Robert and Arlene Kogod Center on Aging and Endocrine Research Unit, Mayo Clinic College of Medicine, Rochester, Minnesota.
Endocrinology. 2020 Aug 1;161(8). doi: 10.1210/endocr/bqaa111.
Provocative mouse studies and observational human data have generated considerable enthusiasm for modulating follicle-stimulating hormone (FSH) action in humans to prevent bone loss and, in addition, to treat obesity. This perspective summarizes the strengths and potential weaknesses of the mouse studies examining the skeletal phenotype of FSHβ or FSH receptor null mice, as well as more recent studies using FSH neutralizing antibodies. Although human observational studies do demonstrate correlation of serum FSH levels with postmenopausal bone loss, these studies cannot distinguish whether serum FSH is simply a better biomarker than estradiol or causally related to the bone loss. Establishing causality requires direct interventional studies either suppressing or infusing FSH in humans and to date, such studies have uniformly failed to demonstrate an effect of FSH on bone turnover independent of changes in sex steroid levels. In addition, suppression of FSH is unable to prevent increases in body fat following the induction of sex steroid deficiency, at least in men. Thus, although the preclinical mouse and human observational data are intriguing, there is currently no direct evidence from interventional studies that FSH regulates bone or fat metabolism in vivo in humans.
刺激性的小鼠研究和观察性的人类数据激发了人们极大的兴趣,即调节人类促卵泡激素(FSH)的作用以预防骨质流失,并治疗肥胖。这一观点总结了检查 FSHβ 或 FSH 受体缺失小鼠骨骼表型的小鼠研究以及使用 FSH 中和抗体的最新研究的优势和潜在弱点。尽管人类观察性研究确实表明血清 FSH 水平与绝经后骨质流失相关,但这些研究无法区分血清 FSH 仅是比雌二醇更好的生物标志物,还是与骨质流失有因果关系。确定因果关系需要在人类中进行直接的干预研究,抑制或输注 FSH,迄今为止,此类研究一致未能证明 FSH 对骨转换具有独立于性激素水平变化的作用。此外,抑制 FSH 无法防止在诱导性激素缺乏后体内脂肪增加,至少在男性中是这样。因此,尽管临床前的小鼠和人类观察性数据很有吸引力,但目前没有来自干预性研究的直接证据表明 FSH 在体内调节人类的骨或脂肪代谢。