Apolipoprotein E (APOE) genotype, dementia, and memory performance among Caribbean Hispanic versus US populations

• Published in: Alzheimer's & dementia Vol. 19; no. 2; pp. 602 - 610
• Main Authors: Llibre‐Guerra, Jorge J., Li, Jing, Qian, Yuting, Llibre‐Rodriguez, Juan de Jesús, Jiménez‐Velázquez, Ivonne Z., Acosta, Daisy, Salas, Aquiles, Llibre‐Guerra, Juan Carlos, Valvuerdi, Adolfo, Harrati, Amal, Weiss, Jordan, Liu, Mao‐Mei, Dow, William H.
• Format: Journal Article
• Language: English
• Published: United States 01.02.2023
• Subjects: admixture; Aged; Alleles; Alzheimer Disease - epidemiology; Alzheimer Disease - genetics; Alzheimer's disease; apolipoprotein E; Apolipoprotein E4 - genetics; Apolipoproteins E - genetics; Blacks; Caribbean Region; cognitive performance; dementia; Female; Genotype; Hispanic or Latino - genetics; Hispanics/Latinos; Humans; Male; Non‐Hispanic Whites; Caribbean Region; admixture; Non-Hispanic Whites; apolipoprotein E; dementia; Blacks; cognitive performance; Alzheimer's disease; Hispanics/Latinos
• ISSN: 1552-5260; 1552-5279
• DOI: 10.1002/alz.12699

Introduction Apolipoprotein E (APOE) is considered the major susceptibility gene for developing Alzheimer's disease. However, the strength of this risk factor is not well established across diverse Hispanic populations. Methods We investigated the associations among APOE genotype, dementia prevalence, and memory performance (immediate and delayed recall scores) in Caribbean Hispanics (CH), African Americans (AA), Hispanic Americans (HA) and non‐Hispanic White Americans (NHW). Multivariable logistic regressions and negative binomial regressions were used to examine these associations by subsample. Results Our final dataset included 13,516 participants (5198 men, 8318 women) across all subsamples, with a mean age of 74.8 years. Prevalence of APOE ε4 allele was similar in CHs, HAs, and NHWs (21.8%–25.4%), but was substantially higher in AAs (33.6%; P < 0.001). APOE ε4 carriers had higher dementia prevalence across all groups. Discussion APOE ε4 was similarly associated with increased relative risk of dementia and lower memory performance in all subsamples.