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Sex differences in Alzheimer's disease blood biomarkers in a Caribbean population of African ancestry: The Tobago Health Study.
Rosano, Caterina; Karikari, Thomas K; Cvejkus, Ryan; Bellaver, Bruna; Ferreira, Pamela C L; Zmuda, Joseph; Wheeler, Victor; Pascoal, Tharick A; Miljkovic, Iva.
  • Rosano C; Department of Epidemiology School of Public Health University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Karikari TK; Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Cvejkus R; Department of Psychiatry and Neurochemistry Institute of Neuroscience and Physiology The Sahlgrenska Academy University of Gothenburg Gothenburg Sweden.
  • Bellaver B; Department of Epidemiology School of Public Health University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Ferreira PCL; Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Zmuda J; Department of Psychiatry University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Wheeler V; Department of Epidemiology School of Public Health University of Pittsburgh Pittsburgh Pennsylvania USA.
  • Pascoal TA; Tobago Health Studies Office Scarborough Tobago Trinidad and Tobago.
  • Miljkovic I; Department of Neurology School of Medicine University of Pittsburgh Pittsburgh Pennsylvania USA.
Alzheimers Dement (N Y) ; 10(2): e12460, 2024.
Article en En | MEDLINE | ID: mdl-38617114
ABSTRACT

INTRODUCTION:

Alzheimer's disease (AD) is increasing in the Caribbean, especially for persons of African ancestry (PAA) and women. However, studies have mostly utilized surveys without AD biomarkers.

METHODS:

In the Tobago Health Study (n = 309; 109 women, mean age 70.3 ± 6.6), we assessed sex differences and risk factors for serum levels of phosphorylated tau-181 (p-tau181), amyloid-beta (Aß)42/40 ratio, glial fibrillary acidic protein (GFAP), and neurofilament light chain (NfL). Blood samples were from 2010 to 2013 for men and from 2019 to 2023 for women.

RESULTS:

Women were more obese, hypertensive, and sedentary but reported less smoking and alcohol use than men (age-adjusted p < 0.04). Compared to men, women had worse levels of AD biomarkers, with higher p-tau181 and lower Aß42/40, independent of covariates (p < 0.001). In sex-stratified analyses, higher p-tau181 was associated with older age in women and with hypertension in men. GFAP and NfL did not differ by sex.

DISCUSSION:

Women had worse AD biomarkers than men, unexplained by age, cardiometabolic diseases, or lifestyle. Studying risk factors for AD in PAA is warranted, especially for women earlier in life.
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