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APOE ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment

BACKGROUND: APOE ɛ4 and sex have been linked to increased risk for conversion to Alzheimer’s disease (AD). However, the relationship between APOE ɛ4 gene dose, sex, and AD biomarkers remains understudied. OBJECTIVE: To investigate the effect of APOE ɛ4 dose on AD biomarkers in a sample of older adul...

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Detalles Bibliográficos
Autores principales: Hobel, Zachary, Isenberg, A. Lisette, Raghupathy, Dhvani, Mack, Wendy, Pa, Judy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839478/
https://www.ncbi.nlm.nih.gov/pubmed/31424388
http://dx.doi.org/10.3233/JAD-180859
Descripción
Sumario:BACKGROUND: APOE ɛ4 and sex have been linked to increased risk for conversion to Alzheimer’s disease (AD). However, the relationship between APOE ɛ4 gene dose, sex, and AD biomarkers remains understudied. OBJECTIVE: To investigate the effect of APOE ɛ4 dose on AD biomarkers in a sample of older adults with mild cognitive impairment (MCI), and to examine whether APOE ɛ4 dose modifies AD risk differently in MCI women and men. METHODS: We examined cross-sectional AD biomarkers for participants with MCI (n = 930, 55–96 years old) from three large aging cohorts. Region of interest MRI volumes, global cognition, and episodic memory were analyzed by number of APOE ɛ4 alleles and stratified by sex. RESULTS: Across all participants, number of APOE ɛ4 alleles was associated with smaller hippocampal and amygdala volumes and poorer cognition. When stratified by sex, women showed an APOE ɛ4 dose effect for bilateral hippocampal and left amygdala volumes and cognition. In contrast, men showed an APOE ɛ4 dose effect for hippocampal volumes with a trend in amygdala, but cognition did not differ between men with 1 and 2 APOE ɛ4 alleles. Women with 2 APOE ɛ4 alleles had poorer memory between 65–69 and poorer global cognition between 70–74 compared to men with 2 APOE ɛ4 alleles. CONCLUSION: APOE ɛ4 confers a dose effect on AD biomarkers in patients with MCI, and the number of APOE ɛ4 alleles has a greater detrimental impact in women than men, which may be specific to a critical time window.