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Journal ArticleDOI

Sex hormones, aging, and Alzheimer's disease.

Anna M. Barron, +1 more
- 01 Jan 2012 - 
- Vol. 4, Iss: 3, pp 976-997
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TLDR
A broad literature that indicates age-related losses of estrogens in women and testosterone in men are risk factors for AD is reviewed, suggesting that hormone therapies have the potential to combat AD pathogenesis.
Abstract
A promising strategy to delay and perhaps prevent Alzheimer's disease (AD) is to identify the age-related changes that put the brain at risk for the disease. A significant normal age change known to result in tissue-specific dysfunction is the depletion of sex hormones. In women, menopause results in a relatively rapid loss of estradiol and progesterone. In men, aging is associated with a comparatively gradual yet significant decrease in testosterone. We review a broad literature that indicates age-related losses of estrogens in women and testosterone in men are risk factors for AD. Both estrogens and androgens exert a wide range of protective actions that improve multiple aspects of neural health, suggesting that hormone therapies have the potential to combat AD pathogenesis. However, translation of experimental findings into effective therapies has proven challenging. One emerging treatment option is the development of novel hormone mimetics termed selective estrogen and androgen receptor modulators. Continued research of sex hormones and their roles in the aging brain is expected to yield valuable approaches to reducing the risk of AD.

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Citations
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Sex differences in cognitive impairment and Alzheimer's disease

TL;DR: This review draws on epidemiological, translational, clinical, and basic science studies to assess the impact of sex differences in cognitive function from young to old, and examines the effects of sex hormone treatments on Alzheimer's disease in men and women.
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Age at surgical menopause influences cognitive decline and Alzheimer pathology in older women.

TL;DR: Early age at surgical menopause was associated with cognitive decline and AD neuropathology, and HRT use for at least 10 years, when administered within a 5-year perimenopausal window, wasassociated with decreased decline in global cognition.
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Sex, hormones and neurogenesis in the hippocampus: hormonal modulation of neurogenesis and potential functional implications.

TL;DR: Early evidence is provided of the functional links between the hormonal modulation of neurogenesis that may contribute to the regulation of cognition and stress in both male and female rodents.
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Role of Estrogen and Other Sex Hormones in Brain Aging. Neuroprotection and DNA Repair

TL;DR: Estrogen anti-aging and neuroprotective mechanisms, which are currently an area of intense study, are reviewed together with the effect they may have on the DNA repair capacity in the brain.
References
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Journal ArticleDOI

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TL;DR: Overall health risks exceeded benefits from use of combined estrogen plus progestin for an average 5.2-year follow-up among healthy postmenopausal US women, and the results indicate that this regimen should not be initiated or continued for primary prevention of CHD.
Journal ArticleDOI

2013 Alzheimer's disease facts and figures

TL;DR: This report provides information to increase understanding of the public health impact of Alzheimer's disease (AD), including incidence and prevalence, mortality rates, health expenditures and costs of care, and effect on caregivers and society in general.
Journal ArticleDOI

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TL;DR: Comparing the distribution of the classical and novel forms of ER mRNA‐expressing neurons in the central nervous system (CNS) of the rat with in situ hybridization histochemistry provides evidence that the region‐specific expression of ER‐α, ER‐β, or both may be important in determining the physiological responses of neuronal populations to estrogen action.
Journal ArticleDOI

Testosterone therapy in men with androgen deficiency syndromes: an Endocrine Society clinical practice guideline.

TL;DR: The guidelines for the evaluation and treatment of androgen deficiency syndromes in adult men published previously in 2006 were updated by the Task Force of the Clinical Guidelines Subcommittee of The Endocrine Society.
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