Evidence map›Paper›PMID 42552753›Full record

Observational studyAlzheimer's & dementia : the journal of the Alzheimer's Association2026

The role of polygenic risk in Alzheimer's disease prediction for African Americans.

Christina G Hutten, Todd Beck, Denis Evans, Kumar B Rajan

Abstract readObservational Study
In one paragraph

Observational study in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2026. 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
–field-weighted citation impact
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

4 authors.

Christina G HuttenInternal Medicine-Epidemiology, Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois, USA.ORCID https://orcid.org/0000-0001-9957-5952
Todd BeckInternal Medicine-Epidemiology, Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois, USA.
Denis EvansInternal Medicine-Epidemiology, Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois, USA.
Kumar B RajanInternal Medicine-Epidemiology, Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois, USA.

Funding

Impact of Neuroinflammation on AD Occurrence: A Bi-Generational Population StudyR01AG073627 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI NEELUM T. AGGARWAL, DENIS A EVANS · 2021 to 2026
$14.0M
Preserving Cognitive Resilience: A Biracial Parent-Offspring Study (18-4674) - Feasibility StudyR01AG058679 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI EVANS, DENIS A, RAJAN, KUMAR B. · 2019 to 2024
$13.8M
A Population-Based Latinx Community Study of Alzheimer’s DiseaseUH2AG083289 · NIA · RUSH UNIVERSITY MEDICAL CENTER · PI KRUEGER, KRISTIN R, RAJAN, KUMAR B. · 2023 to 2024
$1.1M
NIA NIH HHS R01 AG058679NIA NIH HHS R01AG058679NIA NIH HHS R01 AG073627NIA NIH HHS R01AG073627NIA NIH HHS UH2 AG083289NIA NIH HHS UH2AG083289
6 · The paper itself

Abstract

introductionAfrican Americans (AAs) face a higher risk of Alzheimer's disease and related dementias (ADRD) than European Americans (EUs), yet the utility of polygenic risk scores (PRS) in AAs remains underexplored.

methodsA standardized dementia PRS was evaluated in the Chicago Health and Aging Project (n = 4336; 61% AA) for associations with ADRD and cognitive trajectories over 8.4 years.

resultsPRS predicted ADRD more strongly in EUs (c-index 0.86) than AAs (0.77); however, it conferred higher risk in AAs (hazard ratio [HR] = 1.36, 95% confidence interval [CI]: 1.04-1.78) compared to EU (HR = 1.13, 95% CI: 0.88-1.44). The PRS remained predictive among AAs after apolipoprotein E (APOE) ε4 adjustment (HR = 1.53, 95% CI: 1.03-2.27). Higher PRS associated with lower baseline cognition and faster decline (p < 0.05). DISCUSSION: PRS conferred greater ADRD risk in AAs and comparable rates of cognitive decline, despite stronger discrimination in EUs, adding to the limited knowledge of genetic contributions to ADRD risk among AAs beyond APOE ε4 alleles.

Indexed as

Alzheimer DiseaseBlack or African AmericanGenetic Predisposition to DiseaseMultifactorial InheritanceAgedAged, 80 and overApolipoprotein E4ChicagoFemaleGenetic Risk ScoreHumansMaleRisk FactorsWhiteApolipoprotein E4admixtureAlzheimer's disease and related dementiascognitive declinediverse populationspolygenic risk scorerisk stratification

Identifiers

PMID42552753
PMCPMC13438189

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Registered trials

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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.