Abstract

The level of gonadal hormones to which the female brain is exposed considerably changes across the menopausal transition, which in turn, is likely to be of great relevance for neurodegenerative diseases and psychiatric disorders. However, the neurobiological consequences of these hormone fluctuations and of hormone replacement therapy in the menopause have only begun to be understood. The present review summarizes the findings of thirty-five studies of human brain function, including functional magnetic resonance imaging, positron and single-photon computed emission tomography studies, in peri- and postmenopausal women treated with estrogen, or estrogen-progestagen replacement therapy. Seven studies using gonadotropin-releasing hormone agonist intervention as a model of hormonal withdrawal are also included. Cognitive paradigms are employed by the majority of studies evaluating the effect of unopposed estrogen or estrogen-progestagen treatment on peri- and postmenopausal women's brain. In randomized-controlled trials, estrogen treatment enhances activation of fronto-cingulate regions during cognitive functioning, though in many cases no difference in cognitive performance was present. Progestagens seems to counteract the effects of estrogens. Findings on cognitive functioning during acute ovarian hormone withdrawal suggest a decrease in activation of the left inferior frontal gyrus, thus essentially corroborating the findings in postmenopausal women. Studies of the cholinergic and serotonergic systems indicate these systems as biological mediators of hormonal influences on the brain. More, hormonal replacement appears to increase cerebral blood flow in several cortical regions. On the other hand, studies on emotion processing in postmenopausal women are lacking. These results call for well-powered randomized-controlled multi-modal prospective neuroimaging studies as well as investigation on the related molecular mechanisms of effects of menopausal hormonal variations on the brain.

Highlights

  • The change in ovarian hormone levels to which the female brain is exposed during the menopausal transition is likely relevant for neurodegenerative diseases as well as psychiatric disorders

  • The prevention and clinical management of mental health problems during the menopausal transition suffers from uncertainty, which renders research in this field of outmost importance

  • Neuroimaging techniques are certainly suitable tools for investigating potential intermediate phenotypes related to the neurobiological correlates of menopause and hormone replacement therapy (HRT)

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Summary

Introduction

The change in ovarian hormone levels to which the female brain is exposed during the menopausal transition is likely relevant for neurodegenerative diseases as well as psychiatric disorders. The effects of the peri- and postmenopausal estradiol level decline and hormone replacement therapy (HRT) on the brain have only begun to be understood (Mueller et al, 2014). The prevention and clinical management of mental health problems during the menopausal transition suffers from uncertainty, which renders research in this field of outmost importance. During the last two decades menopause researchers have opted for an intermediate phenotype-based approach to further the psychobiological dissection of menopausal hormonal transition and HRT effects on mental health.

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