News
FDA greenlights simple Alzheimer’s test

The US Food and Drug Administration (FDA) has approved a second blood test to detect Alzheimer’s disease, potentially speeding diagnosis for millions of patients.
The Elecsys pTau181 test measures protein levels in blood plasma that act as biomarkers for the degenerative brain disorder, offering a simpler alternative to costly brain scans for people aged 55 and over with symptoms of cognitive decline.
The approval marks another step toward making Alzheimer’s detection more accessible through routine blood testing rather than specialist imaging that can take weeks or months for diagnosis.
Developed by Swiss biotech company Roche with Eli Lilly, the test builds on evidence that certain blood proteins can indicate brain changes linked to Alzheimer’s disease.
The pTau181 protein it measures is a biomarker — a biological indicator of disease activity.
“By bringing Alzheimer’s blood-based biomarker testing into primary care, we can help patients and their clinicians get answers sooner to support them earlier in their journeys,” said Brad Moore, CEO and president of Roche Diagnostics North America.
The FDA approved the first Alzheimer’s blood test, Lumipulse, earlier this year.
That test, made by Japanese company Fujirebio, detects different protein biomarkers linked to the disease.
Alzheimer’s is currently diagnosed using brain scans that detect toxic protein build-up and other hallmarks of the disease. These procedures are expensive, often involve long waiting times, and are not widely available.
Blood tests could make early screening easier in primary care, though experts stress they cannot provide a definitive diagnosis on their own.
“This is another important step toward expanding access to Alzheimer’s disease diagnostic tools,” said Dr Joanne Pike, president and CEO of the Alzheimer’s Association.
“At the same time, it is important to understand this test is designed to rule out the presence of amyloid plaques. It is not a test that will give an Alzheimer’s disease diagnosis, nor is it a standalone tool for detection.”
Amyloid plaques are abnormal protein deposits that form between brain cells and are a hallmark of Alzheimer’s.
The blood test helps determine whether these plaques are likely present, guiding doctors on whether further testing is needed.
Roche said a clinical study involving more than 300 participants showed the test correctly identified people without Alzheimer’s signs in nearly 98 per cent of cases.
his accuracy could help reduce unnecessary brain scans and related costs.
Researchers at UC San Diego recently reported that rises in blood proteins following brain inflammation and nerve cell damage were linked to cognitive decline — evidence supporting development of blood-based early detection tools.
Dr Richard Isaacson, who established one of the first Alzheimer’s prevention clinics in the US, told CNN that additional blood tests would likely be needed to give a full picture of brain health.
“This single Roche test is looking at pTau181 as a single protein marker,” he said.
“But for people who are at risk for Alzheimer’s, to truly have the best accuracy and the most granularity to understand what’s going on, we’re going to need a panel of tests.
“And then we’re going to need to follow these tests over time.”
The Alzheimer’s Association said the test could help avoid unnecessary and expensive diagnostic procedures.
The Elecsys pTau181 test is designed to be used alongside clinical evaluation and other diagnostic tools, not as a replacement for full medical assessment.
Patients with positive results would typically undergo additional testing to confirm a diagnosis.
Both approved blood tests represent progress in improving Alzheimer’s detection, though experts emphasise that diagnosis still requires a combination of clinical, imaging and laboratory assessments.
As blood-based biomarker research advances, scientists hope combining several markers will give a clearer picture of brain health and disease progression — potentially allowing earlier intervention and better patient outcomes.
Wellness
Gut-friendly foods may damage heart, charity warns
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Diabetes patients face increased risk of undiagnosed heart failure

People with diabetes may have undiagnosed heart failure that could be detected by a simple screening blood test, research suggests.
The TARTAN-HF trial found that one in four patients with diabetes who had at least one other risk factor for heart failure had undiagnosed heart failure detected through screening with a blood test and ultrasound scanning of the heart.
Experts said the findings show the extent of unrecognised heart failure in people with diabetes, and how the condition can be detected using a widely available blood test called NT-proBNP, which measures how much strain the heart is under.
They suggest a heart failure screening programme for diabetics could improve diagnosis rates, lead to earlier treatment and potentially reduce the risk of hospitalisation and death.
The study, involving 700 patients, was led by the University of Glasgow in collaboration with AstraZeneca, Roche Diagnostics, Us2.ai, NHS Greater Glasgow and Clyde and NHS Lanarkshire.
Dr Kieran Docherty, clinical senior lecturer at the University of Glasgow’s School of Cardiovascular and Metabolic Health, said: “Our results from the landmark TARTAN-HF trial identified heart failure in a large proportion of people living with diabetes, emphasising the need for a heart failure screening strategy in this group of patients.
“We know that many of the symptoms and signs of heart failure are non-specific, and may go unrecognised as potentially being due to heart failure for a long time.
“The strategy used in our trial is simple and easy to implement in clinical practice, and will aid in the early identification of heart failure in people with diabetes, and facilitate the initiation of medications that we know improve outcomes in patients with heart failure.”
The study, which began more than three years ago, involved more than 700 people with diabetes from the two health board areas who had at least one other risk factor for heart failure.
They were randomly assigned either to receive heart failure screening or to continue with their usual care.
Researchers found screening uncovered a large number of previously unrecognised cases of heart failure. Around one in four, or 24.9 per cent, of those screened were found to have the condition within six months, compared with 1 per cent in the group continuing their usual care.
The study, involving patients with type 1 and type 2 diabetes, found almost all of the participants found to have heart failure had preserved ejection fraction, which can be difficult to detect without dedicated testing.
The findings of the TARTAN-HF trial were presented at the American College of Cardiology conference taking place from 28 to 30 March in New Orleans in the US.
Dr Edward Piper, medical director at AstraZeneca UK, said: “Delayed diagnosis and treatment of heart failure in people with type 2 diabetes contributes to poor long-term outcomes. TARTAN-HF demonstrates that targeted, risk-based screening can identify previously undiagnosed heart failure in approximately one in four high-risk patients with diabetes, enabling earlier intervention with guideline-directed therapy.”
Dr Christian Simon, head of global medical affairs at Roche Diagnostics, said: “We are proud to have supported the landmark TARTAN-HF trial. These findings demonstrate the transformative power of early, accessible diagnostics like the NT-proBNP blood test.
“By identifying unrecognised heart failure in people with diabetes, we enable clinicians to initiate appropriate treatments sooner, ultimately improving patient outcomes and lives.”
News
UK government announces £6.3m fund to boost men’s health

The UK has launched a £6.3m men’s health fund to back local projects aimed at helping men and boys live longer, healthier lives.
The Men’s Health Community Fund is a partnership between the Department of Health and Social Care, Movember and People’s Health Trust.
The government is contributing £3m, while the two charities are more than doubling that to take the total to £6.3m.
Grants will support community projects reaching underserved men and boys aged 16 and over, particularly in the most disadvantaged areas and at key points in their lives such as becoming a father, losing a job or retiring.
Projects could include support for new fathers, activities for men facing loneliness and social isolation, services to help young men engage with the health system, and support for men in work, out of work and moving into retirement.
The programme will bring together voluntary, community and social enterprise organisations to test new ways of reaching men who are least likely to use traditional health services.
An evaluation funded through the National Institute for Health and Care Research will assess what works and help inform future policy and delivery.
Health and social care secretary Wes Streeting said: “Too many men across the country are living shorter, less healthy lives, particularly those in our most disadvantaged communities.
“This new partnership will help men get the support they need in the places they feel most comfortable, their communities, among people they trust.
“By working with expert charities and local organisations, we can reach the men who are too often missed by traditional services and help them take better care of their mental and physical health.”
“It is a key step in delivering our first ever Men’s Health Strategy and driving forward our ambition to halve the gap in healthy life expectancy between the richest and poorest areas.”
The Men’s Health Strategy sets out plans to tackle the physical and mental health challenges men and boys face.
Men can be less likely to seek help and more likely to suffer in silence, while higher rates of smoking, drinking, gambling and drug use are damaging men’s health and affecting families, workplaces and communities.
The government is also investing £3.6m over the next three years in suicide prevention projects for middle-aged men in local communities across areas of England where men are most at risk, many of which are also among the most deprived. Suicide is one of the biggest killers of men under 50, and three-quarters of all suicides are men.
The projects will aim to break down barriers middle-aged men face in seeking support, including stigma around asking for help and a lack of awareness of what is available and how to access it.
They will be co-designed with experts and men with lived experience of mental health crises and suicidal thoughts.








