Estrogens, hormone therapy, and hippocampal volume in postmenopausal women
- PMID: 22858056
- PMCID: PMC3576699
- DOI: 10.1016/j.maturitas.2012.07.001
Estrogens, hormone therapy, and hippocampal volume in postmenopausal women
Abstract
The brain atrophies in late life. However, there are many factors that either magnify or mitigate the rate of atrophy. Loss of estrogens during menopause and administration of hormone therapy have both been hypothesized as sources of individual variation in the prevalence of cortical and subcortical atrophy and loss of cognitive function in late adulthood. In this review we critically summarize and assess the extant rodent and human neuroimaging studies that examine the link between estrogens and hippocampal morphology and function and focus predominantly on human studies of the hippocampus in postmenopausal women. Several cross-sectional studies report that the size of the hippocampus is larger in women receiving hormone therapy while several other cross-sectional studies report either negligible effects or smaller volumes in women receiving hormone therapy. We suggest that these differences might be caused by the variation between studies in the age of the samples studied, the duration of therapy, and the age at which hormone therapy is initiated. Unfortunately, all of the human studies reviewed here are cross-sectional in nature. With the lack of well-controlled randomized trials with neuroimaging measures on postmenopausal women both before and after some exposure interval, the effect of hormone therapy on hippocampal atrophy will remain equivocal and poorly understood.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.
Conflict of interest statement
All authors declare that there are no competing interests for the publications of this paper.
All authors contributed to the writing of this article and declare no conflicts of interest.
Comment in
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Climacteric commentaries.Climacteric. 2013 Apr;16(2):293-302. doi: 10.3109/13697137.2013.769834. Climacteric. 2013. PMID: 23488526 No abstract available.
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