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Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume

BACKGROUND: Alzheimer’s disease (AD) impacts men and women differently, but the effect of sex on predementia stages is unclear. The objective of this study was to examine whether sex moderates the impact of florbetapir positron emission tomography (PET) amyloid positivity (A(+)) on verbal learning a...

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Autores principales: Caldwell, Jessica Z. K., Berg, Jody-Lynn, Cummings, Jeffrey L., Banks, Sarah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596932/
https://www.ncbi.nlm.nih.gov/pubmed/28899422
http://dx.doi.org/10.1186/s13195-017-0300-8
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author Caldwell, Jessica Z. K.
Berg, Jody-Lynn
Cummings, Jeffrey L.
Banks, Sarah J.
author_facet Caldwell, Jessica Z. K.
Berg, Jody-Lynn
Cummings, Jeffrey L.
Banks, Sarah J.
author_sort Caldwell, Jessica Z. K.
collection PubMed
description BACKGROUND: Alzheimer’s disease (AD) impacts men and women differently, but the effect of sex on predementia stages is unclear. The objective of this study was to examine whether sex moderates the impact of florbetapir positron emission tomography (PET) amyloid positivity (A(+)) on verbal learning and memory performance and hippocampal volume (HV) in normal cognition (NC) and early mild cognitive impairment (eMCI). METHODS: Seven hundred forty-two participants with NC and participants with eMCI from the Alzheimer’s Disease Neuroimaging Initiative (second cohort [ADNI2] and Grand Opportunity Cohort [ADNI-GO]) were included. All had baseline florbetapir PET measured, and 526 had screening visit HV measured. Regression moderation models were used to examine whether A(+) effects on Rey Auditory Verbal Learning Test learning and delayed recall and right and left HV (adjusted for total intracranial volume) were moderated by diagnosis and sex. Age, cognition at screening, education, and apolipoprotein E ε4 carrier status were controlled. RESULTS: Women with A(+), but not those with florbetapir PET amyloid negative (A-),eMCI showed poorer learning. For women with NC, there was no relationship of A(+) with learning. In contrast, A(+) men trended toward poorer learning regardless of diagnosis. A similar trend was found for verbal delayed recall: Women with A(+), but not A-, eMCI trended toward reduced delayed recall; no effects were observed for women with NC or for men. Hippocampal analyses indicated that women with A(+), but not those with A(−), eMCI, trended toward smaller right HV; no significant A(+) effects were observed for women with NC. Men showed similar, though nonsignificant, patterns of smaller right HV in A(+) eMCI, but not in men with A(−) eMCI or NC. No interactive effects of sex were noted for left HV. CONCLUSIONS: Women with NC showed verbal learning and memory scores robust to A(+), and women with A(+) eMCI lost this advantage. In contrast, A(+) impacted men’s scores less significantly or not at all, and comparably across those with NC and eMCI. Sex marginally moderated the relationship of A(+) and diagnosis with right HV, such that women with NC showed no A(+) effect and women with A(+) eMCI lost that advantage in neural integrity; the pattern in men was less clear. These findings show that women with A(+) eMCI (i.e., prodromal AD) have differential neural and cognitive decline, which has implications for considering sex in early detection of AD and development of therapeutics.
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spelling pubmed-55969322017-09-15 Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume Caldwell, Jessica Z. K. Berg, Jody-Lynn Cummings, Jeffrey L. Banks, Sarah J. Alzheimers Res Ther Research BACKGROUND: Alzheimer’s disease (AD) impacts men and women differently, but the effect of sex on predementia stages is unclear. The objective of this study was to examine whether sex moderates the impact of florbetapir positron emission tomography (PET) amyloid positivity (A(+)) on verbal learning and memory performance and hippocampal volume (HV) in normal cognition (NC) and early mild cognitive impairment (eMCI). METHODS: Seven hundred forty-two participants with NC and participants with eMCI from the Alzheimer’s Disease Neuroimaging Initiative (second cohort [ADNI2] and Grand Opportunity Cohort [ADNI-GO]) were included. All had baseline florbetapir PET measured, and 526 had screening visit HV measured. Regression moderation models were used to examine whether A(+) effects on Rey Auditory Verbal Learning Test learning and delayed recall and right and left HV (adjusted for total intracranial volume) were moderated by diagnosis and sex. Age, cognition at screening, education, and apolipoprotein E ε4 carrier status were controlled. RESULTS: Women with A(+), but not those with florbetapir PET amyloid negative (A-),eMCI showed poorer learning. For women with NC, there was no relationship of A(+) with learning. In contrast, A(+) men trended toward poorer learning regardless of diagnosis. A similar trend was found for verbal delayed recall: Women with A(+), but not A-, eMCI trended toward reduced delayed recall; no effects were observed for women with NC or for men. Hippocampal analyses indicated that women with A(+), but not those with A(−), eMCI, trended toward smaller right HV; no significant A(+) effects were observed for women with NC. Men showed similar, though nonsignificant, patterns of smaller right HV in A(+) eMCI, but not in men with A(−) eMCI or NC. No interactive effects of sex were noted for left HV. CONCLUSIONS: Women with NC showed verbal learning and memory scores robust to A(+), and women with A(+) eMCI lost this advantage. In contrast, A(+) impacted men’s scores less significantly or not at all, and comparably across those with NC and eMCI. Sex marginally moderated the relationship of A(+) and diagnosis with right HV, such that women with NC showed no A(+) effect and women with A(+) eMCI lost that advantage in neural integrity; the pattern in men was less clear. These findings show that women with A(+) eMCI (i.e., prodromal AD) have differential neural and cognitive decline, which has implications for considering sex in early detection of AD and development of therapeutics. BioMed Central 2017-09-12 /pmc/articles/PMC5596932/ /pubmed/28899422 http://dx.doi.org/10.1186/s13195-017-0300-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Caldwell, Jessica Z. K.
Berg, Jody-Lynn
Cummings, Jeffrey L.
Banks, Sarah J.
Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title_full Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title_fullStr Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title_full_unstemmed Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title_short Moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
title_sort moderating effects of sex on the impact of diagnosis and amyloid positivity on verbal memory and hippocampal volume
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596932/
https://www.ncbi.nlm.nih.gov/pubmed/28899422
http://dx.doi.org/10.1186/s13195-017-0300-8
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