Evidence map›Paper›PMID 40779734›Full record

ArticleNeurology2025

Associations of Longitudinal Changes in Blood Biomarkers of Dementia With the Proportion of Genetically Inferred African Ancestry.

Lu Wang, Huifang Xu, Ronald L Simons, Steven R H Beach, Man-Kit Lei, Mei Ling Ong, Robert A Philibert, Michelle M Mielke, Yitang Sun, Yueqi Lu and 3 more

Abstract read
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Lu WangDepartment of Genetics, University of Georgia, Athens.
Huifang XuDepartment of Genetics, University of Georgia, Athens.
Ronald L SimonsDepartment of Sociology, University of Georgia, Athens.
Steven R H BeachDepartment of Psychology, University of Georgia, Athens.
Man-Kit LeiDepartment of Sociology, University of Georgia, Athens.
Mei Ling OngCenter for Family Research, University of Georgia, Athens.
Robert A PhilibertDepartment of Psychiatry, University of Iowa, Iowa City.
Michelle M MielkeDepartment of Epidemiology and Prevention, Wake Forest University School of Medicine, Winston-Salem, NC.ORCID 0000-0001-7177-1185
Yitang SunDepartment of Genetics, University of Georgia, Athens.
Yueqi LuDepartment of Genetics, University of Georgia, Athens.
Charleston W K ChiangCenter for Genetic Epidemiology, Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles.
Burcu F DarstPublic Health Sciences, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-6205-4632
Kaixiong YeDepartment of Genetics, University of Georgia, Athens.ORCID 0000-0003-4658-7292

Funding

Psychosocial Context and the Biological Clock: Changes in Weathering during Middle-AgeR01AG055393 · NIA · UNIVERSITY OF GEORGIA · PI SIMONS, RONALD L · 2017 to 2021
$3.4M
Social Determinants of Inflammation and Metabolic Syndrom among African AmericansR01HL118045 · NHLBI · UNIVERSITY OF GEORGIA · PI SIMONS, RONALD L · 2014 to 2017
$2.3M
An evolutionary framework to elucidate and interpret the genetic architecture of complex traits in diverse populations - diversity supplementR35GM142783 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHIANG, CHARLESTON · 2021 to 2025
$2.2M
T32 Predoctoral Training Grant in GeneticsT32GM142623 · NIGMS · UNIVERSITY OF GEORGIA · PI Kelly A Dyer, Mary Grace Goll · 2022 to 2026
$2.1M
Gene-Environment Interactions in Human Evolution and Complex TraitsR35GM143060 · NIGMS · UNIVERSITY OF GEORGIA · PI YE, KAIXIONG · 2021 to 2025
$1.9M
Stress, Weathering, and Blood-Based Biomarkers of Alzheimer’s DiseaseR01AG077386 · NIA · UNIVERSITY OF GEORGIA · PI Steven R Beach, Michelle M Mielke · 2025 to 2026
$1.6M
NHLBI NIH HHS R01 HL118045NIA NIH HHS R01 AG055393NIA NIH HHS R01 AG077386NIGMS NIH HHS R35 GM142783NIGMS NIH HHS R35 GM143060NIGMS NIH HHS T32 GM142623
6 · The paper itself

Abstract

BACKGROUND AND

objectivesAfrican American individuals have a higher risk of Alzheimer disease (AD) and related dementia (ADRD) than non-Hispanic White individuals. Some cross-sectional studies with self-reported race and ethnicity have reported racial differences in circulating ADRD biomarkers, including phosphorylated tau181 (p-Tau181), glial fibrillary acidic protein (GFAP), and neurofilament light (NfL). We aimed to examine the associations of genetically inferred African ancestry proportion with the longitudinal changes in these biomarkers and to evaluate the associations of previously identified ADRD-related genetic factors in European cohorts with these biomarkers in an African American cohort.

methodsThis study used longitudinal data from the Family and Community Health Study, which was initiated in 1996, recruited and followed 889 African American families residing in Georgia and Iowa. Circulating p-Tau181, GFAP, and NfL were measured in serum samples collected in 2008 (wave 5) and 2019 (wave 8). Closely related individuals, genetically inferred to be third-degree relatives or closer, were excluded. Genetic ancestry proportions were inferred using the ADMIXTURE analysis. Multivariable regression analyses were performed to test the associations of African ancestry proportion with cross-sectional biomarker levels and their longitudinal changes over 11 years. We also tested the associations of selected genetic variants, polygenic scores, and

resultsOur cross-sectional sample included 573 participants (mean age = 55.1 years; 69% female), whereas our longitudinal sample included 225 (57.2 years; 80% female). African ancestry proportion was not associated with cross-sectional biomarker levels but was inversely associated with the longitudinal change in p-Tau181 (β = -14.50 pg/mL, DISCUSSION: We found suggestive evidence that a higher African ancestry proportion is associated with an attenuated increase in the blood p-Tau181 level over time. More research is needed to characterize the longitudinal dynamics of ADRD biomarkers across ancestry and the driving biological or sociocultural factors.

Indexed as

Black or African AmericanDementiaGlial Fibrillary Acidic ProteinNeurofilament Proteinstau ProteinsAgedAged, 80 and overAlzheimer DiseaseBiomarkersCross-Sectional StudiesFemaleHumansLongitudinal StudiesMaleMiddle AgedBiomarkersGFAP protein, humanGlial Fibrillary Acidic Proteinneurofilament protein LNeurofilament Proteinstau Proteins

Identifiers

PMID40779734
PMCPMC12341075

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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.