Evidence map›Paper›PMID 40297430›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Assessing Cognitive Decline and Dementia Risk in Black and White Older Adults with Blood Biomarkers pTau217, GFAP, NfL, and Aβ ratio.

Ana W Capuano, David A Bennett, Jeffrey L Dage, Kristen Russ, Konstantinos Arfanakis, Melissa Lamar, Lisa Barnes, Julie Schneider

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Ana W Capuano
David A Bennett
Jeffrey L Dage
Kristen Russ
Konstantinos Arfanakis
Melissa Lamar
Lisa Barnes
Julie Schneider

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Alzheimer's disease blood-based biomarkers are a cost-effective early-detection method that, for precision medicine reasons, needs to be studied in both Blackand White. Few studies have a long follow-up of cognition. We studied a blood-biomarkers panel, cognitive decline, and dementia risk in a large number of Black and White participants. Methods: Participants without dementia were followed annually up to 15 years, after plasma biomarker measurement (NfL, GFAP, amyloid-beta 42/40 ratio, pTau217). Data included demographics, medical history, blood tests (e.g., kidney function), MMSE, APOEε4, annual evaluations of cognition, and clinician-based dementia evaluation. The biomarkers' association with comorbidities, cognitive decline, and risk of dementia was examined within race. To examine racial differences, we repeated analyses using a subset Mahalanobis-balanced 1:1 on sex, age, education, Latino/Non-Latino, and clinical status (hypertension, diabetes, GFR, BMI, and heart disease). Results: Biomarkers were measured in 431 Black and 583 White (respectively mean age of 77 and 80, 17% and 21% men), generating a balanced sample of 366:366. Biomarker's levels were similar between races. Within races, the associations of blood biomarkers with multiple comorbidities (especially kidney dysfunction and BMI) remained after controlling for demographics, APOE ε4, and dementia or death within 5 years. Men had lower GFAP levels than women (all p=<0.001). pTau217 was associated with decline in global cognition and all domains within races, and when comparing races, it was associated with a faster decline in global cognition and semantic memory in Black. The discrimination of dementia of pTau217 (AUC Discussion: pTau217 was highly associated with dementia risk and cognitive decline. The association of blood biomarkers with cognitive decline in Black and White participants was similar. Higher levels of pTau217 were, however, associated with semantic memory decline in Black adults. The combination of pTau217 with other biomarkers or MMSE did not improve dementia discrimination.

Identifiers

PMID40297430
PMCPMC12036404

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.