatments

    The results show that the progenitors of adult neurons are similar to those of mice, pigs and monkeys, but that there are some differences in which genes are active. There were also large variations between individuals – some adult humans had many neural progenitor cells, others hardly any at all.

    “This gives us an important piece of the puzzle in understanding how the human brain works and changes during life,” explains Jonas Frisén. “Our research may also have implications for the development of regenerative treatments that stimulate neurogenesis in neurodegenerative and psychiatric disorders.”

    The study was conducted in close collaboration with Ionut Dumitru, Marta Paterlini and other researchers at Karolinska Institutet, as well as researchers at Chalmers University of Technology in Sweden.

    The research was funded by the Swedish Research Council, the European Research Council (ERC), the Swedish Cancer Society, the Knut and Alice Wallenberg Foundation, the Swedish Foundation for Strategic Research, the StratRegen programme, the EMBO Long-Term Fellowship, Marie Sklodowska-Curie Actions and SciLifeLab. Jonas Frisén is a consultant for the company 10x Genomics. See the scientific article for a complete list of potential conflicts of interest.

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  • Multilevel Cervical Epidural Hematoma From C1 to T3 Following C6/C7 Anterior Cervical Discectomy and Fusion (ACDF): A Rare but Reversible Surgical Emergency

    Multilevel Cervical Epidural Hematoma From C1 to T3 Following C6/C7 Anterior Cervical Discectomy and Fusion (ACDF): A Rare but Reversible Surgical Emergency


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  • The way you drink coffee could determine how long you live, study finds

    The way you drink coffee could determine how long you live, study finds

    If your daily routine involves an energizing cup of coffee, you may want to rethink what you choose to put in it.

    Drinking coffee has been linked to a lower risk of death. The catch is, mortality risk based on coffee consumption changes with the amount of sweeteners and saturated fat added, according to a study from the Gerald J. and Dorothy R. Friedman School of Nutrition Science and Policy at Tufts University.

    “Coffee is among the most-consumed beverages in the world, and with nearly half of American adults reporting drinking at least one cup per day, it’s important for us to know what it might mean for health,” Fang Fang Zhang, senior author of the study, said.

    “The health benefits of coffee might be attributable to its bioactive compounds, but our results suggest that the addition of sugar and saturated fat may reduce the mortality benefits.”

    The study found that drinking black coffee and coffee with low levels of added sugar and saturated fat were associated with a 14% lower risk of all-cause mortality as compared to no coffee consumption.

    But for coffee with high amounts of added sugar and saturated fat, results varied.

    The study analyzed data from the National Health and Nutrition Examination Survey from 1999 to 2018 and National Death Index Mortality Data.

    Among the studied 46,332 U.S. adults aged 20 or over, 7,074 people have died. Those deaths were then cross-referenced against coffee consumption, according to reports.

    The researchers found that people who drink coffee showed a lower risk of all-cause mortality, but when more than a little sugar and saturated fat was added, the risks were heightened.

    While limited in scope, the study suggests that drinking caffeinated coffee could help you live longer, while decaffeinated coffee drinkers saw no difference in mortality rates. And taking sugar, milk and cream in your coffee could increase mortality.

    “Few studies have examined how coffee additives could impact the link between coffee consumption and mortality risk, and our study is among the first to quantify how much sweetener and saturated fat are being added,” researcher Bingjie Zhou said.

    “Our results align with the Dietary Guidelines for Americans which recommend limiting added sugar and saturated fat.”

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  • Q2 2025 Recap: Cardiology News and Updates

    Q2 2025 Recap: Cardiology News and Updates

    HCPLive Cardiology
    Q2 2025 Recap

    The second quarter of 2025 brought a steady stream of momentum in cardiology, with developments spanning early-stage innovation, late-phase trial results, and new FDA approvals. This quarter’s recap includes 3 key regulatory milestones—including a major hypertension approval and a fast-tracked gene editing therapy—as well as 3 headline-making trial readouts that challenged, confirmed, or extended the evidence base in high-risk populations.

    Rounding it out, Don’t Miss a Beat delivered 3 episodes from the frontlines of ACC, Heart in Diabetes, and beyond—offering expert commentary on treatment sequencing, cardiorenal strategies, and emerging approaches in ATTR-CM. Here’s a look at what mattered most this past quarter in cardiovascular care.

    FDA News in Cardiology

    FDA Grants Fast Track Designation to VERVE-102 Gene Therapy

    On April 11, 2025, the FDA awarded Fast Track designation to Verve Therapeutics’ VERVE-102 gene editing medicine to lower low-density lipoprotein cholesterol (LDL-C) levels in individuals with hyperlipidemia and high cardiovascular risk. The regulatory agency cleared the Investigational New Drug (IND) application for VERVE-102 in March 2025, when the company provided interim data from the dose–escalation part of the Phase 1b Heart-2 trial.

    FDA Accepts NDA Submission for Oral Semaglutide 25 mg

    On May 2, 2025, Novo Nordisk announced the FDA accepted its NDA for a once-daily 25 mg oral formulation of semaglutide (Wegovy) for chronic weight management in adults with obesity or overweight. Based on Phase 3 OASIS 4 trial results, the pill showed significant efficacy in reducing weight in patients with at least one comorbidity. According to Novo Nordisk, this could become the first oral GLP-1 therapy approved for obesity treatment. The drug also aims to reduce cardiovascular risk in patients with established heart disease. The FDA decision is expected in Q4 2025.

    FDA Approves Triple Combination Drug GMRx2 (Widaplik) for Hypertension Treatment

    On June 9, 2025, the FDA approved GMRx2 (Widaplik), the first single-pill triple combination therapy—telmisartan, amlodipine, and indapamide—approved for initial treatment of hypertension in adults likely needing multiple drugs. Based on positive results from 2 phase 3 trials and the VERONICA study, Widaplik demonstrated superior blood pressure control and good tolerability. According to George Medicines, the pill’s design aligns with global guidelines recommending early use of combination therapy. A US launch is expected in Q4 2025.

    Trial Updates

    VERVE-102 Safely Cuts LDL-C Levels in Early Phase 1b Results

    On April 14, 2025, Verve Therapeutics announced data from their phase 1b Heart-2 trial of VERVE-102 for the treatment of patients with heterozygous familial hypercholesterolemia (HeFH) and/or premature coronary artery disease (CAD). A single infusion of the in vivo gene editing medicine achieved dose-dependent reductions in blood PCSK9 and LDL-C, with a mean LDL-C reduction of ≥50% and a maximum decrease of nearly 70% at the highest dose.

    Phase 3 Trial Results Announced for Sotatercept-csrk in Pulmonary Arterial Hypertension

    On June 23, 2025, Merck announced positive topline results from the Phase 3 HYPERION trial, showing sotatercept-csrk (WINREVAIR) significantly reduced time to clinical worsening in newly diagnosed PAH patients at intermediate or high risk. Based on a composite primary endpoint, the trial met its goal, with additional benefits seen in walking distance, NT-proBNP levels, and functional class. According to Merck, these findings extend sotatercept’s evidence base to earlier-stage patients, building on prior success in advanced PAH. On July 02, 2025, Merck announced the FDA’s acceptance of their BLA for a label expansion, which was granted Priority Review.

    ACHIEVE: Spironolactone Fails to Reduce Cardiovascular Risk in Dialysis Patients

    On June 6, 2025, results from the ACHIEVE trial presented at ERA 2025 showed that spironolactone did not significantly reduce cardiovascular death or heart failure hospitalization in dialysis patients. Based on data from over 2,500 participants, the primary outcome occurred in 20.5% of the spironolactone group vs. 21.6% in the placebo group (HR 0.92; P = .35). According to investigators, the findings challenge earlier studies suggesting large cardioprotective benefits. Additionally, spironolactone was associated with a higher rate of severe hyperkalemia, occurring in 6.6% of patients.

    Don’t Miss a Beat

    During the second quarter of 2025, Don’t Miss a Beat released a trio of episodes, including a pair of in-person episodes from the floor at the American College of Cardiology and the Heart in Diabetes meeting. Check out our episode summaries below!

    Treatment Sequencing in New Era of Heart Failure Management

    In this episode recorded at ACC 2025, the hosts examine the expanding treatment landscape for HFpEF, advocating for early combination therapy using SGLT2 inhibitors, MRAs, and incretin-based drugs to improve outcomes. They debate rapid versus risk-based implementation, highlight phenotyping for tailored care, and discuss upcoming trials and the promise of fixed-dose combinations to enhance adherence.

    CONFIDENCE Trial and Combination T2D, CKD Therapy at Heart in Diabetes 2025

    In this episode, the hosts review findings from the CONFIDENCE trial showing that combination therapy with finerenone and empagliflozin significantly outperformed either drug alone in reducing albuminuria in patients with CKD and type 2 diabetes. They discuss the trial’s design, safety profile, and implications for rapid implementation strategies and future fixed-dose combination treatments in cardiorenal care.

    Don’t Miss a Beat: Navigating the ATTR-CM Care Landscape, With Ahmad Masri, MD

    In this episode, the hosts and their guest discuss major advances in treating transthyretin amyloid cardiomyopathy, highlighting FDA-approved agents like tafamidis, acoramidis, and vutrisiran, while examining challenges such as residual risk, late-stage symptom limitations, and lack of head-to-head data. They also explore future strategies including amyloid-clearing therapies and early intervention trials like ACT-EARLY, which could shift the focus toward prevention in high-risk patients.

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  • U.S. researchers develop AI model improving sudden cardiac death prediction

    LOS ANGELES, July 4 (Xinhua) — Researchers at Johns Hopkins University have developed a new artificial intelligence (AI) model that significantly outperforms current clinical guidelines in identifying patients at high risk of sudden cardiac death, according to a newly published study.

    The AI system, known as Multimodal AI for ventricular Arrhythmia Risk Stratification (MAARS), integrates cardiac MRI images with a wide range of patient health records to detect hidden warning signs, offering a new level of precision in cardiovascular risk prediction.

    The study, published this week in Nature Cardiovascular Research, focused on hypertrophic cardiomyopathy, one of the most common inherited heart conditions and a leading cause of sudden cardiac death in young people.

    “Currently we have patients dying in the prime of their life because they aren’t protected and others who are putting up with defibrillators for the rest of their lives with no benefit,” said senior author Natalia Trayanova, a researcher focused on using AI in cardiology. “We have the ability to predict with very high accuracy whether a patient is at very high risk for sudden cardiac death or not.”

    Clinical guidelines used in the United States and Europe currently have an estimated accuracy of only 50 percent in identifying at-risk patients. In contrast, the MAARS model demonstrated an overall accuracy of 89 percent, and 93 percent for patients aged 40 to 60 — the group at the greatest risk.

    The AI model analyzes contrast-enhanced MRI scans for patterns of heart scarring — something that physicians have traditionally found difficult to interpret. By applying deep learning to this previously underused data, the model identifies key predictors of sudden cardiac death.

    “Our study demonstrates that the AI model significantly enhances our ability to predict those at highest risk compared to our current algorithms and thus has the power to transform clinical care,” said co-author Jonathan Chrispin, a Johns Hopkins cardiologist.

    The team plans to further test the new model on more patients and expand the new algorithm to use with other types of heart diseases, including cardiac sarcoidosis and arrhythmogenic right ventricular cardiomyopathy. Enditem

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  • U.S. researchers develop AI model improving sudden cardiac death prediction-Xinhua

    LOS ANGELES, July 4 (Xinhua) — Researchers at Johns Hopkins University have developed a new artificial intelligence (AI) model that significantly outperforms current clinical guidelines in identifying patients at high risk of sudden cardiac death, according to a newly published study.

    The AI system, known as Multimodal AI for ventricular Arrhythmia Risk Stratification (MAARS), integrates cardiac MRI images with a wide range of patient health records to detect hidden warning signs, offering a new level of precision in cardiovascular risk prediction.

    The study, published this week in Nature Cardiovascular Research, focused on hypertrophic cardiomyopathy, one of the most common inherited heart conditions and a leading cause of sudden cardiac death in young people.

    “Currently we have patients dying in the prime of their life because they aren’t protected and others who are putting up with defibrillators for the rest of their lives with no benefit,” said senior author Natalia Trayanova, a researcher focused on using AI in cardiology. “We have the ability to predict with very high accuracy whether a patient is at very high risk for sudden cardiac death or not.”

    Clinical guidelines used in the United States and Europe currently have an estimated accuracy of only 50 percent in identifying at-risk patients. In contrast, the MAARS model demonstrated an overall accuracy of 89 percent, and 93 percent for patients aged 40 to 60 — the group at the greatest risk.

    The AI model analyzes contrast-enhanced MRI scans for patterns of heart scarring — something that physicians have traditionally found difficult to interpret. By applying deep learning to this previously underused data, the model identifies key predictors of sudden cardiac death.

    “Our study demonstrates that the AI model significantly enhances our ability to predict those at highest risk compared to our current algorithms and thus has the power to transform clinical care,” said co-author Jonathan Chrispin, a Johns Hopkins cardiologist.

    The team plans to further test the new model on more patients and expand the new algorithm to use with other types of heart diseases, including cardiac sarcoidosis and arrhythmogenic right ventricular cardiomyopathy.

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  • First report of Aedes albopictus in Saint Barthélemy (French West Indies) confirmed by morphological, molecular and MALDI-TOF mass spectrometry approaches | Parasites & Vectors

    First report of Aedes albopictus in Saint Barthélemy (French West Indies) confirmed by morphological, molecular and MALDI-TOF mass spectrometry approaches | Parasites & Vectors

    The French Territories of the Americas are regions frequently impacted by arthropod-borne viruses transmitted by Aedes aegypti mosquitoes, such as dengue, chikungunya, and Zika viruses [1]. However, the presence of Aedes albopictus, another important mosquito vector for arboviruses [2], had never been reported in any of these territories, despite the impressive spread of this mosquito in mainland France since 2004 [3]. In the Caribbean, Ae. albopictus was first reported in the Dominican Republic in 1993 [4].

    On 30 September 2024, two vector control agents collected mosquito larvae from a floor siphon (17°54′20″N, 62°49′28″W) near the Lorient post office on the island of Saint Barthélemy, as part of their routine entomological surveillance activities that include weekly larval prospections and ovitrapping. The larvae were brought to the Vector Control Agency office (Agence Régionale de Santé [ARS]) in Saint Barthélemy and reared until adulthood. After emergence, the agents noted the presence of adult mosquitoes that did not match morphological criteria for Ae. aegypti and photographed the mosquitoes. Entomologists from ARS Guadeloupe, ARS Martinique and from local research institutions examined the photographs and confirmed the agents’ suspicion that the mosquitoes were Ae. albopictus.

    Two weeks later, an exploration mission was organized, during which agents from ARS Guadeloupe, ARS Saint Barthélémy, and the Institut Pasteur of Guadeloupe (IPG) traveled to Saint Barthélémy to confirm the species’ identity and to inform about its distribution area on the island. Larval prospections conducted from 14 to 16 October identified five breeding sites within a 400-m radius of the initial detection site, all containing mosquitoes morphologically identified as Ae. albopictus (Table 1).

    Table 1 Aedes albopictus breeding sites identified in Saint Barthélemy (French West Indies) between 14 and 16 October 2024

    Morphological criteria described by Darsie [5] were initially used during the missions to identify Ae. albopictus at both the larval and adult stages (Fig. 1a–c). However, since Ae. albopictus shares morphological similarities with other members of the Scutellaris group, further identification steps were performed on two collected specimens using matrix-assisted laser desorption ionization—time-of-flight mass spectrometry (MALDI-TOF MS) and cytochrome c oxidase 1 (cox1) gene barcoding to confirm the species. Briefly, the two specimens were individually dissected to separate the head and thorax from the rest of the body, and then homogenized 3 × 1 min at 30 Hz in a tissue lyzer (Retsch GmbH, Haan Germany). Legs and/or thoraxes were separately treated for identification by MALDI-TOF MS as previously described [6]. Protein mass profiles were acquired using a Maldi Biotyper Sirius Mass Spectrometer (Bruker Daltonics, Bremen, Germany), operating in linear positive-ion mode, with detection at a laser frequency of 50 Hz within a mass range of 2–20 kDa. MALDI-TOF spectra databases shared between entomologists from the Institut Pasteur of New Caledonia and the IHU Méditerranée enabled almost instantaneously confirmation of the samples as Ae. albopictus species, with the relevant score for the two specimens (log-score identification value = 2.05, matching spectra of Ae. albopictus from Cameroon [using mosquito legs from specimen 1] and from Marseille [using mosquito thorax from specimen 2]). To evaluate spectral similarity between specimen 1, which was collected in Saint-Barthélemy, and those from other Ae. albopictus, we generated a clustering analysis via the MSP (main spectra library) dendrogram function in MALDI-Biotyper v3.0 software. (Bruker Daltonics) using MS spectra from Ae. albopictus and five other Aedes species from the Scutellaris group (Aedes scutellaris, Aedes pseudoscutellaris, Aedes futunae, Aedes malayensis and Aedes polynesiensis). The resulting MSP dendrogram showed that the spectrum of the Saint-Barthélemy specimen clustered together with those of other Ae. albopictus, ruling out the possibility of other species from the Scutellaris group (Fig. 1d). These results highlighted the high reproducibility and the specificity of protein profiles among Aedes species, allowing a rapid and relevant identification of the specimen.

    Fig. 1

    Identification of adult Aedes albopictus specimens found in Saint Barthélémy (French West Indies) according to morphological criteria (A, B, C), MALDI-TOF MS analysis (D) and cox1 gene barcoding (E). A Abdomen view: abdominal terga with complete basal white bands (red arrow), B thorax view: scutum with a medial-longitudinal white stripe (red arrow), C thorax view: mesepimeron with non-separated white scales, forming a V-shaped white spot (red arrow). D Main spectrum profile (MSP) dendrogram of Aedes Scutellaris Group. Spectrum from the mosquito specimen collected in Saint Barthélémy was obtained with a Maldi Biotyper Sirius mass spectrometer (Bruker Daltonics), and the dendrogram was generated by MALDI Biotyper Compas Explorer software. Distance units correspond to the relative similarity between spectra of Ae. albopictus from Saint Barthélémy and those from IHU Méditérranée and Institut Pasteur New Caledonia databases. E Molecular phylogenetic tree generated by the maximum likelihood method. The percentage bootstrap values shown at the nodes were calculated with 1000 replicates, and only bootstrap values > 70 are shown. Scale bar indicates nucleotide substitutions per site. Aedes albopictus sequences or spectra from Saint Barthelemy specimens are indicated in red and bold. cox1, Cytochrome c oxidase 1 gene; IHU, Institut hospitalo-universitaire; MALDI-TOF MS, matrix-assisted laser desorption ionization—time-of-flight mass spectrometry. Mosquito pictures were taken by Fabrice Sonor

    We subsequently used the remaining body parts from the two specimens to conduct cox1 barcoding. Total DNA was extracted using the cetyltrimethylammonium bromide technique as previously described [7] and sequenced by Eurofins Genomics Europe (Sanger sequencing) using the primers HCO2198 and LCO1490 [6]. Sequences were analyzed, and multiple sequence alignment (Clustal W) was conducted using BioEdit version 7.0.5.3 software (BioEdit, Manchester, UK) [8, 9]. A molecular phylogenetic tree was generated by the maximum likelihood method based on the Timura 3-parameter model (best-fit nucleotide substitution pattern determined according to the corrected Akaike Information Criterion) using MEGA (http://www.megasoftware.net) with a bootstrap of 1000 replications [10]. Barcoding results indicated that the sequences from the mosquitoes collected in Saint Barthélemy (GenBank accession no. PQ644904 and PQ644905) shared 100% homology with sequences from Ae. albopictus collected in Europe and the Americas (Fig. 1e).

    In the following weeks, weekly entomological surveillance continued, and the number of Ae. albopictus-positive breeding sites on Lorient increased to 18 in a 665-m2 area. The species’ presence was also detected in five breeding sites within a 150-m2 area in Saint Jean (17°53′50″N, 62°50′14″W). The discovery of this second hotspot, located 1.6 km from Lorient and near the airport, suggests a broader distribution of the species on the island. The presence of this invasive mosquito species in Saint Barthélémy, an island with daily aerial or maritime connections to the French Departments of the Americas [11], raises concerns about the risk of its introduction into these territories, as well as into other Caribbean countries. After the first detection of Ae. albopictus in the Dominican Republic in 1993 [4], the species has been reported in an increasing number of Caribbean territories, including Cuba in 1995 [12], Cayman Islands in 1997 [13, 14], Trinidad in 2002 [15], Haiti in 2010 [16], and Jamaica in 2018 [17] (Fig. 2).

    Fig. 2
    figure 2

    Aedes albopictus distribution in the Caribbean. Countries or territories reporting the species have been marked with red location pins. Date of first detection is given in parentheses. Asterisks indicate the first detection in Saint Barthélemy. cox1, Cytochrome c oxidase 1 gene; IHU, Institut hospitalo-universitaire; MALDI-TOF MS, matrix-assisted laser desorption ionization—time-of-flight mass spectrometry. Created with BioRender.com

    It is noteworthy that in Cuba, from 1995 to 1999, Ae. albopictus was mainly distributed in peripheral municipalities with abundant vegetation rather that in more urbanized areas (i.e. city center). However, an increase in the species’ distribution in more urbanized areas, in association with Ae. aegypti, was observed from 2010 to 2018, highlighting the competitiveness of Ae. albopictus in the Caribbean context and an invasion process that can take several years [18]. In Saint Barthélemy, a 25-km2 island, Ae. albopictus is already present in artificial breeding sites from urban settings. In addition, half of these breeding sites contained the species in association with Ae. aegypti individuals (Table 1). In this context, the ecological plasticity of Ae. albopictus [19, 20] will likely facilitate its rapid invasion of Saint Barthélémy, emphasizing the urgent need to locally reinforce vector surveillance and control measures to prevent the further spread of this mosquito.

    This work also highlights the efficiency of MALDI-TOF MS for rapidly identifying mosquito specimens in a real-life surveillance situation. The value of this approach for entomological surveillance has been repeatedly shown [21, 22]. Although MALDI-TOF MS-based identification requires reference spectra databases to identify specimens, as well as standardized protocols for spectrum acquisition [23], the exchange of databases between regions and institutes with access to different mosquito species represents a key development perspective. This is particularly relevant in our increasingly globalized world, where the potential for transcontinental movements of viruses and vectors continues to grow.

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  • ‘Very Healthy and Fit’ Mom, 39, Ignored Multiple Bowel Cancer Symptoms For Months

    ‘Very Healthy and Fit’ Mom, 39, Ignored Multiple Bowel Cancer Symptoms For Months

    NEED TO KNOW

    • Krystal Maeyke has been documenting her battle with bowel cancer on TikTok

    • In May 2023, Maeyke was diagnosed with stage 4 bowel cancer

    • She shared that she ignored her symptoms of night sweats and abdominal pain for months

    Krystal Maeyke believed the sharp stabbing pains in her stomach were a food allergy.

    Maeyke, 39, tried to ignore the uncomfortable sensations in her lower abdomen for three months until the pain became unbearable.

    The mom of one has been documenting her battle with cancer on her TikTok account. In a video, she describes her diagnosis and shares that “three months” before she got the news, “I was having sharp stabbing pains, very tired, unexplained night sweats, loss of appetite, irregular bowel movements, and feeling like s—.”

    She thought she was just “overworked, and being a busy mum.” She said that she was “very healthy and fit.”

    After her symptoms became unbearable, she was airlifted by the Royal Flying Doctors Service to the nearest hospital, which was 280 miles away.

    At Alice Springs Hospital, she was given a series of tests. On May 30, 2023, Krystal Maeyke was diagnosed with metastatic bowel cancer.

    gofundme Krystal Maeyke

    In the same video, Maeyke shared, “I underwent a series of tests. That’s when I knew it was something serious. I was woken up later that night by a doctor whose words I will never forget.”

    ” ‘Krystal, I’ve got bad news…. You have cancer,’ ” she recalled the doctor telling her. “The weight of those words, accompanied by my question of ‘How do you know?’ and the doctor’s response, ‘It’s everywhere,’ shook me to my core.”

    According to the Cleveland Clinic, stage 4 is characterized by the cancer having spread to other “distant” parts of the body than where it originated. In this stage, it is considered metastatic or advanced cancer.

    Maeyke also said that before her diagnosis, she had months of night sweats, which she “ignored.”

    “I was experiencing persistent night sweats a few months before I was diagnosed. I would wake up during the night drenched in sweat, enough so I had to change clothes and sheets.” She described that “some nights it would happen a few times.”

    “It was summertime, and I slept with the air [conditioner] on and a fan, so I just thought it was my air [conditioner] not keeping up with the summer heat. So I ignored this sign,” the mom shared.

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    Maeyke continues to share her ongoing battle against cancer on her TikTok account, sharing with almost 50,000 people the key signs of bowel cancer and the treatment that she is undergoing, including multiple rounds of chemotherapy.

    Maeyke has been transparent in her struggle with cancer and candidly shared that one of the most complex parts is planning for the future of her son, Maison.

    Maeyke set up a GoFundMe to develop a financial cushion for her family during her illness. In the post, she wrote, “The true weight of my struggle lies not in my own pain, but the potential loss for my 12-year-old son, Maison.”

    According to Cancer Research UK, some symptoms of bowel cancer can be bleeding from the rectum or blood in your poop, a change in bowel habits, a lump in your abdomen, tiredness and breathlessness. It can also feel like cramping pains in the abdomen, feeling bloated, constipation and being sick.

    Read the original article on People


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