多囊卵巢综合征:一种进化代谢适应。

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2025-03-24 Print Date: 2025-04-01 DOI:10.1530/REP-25-0021
Daniel A Dumesic, Vasantha Padmanabhan, David H Abbott
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引用次数: 0

摘要

多囊卵巢综合征(PCOS)是育龄妇女常见的内分泌疾病,以雄激素分泌过多、无排卵少和胰岛素抵抗为特征,并伴有腹部脂肪优先堆积。作为灵长类祖先的一种特征,人类多囊卵巢综合征可能经历了相对较近的优先选择,当更新世狩猎采集者食物匮乏时,他们选择了增强脂肪储存和胰岛素抵抗作为维持大脑和生殖功能葡萄糖稳态的生存优势。作为多囊卵巢综合征的进化模型,患有高雄激素性多囊卵巢综合征的健康正常体重女性具有皮下(SC)腹部脂肪干细胞,在体外脂肪细胞发育过程中倾向于过度的脂质积累,并伴有全身胰岛素敏感性降低和腹内高脂性脂肪优先积累。多囊卵巢综合征(PCOS)的这种代谢适应由生命早期的遗传和表观遗传事件决定,提供了SC脂肪储存增强和循环葡萄糖和游离脂肪酸可用性增加之间的平衡,作为关键靶组织的能量底物。古代多囊卵巢综合征妇女伴随的肌肉力量增加和少排卵也使耐力活动中持续的能量消耗与更长的时间相结合,作为抚养孩子的优势和更低的孕产妇死亡率风险。遗传性多囊卵巢综合征(PCOS)的特征最初是在灵长类动物中进化而来的,是一种遗传和表观遗传增强的代谢适应,有利于脂肪储存,现在却易导致脂肪毒性和妊娠并发症,这要求我们通过早期生活方式和治疗选择来改善预防保健,以优化多囊卵巢综合征妇女及其子女在当今肥胖环境中的长期健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
POLYCYSTIC OVARY SYNDROME: ORIGINS AND IMPLICATIONS: Polycystic ovary syndrome: an evolutionary metabolic adaptation.

In brief: Polycystic ovary syndrome has ancient genetic origins that favored preferential abdominal fat accumulation, ovarian hyperandrogenism and insulin resistance. This review examines how endocrine-metabolic changes in normal-weight hyperandrogenic PCOS women originated as an evolutionary metabolic adaptation to balance enhanced fat storage with increased glucose and fatty acid availability for optimal energy use for survival and reproduction.

Abstract: Polycystic ovary syndrome (PCOS) is a common endocrinopathy of reproductive-aged women, characterized by hyperandrogenism, oligo-anovulation and insulin resistance in combination with preferential abdominal fat accumulation. As an ancestral primate trait, PCOS in humans likely underwent relatively recent preferential selection when scarcity of food in hunter-gatherers of the Pleistocene selected for enhanced fat storage and insulin resistance as a survival advantage to maintain glucose homeostasis for brain and reproductive function. As an evolutional model for PCOS, healthy normal-weight women with hyperandrogenic PCOS have subcutaneous (SC) abdominal adipose stem cells that favor exaggerated lipid accumulation during adipocyte development in vitro accompanied by reduced systemic insulin sensitivity and preferential accumulation of highly lipolytic intra-abdominal fat. Programmed by genetic inheritance and epigenetic events during early life, such a metabolic adaptation in PCOS, provides a balance between enhanced SC adipose fat storage and increased circulating glucose and free fatty acid availability as energy substrate for crucial target tissues. The accompanying increased muscle strength and oligo-anovulation in PCOS women of antiquity also enabled sustained energy use during endurance activities in combination with greater time as a rearing advantage for children and a lower risk of maternal mortality. Heritable PCOS characteristics that originally evolved in primates as a genetically and epigenetically enhanced metabolic adaptation to favor fat storage now predispose to lipotoxicity and pregnancy complications, calling for improved preventive healthcare, with early lifestyle and therapeutic choices to optimize the long-term health of PCOS women and their children in today's obesogenic environment.

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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
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