分类: health

  • US military to start testosterone  testing, Hegseth says

    US military to start testosterone testing, Hegseth says

    The U.S. Department of Defense has launched a new initiative that marks a significant shift in military healthcare policy, mandating annual testosterone screenings for all active duty and reserve service members aged 30 and older, while offering voluntary testing for younger troops. Defense Secretary Pete Hegseth made the announcement official in a video posted to the social platform X, framing the program as a core commitment to delivering the highest standard of care for the nation’s armed forces.

    In the video titled “High-T Department”, Hegseth authorized the new screening protocol, emphasizing that the program’s core goal is to help troops operate at peak physical performance, rather than enabling artificial performance enhancement. “We owe our warriors the absolute best medical care in the world, and this program delivers on that obligation,” Hegseth said. He added that supporting long-term troop health ensures service members remain strong, resilient, and capable not only through deployments but for life after they leave military service. Service members found to have clinically low testosterone levels will be offered voluntary testosterone replacement therapy (TRT), while non-medical use of testosterone for artificial muscle growth remains strictly prohibited under military rules.

    Pentagon spokesperson Sean Parnell confirmed in a Wednesday statement that the mandatory screening for testosterone deficiency is effective immediately for all eligible personnel. Parnell noted that the protocol will allow the Department of Defense to build a comprehensive health baseline for troops and deliver targeted care when needed, with the end goal of sustaining a healthy, highly capable fighting force.

    The initiative aligns with broader pushes from the current Trump administration to expand access to testosterone therapy across the U.S. U.S. Health Secretary Robert F. Kennedy Jr. has led efforts to remove regulatory barriers for clinicians prescribing TRT, even positioning expanded access as a potential response to what the administration has called a national “fertility crisis”. Just last month, the U.S. Food and Drug Administration (FDA) moved to revise labeling requirements for TRT products, removing mandatory safety and effectiveness disclosures and proposing looser limits on how the products can be prescribed.

    Medical experts have broadly supported the core idea of routine testosterone screening for older men, while raising important cautions about overprescription. Dr. Mohit Khera, a urology professor at Baylor College of Medicine who led an FDA expert panel on military testosterone screening and use last year, told the BBC that routine screening for all men over 30 is clinically justified, as testosterone levels are a key marker of both current and long-term overall health. Khera explained that undiagnosed low testosterone can reduce muscle mass and energy levels, disadvantages that carry particular risk for service members in combat situations. When prescribed appropriately to patients with confirmed deficiency, TRT offers meaningful benefits: increased muscle mass, reduced body fat, lower depression risk, and improved long-term bone mineral density.

    However, Khera emphasized that TRT is not appropriate for everyone, and carries measurable risks for certain groups. For younger men in their reproductive years, testosterone supplementation can cause infertility, a side effect that must be clearly communicated before treatment begins. The treatment also carries a theoretical increased risk of cardiovascular events that providers and patients must take into account when weighing treatment options. “You have to be careful not to just give someone testosterone unless they do have some kind of symptoms,” Khera noted, highlighting the need for targeted, clinically justified care rather than widespread routine supplementation.

  • More health workers strike as Ebola cases in Congo exceed 2,000, including 754 deaths

    More health workers strike as Ebola cases in Congo exceed 2,000, including 754 deaths

    In the conflict-wracked eastern region of the Democratic Republic of the Congo, a devastating Ebola outbreak driven by the rare Bundibugyo virus has reached a grim milestone, with confirmed cases climbing to 2,011 and total deaths hitting 754, according to newly released official government data. World Health Organization (WHO) officials confirm this is the fastest-expanding Ebola event ever recorded, outpacing containment efforts at every turn.

    The crisis has been compounded by growing unrest among frontline medical teams, who have walked off the job over unmet pay promises. On Wednesday, staff at Bunia General Hospital — the largest medical facility in the outbreak’s epicenter — launched a strike, barricading the hospital entrance to demand long-delayed wages earned while working in high-risk, resource-strapped conditions. This industrial action follows a similar strike just two days earlier at an Ebola treatment center in Rwampara, another Ituri Province hotspot that has borne the brunt of the outbreak. That strike ended after workers secured a government commitment to issue back pay within 72 hours, but many frontline staff report they have not received any compensation since the outbreak began in mid-May, leaving deep lingering frustration.

    Public health experts warn multiple overlapping barriers are making the outbreak extremely difficult to contain. The most pressing issue is the unprecedented rate of spread: roughly 80% of all new confirmed cases stem from unknown transmission chains that officials have been unable to map. To date, authorities have only successfully traced 67% of known close contacts of infected patients, a rate far too low to halt transmission. Complicating tracing efforts further, health teams have still not identified the outbreak’s index case (patient zero), while widespread population displacement from ongoing armed conflict and frequent cross-community movement of artisanal miners have scattered thousands of potentially exposed people across the region.

    Unlike previous Ebola outbreaks in Congo that were caused by the more common Zaire strain — for which effective, approved vaccines and treatments already exist — there are no licensed medical countermeasures for the Bundibugyo virus driving this current event. In a small glimmer of hope for the response, enrollment for a clinical trial testing two promising investigational treatments has recently launched in Ituri, though results will not be available for months.
    Additional systemic challenges continue to undermine response work: a critical funding gap has left operations under-resourced, repeated attacks on health facilities have forced care closures in high-risk areas, ongoing armed violence in eastern Congo prevents teams from reaching remote communities, and deep-seated mistrust between local populations and public health workers has reduced cooperation with contact tracing and isolation efforts.
    As of the latest data release, 753 patients remain in isolation care at hospitals across the region, while 366 people have recovered from infection so far. More than 100 frontline healthcare workers have already contracted the virus since the outbreak began, according to WHO figures. WHO’s emergencies chief Dr. Chikwe Ihekweazu, who recently completed an assessment visit to Bunia, noted that many of the newly recorded deaths are people who never accessed care, dying in their home communities before medical teams could intervene.

  • Health officials issue urgent vaccine call as RSV cases grip Australia

    Health officials issue urgent vaccine call as RSV cases grip Australia

    As Australia heads toward the final stretch of winter, public health authorities are sounding a clear alarm: a highly contagious, cold-like respiratory virus is spreading at record-breaking rates, surpassing both COVID-19 and influenza to become the country’s dominant seasonal respiratory illness this year. As of this week, official data from the Immunisation Foundation of Australia (IFA) and the Australian Medical Association (AMA) shows more than 83,000 confirmed cases of respiratory syncytial virus, better known as RSV, have already been logged across the nation. By comparison, confirmed COVID-19 cases sit at just over 51,000, while influenza has infected nearly 50,000 Australians this winter.

    With an average of 890 new confirmed RSV cases reported daily since winter began, national projections show Australia is on track to exceed 127,000 total cases by the time winter draws to a close. While RSV often causes mild, cold-like symptoms similar to influenza or COVID-19, it poses severe life-altering risks to the most vulnerable groups: infants and older adults with weakened immune systems. For these populations, the infection can quickly progress to serious lower respiratory tract complications, making RSV the leading cause of preventable hospitalisation for both young children and senior Australians.

    Australia launched a national free RSV vaccination program in recent years, expanding eligibility to cover high-risk groups in incremental steps. Since February 2025, the vaccine has been available at no cost to pregnant people, and starting in May 2026, all Australians aged 75 and older became eligible for free doses. The program for infants has already delivered dramatic, positive results: since it launched nationwide in 2024, it has cut infant RSV hospital admissions by 70% during autumn and early winter, protecting more than 360,000 babies and preventing thousands of critical care admissions.

    “The fact that more than 700,000 vulnerable older Australians received the RSV vaccine in the first two months of the vaccination program is an outstanding effort by the community and immunisation providers,” said IFA founder and executive director Catherine Hughes. Despite this early progress, a major gap in protection remains: more than one million eligible older Australians have yet to get their free jab. Hughes noted that rollout timing created an unintended barrier, as the vaccine was not widely available in April and early May, when most seniors typically get their annual flu shot, leaving many people unaware they are still unprotected.

    “However, there is still a massive gap in RSV vaccination coverage and an urgent need for older adults to roll up their sleeves,” Hughes added.
    AMA president Dr. Danielle McMullen echoed this call to action, emphasizing that the vaccine is a simple, effective tool to cut the risk of serious illness and hospitalisation this winter. “With so many Australians yet to be protected against RSV, it’s essential that people speak to a healthcare professional about RSV protection. Now is the time to act – winter is far from over,” Dr. McMullen said. “Getting protected against RSV is an incredibly simple yet effective way to help prevent serious illness and stay out of hospital.”

    Eligible Australians can access their free RSV vaccine through participating general practitioners, local pharmacies, and community health centres, with public health officials stressing that getting vaccinated now can still prevent severe illness as cases continue to climb through the end of winter.

  • The new malaria vaccine helps in Africa but faces a test: Completing all 4 doses

    The new malaria vaccine helps in Africa but faces a test: Completing all 4 doses

    In the sweltering hills of central Cameroon, Mabel Djoumessi trekked for miles along rain-soaked, mud-caked dirt roads, her 9-month-old son Kenfack strapped securely to her back. Her destination: a local clinic, where Kenfack was scheduled for his malaria vaccine — an appointment too urgent to skip, even in poor conditions.

    For generations, malaria has reigned as one of the deadliest threats to young children across the African continent, leaving millions of families grappling with repeated sickness and unmanageable medical costs. Today, Kenfack has never contracted the disease, a outcome his mother credits directly to the new malaria vaccine that has entered routine childhood immunization schedules across the country. “My other children, who never had access to the vaccine, get sick all the time,” Djoumessi explained, as she sat alongside other mothers holding their infants at Soa District Hospital.

    It has now been more than two years since Cameroon made history as the first nation to integrate the RTS,S malaria vaccine into its standard routine immunization program, and frontline health workers are already documenting clear public health gains: severe malaria cases among children have dropped noticeably, and pediatric hospital wards that once overflowed with sick young patients are now far emptier. But a critical gap threatens to undermine these hard-won gains: too few families are returning for the fourth and final booster dose that the World Health Organization (WHO) confirms is essential to sustaining long-term immunity against the parasite.

    This low fourth-dose coverage is not an isolated challenge limited to Cameroon. It reflects a systemic issue that plagues multidose vaccine rollouts across the entire African continent, where barriers ranging from travel costs to competing work and childcare responsibilities keep families from returning for follow-up doses months after the initial rounds of vaccination.

    Global public health data underscores just how high the stakes are: the WHO and UNICEF estimate that malaria kills one child under the age of five every single minute worldwide, with more than 90% of those deaths occurring in Africa. Cameroon alone is among 11 nations that bear roughly 70% of the world’s total malaria burden; the country recorded an estimated 7.6 million cases and 11,700 deaths from the disease in 2024. Early 2025 data from Cameroon’s National Malaria Control Program shows a 33,000-drop in cases compared to the previous year, though experts caution that the vaccine is not the sole driver of this decline.

    “Isolating the specific impact of malaria interventions requires advanced statistical modeling, and we do not yet have a framework to quantify the vaccine’s exclusive contribution,” explained Dr. Bomba Amougou, head of prevention at the National Malaria Control Program. “It is accurate to say the vaccine has contributed to falling cases and deaths, but it is not the only cause.”

    The WHO first endorsed broad use of the RTS,S vaccine in 2021, after multi-year pilot programs in Ghana, Kenya and Malawi found the shot cut child mortality from malaria by 13% among eligible children. Separate clinical trials across several African nations found that both RTS,S and the newer R21 vaccine reduced clinical malaria cases by more than 50% in the first year after three doses. To date, more than 52 million doses have been delivered to 25 high-risk African nations, supported by Gavi, the Vaccine Alliance. But the rollout faces major funding constraints following sweeping cuts to foreign aid from the Trump administration and other donors. Currently, Gavi is only able to guarantee vaccine supplies to cover up to 70% of eligible children in the world’s lowest-income countries.

    In Cameroon, coverage for the first three doses of the vaccine — given at six, seven, and nine months of age — has slowly improved since the program launched, climbing from 66% to 68% for first doses, 53% to 58% for second doses, and 48% to 59% for third doses between 2024 and 2025, according to Amougou. But coverage for the fourth dose, scheduled when a child turns two years old, remains stuck at just 25% as of 2025.

    Amougou noted that gaps stem from both parent and provider awareness issues: “Parents and even some health workers sometimes forget the fourth dose, particularly because it is administered more than a year after the third, and this is still a relatively new vaccine.” Receiving all four doses is critical, he emphasized: “Getting every shot makes the protection far more potent, and vaccination must work alongside other tools like bed nets, early treatment, and improved sanitation to beat malaria.”

    Data from the earlier pilot programs across Ghana, Kenya and Malawi confirms that the low fourth-dose coverage problem is widespread. While 80% of eligible children received their first dose in those countries, coverage dropped to just 46% for the fourth dose, according to a 2024 study published in the peer-reviewed Malaria Journal. Researchers found that high parent acceptance of the vaccine itself — driven by widespread familiarity with malaria’s deadly toll — but barriers like transport costs, lack of appointment reminders, poor care follow-up, and competing work and family obligations keep families from returning for the final booster months later.

    Gavi Chief Executive Officer Dr. Sania Nishtar emphasized that low late-dose coverage is an early, solvable challenge that should not overshadow the vaccine’s life-saving value. Nishtar noted that malaria vaccine actually has the lowest rate of parental hesitancy of any routine vaccine, a reflection of how desperate communities are for tools to protect their children from a preventable killer. “There is huge demand from governments and communities for this vaccine,” she said.

    In response to the coverage gap, Cameroon and other affected African nations have launched national “Big Catch-up” campaigns to remind parents and health workers to prioritize the fourth dose and bring eligible children who have missed their booster in for vaccination. Looking ahead, global health researchers are actively developing a single-dose malaria vaccine, which would eliminate the need for multiple follow-up visits and dramatically improve coverage. “The fewer the doses of a vaccine to be administered, the higher the uptake and the easier the administration,” Nishtar explained.

    For many low-income families across Cameroon, preventing malaria is not just a matter of child health — it is also a matter of financial survival. Georgette Caroline Mengbwa, a mother of three waiting for her youngest daughter’s third dose at Soa District Hospital, explained that her two older children were born before the vaccine was available, and face repeated bouts of sickness that drain the family’s limited income. “They fall ill every two or three months, and I have to spend between $53 and $107 every time one or all of them get sick,” she said. “It’s a lot of money.” Those costs are devastating in a country where the official monthly minimum wage is just $76, and nearly 40% of the population lives below the poverty line.

    For mothers like Djoumessi, the vaccine is already a life-changing tool, and she says she has every intention of returning for Kenfack’s fourth dose when he turns two. “I don’t want him to suffer like the others,” she said.

  • ‘Miracle on the Hudson’ pilot Captain Sully diagnosed with Alzheimer’s disease

    ‘Miracle on the Hudson’ pilot Captain Sully diagnosed with Alzheimer’s disease

    Seventeen years after he pulled off one of the most miraculous emergency landings in modern aviation history, retired Captain Chesley “Sully” Sullenberger III — the pilot who saved all 155 lives aboard US Airways Flight 1549 — has announced he is living with early-stage Alzheimer’s disease. The 75-year-old aviation icon shared the diagnosis in a heartfelt public post on his personal website Tuesday, opening up about his early symptoms and his decision to speak out to destigmatize the neurodegenerative condition.

    “For now, this means a name may not come easily to me, I forget a story I have recently told, or I don’t sleep as well, but I am in the beginning of this long journey,” Sullenberger wrote in his post.

    Sullenberger cemented his place as a national hero on January 15, 2009, just minutes after Flight 1549 departed New York’s LaGuardia Airport for Charlotte, North Carolina. The plane struck a flock of Canada geese shortly after takeoff, disabling both of its jet engines in an instant. With too little altitude to reach a nearby airport and a high risk of crashing into densely populated Manhattan neighborhoods, Sullenberger made a quick, life-saving decision to ditch the aircraft intact in the frigid waters of the Hudson River. Thanks to his calm expertise and split-second decision-making, every passenger and crew member on board survived the incident, which quickly became known across the globe as the “Miracle on the Hudson.”

    A former U.S. Air Force fighter pilot with 40 years of flying experience when the emergency landing occurred, Sullenberger retired from commercial aviation in 2010, one year after the incident. He never stepped back from public life, however, continuing a decades-long advocacy work to improve aviation safety standards across the industry. In 2016, his extraordinary feat was adapted into the Clint Eastwood-directed Hollywood feature film *Sully*, starring Tom Hanks as the quick-thinking captain.

    In his latest announcement, Sullenberger reflected that his Alzheimer’s diagnosis has forced him to reexamine what it means to live a life of service. His conclusion, he said, was to speak openly about his experience rather than stay private. Echoing the words he has shared for years about the 2009 emergency, he emphasized that courage is a contagious force that can bind communities together.

    “Over the years, when people would ask about the successful outcome of Flight 1549, I would say that ‘courage can be contagious,’ and on that day it helped everyone band together to get everyone off that airplane successfully,” he wrote. “Now we need that courage to battle this disease. I am now part of a larger community with many of you, and we will be courageous together.”

  • ‘Explosive diarrhoea’ outbreak remains a mystery as officials struggle to find sources

    ‘Explosive diarrhoea’ outbreak remains a mystery as officials struggle to find sources

    A summer outbreak of cyclosporiasis, a parasitic infection spread via contaminated food and water, has spread across 31 U.S. states and sickened more than 3,000 people, leaving public health experts scrambling to identify its source and slow transmission amid unique investigative challenges and strained public health resources.

    The illness, which is rarely fatal, is defined by its primary symptom: severe, watery diarrhea that strikes abruptly. As of current reports, Michigan has borne the brunt of the outbreak with more than 2,600 confirmed cases, followed by New York State with a smaller but still significant caseload. Despite weeks of investigation, health officials have not yet pinpointed the original contaminated source of the parasite, and have only issued general guidance to the public: thoroughly wash all produce, avoid certain high-risk fruits including raspberries, and cook vegetables thoroughly to destroy the pathogen.

    Public health investigators have described tracing the parasite as an extraordinarily difficult task, compounded by multiple biological and systemic barriers. “This isn’t like detecting a needle in a haystack. It’s like detecting a microscopic portion of a needle in a haystack,” explained Steven Manderach, executive director of the Association of Food and Drug Officials, who previously addressed cyclosporiasis outbreaks as a food safety official in Iowa.

    Biologically, the parasite’s long incubation period creates a major hurdle for investigators. Unlike most foodborne illnesses that cause symptoms within hours of consumption, cyclosporiasis takes one to two weeks to trigger illness in infected people, explained Jodie Guest, senior vice chair of epidemiology at Emory University’s Rollins School of Public Health. By the time most people seek care and report their illness, they often cannot recall every food they ate in the preceding two weeks, breaking a key link investigators rely on to trace contamination sources.

    Testing for the parasite in food supplies is also far more labor-intensive and complex than testing for other common pathogens. To isolate cyclospora, investigators must wash massive quantities of potentially contaminated produce to collect any parasite particles present, then concentrate the sample before testing can begin. “You’d have to have truckloads of lettuce to get to that point,” Manderach noted. The broad geographic spread of cases, spanning 31 states, also suggests multiple contamination points in the national food supply, a factor that further complicates coordinated investigations.

    Many public health experts point to recent federal budget and staffing cuts to U.S. Department of Health and Human Services (HHS) agencies as a critical additional barrier to solving the outbreak. As part of Elon Musk’s Department of Government Efficiency cost-cutting initiative, Health Secretary Robert F. Kennedy Jr has implemented widespread cuts that have reduced capacity for key foodborne illness surveillance programs. Most notably, the Foodborne Diseases Active Surveillance Network (FoodNet)—a federal program that previously tracked cyclospora, salmonella, listeria and other pathogens nationwide—scaled back monitoring last year to only track two pathogens, ending its systematic surveillance for cyclospora.

    In an internal memo to the state of Connecticut obtained by NBC News, the CDC acknowledged that “Funding has not kept pace” with the resources required to run the full FoodNet program. Guest, who previously worked on FoodNet operations, explained that the program previously collected patient data, tested food samples from state labs, and collated information at a national level to speed outbreak investigations. “When we see an outbreak or a cluster or something, we don’t have the data we normally expect to go back to use to help us, and this is one of those consequences,” she said. “You’re starting in the dark.”

    HHS officials have pushed back on criticism, telling the BBC that the CDC continues to collaborate with more than 3,000 local and state health departments to collect cyclospora data through alternative surveillance systems, and that overall health funding for foodborne illness work has “remained stable”. However, state health departments across the country report feeling the impact of reduced federal support. In Colorado, which has recorded 90 cases this year in line with typical annual totals, the state health department confirmed it has received less federal funding and operates with fewer staff assigned to case monitoring. “While our colleagues at the CDC are working hard to support state partners, we have had to adapt to federal changes,” said Hope Shuler, a spokesperson for Colorado’s public health department. The state has continued all core testing, monitoring and data reporting to the CDC despite the cuts, she added.

    Not all experts agree that the post-cut system is failing: Manderach noted that federal food safety agencies have largely maintained previous performance standards despite restructuring that began during the Trump administration, adding that “while yes, I do think there were challenges early on, most of those seem to have resolved.”

    Other public health leaders point to competing priorities that have stretched federal resources thin, including the ongoing deadly Ebola outbreak in the Democratic Republic of the Congo that has demanded significant attention and funding. This resource strain has shifted more responsibility for foodborne illness outbreak investigations to state governments, explained Nancy Glick of the National Consumers League. “States are doing that now, but they don’t have the resources that the CDC had,” she said.

    Currently, the core investigative work relies on time-consuming interviews with every person who tests positive for cyclospora, asking them to recount every food they consumed in the two weeks before they developed symptoms. Investigators hope to identify a common contaminated product or exposure point that can be pulled from the market to end the outbreak. But experts note that this work requires extensive staffing, a resource many small local health departments simply do not have available. “It is pretty straightforward, but it takes a lot of person power to do it,” said David Weber, a professor of medicine, pediatrics and epidemiology at University of North Carolina at Chapel Hill.

    For American consumers, the ongoing uncertainty has left them to rely on general prevention measures to avoid the uncomfortable illness. “At the moment, the list of things that you need to be concerned about is unfortunately quite long, making it feel really hard to control,” Guest said.

  • An experimental Alzheimer’s drug shows promise targeting a different brain protein, new study shows

    An experimental Alzheimer’s drug shows promise targeting a different brain protein, new study shows

    LONDON – Researchers unveiled groundbreaking new findings Tuesday at the Alzheimer’s Association International Conference, revealing that an experimental drug from Biogen offers a novel path to slow early-stage Alzheimer’s disease by targeting a destructive brain protein long considered difficult to treat. Unlike today’s approved therapies that focus on clearing a different toxic protein linked to the condition, this new candidate works by reducing the production of tau, a protein that forms deadly tangles in neurons and drives cognitive decline.

    Alzheimer’s, the leading cause of dementia worldwide, impacts more than 7 million people in the United States alone and tens of millions globally. For years, the majority of approved treatments have centered on clearing amyloid, a sticky protein that forms plaques in the brain up to two decades before symptoms emerge. While the two currently approved drugs, lecanemab and donanemab, can modestly slow cognitive decline by removing amyloid buildup, scientists have long recognized that amyloid alone does not cause Alzheimer’s. The dominant scientific model holds that amyloid accumulation ultimately triggers abnormal tau to clump into tangles that kill brain cells, making tau a critical yet underexploited target for new therapies. Prior attempts to develop tau-targeting drugs have repeatedly failed, leaving a critical gap in treatment development.

    Biogen’s new candidate, diranersen, works through a fundamentally different mechanism than existing amyloid-focused drugs. Classified as an antisense oligonucleotide, the drug does not attack existing tau buildup; instead, it instructs the gene that produces tau to generate less of the protein. “If you lower tau production, you are lowering the amount of the abnormal tau that needs to be cleared by the microglia, by the clearance mechanism in the brain. And so you are enabling the normal clearance mechanism to have more capacity to clear the tau,” explained Dr. Cath Mummery of University College London, who led the phase 2 study of the drug. Unlike approved amyloid drugs that are delivered via intravenous infusions or injections into the bloodstream, diranersen is administered via injection into the fluid surrounding the spinal cord, providing a more direct route to brain tissue.

    The phase 2 trial enrolled roughly 400 patients with mild cognitive impairment or early-stage Alzheimer’s, who were randomly assigned to receive varying doses of diranersen or a placebo. In an unexpected finding announced earlier this year by Biogen and its development partner Ionis Pharmaceuticals, the lowest dose – given just twice per year – produced the strongest effect, meaning the study did not meet its pre-planned endpoint of demonstrating greater benefit from higher doses. Despite this miss, new data presented this week shows encouraging signs of cognitive benefit: five out of six cognitive tests showed that patients receiving diranersen still experienced cognitive decline, but at a markedly slower rate than patients given a placebo. For the lowest dose group, the decline rate slowed by 26% – a reduction comparable to the benefits seen in clinical trials of approved amyloid drugs.

    Notably, side effects reported in the trial were mild, including injection site pain and temporary confusion that resolved within roughly a week of treatment. Crucially, researchers observed no cases of brain swelling or inflammation, a common and potentially dangerous side effect linked to amyloid-targeting drugs.

    Independent researchers not involved with the Biogen study called the results a promising step forward for the field. “This is really quite promising if it were to hold up” in larger-scale confirmatory testing, said Jessica Langbaum of the Banner Alzheimer’s Institute in Phoenix. While Dr. Reisa Sperling of Mass General Brigham emphasized that the results are still early, she noted that the findings “will reinvigorate interest and investment in lots of tau mechanisms, and the field needs that.” Biogen has confirmed it plans to launch a large-scale phase 3 trial to confirm the drug’s clinical benefit.

    Diranersen is just one of multiple innovative new approaches to Alzheimer’s treatment presented at the conference, reflecting a growing shift in the field toward targeting tau and exploring combination therapies. Last week, the University of California, San Francisco launched the first-of-its-kind Alzheimer’s Tau Platform, a National Institutes of Health-funded study that will test multiple experimental anti-tau therapies, both alone and in combination with approved amyloid treatments. The first candidate to be tested through the platform is AADvac1, a tau vaccine designed to train the body’s immune system to recognize and attack abnormal tau. The platform will expand to sites across the U.S. and will even include patients who have tau and amyloid buildup but have not yet developed cognitive symptoms, allowing researchers to test the potential of early intervention.

    Other researchers are exploring repurposing existing drug candidates for Alzheimer’s prevention. Scientists reported that obicetrapib, an experimental cholesterol-lowering drug, may hold promise for reducing Alzheimer’s protein buildup in people with a genetic risk for the disease. The APOE4 gene, the strongest known genetic risk factor for late-onset Alzheimer’s, also impacts how the body processes cholesterol, leading researchers to hypothesize that cholesterol-lowering drugs could mitigate this elevated risk. NewAmsterdam Pharma, the developer of obicetrapib, plans to launch a clinical trial soon to test this hypothesis in carriers of one or two copies of the APOE4 gene.

    Companies are also advancing new technologies to overcome one of the biggest barriers to Alzheimer’s drug development: penetrating the blood-brain barrier, a protective lining that blocks most large molecules from entering brain tissue. Denali Therapeutics is developing technology that “hitches a ride” on iron, a molecule that naturally crosses the blood-brain barrier, to deliver both anti-tau and anti-amyloid drugs to the brain in higher concentrations.

    The new wave of tau-focused research comes as the field continues to search for more effective treatments for a disease that is projected to see a sharp rise in cases globally as populations age. While diranersen still requires years of additional testing before it could win regulatory approval, researchers say its early success has already re-energized work on a long-overlooked target that could be key to slowing or stopping Alzheimer’s progression.

    This reporting was supported by the Howard Hughes Medical Institute’s Department of Science Education and the Robert Wood Johnson Foundation, with the Associated Press taking sole responsibility for all content.

  • Majority of new Ebola cases are ‘from unknown chains of transmission,’ WHO official says

    Majority of new Ebola cases are ‘from unknown chains of transmission,’ WHO official says

    GENEVA — The World Health Organization’s top emergencies official issued a stark warning Tuesday, stating that the ongoing Ebola outbreak in the eastern region of the Democratic Republic of the Congo is still moving faster than international and local response teams can contain, following a firsthand assessment trip to one of the crisis’s hardest-hit areas. Chikwe Ihekweazu, WHO’s emergencies chief, returned this week from Bunia, located in Ituri province, the epicenter of the current outbreak, where he uncovered deeply troubling trends driving the virus’s spread.

    According to Ihekweazu, the most worrying observation from his visit is that a large share of newly reported fatalities are people who never accessed formal medical care, passing away in their home communities before they could reach a treatment facility. As of this week, he added, roughly 80 percent of all new confirmed cases are not linked to existing contact tracing lists, meaning they originate from unknown transmission chains that response teams have not been able to track or pre-empt.

    The DRC has been fighting this outbreak of the rare Bundibugyo Ebola variant since undetected community transmission began in early May, with no approved vaccine or specific antiviral treatment currently available for this strain. The Africa Centres for Disease Control and Prevention labeled the event the fastest-expanding Ebola outbreak the African continent has ever seen last week.

    Congolese health authorities released updated figures Monday showing at least 1,926 confirmed and probable infections across three affected provinces, with a total of 702 recorded deaths. The outbreak has already spilled across national borders, with confirmed cases detected in neighboring Uganda, raising concerns of a wider regional spread. Last week, the U.S. Centers for Disease Control and Prevention announced that a U.S. citizen working for a humanitarian organization in the DRC had tested positive for the virus, though no additional details about the patient’s condition or location were released.

    Ihekweazu noted that his trip to Bunia revealed mixed progress: while response capacity has expanded significantly in recent weeks, systemic barriers continue to prevent teams from getting ahead of the virus. Local treatment capacity now stands at nearly 800 beds, with new spaces added every week, and laboratory testing capacity has jumped dramatically from just one operational lab at the start of the outbreak to 14 fully functional facilities. Other core response operations have also seen incremental improvements.

    Still, Ihekweazu emphasized that even with these gains, response teams have not managed to overtake the virus’s spread. “Despite our best efforts … we have not caught up in the race,” he told reporters in Geneva.

    The response effort has been held back by a range of interconnected challenges, including a critical shortfall in funding, repeated violent attacks on health facilities operating in the region, ongoing armed conflict that makes large parts of eastern DRC inaccessible to response teams, and widespread mistrust of medical authorities among local communities. These barriers compounded this week, when dozens of staff members at an Ebola treatment center in northeastern DRC launched a strike Monday over months of unpaid salaries and performance bonuses, further disrupting care delivery.

    The Congolese government only officially declared the outbreak on May 15, after the virus had been spreading undetected through local communities for multiple weeks, the WHO confirmed. Last week, researchers finally launched long-awaited clinical trials for experimental treatments, marking the first formal effort to test targeted interventions against the current circulating strain.

  • Hours each day in an iron lung kept her breathing, her will to live kept her alive

    Hours each day in an iron lung kept her breathing, her will to live kept her alive

    Martha Lillard, the United States’ last remaining person who relied on an iron lung to breathe after contracting polio, died at her home in Oklahoma at the age of 78 on June 26. For nearly three-quarters of her life, the large metal breathing device defined her daily routine — but it never defined her spirit, her family says.

    Lillard was just 5 years old when she was diagnosed with paralytic polio in the mid-1950s, one year before the first widespread polio vaccine rolled out across the U.S. Waking up one morning unable to lift her head from her pillow, she already understood what her symptoms meant: widespread public fear of the incurable disease dominated conversations at the time, and the young girl immediately recognized the signs of the infection that had already left so many children dead or disabled.

    After her diagnosis, Lillard spent decades dependent on the iron lung, a negative-pressure respiratory device that works by adjusting air pressure inside a sealed metal cylinder to force the lungs to expand and contract, doing the work of weakened respiratory muscles automatically. While many children who relied on the machine feared it, Lillard never shared that anxiety, according to her younger sister Cindy McVey. Instead, the device felt like a recharge, leaving her feeling refreshed after daily sessions inside it.

    Against all odds, Lillard and her family refused to let her condition limit the life she built. Determined to let her live as independently as possible, her uncle and grandfather engineered a custom modification to the iron lung that let Lillard open and close the device on her own, granting her the ability to live alone that most other iron lung users never had. Loved ones also retrofitted a car to match her limited mobility: the steering wheel was repositioned to rest in her lap, and turn signals were moved to the floor, letting Lillard drive herself wherever she wanted to go.

    Over her decades of life, Lillard cultivated a rich set of passions. She became a skilled painter, creating detailed landscape works, and was an avid learner who constantly asked questions of her smart speaker to expand her knowledge. She also shared more than 20 years with her partner Baha Salh, who moved to the U.S. from Egypt after securing a visa earlier this year. The pair married in February, just four months before Lillard’s death.

    While her official cause of death is listed as post-polio syndrome and chronic pulmonary failure, McVey says long COVID-19 ultimately contributed to her sister’s passing. Even so, McVey says her sister remained resilient and resourceful throughout her entire life: “She was resilient, she would find a way, or make do.”

    Lillard’s story comes amid a renewed reckoning over polio and vaccine access in the U.S. After the polio vaccine was introduced in 1955, a nationwide mass vaccination campaign eliminated endemic polio in the U.S. by 1979, a major public health victory that ended the regular outbreaks that killed and paralyzed thousands of children annually. According to the World Health Organization, roughly 1 in 200 polio infections result in permanent paralysis, and 5 to 10 percent of paralyzed patients die when their breathing muscles become immobilized.

    Today, however, growing vaccine hesitancy across the U.S. has put that progress at risk. Earlier this year, Kirk Milhoan, chair of the Centers for Disease Control and Prevention’s Advisory Committee on Immunization Practices, drew controversy after suggesting that polio vaccination should be made optional, arguing that improved sanitation and lower current risk mean the tradeoff between vaccine risk and disease risk has shifted.

    That rhetoric and the trend of declining childhood vaccination leave McVey deeply worried. Speaking through tears, she warned that fading cultural memory of polio’s devastation has led generations to underestimate the danger of the disease. “Polio is terrible. The disease disfigures, disables and leaves people trapped. We had it under control here and now we have all these people who aren’t vaccinating their children,” she said. “They may think there’s problems with the vaccine, but there’s a whole lot more problems if they don’t vaccinate.”

    McVey also noted just how narrow the gap was between her sister’s fate and a polio-free life: Lillard was infected the year before the vaccine became widely available, and McVey had friends who participated in the vaccine trials that same year. “It was that close,” she said.

  • Why the fastest-growing Ebola outbreak in history is becoming more challenging

    Why the fastest-growing Ebola outbreak in history is becoming more challenging

    What is already the fastest-expanding Ebola outbreak in recorded history is pushing response teams to their breaking point in eastern Democratic Republic of the Congo, where overlapping security, logistical and social crises have collided just as researchers launch the first clinical trial for life-saving treatments targeting this rare, untreatable strain of the virus.

    The outbreak, driven by the little-studied Bundibugyo Ebola virus, a subtype with no licensed vaccines or proven treatments, has already reached a grim milestone: the DRC Ministry of Health has confirmed nearly 2,000 cases and 702 deaths to date. Worse, suspected cases have now been detected in two additional provinces, including Kisangani, one of the country’s largest urban centers, leaving responders scrambling to map the full scope of the outbreak. Experts now confirm the initial spread went undetected for weeks, as health teams initially tested for more common Ebola subtypes, and the outbreak’s zoonotic origin remains a mystery.

    Unlike better-documented Ebola strains, Bundibugyo is a rare variant that spreads through direct contact with infected bodily fluids—including blood, vomit, and semen—or contact with contaminated materials such as bedding and clothing. Like other Ebola variants, it causes severe, often fatal symptoms ranging from high fever, muscle pain, vomiting and diarrhea to internal and external bleeding. Outbreaks of this strain have historically been limited to remote Central African villages near tropical rainforests, and public health guidance has restricted traditional local funeral practices that involve close contact with deceased loved ones—a measure that has sparked significant anger among local communities.

    Compounding every challenge of this outbreak is the volatile, conflict-ravaged landscape where it is unfolding. Decades of violence by armed rebel groups have left local populations traumatized and deeply distrustful of outside authorities, leading to widespread misinformation that claims the Ebola outbreak is a hoax. Community outreach workers have faced threats and abuse while trying to spread prevention information, and attacks on health facilities have repeatedly disrupted response work. A portion of the outbreak is centered in Goma, a major humanitarian hub and key city that was seized by Rwanda-backed rebel forces more than a year ago, creating further barriers to coordinated relief efforts.

    The latest and most urgent threat to containment efforts came this week, when unpaid frontline workers at the outbreak’s epicenter Ituri province walked off the job. The strike shuttered a core treatment center, with workers blocking access to the facility and burning tires to protest weeks of unfulfilled pay from the Congolese government, after weeks of high-risk work. Striking staff include epidemiologists, contact tracers, drivers, and gravediggers—all critical roles in stopping transmission. Congolese health officials have confirmed they are currently negotiating with workers to resolve the dispute, but public health experts warn that if the strike spreads to other overstretched, underfunded facilities across the region, it could deliver a catastrophic blow to already strained containment efforts. Infrastructure across the affected area is already extremely limited, leaving even fully staffed facilities struggling to operate.

    This unrest has erupted at an exceptionally vulnerable moment for the response. Just weeks before the strike, researchers officially launched the first clinical trial for two promising experimental treatments targeting Bundibugyo Ebola, and have already begun enrolling the first participants.

    The two candidate therapies are remdesivir, a broad-spectrum antiviral developed by Gilead Sciences that is already approved for COVID-19 treatment and has shown preliminary antiviral activity against Bundibugyo in laboratory testing, and MBP134, an experimental monoclonal antibody therapy developed by Mapp Biopharmaceutical that is specifically engineered to target multiple Ebola strains, including Bundibugyo.

    Under the trial protocol overseen by the World Health Organization, patients will be randomly assigned to receive either the current standard of care alone, standard care plus remdesivir, standard care plus MBP134, or standard care plus both investigational treatments. The WHO has cautioned that it could take months of data collection and up to 1,000 trial participants before researchers can confirm whether either treatment is effective. Currently, the trial is only being run at one Ituri province treatment center—an unaffected facility separate from the strike site—and officials plan to expand the trial to additional sites only once security and staffing conditions allow.