Abstract

Many investigations have found common occurrences of benign paroxysmal positional vertigo (BPPV) in women, and clinical experience has shown that BPPV can develop due to increased hormonal fluctuations, especially during menopause. Therefore, knowledge about neurochemicals and their involvement with BPPV is imperative for the management of neurological issues in women. This review will discuss appropriate gender-based considerations of BPPV based on experimental and clinical evidence. The studies describe 2 lines of evidence regarding the association of perimenopause in women and the development of BPPV: (1) experimental evidence: the existence of estrogen receptors in the inner ear, otoconial malformations in osteopenic/osteoporotic rats, changes in otoconin 90 caused by hormone replacement therapy, and impaired calcium absorption following estrogen deprivation corrected by estrogen replacement therapy and (2) clinical evidence: epidemiological aspects, osteoporosis and estrogen deficiency. Future studies are necessary to validate the effects of hormonal replacement therapy and phytoestrogen in women with recurrent BPPV.

Highlights

  • Known as the most common cause of recurrent vertigo [1], benign paroxysmal positional vertigo (BPPV) is an important health problem affecting more than 420 million adults worldwide, based on an international consensus that BPPV has a lifetime prevalence of 10% [2]

  • Hormonal changes, external estrogens, and pregnancy exposure are only experienced by women

  • It is not fully understood why postmenopausal women show a higher prevalence of BPPV

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Summary

INTRODUCTION

Known as the most common cause of recurrent vertigo [1], benign paroxysmal positional vertigo (BPPV) is an important health problem affecting more than 420 million adults worldwide, based on an international consensus that BPPV has a lifetime prevalence of 10% [2]. Many neurotology studies have shown an increased incidence of BPPV in women, and experience with older people suggests that hormonal fluctuations, during menopause, may increase, resulting in the development of BPPV [3,4,5,6,7,8]. Many studies have shown a common occurrence in women, and clinical experience with older people has shown that BPPV can develop due to increased hormonal fluctuations, especially during menopause [3,4,5,6,7,8]. Type I primary osteoporosis occurs during the postmenopausal period when estrogen output and the bone formation rate are reduced and bone loss is accelerated [51]. Fractures and injuries due to osteoporosis could harm a person’s life and incapacitate

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