Hormonal changes in the menopause transition.

H. Burger, E. Dudley, D. Robertson, L. Dennerstein
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引用次数: 431

Abstract

The menopause is the permanent cessation of menstruation resulting from the loss of ovarian follicular activity. It is heralded by the menopausal transition, a period when the endocrine, biological, and clinical features of approaching menopause begin. A common initial marker is the onset of menstrual irregularity. The biology underlying the transition to menopause includes central neuroendocrine changes as well as changes within the ovary, the most striking of which is a profound decline in follicle numbers. Follicle-stimulating hormone (FSH) is an established indirect marker of follicular activity. In studies of groups of women, its concentration, particularly in the early follicular phase of the menstrual cycle, begins to increase some years before there are any clinical indications of approaching menopause. The rise in FSH is the result of declining levels of inhibin B (INH-B), a dimeric protein that reflects the fall in ovarian follicle numbers, with or without any change in the ability of the lining granulosa cells to secrete INH-B. Estradiol levels remain relatively unchanged or tend to rise with age until the onset of the transition and are usually well preserved until the late perimenopause, presumably in response to the elevated FSH levels. During the transition, hormone levels frequently vary markedly - hence, measures of FSH and estradiol are unreliable guides to menopausal status. Concentrations of testosterone have been reported to fall by about 50% during reproductive life, between the ages of 20 and 40. They change little during the transition and, after menopause, may even rise. Dehydroepiandrosterone (DHEA) and DHEAS, its sulphate, on the other hand, decline with age, without any specific influence of the menopause. Symptoms of the menopause can be interpreted as resulting primarily from the profound fall in estradiol, occurring over a 3- to 4-year period around final menses, a fall that presumably contributes importantly to the beginning, in the late perimenopause, of loss of bone mineral density.
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绝经过渡期荷尔蒙的变化。
更年期是由于卵巢卵泡活动丧失而导致的月经永久停止。它预示着更年期的过渡,这是一个内分泌、生物学和临床特征开始接近更年期的时期。一个常见的初始标志是月经不规律的开始。更年期过渡的生物学基础包括中枢神经内分泌的变化以及卵巢的变化,其中最引人注目的是卵泡数量的急剧下降。促卵泡激素(FSH)是卵泡活性的间接标志物。在对妇女群体的研究中,其浓度,特别是在月经周期的早期卵泡阶段,在任何接近更年期的临床迹象出现前几年就开始增加。FSH的升高是抑制素B (INH-B)水平下降的结果,抑制素B是一种二聚体蛋白,反映了卵巢卵泡数量的下降,衬里颗粒细胞分泌INH-B的能力有或没有任何变化。雌二醇水平保持相对不变或随着年龄的增长而上升,直到转变开始,通常保持良好,直到晚期围绝经期,可能是对FSH水平升高的反应。在过渡期间,激素水平经常发生显著变化——因此,测量FSH和雌二醇是绝经状态的不可靠指南。据报道,在20岁至40岁之间的生育期,睾丸激素浓度下降了约50%。它们在过渡期间变化不大,绝经后甚至可能上升。另一方面,脱氢表雄酮(DHEA)及其硫酸盐脱氢表雄酮(DHEAS)随着年龄的增长而下降,而不受更年期的具体影响。更年期的症状可以解释为雌二醇水平的急剧下降,发生在最后一次月经前后的3到4年的时间里,这种下降可能对绝经后期骨密度的下降起了重要作用。
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