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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2019
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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 |
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author | Hobel, Zachary Isenberg, A. Lisette Raghupathy, Dhvani Mack, Wendy Pa, Judy |
author_facet | Hobel, Zachary Isenberg, A. Lisette Raghupathy, Dhvani Mack, Wendy Pa, Judy |
author_sort | Hobel, Zachary |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6839478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68394782019-11-20 APOE ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment Hobel, Zachary Isenberg, A. Lisette Raghupathy, Dhvani Mack, Wendy Pa, Judy J Alzheimers Dis Research Article 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. IOS Press 2019-09-17 /pmc/articles/PMC6839478/ /pubmed/31424388 http://dx.doi.org/10.3233/JAD-180859 Text en © 2019 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hobel, Zachary Isenberg, A. Lisette Raghupathy, Dhvani Mack, Wendy Pa, Judy APOE ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title | APOE
ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title_full | APOE
ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title_fullStr | APOE
ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title_full_unstemmed | APOE
ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title_short | APOE
ɛ4 Gene Dose and Sex Effects on Alzheimer’s Disease MRI Biomarkers in Older Adults with Mild Cognitive Impairment |
title_sort | apoe
ɛ4 gene dose and sex effects on alzheimer’s disease mri biomarkers in older adults with mild cognitive impairment |
topic | Research Article |
url | 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 |
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