Scientists identify new dementia affecting millions of elderly

A recently recognized form of dementia, known as LATE, is reshaping understanding of cognitive decline in the elderly, with rising diagnoses and guidelines for doctors published this year. It is estimated to affect about one-third of people aged 85 or older and 10% of those aged 65 or older, often mistaken for Alzheimer's. Experts emphasize the need for a broader range of treatments for this condition.

Limbic-predominant age-related TDP-43 encephalopathy (LATE) is emerging as a distinct disease from Alzheimer's, though it often coexists with it. According to recent guidelines, it affects about one-third of people aged 85 or older and 10% of those aged 65 or older. "In about 1 in 5 people who come to our clinic, what was previously thought to be Alzheimer's disease actually appears to be LATE," says Greg Jicha, a neurologist at the University of Kentucky.

LATE progresses more slowly than pure Alzheimer's and mainly impacts memory, with symptoms like difficulty finding words. However, when combined with Alzheimer's, the condition worsens, leading to faster decline and severe symptoms such as psychosis and incontinence. About half of 85-year-olds with severe Alzheimer's also have LATE, according to Pete Nelson of the Sanders-Brown Center.

The recognition of LATE followed a 2018 meeting of 35 Alzheimer's researchers, resulting in a 2019 report defining it by abnormal TDP-43 protein accumulations, unlike amyloid plaques and tau tangles in Alzheimer's. Identified in 2006, TDP-43 is linked to disorders like amyotrophic lateral sclerosis.

In the case of Ray Hester, 79, initial tests suggested Alzheimer's, but detailed exams revealed LATE, without amyloid buildup. Diagnosis involves hippocampus imaging, which shrinks more in LATE, and symptom assessment.

Patients with pure LATE do not qualify for recently approved anti-amyloid drugs. A clinical trial at the University of Kentucky is testing nicorandil, an angina medication, in 64 participants with mild memory issues. The cause remains unknown, but the APOE4 gene raises risk.

Experts like David Wolk and Reisa Sperling note that mixed pathologies may explain modest results in Alzheimer's treatments, underscoring the need for LATE-specific research.

Makala yanayohusiana

Illustration of an elderly woman reviewing medical charts linking late-life depression to early signs of Parkinson’s disease or Lewy body dementia.
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Late-life depression may precede Parkinson’s disease or Lewy body dementia, Danish registry study suggests

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Depression diagnosed for the first time in older adults was more common in the years leading up to a diagnosis of Parkinson’s disease or Lewy body dementia and remained elevated for years afterward, according to a large Danish registry study. The authors said the pattern—stronger than in several other chronic illnesses—supports the possibility that depression can be an early feature of these neurodegenerative conditions rather than only an emotional response to disability.

As the population ages, more people are affected by memory diseases like Alzheimer's. However, research in the field is progressing slowly, and only about half of those affected receive the available treatment.

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Researchers at Scripps Research have developed a blood test that detects Alzheimer's disease by analyzing structural changes in blood proteins. The method identifies differences in three specific proteins, allowing accurate distinction between healthy individuals, those with mild cognitive impairment, and Alzheimer's patients. Published in Nature Aging on February 27, 2026, the findings could enable earlier diagnosis and treatment.

Researchers at University College London have found that up to 93 percent of Alzheimer's cases may be linked to variants of the APOE gene, far more than previously estimated. The analysis, published in npj Dementia, also indicates that nearly half of all dementia cases could depend on this gene. The discovery underscores APOE as a key target for future treatments.

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Scientists at Brown University have identified a subtle brain activity pattern that can forecast Alzheimer's disease in people with mild cognitive impairment up to two and a half years in advance. Using magnetoencephalography and a custom analysis tool, the researchers detected changes in neuronal electrical signals linked to memory processing. This noninvasive approach offers a potential new biomarker for early detection.

New research finds that blood biomarkers associated with Alzheimer’s disease increase significantly faster in people with obesity than in those without. Drawing on five years of data from 407 volunteers, the study suggests that blood tests can detect obesity‑related changes earlier than brain scans, underscoring obesity as a major modifiable risk factor for Alzheimer’s.

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Researchers at Brazil’s Federal University of ABC report a simple copper-chelating molecule that reduced beta-amyloid–linked pathology and improved memory in rats. The compound showed no detectable toxicity in preclinical tests and, based on computer modeling, is predicted to cross the blood–brain barrier. The team is seeking industry partners for clinical development.

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