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2
FSH directly regulates bone mass.促卵泡激素直接调节骨量。
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Altered ovarian function affects skeletal homeostasis independent of the action of follicle-stimulating hormone.卵巢功能改变会独立于促卵泡激素的作用而影响骨骼稳态。
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Effects of castration and chronic steroid treatments on hypothalamic gonadotropin-releasing hormone content and pituitary gonadotropins in male wild-type and estrogen receptor-alpha knockout mice.去势和长期类固醇治疗对雄性野生型和雌激素受体α基因敲除小鼠下丘脑促性腺激素释放激素含量及垂体促性腺激素的影响。
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本文引用的文献

1
Effect of Androgen-Deprivation Therapy on Bone Mineral Density in Patients with Prostate Cancer: A Systematic Review and Meta-Analysis.雄激素剥夺疗法对前列腺癌患者骨密度的影响:一项系统评价和荟萃分析。
J Clin Med. 2019 Jan 18;8(1):113. doi: 10.3390/jcm8010113.
2
Metabolic consequences of gonadotropin-releasing hormone agonists vs orchiectomy: a randomized clinical study.促性腺激素释放激素激动剂与去势治疗的代谢后果:一项随机临床研究。
BJU Int. 2019 Apr;123(4):602-611. doi: 10.1111/bju.14609. Epub 2018 Nov 28.
3
FSH, Bone Mass, Body Fat, and Biological Aging.促卵泡激素(FSH)、骨量、体脂肪与生物老化。
Endocrinology. 2018 Oct 1;159(10):3503-3514. doi: 10.1210/en.2018-00601.
4
Progesterone for the prevention and treatment of osteoporosis in women.孕酮用于预防和治疗女性骨质疏松症。
Climacteric. 2018 Aug;21(4):366-374. doi: 10.1080/13697137.2018.1467400. Epub 2018 Jul 2.
5
Epitope-specific monoclonal antibodies to FSHβ increase bone mass.针对 FSHβ 的表位特异性单克隆抗体可增加骨量。
Proc Natl Acad Sci U S A. 2018 Feb 27;115(9):2192-2197. doi: 10.1073/pnas.1718144115. Epub 2018 Feb 12.
6
Extragonadal Actions of FSH: A Critical Need for Novel Genetic Models.促卵泡生成素的性腺外作用:对新型遗传模型的迫切需求
Endocrinology. 2018 Jan 1;159(1):2-8. doi: 10.1210/en.2017-03118.
7
New hope for symptom management during natural and iatrogenic menopause transitions.自然绝经和医源性绝经过渡期间症状管理的新希望。
Biol Reprod. 2017 Aug 1;97(2):177-178. doi: 10.1093/biolre/iox079.
8
Blocking FSH induces thermogenic adipose tissue and reduces body fat.阻断促卵泡激素可诱导产热脂肪组织并减少体脂。
Nature. 2017 Jun 1;546(7656):107-112. doi: 10.1038/nature22342. Epub 2017 May 24.
9
Estrogens and Androgens in Skeletal Physiology and Pathophysiology.雌激素与雄激素在骨骼生理和病理生理中的作用
Physiol Rev. 2017 Jan;97(1):135-187. doi: 10.1152/physrev.00033.2015.
10
Androgen deprivation increases the risk of fracture in prostate cancer patients: a population-based study in Chinese patients.雄激素剥夺增加前列腺癌患者骨折风险:一项基于中国患者人群的研究。
Osteoporos Int. 2015 Sep;26(9):2281-90. doi: 10.1007/s00198-015-3135-9. Epub 2015 May 20.

雌激素与促卵泡激素对骨代谢的影响:来自干预性人体研究的证据。

Estrogen Versus FSH Effects on Bone Metabolism: Evidence From Interventional Human Studies.

机构信息

Robert and Arlene Kogod Center on Aging and Endocrine Research Unit, Mayo Clinic College of Medicine, Rochester, Minnesota.

出版信息

Endocrinology. 2020 Aug 1;161(8). doi: 10.1210/endocr/bqaa111.

DOI:10.1210/endocr/bqaa111
PMID:32602895
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7371389/
Abstract

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.

摘要

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。