Sexual dimorphism in predisposition to Alzheimer's disease

被引:181
作者
Fisher, Daniel W. [1 ,2 ]
Bennett, David A. [3 ]
Dong, Hongxin [1 ,2 ]
机构
[1] Northwestern Univ, Dept Psychiat, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Behav Sci, Feinberg Sch Med, Chicago, IL 60611 USA
[3] Rush Med Coll, Dept Neurol Sci, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
关键词
Sex difference; Cognition; APOE; Brain structure; Hormones; Stress; Alzheimer's disease; CORTICOTROPIN-RELEASING-FACTOR; APOLIPOPROTEIN-E EPSILON-4; CARDIOVASCULAR RISK-FACTORS; GENOME-WIDE ASSOCIATION; TRANSGENIC MOUSE MODEL; AMYLOID-BETA; A-BETA; GENDER-DIFFERENCES; TAU PHOSPHORYLATION; COGNITIVE DECLINE;
D O I
10.1016/j.neurobiolaging.2018.04.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Clinical studies indicate that Alzheimer's disease (AD) disproportionately affects women in both disease prevalence and rate of symptom progression, but the mechanisms underlying this sexual divergence are unknown. Although some have suggested this difference in risk is a reflection of the known differences in longevity between men and women, mounting clinical and preclinical evidence supports women also having intrinsic susceptibilities toward the disease. Although a number of potential risk factors have been hypothesized to mediate these differences, none have been definitively verified. In this review, we first summarize the epidemiologic studies of prevalence and incidence of AD among the sexes. Next, we discuss the most likely risk factors to date that interact with biological sex, including (1) genetic factors, (2) sex hormones (3) deviations in brain structure, (4) inflammation and microglia, and (5) and psychosocial stress responses. Overall, though differences in life span are likely to account for part of the divide between the sexes in AD prevalence, the abundance of preclinical and clinical evidence presented here suggests an increase in intrinsic AD risk for women. Therefore, future studies focusing on the underlying biological mechanisms for this phenomenon are needed to better understand AD pathogenesis in both sexes, with the eventual goal of sex-specific prevention and treatment strategies. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:308 / 324
页数:17
相关论文
共 177 条
[1]
Sex Modifies the APOE-Related Risk of Developing Alzheimer Disease [J].
Altmann, Andre ;
Tian, Lu ;
Henderson, Victor W. ;
Greicius, Michael D. .
ANNALS OF NEUROLOGY, 2014, 75 (04) :563-573
[2]
Alzheimers Association, 2015, Alzheimers Dement, V11, P332
[3]
GENETIC-CONTROL OF THE CD4/CD8 T-CELL RATIO IN HUMANS [J].
AMADORI, A ;
ZAMARCHI, R ;
DESILVESTRO, G ;
FORZA, G ;
CAVATTON, G ;
DANIELI, GA ;
CLEMENTI, M ;
CHIECOBIANCHI, L .
NATURE MEDICINE, 1995, 1 (12) :1279-1283
[4]
Analysis of the MIRIAD Data Shows Sex Differences in Hippocampal Atrophy Progression [J].
Ardekani, Babak A. ;
Convit, Antonio ;
Bachman, Alvin H. .
JOURNAL OF ALZHEIMERS DISEASE, 2016, 50 (03) :847-857
[5]
High-dose estradiol improves cognition for women with AD - Results of a randomized study [J].
Asthana, S ;
Baker, LD ;
Craft, S ;
Stanczyk, FZ ;
Veith, RC ;
Raskind, MA ;
Plymate, SR .
NEUROLOGY, 2001, 57 (04) :605-612
[6]
INCIDENCE OF DEMENTIA AND PROBABLE ALZHEIMERS-DISEASE IN A GENERAL-POPULATION - THE FRAMINGHAM-STUDY [J].
BACHMAN, DL ;
WOLF, PA ;
LINN, RT ;
KNOEFEL, JE ;
COBB, JL ;
BELANGER, AJ ;
WHITE, LR ;
DAGOSTINO, RB .
NEUROLOGY, 1993, 43 (03) :515-519
[7]
Corticotropin-releasing factor overexpression gives rise to sex differences in Alzheimer's disease-related signaling [J].
Bangasser, D. A. ;
Dong, H. ;
Carroll, J. ;
Plona, Z. ;
Ding, H. ;
Rodriguez, L. ;
McKennan, C. ;
Csernansky, J. G. ;
Seeholzer, S. H. ;
Valentino, R. J. .
MOLECULAR PSYCHIATRY, 2017, 22 (08) :1126-1133
[8]
Sex differences in the clinical manifestations of Alzheimer disease pathology [J].
Barnes, LL ;
Wilson, RS ;
Bienias, JL ;
Schneider, JA ;
Evans, DA ;
Bennett, DA .
ARCHIVES OF GENERAL PSYCHIATRY, 2005, 62 (06) :685-691
[9]
DISPLACEMENT OF CORTICOTROPIN-RELEASING FACTOR FROM ITS BINDING-PROTEIN AS A POSSIBLE TREATMENT FOR ALZHEIMERS-DISEASE [J].
BEHAN, DP ;
HEINRICHS, SC ;
TRONCOSO, JC ;
LIU, XJ ;
KAWAS, CH ;
LING, N ;
DESOUZA, EB .
NATURE, 1995, 378 (6554) :284-287
[10]
Sex differences in the association of the apolipoprotein E epsilon 4 allele with incidence of dementia, cognitive impairment, and decline [J].
Beydoun, May A. ;
Boueiz, Adel ;
Abougergi, Marwan S. ;
Kitner-Triolo, Melissa H. ;
Beydoun, Hind A. ;
Resnick, Susan M. ;
O'Brien, Richard ;
Zonderman, Alan B. .
NEUROBIOLOGY OF AGING, 2012, 33 (04)