Lower Prevalence of Asymptomatic Alzheimer's Disease Among Healthy African Americans

Author:

Lah James J.123ORCID,Tian Ganzhong4,Risk Benjamin B.4,Hanfelt John J.24,Wang Liangkang4ORCID,Zhao Liping24,Hales Chadwick M.123,Johnson Erik C.B.123,Elmor Morgan B.12,Malakauskas Sarah J.12,Heilman Craig12,Wingo Thomas S.123ORCID,Dorbin Cornelya D.12,Davis Crystal P.12,Thomas Tiffany I.12,Hajjar Ihab M.12,Levey Allan I.123ORCID,Parker Monica W.12

Affiliation:

1. Department of Neurology Emory University School of Medicine, Emory Brain Health Center Atlanta GA USA

2. Emory Goizueta Alzheimer's Disease Research Center Emory University Atlanta GA USA

3. Center for Neurodegenerative Disease Emory University Atlanta GA USA

4. Department of Biostatistics and Bioinformatics, Rollins School of Public Health Emory University Atlanta GA USA

Abstract

ObjectiveAlzheimer's disease (AD) is believed to be more common in African Americans (AA), but biomarker studies in AA populations are limited. This report represents the largest study to date examining cerebrospinal fluid AD biomarkers in AA individuals.MethodsWe analyzed 3,006 cerebrospinal fluid samples from controls, AD cases, and non‐AD cases, including 495 (16.5%) self‐identified black/AA and 2,456 (81.7%) white/European individuals using cutoffs derived from the Alzheimer's Disease Neuroimaging Initiative, and using a data‐driven multivariate Gaussian mixture of regressions.ResultsDistinct effects of race were found in different groups. Total Tauand phospho181‐Tau were lower among AA individuals in all groups (p < 0.0001), and Aβ42 was markedly lower in AA controls compared with white controls (p < 0.0001). Gaussian mixture of regressions modeling of cerebrospinal fluid distributions incorporating adjustments for covariates revealed coefficient estimates for AA race comparable with 2‐decade change in age. Using Alzheimer's Disease Neuroimaging Initiative cutoffs, fewer AA controls were classified as biomarker‐positive asymptomatic AD (8.0% vs 13.4%). After adjusting for covariates, our Gaussian mixture of regressions model reduced this difference, but continued to predict lower prevalence of asymptomatic AD among AA controls (9.3% vs 13.5%).InterpretationAlthough the risk of dementia is higher, data‐driven modeling indicates lower frequency of asymptomatic AD in AA controls, suggesting that dementia among AA populations may not be driven by higher rates of AD. ANN NEUROL 2024;96:463–475

Funder

Roche Diagnostics

National Institute on Aging

Publisher

Wiley

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