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ABSTRACT: Background/objective
The aim of this study was to determine if plasma concentrations of 5 surrogate markers of Alzheimer's disease (AD) pathology and neuroinflammation are associated with disease status in African Americans.Methods
We evaluated 321 African Americans (159 AD, 162 controls) from the Florida Consortium for African-American Alzheimer's Disease Studies (FCA3DS). Five plasma proteins reflecting AD neuropathology or inflammation (A?42, tau, IL6, IL10, TNF?) were tested for associations with AD, age, sex, APOE and MAPT genotypes, and for pairwise correlations.Results
Plasma tau levels were higher in AD when adjusted for biological and technical covariates. APOE?4 was associated with lower plasma A?42 and tau levels. Older age was associated with higher plasma A?42, tau, and TNF?. Females had lower IL10 levels. Inflammatory proteins had strong pairwise correlations amongst themselves and with A?42.Conclusion
We identified effects of demographic and genetic variants on five potential plasma biomarkers in African Americans. Plasma inflammatory biomarkers and A?42 may reflect correlated pathologies and elevated plasma tau may be a biomarker of AD in this population.
SUBMITTER: Deniz K
PROVIDER: S-EPMC7902984 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
Deniz Kaancan K Ho Charlotte C G CCG Malphrus Kimberly G KG Reddy Joseph S JS Nguyen Thuy T Carnwath Troy P TP Crook Julia E JE Lucas John A JA Graff-Radford Neill R NR Carrasquillo Minerva M MM Ertekin-Taner Nilüfer N
Journal of Alzheimer's disease : JAD 20210101 1
<h4>Background/objective</h4>The aim of this study was to determine if plasma concentrations of 5 surrogate markers of Alzheimer's disease (AD) pathology and neuroinflammation are associated with disease status in African Americans.<h4>Methods</h4>We evaluated 321 African Americans (159 AD, 162 controls) from the Florida Consortium for African-American Alzheimer's Disease Studies (FCA3DS). Five plasma proteins reflecting AD neuropathology or inflammation (Aβ42, tau, IL6, IL10, TNFα) were tested ...[more]