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Researchers find a hint at how to delay Alzheimer's symptoms. Now they have to prove it

Researchers find a hint at how to delay Alzheimer's symptoms. Now they have to prove it

An experimental treatment appears to delay Alzheimer's symptoms in some people genetically destined to get the disease in their 40s or 50s, according to new findings from ongoing research now caught up in Trump administration funding delays.
The early results — a scientific first — were published Wednesday even as study participants worried that politics could cut their access to a possible lifeline.
'It's still a study but it has given me an extension to my life that I never banked on having,' said Jake Heinrichs of New York City.
Now 50, Heinrichs has been treated in that study for more than a decade and remains symptom-free despite inheriting an Alzheimer's-causing gene that killed his father and brother around the same age.
If blocked funding stops Heinrichs' doses, 'how much time do we have?' asked his wife, Rachel Chavkin. 'This trial is life.'
Two drugs sold in the U.S. can modestly slow worsening of early-stage Alzheimer's by clearing the brain of one of its hallmarks, a sticky gunk called amyloid. But until now, there haven't been hints that removing amyloid far earlier – many years before the first symptoms appear – just might postpone the disease.
The research led by Washington University in St. Louis involves families that pass down rare gene mutations almost guaranteeing they'll develop symptoms at the same age their affected relatives did – information that helps scientists tell if treatments are having any effect.
The new findings center on a subset of 22 participants who received amyloid-removing drugs the longest, on average eight years. Long-term amyloid removal cut in half their risk of symptom onset, researchers reported Wednesday in the journal Lancet Neurology.
Despite the study's small size, 'it's incredibly important,' said Northwestern University neuroscientist David Gate, who wasn't involved with the research.
Now participants have been switched from an earlier experimental drug to Leqembi, an IV treatment approved in the U.S., to try to answer the obvious next question.
'What we want to determine over the next five years is how strong is the protection,' said Washington University's Dr. Randall Bateman, who directs the Dominantly Inherited Alzheimer's Network of studies involving families with these rare genes. 'Will they ever get the symptoms of Alzheimer's disease if we keep treating them?'
Here's the worry: Bateman raised money to start that confirmatory study while seeking National Institutes of Health funding for the full project but his grant has been delayed as required reviews were canceled. It's one example of how millions of dollars in research have been stalled as NIH grapples with funding restrictions and mass firings.
At the same time researchers wonder if NIH will shift focus away from amyloid research after comments by Dr. Jay Bhattacharya, nominated as the agency's new director.
'One of the reasons I think that we have not made progress in Alzheimer's, as much as we ought to have, is because the NIH has not supported a sufficiently wide range of hypotheses,' Bhattacharya told senators, responding to one who brought up an example of earlier science misconduct unrelated to current research.
Scientists don't know exactly what causes Alzheimer's, a mind-destroying disease that affects nearly 7 million Americans, mostly late in life. What's clear is that silent changes occur in the brain at least two decades before the first symptoms -- and that sticky amyloid is a major contributor. At some point amyloid buildup appears to trigger a protein named tau to begin killing neurons, which drives cognitive decline.
Tau-fighting drugs now are being tested. Researchers also are studying other factors including inflammation, the brain's immune cells and certain viruses.
NIH's focus expanded as researchers found more potential culprits. In 2013, NIH's National Institute on Aging funded 14 trials of possible Alzheimer's drugs, over a third targeting amyloid. By last fall, there were 68 drug trials and about 18% targeted amyloid.
Northwestern's Gate counts himself among scientists who 'think amyloid isn't everything,' but said nothing has invalidated the amyloid hypothesis. He recently used brain tissue preserved from an old amyloid study to learn how immune cells called microglia can clear those plaques and then switch to helping the brain heal, possible clues for improving today's modest therapies.
For now, amyloid clearly is implicated somehow and families with Alzheimer's-causing genes are helping answer a critical question for anyone at risk: Can blocking amyloid buildup really stave off symptoms? Without NIH funding, Bateman said, that opportunity will be lost.
'It's absolutely insane,' said longtime study participant June Ward, who lives near Asheville, North Carolina, and plans to ask friends to complain to lawmakers.
Ward turns 64 in June and is healthy, two years older than when her mother's symptoms appeared. 'It is exciting to think about the possibility that Alzheimer's disease might not be what gets me,' she said.
In New York, Heinrichs said he has hope that his 3-year-old son won't 'experience the stress and sorrow that I lived through as a young man to watch my father fade away.'
'We need the NIH to be not politicized,' added Chavkin, his wife. 'It's just about keeping people alive or helping them live better. And in this case, it's helping my husband survive.'
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Trump's palace coup leaves NASA in limbo
Trump's palace coup leaves NASA in limbo

The Hill

time33 minutes ago

  • The Hill

Trump's palace coup leaves NASA in limbo

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Endangered species deserve a home, too
Endangered species deserve a home, too

The Hill

time3 hours ago

  • The Hill

Endangered species deserve a home, too

The elusive Northern Spotted Owl. The majestic Whooping Crane. Charismatic Florida panthers and beloved Monarch butterflies. These and many other endangered species now face even graver threats in the wake of two recent developments in the world of conservation. On Apr. 7, the billion-dollar biotech firm Colossal announced the 'de-extinction' of the dire wolf, a canine species that vanished in the Late Pleistocene (approximately 13,000 years ago). And on Apr. 17, the Trump administration revealed its intention to weaken decades-old endangered species protections by redefining a key word: harm. This narrower definition effectively rescinds protection of an endangered species' habitat, limiting harm to actions that 'directly' harass, injure or kill organisms. What these two developments have in common is a disregard for the vital connection that exists between species and the places they call home. Habitat refers to the place where an organism naturally or normally lives. Removal of habitat protection opens the door to logging, development and extraction of oil and minerals. The proposed definition of harm could convert fragile wetlands into farmland, migration corridors into freeways and nesting sites into beachfront property — and none of this would qualify as harm to the creatures who live there. A habitat includes the specific resources and conditions that a given species needs to survive — the plants or animals it feeds on, and particular features of topography, soil, climate and water. Some species are especially vulnerable to extinction because they require a very rare or specific type of habitat. Others are at risk because they range across several. Many butterfly species, for example, are reliant on a single host plant for every stage of their life cycle — mating, laying eggs and feeding their young. Even plants closely related to the host plant cannot replace these vital functions, however indistinguishable they may appear to the human eye. Migratory creatures, meanwhile, depend upon many habitats in far-flung geographic locations. A recent study found that approximately half of all migratory species are in decline. Annually, billions of migratory birds crisscross state and national boundaries, with varying degrees of legal protections for the places where they nest, feed or rest. Further erosion of habitat protection could be the death knell for these and other vulnerable species. Were species not so intimately tied to their environments, it might make sense to regard lab-created or genetically engineered organisms, like the recently unveiled dire wolves, as suitable replacements for endangered or extinct species. Conservation would be akin to curating museum or zoo specimens, with living representatives of endangered species, or mere samples of their genetic material, maintained in artificial environments. Disregard for the importance of habitat is evident in the fanfare over Colossal's so-called dire wolves — more accurately, grey wolves with dire wolf DNA spliced into their genome. Consider that in their original Pleistocene environments, true dire wolves preyed upon large herbivorous megafauna that are now extinct: sloths, mastodons, giant bison and camels. By contrast, Remus, Romulus and Khaleesi, the telegenic trio of fluffy white wolves created by Colossal, will live their entire lives in a highly secured, undisclosed site, subsisting on a hand-fed diet of ground meats and kibble. In short, the same flawed logic lies behind the dire wolf 'de-extinction' and the Trump proposal to redefine harm: Both treat species as if they live in a vacuum. Doug Burgum, the Trump-appointed secretary of the Interior, exemplified this sort of thinking when he took to social media to hail de-extinction as the 'bedrock' of future conservation, arguing simultaneously for re-think of endangered species protections: 'It has been innovation—not regulation—that has spawned American greatness,' he said. Citing Colossal's breakthrough, Burgum questioned the need for an endangered species list. Ten days later, the administration moved to weaken endangered species regulation by excluding habitat from the definition of harm. Yet, habitat loss remains the primary culprit of species endangerment and extinction. While these losses can occur naturally through periodic events like fires or earthquakes, the vast majority of habitat degradation, fragmentation and loss stems from human activity: land development, deforestation, large-scale agriculture, air and water pollution, and human-caused climate change, among other factors. 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New Alzheimer's blood tests make diagnosis easier — but they're not right for everyone
New Alzheimer's blood tests make diagnosis easier — but they're not right for everyone

San Francisco Chronicle​

time4 hours ago

  • San Francisco Chronicle​

New Alzheimer's blood tests make diagnosis easier — but they're not right for everyone

The number of Americans with Alzheimer's disease, the most common cause of dementia in the U.S., is projected to rise significantly in the coming decades. The devastating disease has no cure, but the past several years have brought promising developments in new drug therapies and blood tests that help doctors treat and diagnose the disease. Here's what to know about the blood tests that diagnose Alzheimer's, one of which got full FDA approval in May. How they work Several commercially available blood tests have become available the past few years, most recently from biotech company Fujirebio Diagnostics, which got full approval from the FDA last month. Each test measures slightly different things, but overall they look for abnormal levels of certain proteins — amyloid and tau — in the blood. The accumulation of amyloid and tau proteins in the brain, often called plaques, are hallmark signs of Alzheimer's. If someone has tau plaques in the brain, for instance, some of that will leak out of the brain into the blood, resulting in a blood test result showing higher than normal levels of tau. In patients with symptoms of cognitive impairment, the tests predict an Alzheimer's diagnosis with about 90% accuracy. Why they're important The blood tests are a notable development because they are less expensive and less invasive than other types of testing that doctors have long used to diagnose patients with Alzheimer's. One is a PET scan, which involves injecting a patient with a radioactive tracer that binds to amyloid or tau in the brain so the presence of the proteins can be seen in a scan. It can cost several thousand dollars, compared to several hundred dollars for a blood test. The other is a spinal tap, which is painful or uncomfortable for many people. This method measures different forms of amyloid and tau in the spinal fluid. 'Up until these blood tests came out, a physician was stuck doing a PET scan or spinal tap, so not great options,' said Dr. Frank Longo, a professor of neurology at Stanford Medicine. 'The big breakthrough is finding something to measure in the blood that's about 90% accurate of what's going on in the brain, about as accurate as spinal fluid or a PET scan.' Doctors use the blood test as part of a broader medical evaluation that also includes a patient history, neurological exam and other testing. The blood test can help rule out Alzheimer's as the cause of a patient's cognitive impairment and potentially avoid unnecessary further testing. If someone's blood test comes back normal, for example, they may not have to undergo the PET scan or spinal tap, and their doctor can look into other potential causes of the cognitive impairment. 'That's the biggest practical thing it's doing now,' Longo said. It's important to distinguish Alzheimer's from other types of dementia because there are Alzheimer's treatments that have come out the last few years that help slow the progression of Alzheimer's. But patients must be in relatively early stages of the disease, with mild impairment or mild dementia, to be eligible. Some of the therapies have significant side effects, so patients would not want to start them unless they knew it was Alzheimer's, and not something else, causing the dementia. They're not for everyone The tests are approved only for people who already have symptoms of cognitive impairment and are of a certain age — 55 and over or 60 and over, depending on the test. They are not approved for healthy adults with normal cognition who want to diagnose or rule out Alzheimer's, or who are simply curious if they are at risk for developing Alzheimer's. They must be ordered by a doctor. They're becoming more common, but may not be covered by insurance Some of the blood tests have been available for a year or two, Longo said, but they were under an earlier and more limited type of FDA approval, not the full approval that the agency granted last month to the Fujirebio test. So they are poised to become more common. 'A year ago, most of my colleagues and I were not ordering these,' Longo said. 'I'd say less than 5% or 10% of the time we were ordering these. Now people are starting to order them in symptomatic patients. It's not rare now. They're starting to be recognized more.' Some primary care doctors are starting to order the tests as well, said Dr. Armen Moughamian, medical director of Sutter Health's Ray Dolby Brain Center at CPMC in San Francisco. The center treats patients with memory disorders. 'It's definitely a minority, but I've been seeing it done,' he said. As with many new medical tests, insurers may not cover them yet, but that usually evolves over time. Full FDA approval may help make the case for the tests to be covered, Longo said. 'There is some uncertainty and lack of clarity about whether insurance and Medicare pay,' Moughamian said. 'That creates some hesitancy for providers to order it.' They may one day be used to screen and diagnose healthy people earlier In people with Alzheimer's, amyloid plaques begin to form in the brain as many as 20 years before they show symptoms. Right now, newer therapies for Alzheimer's — like lecanemab and donanemab, which slow the progression of the disease — are approved only for people with symptoms. Those symptoms are mild cognitive impairment or mild dementia, the early stages of symptomatic Alzheimer's. This means people who have not yet developed symptoms, but who have amyloid plaques in the brain, cannot get these treatments. So if a blood test could be used in pre-symptomatic people, it could mean better screening and earlier diagnosis to larger groups of people. 'What we want to push for is earlier diagnosis because new therapies are available when we catch people in earlier stages,' Moughamian said. Moughamian is leading two clinical trials that examine whether drugs that remove amyloid in the brain, donanemab and another drug remternetug, can work in people who have amyloid plaques but have not yet developed symptoms. They are using an Alzheimer's blood test to see whether patients are eligible for the trial.

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