TY - JOUR
T1 - Sex differences in chronic stress responses and Alzheimer's disease
AU - Yan, Yan
AU - Dominguez, Sky
AU - Fisher, Daniel W.
AU - Dong, Hongxin
N1 - Funding Information:
This work was supported by the National Institutes of Health ( 1R56AG053491-01 , Dong, H) and ( 1 R01 AG057884-01 Dong, H).
Publisher Copyright:
© 2018 The Authors
PY - 2018/2
Y1 - 2018/2
N2 - Clinical studies indicate that Alzheimer's disease (AD) disproportionately affects women in both disease prevalence and severity, but the mechanisms underlying this sex divergence are unknown. Though some have suggested this difference in risk is a reflection of known differences in longevity between men and women, mounting clinical and preclinical evidence supports women also having intrinsic susceptibilities towards the disease. While a number of potential risk factors have been hypothesized to affect these differences in risks, none have been definitively verified. In this review, we discuss a novel hypothesis whereby women's susceptibility to chronic stress also mediates increased risk for AD. As stress is a risk factor for AD, and women are twice as likely to develop mood disorders where stress is a major etiology, it is possible that sex dimorphisms in stress responses contribute to the increase in women with AD. In line with this, sex divergence in biochemical responses to stress have been noted along the hypothalamic-pituitary-adrenal (HPA) axis and among known molecular effectors of AD, with crosstalk between these processes also being likely. In addition, activation of the cortical corticotrophin-releasing factor receptor 1 (CRF1) signaling pathway leads to distinct female-biased increases in molecules associated with AD pathogenesis. Therefore, the different biochemical responses to stress between women and men may represent an intrinsic, sex-dependent risk factor for AD.
AB - Clinical studies indicate that Alzheimer's disease (AD) disproportionately affects women in both disease prevalence and severity, but the mechanisms underlying this sex divergence are unknown. Though some have suggested this difference in risk is a reflection of known differences in longevity between men and women, mounting clinical and preclinical evidence supports women also having intrinsic susceptibilities towards the disease. While a number of potential risk factors have been hypothesized to affect these differences in risks, none have been definitively verified. In this review, we discuss a novel hypothesis whereby women's susceptibility to chronic stress also mediates increased risk for AD. As stress is a risk factor for AD, and women are twice as likely to develop mood disorders where stress is a major etiology, it is possible that sex dimorphisms in stress responses contribute to the increase in women with AD. In line with this, sex divergence in biochemical responses to stress have been noted along the hypothalamic-pituitary-adrenal (HPA) axis and among known molecular effectors of AD, with crosstalk between these processes also being likely. In addition, activation of the cortical corticotrophin-releasing factor receptor 1 (CRF1) signaling pathway leads to distinct female-biased increases in molecules associated with AD pathogenesis. Therefore, the different biochemical responses to stress between women and men may represent an intrinsic, sex-dependent risk factor for AD.
KW - Alzheimer's disease
KW - Corticotrophin-releasing factor receptor 1 signaling
KW - HPA axis
KW - Sex difference
KW - Stress
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U2 - 10.1016/j.ynstr.2018.03.002
DO - 10.1016/j.ynstr.2018.03.002
M3 - Review article
C2 - 29888307
AN - SCOPUS:85046808899
SN - 2352-2895
VL - 8
SP - 120
EP - 126
JO - Neurobiology of Stress
JF - Neurobiology of Stress
ER -