Category: 8. Health

  • Eating Meat May Help Protect Against Cancer-Related Deaths

    Eating Meat May Help Protect Against Cancer-Related Deaths

    Share on Pinterest
    A new study suggests that eating meat could slightly lower cancer-related death risk. Davide Illini/Stocksy United
    • A new study has found no increased death risk from eating plant or animal protein.
    • The findings also suggest that animal protein may slightly lower cancer-related death risk.
    • Nutrition experts say there’s no need to alter general protein recommendations, but individual needs may vary based on age, activity level, health status, or dietary pattern.

    For decades, the question of whether animal protein is harmful has sparked debate.

    Some studies have suggested that eating a lot of meat, eggs, or dairy might increase the risk of death from cancer or heart disease.

    On the other hand, plant protein has been praised as a safer and healthier option.

    The findings of this study come from the Third National Health and Nutrition Examination Survey (NHANES III), which gathered information from more than 15,000 American adults between 1988 and 1994.

    Participants were 19 years or older at the time of enrollment and were followed for 12 years to track mortality outcomes.

    During this follow-up period, researchers recorded deaths from all causes, including cancer or cardiovascular disease.

    The authors noted that measuring protein intake accurately is a challenge, since diets change from day to day, and surveys that rely on food recall are prone to error.

    To address this, the research team used an advanced statistical approach known as the multivariate Markov Chain Monte Carlo (MCMC) model.

    This method helps estimate a person’s “usual” nutrient intake by adjusting for normal daily variation and common reporting mistakes.

    Using this method allowed the investigators to distinguish between protein coming from animal sources — such as meat, dairy, and eggs — and protein coming from plant sources, including beans, nuts, and grains.

    The study went a step further by incorporating blood measurements of insulin-like growth factor 1 (IGF-1).

    This hormone has attracted attention in earlier studies, where higher levels were sometimes associated with cancer development and greater mortality risk.

    By looking at IGF-1 alongside dietary data, the researchers were able to explore whether the hormone helped explain any potential connection between protein intake and death rates.

    Because many lifestyle factors also influence health outcomes, the analysis adjusted for age, sex, smoking, physical activity, and total calorie intake.

    These adjustments are important for teasing apart the role of protein itself rather than mistaking other behaviors for dietary effects.

    After examining years of follow-up data, the researchers found no evidence that eating more animal or plant protein increased the risk of dying early.

    This was true when considering overall mortality as well as deaths caused specifically by cancer or cardiovascular disease.

    The results even suggested a small protective effect: participants with higher animal protein intake showed a slightly lower risk of dying from cancer.

    When IGF-1 levels were factored in, the story did not change. No significant relationship emerged between this hormone and the risk of death, contradicting some earlier concerns.

    The consistency of the results across age groups also stood out. Whether participants were younger adults under 65, older adults over 65, or in the 50-to-65 range, protein intake was not associated with an elevated risk of mortality.

    This detail is notable because prior studies had suggested that middle-aged adults might face more danger from higher protein diets.

    The research team additionally compared their findings with earlier work that reported strong links between protein and mortality.

    They speculated that differences in methodology may explain the contrasting results. Whereas older studies often relied on less precise ways of estimating intake, this analysis used more advanced modeling techniques to better capture long-term dietary patterns.

    In addition, the study’s balanced group sizes helped reduce bias that can occur when too few participants fall into certain categories.

    Taken together, the evidence suggests that usual protein consumption, regardless of source, does not shorten life expectancy.

    By accounting for both dietary variation and biological markers like IGF-1, the researchers provided one of the more thorough examinations to date of the relationship between protein and mortality in a large, nationally representative population.

    Avery Zenker, a medical and health writer with MyHealthTeam, said that, based on these findings, people don’t need to make any adjustments in planning their daily protein intake. Zenker wasn’t involved in the new study.

    “This study found that going beyond the minimum daily recommended intake of 0.8 grams of protein per kilogram of body weight per day didn’t appear to shorten life span,” she told Healthline, noting that higher protein intakes were still within the recommended ranges of between 10–35% of total calories.

    “Plan protein intake based on individual goals, including muscle maintenance [and] growth, health needs, and satiety,” she added.

    Zenker said the main takeaway from this study is not to fear higher total protein intakes when it comes to cancer or cardiovascular disease risk.

    “It doesn’t mean that all protein sources are made equal, though,” she said. “Previous research has linked high intakes of processed meat with negative health outcomes like cardiovascular disease and certain cancers.”

    She further noted the importance of not taking these findings as “rules.”

    “As with most nutrition research, correlation does not always indicate causation,” cautioned Zenker, explaining that the way the study was structured can make it difficult to exclude other factors that might be influencing the results.

    However, this study does contribute to our overall understanding of optimal eating patterns, she said.

    Finally, Zenker pointed out that protein sources are not just composed of protein.

    There are “many other compounds in protein foods that impact health, like vitamins, minerals, fiber, fats, carbohydrates, and phytonutrients,” she said.

    Of course, there is no one-size-fits-all recommendation for protein consumption.

    “In addition to the information provided in this study, we also know that certain groups may need to adjust their protein intake based on their circumstances and lifestyle,” explained Maura Donovan, a board certified sports dietitian and Medical Education Specialist for Sports Nutrition at Thorne. Maura wasn’t involved in the study.

    Donovan said older adults can benefit from a higher protein intake. This can help them maintain muscle mass and daily function as they age.

    “[Athletes] have increased protein needs due to the need for quick muscle repair and recovery after physical activity,” she added.

    “Additionally, individuals recovering from illness or injury can benefit from additional protein for immune support, and vegetarians and vegans should combine different plant sources to ensure they’re receiving a complete amino acid profile,” Donovan advised.

    Working with a registered dietitian is a good way to figure out your own personal needs. The Academy of Nutrition and Dietetics maintains a database of certified nutrition experts in your area.

    Continue Reading

  • Large-Scale Study Highlights Therapeutic Benefits of GLP-1 Receptor Agonists in Idiopathic Intracranial Hypertension

    Large-Scale Study Highlights Therapeutic Benefits of GLP-1 Receptor Agonists in Idiopathic Intracranial Hypertension

    A recently published study of more than 44,000 patients with idiopathic intracranial hypertension (IIH) showed that glucagon-like peptide 1 receptor agonists (GLP-1 RAs) offer therapeutic benefits including lowered medication use, procedures, and improved symptoms. While more prospective studies are needed to confirm these findings, the data support the potential of these medications as a management strategy.

    The retrospective study identified 44,373 patients with IIH from the TriNetX US Collaborative Network who started GLP-1 RAs within 6 months of diagnosis (n = 603) and compared them with nonusers (n = 43,770) on various outcomes. After matching, the analysis included 550 patients for each group, with the GLP-1 group using the following medications: lixisenatide, albiglutide, dulaglutide, semaglutide, liraglutide, and exenatide.

    Published in JAMA Neurology, results showed that those on GLP-1s were less likely to require any medication compared with the control group (29.7% vs 56.4%; P <.001), and demonstrated significantly lower mortality (≤2.0% vs 5.0%; P = .003). In addition, those on these medications had a lower prevalence of IIH symptoms such as headache (12.3% vs 27.4%; P <.001), visual disturbances/blindness (7.0% vs 11.7%; P = .007), and papilledema (2.2% vs 11.5%; P <.001).

    “We know every guideline for IIH emphasizes weight loss, but getting patients to achieve it is incredibly difficult,” senior author Dennis Rivet, MD, told NeurologyLive. “GLP-1 agonists are very effective for weight loss, and there’s already evidence they work on multiple systems, including the brain. Receptors in the choroid plexus, which helps regulate spinal fluid, suggest a possible direct mechanism beyond just weight loss, making them especially interesting for this disease.”

    Rivet, the Harold I. Nemuth Chair in Neurological Disorders at Virginia Commonweath University, believes these data hold significant implications for the use of GLP-1 RAs, which have gained attention in other areas of neurodegenerative disorders, sleep disorders, and weight loss.

    In the study, those on GLP-1 RAs had fewer procedures overall (6.8% vs 15.7%; P <.001), including bariatric surgery (5.4% vs 10.1%; P = .004) and cerebrospinal fluid shunt procedures (≤1.8% vs 5.2%; P = .002) than nonusers. In terms of specific medications, investigators noticed a significant decline in use of tricyclic antidepressants (6.8% vs 12.3%; P = .002), furosemide (6.8% vs 14.4%; P <.001), and acetazolamide (8.6% vs 24.0%; P <.001). There was no change in the use of valproate (GLP-1: 2.7% vs nonusers: 3.4%; P = .49).

    READ MORE: Real-World Data Points to Greater Impact of Semaglutide Over Tirzepatide in Reducing Heart Attack, Stroke Risk

    “Bariatric surgery is effective in IIH, but it carries significant morbidity,” Rivet noted. “What surprised us was that while surgery worked, we didn’t see the same mortality benefit. In contrast, patients on GLP-1 agonists had lower all-cause mortality at one year, which is an intriguing and unexpected finding.”

    A subgroup analysis stratifying patients based on body mass index (BMI)–using a benchmark of 40–was conducted, with data confirming all significant associations from the primary analysis except for dizziness, which did not differ in GLP-1 RA users and nonusers with a BMI of 40 or greater. When looking at bariatric surgery and conventional management with bariatric surgery, there were some noted differences, with bariatric surgery associated with greater weight loss in both comparisons.

    Overall, the subgroup findings revealed that despite lower 1-year BMI in the surgery group, GLP-1 RA users had lower medication use, fewer symptoms/signs, and procedures. Conversely, among GLP-1 RA nonusers, bariatric surgery resulted in lower medication use and fewer symptoms/signs but required more procedures and had higher mortality. Overall, this suggested that while greater weight loss may be achieved through bariatric surgery, GLP-1 RAs may provide better outcomes through other means.

    Rivet added, “A retrospective database study is a signal—it’s encouraging, but it’s not definitive. The obvious next step is a placebo-controlled trial, and I think it could be done, even in a rare condition like IIH. But the reality is many of these patients already meet on-label indications for GLP-1 use, so clinical practice may shift before such a trial is ever performed.”

    In terms of where else GLP-1 agonists might play a role, Rivet noted that secondary stroke prevention is an area of need that holds promise. In addition, he suggested that beyond stroke, the rapid effect of these medications on inflammatory markers could leave for potential in diseases like psoriatic arthritis and other inflammatory conditions.

    REFERENCE
    1. Sioutas GS, Mualem W, Reavey-Cantwell J, et al. GLP-1 Receptor Agonists in Idiopathic Intracranial Hypertension. JAMA Neurol. Published July 14, 2025. doi:10.1001/jamaneurol.2025.2020

    Continue Reading

  • High Coronary Artery Calcium Scores Associated with Double the Cardiovascular Mortality Risk at 25 Years

    High Coronary Artery Calcium Scores Associated with Double the Cardiovascular Mortality Risk at 25 Years

    Coronary artery calcium (CAC) scoring derived from non-gated low-dose computed tomography (LDCT) scans demonstrates significant capability for predicting long-term cardiovascular mortality, according to a new study involving over 8,700 participants.

    For the prospective study, recently published in Radiology, researchers reviewed Early Lung and Cardiac Action Program (ELCAP) CAC scoring for 8,782 participants who underwent LDCT screening between 2000 and 2004. The cohort was comprised of current and former smokers between the ages of 40-85, and there was a median follow-up period of 22.6 years, according to the study.

    The researchers found that the cumulative incidence of cardiovascular disease (CVD) death for those with high-risk CAC scoring (4-12) was 30.5 percent in comparison to 16.5 percent for participants with intermediate risk CAC scoring (1-3) and 9.4 percent for people with low-risk CAC scoring (0).

    High-risk ELCAP-CAC scoring on baseline low-dose CT scans was associated with significantly higher cardiovascular disease mortality and all-cause mortality, according to a new study involving over 8,700 current and past smokers with a median follow-up period of 22.6 years.

    Cumulative all-cause mortality incidence was 63.2 percent for those with high-risk CAC scores, 44.5 percent for cohort participants with intermediate-risk CAC scoring and 30.3 percent for people with low-risk CAC scores, according to the study authors.

    The study authors pointed out that adjusted multivariable analysis revealed that high ELCAP-CAC scoring was associated with nearly double the risk of CVD mortality and over a 2.8-fold higher risk of all-cause mortality in contrast to low ELCAP-CAC scoring.

    “Our findings show that a single ELCAP-CAC score at LDCT is a powerful long-term predictor of CVD death (hazard ratio, 1.98), while also confirming the prognostic value of absent CAC. Our study brings to light the potential for combining early detection of CVD and lung cancer, which are the top causes of death in the United States,” wrote lead study author Joseph Shemesh, M.D., who is affiliated with the Department of Cardiology at Sheba Medical Center in Ramat Gan, Israel, and colleagues.

    Three Key Takeaways

    1. CAC scoring from non-gated LDCT strongly predicts long-term cardiovascular and all-cause mortality. High-risk scores nearly doubled CVD death risk and nearly tripled all-cause mortality compared to low CAC scores.
    2. Absent CAC on LDCT confers favorable long-term prognosis. This reinforces the prognostic value of CAC scoring even in a high-risk cohort of current and former smokers.
    3. Integrating CAC scoring into lung cancer screening programs may enhance preventive care. This could provide additive risk stratification beyond traditional methods and supporting its use as a potential public health measure.

    Emphasizing the additive benefit with chest CT screening for lung cancer in current and past smokers, the researchers posited that CAC scoring can significantly enhance risk stratification beyond traditional laboratory-based methods for evaluating the potential for CVD.

    “Given the risk stratification afforded by ELCAP-CAC scoring, it becomes even more urgent that CAC scoring be acted on in the context of a screening program and perhaps even as a public health measure,” implored Shemesh and colleagues.

    (Editor’s note: For related content, see “CT-Based Coronary Artery Calcium Score Helps Predict Post-Op Survival Risks in Elderly Lung Cancer Patients,” “Computed Tomography Study Examines Potential of Automated Coronary Artery Calcium Scoring with Deep Learning” and “Study Says CT Scan is More Predictive than Genetic Risk Factors for Coronary Heart Disease Risk.”)

    In regard to study limitations, the authors noted that subtle calcifications may have been missed with thicker section thickness thresholds (up to 5 mm) in older image acquisition with LDCT. Not only could this have led to misclassification of participants having an ELCAP-CAC of zero, but the researchers conceded the potential impact in reducing the predictive value associated with higher ELCAP-CAC scores.

    Continue Reading

  • Sacubitril/valsartan shows benefit over enalapril in heart failure caused by Chagas disease

    Sacubitril/valsartan shows benefit over enalapril in heart failure caused by Chagas disease

    In patients with heart failure (HF) caused by Chagas disease, sacubitril/valsartan was superior to enalapril for the composite primary endpoint, predominantly driven by a significant reduction in N-terminal pro-B-type natriuretic peptide (NT-proBNP), according to late-breaking research presented in a Hot Line session today at ESC Congress 2025.

    Chagas disease, caused by Trypanosoma cruzi infection, remains a serious health problem affecting more than 7 million people, primarily from Latin America. T. cruzi parasites are mainly transmitted by contact with faeces/urine of infected triatomine bugs. T. cruzi can also be transmitted by consumption of contaminated food/beverages, during pregnancy or birth, through blood/blood products, organ transplantation and laboratory accidents. Chagas disease is spreading around the world, predominantly due to migration of infected patients to other regions, including North America, Europe, Asia and Australia. Chagas cardiomyopathy is considered the most common and serious manifestation of chronic Chagas disease, occurring in 30-40% of infected people during long-term follow-up.

    HF caused by Chagas disease has unique clinical features with worse prognosis than other causes of HF despite the fact that patients are often younger and have fewer comorbidities. There have been no prospective randomized trials testing the effects of standard treatments in patients with Chagas disease and HF. In the general HF population, the angiotensin receptor-neprilysin inhibitor, sacubitril/valsartan improved HF outcomes vs. the angiotensin-converting enzyme inhibitor, enalapril, and we compared these two agents in the largest trial in patients with Chagas disease and HF conducted to date.”


    Professor Renato Lopes from Duke University Medical Center, Durham, USA, Principal Investigator of the PARACHUTE-HF trial

    PARACHUTE-HF was an academic-led, open-label, blinded-endpoint adjudication, randomized trial conducted at more than 80 sites in Brazil, Argentina, Mexico and Colombia. Eligibility criteria included a diagnosis of Chagas disease confirmed by at least two different serological tests positive for Trypanosoma cruzi infection, left ventricular ejection fraction (LVEF) ≤40%, New York Heart Association functional class II to IV symptoms and NT-proBNP ≥600 pg/ml or ≥400 pg/ml and hospitalization for HF within the last 12 months. Participants were randomized 1:1 to either sacubitril/valsartan (50 or 100 mg twice daily titrated to a target of 200 mg twice daily) or enalapril (2.5 or 5 mg twice daily titrated to a target of 10 mg twice daily). The primary endpoint was a hierarchical composite outcome consisting of cardiovascular death, first hospitalization for HF and the relative change from baseline to week 12 in NT-proBNP, analysed using a win ratio approach.

    In total, 922 patients were randomized. The mean age was 64 years, 42.0% were women, mean LVEF was 29.8% and 44.4% had had prior hospitalization for HF.

    Following pairwise comparisons, sacubitril/valsartan was associated with a 52% higher likelihood of a better primary outcome compared with enalapril (stratified unmatched win ratio 1.52; 95% confidence interval [CI] 1.28 to 1.82; p<0.001). Over a median of 25 months’ follow-up, rates were similar for sacubitril/valsartan vs. enalapril for cardiovascular death (hazard ratio [HR] 0.95; 95% CI 0.73 to 1.23) and first HF hospitalization (HR 0.92; 95% CI 0.70 to 1.20). The significant difference in the primary outcome was predominantly driven by the percent change in NT-proBNP from baseline to 12 weeks: logarithmic median change from baseline was −30.6% in those assigned to sacubitril-valsartan and −5.5% in those assigned to enalapril (ratio of adjusted geometric mean change 0.68; 95% CI 0.62 to 0.75).

    The safety profiles of the two agents were similar, with discontinuations due to adverse events occurring in 6.1% of patients with sacubitril/valsartan and 9.8% with enalapril.

    Concluding, Professor Lopes said: “In patients with HF caused by Chagas disease, sacubitril/valsartan was superior to enalapril with respect to the primary outcome, predominantly driven by the 32% reduction in NT-proBNP levels at week 12. Our study provides the first randomized trial evidence to support a pharmacological treatment specifically in this high-risk population. PARACHUTE-HF shows that much-needed studies to better characterise chronic Chagas cardiomyopathy and to define the benefit/risk of new therapies in this condition are possible. In line with the global health spotlight of ESC Congress, the PARACHUTE-HF trial provides a successful model for international collaborations – in this field among cardiologists and infectious disease physicians − with the shared goal of evaluating the impact of new therapies on cardiovascular outcomes in patients with neglected diseases.”

    Source:

    European Society of Cardiology (ESC)

    Continue Reading

  • How the COVID-19 Pandemic Disrupted Melanoma Diagnosis and Treatment

    How the COVID-19 Pandemic Disrupted Melanoma Diagnosis and Treatment

    Image Credit: © WavebreakmediaMicro – stock.adobe.com

    A recent systematic review analyzed how the COVID-19 pandemic disrupted melanoma diagnosis and treatment.1 Researchers found an increase in disease incidence, severity, and diagnostic delays when comparing results pre- and post-pandemic. This is one of the first systematic reviews to explore the impact of COVID-19 on melanoma treatment practices.

    Background

    During the unprecedented time of the COVID-19 global pandemic, lockdowns and curfews were implemented, limiting the scheduling of routine appointments like cancer screenings, skin checks, and follow-ups. Melanoma diagnoses dropped by up to 67% in April 2020.2 Other cancers, such as breast and colorectal, saw up to a 90% decline in screenings.3 Although cancer and melanoma rates appeared to decrease during this time, it’s likely due to the delayed diagnosis rather than an actual reduction in cases.

    Methods & Materials

    A literature search of the PubMed, Scopus, Web of Science, and Cochrane Library databases was conducted in September 2024. Investigators compared study findings from pre-pandemic and pandemic periods. Pre-COVID-19 was considered to be between the years 2015 and 2019 while COVID-19/post-COVID-19 included years between 2019 and 2024.

    The analysis included clinical trials, observational studies, reviews, and case studies. Of the 503 studies initially screened, 55 were eligible and included in the final review. One was a modeling study while the rest were observational studies. These were conducted in Europe (particularly the United Kingdom), Canada, the United States, Australia, Israel, and South America (particularly in Brazil). In both pre- and post-pandemic periods, the majority of patients were between the ages of 58 and 69, with a slight male predominance.

    Authors extracted patient population characteristics along with incidence rates, Breslow thickness, ulceration, stage at diagnosis, mortality, treatment changes, and adaptations. The Newcastle–Ottawa Scale and the Joanna Briggs Institute (JBI) Critical Appraisal Checklist were used to assess the risk of bias.

    Results & Critical Findings

    Diagnosed melanoma cases decreased during the pandemic, with referrals and biopsies falling dramatically in 53 of the studies. Monthly referrals in Australia declined by 48% with Canada saw a 27% drop in biopsy rates. Initial visits to a dermatologist decreased by up to 37% in Italy. Italy also observed a 29% decrease in sentinel lymph node biopsies.

    With this, Breslow thickness and ulceration rates increased, indicating delayed presentations and more advanced, aggressive disease. In some cases, mean Breslow thickness increased from 1.1 mm in the pre-COVID-19 era to 1.8 mm during the pandemic. Ulceration rates nearly doubled in some findings as well (~ 11.7% to 22.6%).

    Additionally, less surgical excisions were performed, with a decrease of up to 20%. This could be due to limited surgical resources, reduced hospital capacities, and hesitancy among patients. Many countries saw an increase in presentations with inoperable tumors. These findings are consistent with what was researched in other cancer types, specifically breast, colorectal, prostate, and cervical cancers.

    Future Planning for Global Emergencies

    With this proven increase in severe melanoma during the pandemic period, it is imperative for health providers to be more prepared and strengthen future pandemic responses. The study authors outlined several methods to help mitigate diagnosis delays and prevent stage migration in melanoma and other cancers.

    Clinics should create clear policies and frameworks for cancer care, especially for high-risk patients. This could include clear communication and follow-up methods with patients as well as ensuring there is an adequate number of staff members for procedures, if needed.

    The authors also introduced the early implementation of innovative diagnostic methods like teledermatology and artificial intelligence. Although telemedicine is not a substitute, it can be beneficial during public emergencies as an initial check. Additionally, more public education on self-conducted skin checks or other prevention practices can promote earlier intervention in case another global emergency like the COVID-19 pandemic occurs.

    References

    1.Soni, A., Purcell, E., Lim, B., Marcaccini, G., Seth, I. and Rozen, W.M. (2025), The Silent Spread: A Systematic Review of Delayed Melanoma Diagnosis and Disease Progression During the COVID-19 Pandemic. JEADV Clinical Practice. https://doi.org/10.1002/jvc2.70154

    2. McBain RK, Cantor JH, Jena AB, Pera MF, Bravata DM, Whaley CM. Decline and Rebound in Routine Cancer Screening Rates During the COVID-19 Pandemic. J Gen Intern Med. 2021;36(6):1829-1831. doi:10.1007/s11606-021-06660-5

    3. Schadendorf D, van Akkooi ACJ, Berking C, et al. Melanoma. Lancet. 2018;392(10151):971-984. doi:10.1016/S0140-6736(18)31559-9

    Continue Reading

  • No clear benefit from surgical left atrial appendage occlusion in non-AF patients after valve surgery

    No clear benefit from surgical left atrial appendage occlusion in non-AF patients after valve surgery

    No benefit in terms of prevention of ischemic stroke, transient ischemic attack and cardiovascular mortality after 1 year was observed when surgical left atrial appendage occlusion was performed in high-risk non-atrial fibrillation patients after valvular surgery, according to late-breaking research presented in a Hot Line session today at ESC Congress 2025.

    Surgical left atrial appendage occlusion (SLAAO) is a procedure designed to block the left atrial appendage, which is a common site for clot formation.

    While SLAAO reduces stroke in atrial fibrillation (AF) patients, its efficacy in high-risk non-AF patients remains uncertain. We conducted the OPINION trial to address this important clinical question – does SLAAO reduce thromboembolic events in non-AF patients at high risk of stroke after valvular surgery?”


    Professor Yang Wang, trial presenter, from the State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Beijing, China

    OPINION was an open-label, randomised, superiority trial conducted at three cardiac surgery centres in China. Eligibility criteria included age >18 years, no AF diagnosis, CHA₂DS₂VASc ≥2 and an indication for valvuloplasty or replacement due to mitral or aortic valve lesions. Participants were randomised 1:1 to standard surgical care with concomitant SLAAO or without SLAAO. Intraoperative transoesophageal echocardiography was mandatory to assess the SLAAO, with immediate surgical revision required if the residual appendage stump exceeded 1 cm after the initial closure attempt. The primary endpoint was a composite of ischaemic stroke, transient ischaemic attack (TIA) or cardiovascular mortality assessed at 1 year using the intention-to-treat (ITT) principle.

    The ITT population included 2,118 patients who had a mean age of 56 years and 33% were female. The mean CHA₂DS₂VASc score was 2.9.

    The primary endpoint of ischaemic stroke, TIA or cardiovascular mortality was not significantly different between the groups, occurring in 6.9% of patients in the SLAAO group and 8.2% of patients in the control group (hazard ratio [HR] 0.83; 95% confidence interval [CI] 0.61 to 1.14; p=0.25).

    There was no significant difference in secondary endpoints, including components of the primary endpoint and bleeding events. Prespecified subgroup analyses were generally consistent, although there was a suggestion of benefit with SLAAO in high-risk patients with CHA₂DS₂VASc ≥3 (HR 0.81; 95% CI 0.56 to 1.17).

    Summarizing the results, first author, Doctor Xin Yuan, also from the State Key Laboratory of Cardiovascular Disease, said: “The trial found no significant benefit of routine SLAAO in the overall study population. Our results may help avoid unnecessary procedures and guide future research. We have planned further analyses of SLAAO in high-risk subgroups and, given the divergence in primary endpoint event curves observed after 6 months, we are extending follow-up to 3 years. Beyond SLAAO, optimisation of stroke prevention in high-risk patients after valvular surgery may lie in other strategies, including anticoagulation.”

    Source:

    European Society of Cardiology (ESC)

    Continue Reading

  • Spacecraft Surveys Shed New Light on Auroral Kilometric Radiation

    Spacecraft Surveys Shed New Light on Auroral Kilometric Radiation

    Editors’ Highlights are summaries of recent papers by AGU’s journal editors.
    Source: AGU Advances

    Auroral Kilometric Radiation (AKR) is a type of radio wave emitted from Earth’s auroral regions. It is the dominant radio emission from Earth and has been extensively studied, though previous analyses were constrained by limited spacecraft coverage.

    Today, with the availability of more spacecraft observations, it is possible to improve our understanding of the Earth’s most intense natural radio emission. Thanks to these data, Wu et al. [2025]  find that Auroral Kilometric Radiation preferentially occurs at high-latitudes and on the Earth’s night-side. They also found that the dense plasmasphere, which is a region of high-density plasma around Earth, blocks AKR from traveling, thus forming an equatorial shadow zone around the plasmasphere. Furthermore, the authors discover that the low-density ducts within the plasmasphere act as waveguides, enabling AKR to penetrate the dense plasmasphere and propagate along these channels.

    The findings provide valuable insights into Earth’s electromagnetic environments, space weather events and geomagnetic storms that may adversely affect satellites, communication systems, GPS, and power grids on Earth.  

    Citation: Wu, S., Whiter, D. K., Zhang, S., Taubenschuss, U., Zarka, P., Fischer, G., et al. (2025). Spatial distribution and plasmaspheric ducting of auroral kilometric radiation revealed by Wind, Polar, and Arase. AGU Advances, 6, e2025AV001743. https://doi.org/10.1029/2025AV001743

    —Alberto Montanari, Editor-in-Chief, AGU Advances

    Text © 2025. The authors. CC BY-NC-ND 3.0
    Except where otherwise noted, images are subject to copyright. Any reuse without express permission from the copyright owner is prohibited.

    Continue Reading

  • MSU’s cisplatin cancer drug wins national award | MSUToday

    MSU’s cisplatin cancer drug wins national award | MSUToday

    In 1965, a group of Michigan State University researchers accidentally discovered a new cancer-fighting drug: cisplatin. Since then, cisplatin has become the industry standard for cancer-fighting chemotherapy treatments.

    As announced today, MSU will receive a 2025 Golden Goose Award for the scientific success and global impact of cisplatin. The Golden Goose Award is meant to highlight the practical value of curiosity-driven research. The idea is that fundamental research can lead to unexpected, but profound, societal benefits.

    The Golden Goose award committee is housed within the American Association for the Advancement of Science and includes organizations like the Association of American Universities as well as previous winners.

    The award will be presented to MSU on Tuesday, Sept. 16, at the Library of Congress in Washington, D.C. During the award ceremony, members of both parties of the U.S. Congress will speak about the importance of the award and the federal funding of scientific research.

    “We are thrilled to have this important discovery by Barney Rosenberg honored, but what is truly significant are the countless lives saved by Cisplatin,” said Doug Gage, vice president for MSU Research and Innovation. “This is a stellar example of how fundamental research can have unexpected, profound impact in a completely different domain. The combination of curiosity driven research and applied research toward a specific outcome has been at the heart of the nation’s international leadership in science and technology. Strong federal support of both basic and applied research is essential for our continued dominance.”

    In addition to cisplatin, another research group — one that was led by the late Joseph Gall at Carnegie Science — will be honored with a Golden Goose Award. Gall is often referred to as the father of modern cell biology for his contributions to our understanding of chromosomes and the cellular nucleus.

    How cisplatin was discovered

    Barnett “Barney” Rosenberg. Credit: MSU Archives and Historical Collections

    Cisplatin was first created in 1844 by Italian chemist Michele Peyrone and was largely forgotten until 1965 when MSU Professor of Biochemistry Barnett “Barney” Rosenberg and his lab team discovered its use as a breakthrough cancer treatment.

    Rosenberg, in the College of Natural Science, and his lab technician Loretta VanCamp and a team of postdocs including Thomas Krigas were studying how electricity affects bacterial growth, not cancer drug development. He noticed that bacteria did not grow well around the platinum electrode he was using. Rosenberg then isolated some platinum containing compounds from the media and tested them in cell culture. He noticed that cell division was slowed — and only then did he consider its application to cancer.

    After a couple years of follow-up experiments, they discovered the true cause: platinum compounds released from the electrodes, not the electric field itself. As a result, the chemical compound prevents the DNA in cancer cells from replicating, confusing them and causing them to die. This accidental discovery led to the development of cisplatin, a platinum-based chemotherapy drug approved in 1978.

    Loretta Van Camp - Credit - MSU Archives and Historical Collections
    Loretta VanCamp. Credit: MSU Archives and Historical Collections

    The discovery, patenting and FDA approval of cisplatin was a 13-year process made possible by federal funding from the National Institutes of Health and the National Science Foundation, an unusually brief period of time in the research world prior to the development of the COVID-19 vaccine.

    “The discovery of cisplatin is a powerful example of how basic scientific curiosity can save lives,” said Eric Hegg, dean of the College of Natural Science. “What began as an unexpected result in a Michigan State University lab led to one of the most effective cancer treatments in the world. It is a testament to the power of exploratory-driven research and the transformative impact it can have on humanity.”

    Thomas Krigas - Credit - Krigas Family
    Thomas Krigas. Credit: Krigas Family

    While cisplatin is used to treat many types of cancer, it is most widely prescribed for testicular, ovarian, bladder, lung and stomach cancers. Most notably, cisplatin increased the cure rate for testicular cancer from around 10% to over 90%. Cisplatin’s impact has been especially profound in treating testicular cancer, which:

    • affects about 9,760 new patients who are diagnosed each year, and is responsible for the death of 500 men annually;  

    • is the most common cancer in males aged 15–34 at a time when cancer cases and deaths among men are predicted to increase 93% by 2050, according  to a new study; 

    • if in the 1960s had metastasized, resulted in a 90% death rate within one year of diagnosis. Today, the survival rate for testicular cancer is about 95%.  

    Cisplatin has saved countless lives, including that of legendary figure skater Scott Hamilton, who has been diagnosed with cancer three times.

    In 1997, Hamilton, who won gold at the 1984 Winter Olympics, was diagnosed with stage 3 testicular cancer, which had spread to his stomach.

    “When they told me, I was like, ‘I want it to be something else,’” said Hamilton in an interview in 2018. “But they said, ‘No, this is a good one to get, if you had to choose one,’ which is kind of crazy. But I’m grateful there was a proven treatment. I know many cancers don’t really have one.”

    Cisplatin’s impact today

    Cisplatin is responsible for saving millions of lives and remains one of the most effective chemotherapy treatments. In fact, cisplatin was added to the World Health Organization’s Essential Medicines List in 2015 for the treatment of early-stage cervical cancer, concurrently with radiotherapy.

    Cisplatin also has paved the way for new cancer-fighting drugs and continues to fund scientific breakthroughs at MSU. Royalties earned from sales of cisplatin and its derivative, carboplatin, fuel the work of and investments by the MSU Research Foundation, an independent, nonprofit corporation through offices such as MSU Technologies. There, it supports investments in research and economic development initiatives through the commercialization of cutting-edge technologies invented by MSU faculty, staff and students.

    Continue Reading

  • Not getting enough iodine? Brown pediatric endocrinologist reveals why iodine deficiency is on the rise

    Not getting enough iodine? Brown pediatric endocrinologist reveals why iodine deficiency is on the rise

    PROVIDENCE, R.I. [Brown University] — Doctors and researchers are puzzled by a recent rise in what might seem like an antiquated problem: iodine deficiency.

    Iodine, a trace element that helps regulate metabolism and produce vital hormones, is essential for many aspects of human development, especially in children. Specialists like Dr. Monica Serrano-Gonzalez, a pediatric endocrinologist and associate professor of pediatrics, clinician educator, at Brown University’s Warren Alpert Medical School, are hoping that studies like one she recently led can shed light on how to combat a growing challenge that transcends many population groups.

    In a Q&A, Serrano-Gonzalez shared how experiences with patients inspired her and other Brown-affiliated colleagues to study iodine deficiency, and how they’re educating the public on how to get enough.

    Q: Why are physicians seeing an increase in patients with iodine deficiency?

    There are very few food sources for iodine. The main ones are dairy products, seafood and eggs, as well as meat and poultry. In some countries, grain products like bread are made with iodized salt, but this is usually not the practice in the United States. Other foods like fruits and vegetables have very low levels as they depend on the soil iodine content. 

    In the 1920s, American manufacturers began adding iodine to table salt widely available in stores. Part of the problem is that now there are a lot of trendy salts — Himalayan, sea, kosher and others — so many people have moved away from eating iodized salts. Organic dairy also has less iodine, as do processed foods and bread. Patients who have restricted diets, such as practicing vegans or people with dairy intolerance, food allergies or autism spectrum disorder, are also at higher risk for deficiency. Children and pregnant or breastfeeding women are more susceptible, as their iodine requirements are higher.

    There is no public health mandate for iodization in the U.S., so many of the salts you buy in the grocery store don’t have iodine, and the salts that do have varying concentrations. The public health messaging has been so strong against salt due to its connection with blood pressure issues, and people appear to be hyper-aware of that. In the clinic, we have noticed that patients often think that iodized salt, specifically, is bad for health, as opposed to all types of salt. 

    Q: Why do we need iodine?

    Our bodies need iodine to make thyroid hormone, which helps regulate metabolism and is key to brain development. Without adequate iodine, the gland has to figure out ways of compensating, which is why someone can have a goiter — enlarged thyroid — and be otherwise okay. But if you reach a point of chronic deficiency where you can no longer compensate, the thyroid hormone levels go down, so the pituitary gland makes more of another hormone that stimulates the thyroid. The thyroid gland grows as it tries to keep up, but simply can’t. 

    In children, low thyroid function can significantly affect linear growth and cognitive development, causing irreversible intellectual disability, and it affects metabolism overall at any age. There are thyroid hormone receptors all throughout the body, and if thyroid hormone levels are severely low for a long time, that could lead to the worst case scenario of a coma.

    Before iodine fortification in the 1920s, there were “goiter belts” around the Great Lakes, the Appalachian and Northwestern regions. There are reports that analyzed military data from the first world war that found 30% of young people from iodine-deficient areas couldn’t be recruited into the military because they had large goiters, as it was so common back then. Salt fortification made a big difference.

    Q: Why did you start studying this issue?

    I saw a 13-year-old patient a few years ago who had a goiter that rapidly enlarged over the course of a few weeks. We often see patients with goiters in the clinic, but the vast majority of the time it’s from an autoimmune condition called Hashimoto’s disease, where the immune system is misfiring and attacking the thyroid gland. However, the patient’s blood tests for the disease were all negative, so we were puzzled. This boy had autism spectrum disorder and had a highly restricted diet, so we started thinking it could be iodine deficiency. He wasn’t eating eggs, dairy or seafood, and his family cooked with non-iodized salt. A urine test confirmed he was deficient, so we added an iodine supplement to his diet and the goiter decreased in size over the next few weeks. Eventually, his family managed to expand his diet so that he wouldn’t need the supplement anymore.

    This incident sparked interest among me and my colleagues, so we began paying attention to iodine deficiency. We eventually published a case series reporting our experience with six patients, who we tracked from diagnosis to follow-up care. All of the patients shared a restricted diet, due to reasons like developmental delays, autism, vegan diets and dairy intolerance. We are seeing iodine deficiency spanning all ages, from toddlers to adolescents, and in patients belonging to different socioeconomic groups.

    Q: How can physicians address the risk of iodine deficiency?

    One of the things we are learning about is the stigma associated with iodine deficiency. Diet is always a tricky subject to discuss with patients, but I also think that there is a stigma in this case due to the association of iodine deficiency with poverty in underdeveloped countries. 

    In our pediatric endocrine practice, we are educating our patients about the risks of an iodine-free diet. We’re also educating pediatricians as well as medical residents and fellows who work with us in the clinic, and we will give a hospital-wide grand rounds presentation at Hasbro Children’s on the topic of deficiencies of micronutrients such as iodine. 

    To avoid deficiency of iodine and other micronutrients, we encourage patients to diversify their diets. If you have a mix of foods in your diet including seafood, eggs, chicken and dairy, you are likely okay in terms of iodine intake. But especially for patients who have a low dietary diversity because of food allergies, autism, developmental delay, dietary preferences or other reasons, we recommend that they use iodized salt when cooking — in moderation and in the context of a healthy diet.

    This Q&A was originally published on the Warren Alpert Medical School website.

    Continue Reading

  • Regardless of Kidney Function, Abelacimab Consistently Reduced Bleeding Risk in Patients With AF

    Regardless of Kidney Function, Abelacimab Consistently Reduced Bleeding Risk in Patients With AF

    Regardless of patients’ kidney function, abelacimab (Anthos Therapeutics) had consistently reduced the risk of bleeding compared with rivaroxaban (Xarelto; Bayer HealthCare; Johnson & Johnson), wrote investigators of the AZALEA-TIMI 71 clinical trial (NCT04755283). The findings, which were published in JAMA Cardiology, suggested that abelacimab might offer a notably favorable safety profile, especially among those with chronic kidney disease (CKD), but larger studies are needed.1,2

    Image credit: NanSan | stock.adobe.com

    About the Trial

    Trial Name: Safety and Tolerability of Abelacimab (MAA868) vs. Rivaroxaban in Patients With Atrial Fibrillation (AZALEA-TIMI 71)

    ClinicalTrials.gov ID: NCT04755283

    Sponsor: Anthos Therapeutics, Inc.

    Completion Date (Estimated): December 29, 2028

    CKD is a common disease present in patients with atrial fibrillation (AF) and is often associated with higher rates of bleeding with anticoagulation, explained the authors. Although direct oral anticoagulants (DOACs) are safer than vitamin K antagonists (VKAs) regarding bleeding across a range of kidney function, bleeding risk with DOACs in those with impaired kidney function remains a considerable risk.1

    The authors explain that factor XI (FXI) inhibitors are an experimental class of anticoagulants that cause less bleeding than DOACs. Abelacimab, a novel FXI inhibitor, is a monoclonal antibody without renal elimination, whereas about one-third of rivaroxaban is directly renally excreted. In the multicenter, randomized, active-controlled phase 2b AZALEA-TIMI 71 trial, the investigators evaluated the safety and tolerability of 2 blinded doses of abelacimab compared with open-label rivaroxaban in patients with AF who had a range of kidney function.1,2

    The trial enrolled 1284 patients aged 55 years and older (median age: 74 years) with AF and a CHA₂DS₂VASc score of 4 or higher, or 3 or higher for those with planned concomitant antiplatelet use or creatinine clearance (CrCl) of 50 mL/min or less, who were randomly assigned to receive either 150 mg or 90 mg of abelacimab administered subcutaneously monthly or to rivaroxaban daily. Patients with a CrCl less than 15 mL/min or receiving dialysis were not eligible for enrollment.1,2

    The primary end point for this analysis was International Society on Thrombosis and Haemostasis (ISTH) major or clinically relevant or nonmajor (CRNM) bleeding. Other outcomes for this analysis included ISTH major bleeding alone and a broader bleeding composite of ISTH major, CRNM bleeding, or minor bleeding. Further, exploratory efficacy outcomes—including stroke or systemic embolism and a net clinical outcome composite of ischemic stroke, systemic embolism, major or CRNM bleeding, or death—were also evaluated. Outcomes were prospectively captured during trial follow-up and adjudicated by an independent clinical events committee who were blinded to treatment assignment.1,2

    The findings demonstrated that, in the rivaroxaban group, patients with a CrCl of 50 mL/min or less experienced higher rates of major or CRNM bleeding compared with those with a CrCl greater than 50 mL/min despite dose reduction (incidence rates: 13.6 vs 7.0/100 person-years). Additionally, abelacimab reduced major or CRNM bleeding compared with rivaroxaban regardless of CrCl (CrCl ≤50 mL/min: hazard ratio [HR], 0.26 [95% CI, 0.12–0.54]; >50 mL/min: HR, 0.40 [95% CI, 0.26–0.62]; P value for interaction = .33), with absolute risk reductions of about 10.1 and 4.2 per 100 person-years in those with CrCl of 50 mL/min or less and greater than 50 mL/min, respectively (P value for interaction = .09).1

    This risk reduction was consistent for major bleeding alone and for a broader composite inclusive of major, CRNM, and minor bleeding, wrote the study authors. Notably, results were similar when comparing the individual abelacimab doses to rivaroxaban.1

    “[Limitations include] AZALEA-TIMI 71[’s design] to assess the bleeding profile of abelacimab relative to rivaroxaban; larger studies are necessary to examine the efficacy of abelacimab for stroke prevention. Each of the 4 approved DOACs for AF have variable renal elimination and may differ in their bleeding profiles; thus, our results may not be generalizable to other DOACs,” wrote the study authors. “In this secondary analysis of the AZALEA-TIMI 71 randomized clinical trial, abelacimab consistently reduced the risk of bleeding compared with rivaroxaban across a range of kidney function and irrespective of rivaroxaban dose reduction among patients with AF; however, further data are necessary to evaluate the efficacy of abelacimab for stroke prevention in AF.”1

    REFERENCES
    1. Patel SM, Giugliano RP, Morrow DA, et al. Safety of Factor XI Inhibition With Abelacimab in Atrial Fibrillation by Kidney Function: A Prespecified Analysis of the AZALEA-TIMI 71 Randomized Clinical Trial. JAMA Cardiol. Published online September 01, 2025. doi:10.1001/jamacardio.2025.3393
    2. Safety and Tolerability of Abelacimab (MAA868) vs. Rivaroxaban in Patients With Atrial Fibrillation (AZALEA-TIMI 71). ClinicalTrials.gov identifier: NCT04755283. Updated September 2, 2025. Accessed September 3, 2025. https://clinicaltrials.gov/study/NCT04755283

    Continue Reading