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首页> 外文期刊>Gynecological endocrinology: the official journal of the International Society of Gynecological Endocrinology >Combining treatment with myo-inositol and D-chiro-inositol (40:1) is effective in restoring ovary function and metabolic balance in PCOS patients
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Combining treatment with myo-inositol and D-chiro-inositol (40:1) is effective in restoring ovary function and metabolic balance in PCOS patients

机译:用肌肌醇和D-甲基肌醇(40:1)结合处理在PCOS患者中恢复卵巢功能和代谢平衡有效

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Polycystic ovary syndrome (PCOS), a relevant cause of infertility, is a heterogeneous, endocrine disorder affecting up to 10-15% of women in reproductive age. Besides hyperandrogenism, insulin resistance (IR) plays a key role in such syndrome. Insulin-sensitizing drugs, such as Metformin, are effective in treating hyper-insulinemic PCOS patients. Recently, inositols - myo-inositol (MI) and D-chiro-inositol (DCI) - have shown to be an efficient and safe alternative in PCOS management, as both inositol isoforms are able to counteract downstream consequences of insulin resistance. Yet, whereas DCI contributes in mediating insulin activity mainly on non-ovarian tissues, MI displays specific effects on ovary, chiefly by modulating glucose metabolism and FSH-signaling. Moreover, MI may also improve ovarian functions by modulating steroid metabolism through non-insulin-dependent pathways. As DCI and MI activity likely involves different biological mechanisms, both inositol isoforms can be synergistically integrated according to a multitargeted design, by combining MI and DCI in a ratio corresponding to their physiological plasma relative amount (40:1). New experimental and clinical evidence with MI plus DCI evidenced the suitability of such integrated approach, and provided promising results. Further studies need to investigate thoroughly the molecular mechanism and confirm such preliminary data.
机译:多囊卵巢综合征(PCOS),不孕症的相关原因是一种异质,内分泌疾病,影响繁殖年龄的10-15%的妇女。除高腺激素外,胰岛素抵抗(IR)在这种综合征中起着关键作用。胰岛素敏化药物如二甲双胍,可有效治疗超胰岛素血糖患者。最近,肌醇 - 肌醇 - 肌醇(MI)和D-Chiro-intositol(DCI) - 已显示在PCOS管理中是一种有效和安全的替代品,因为肌醇同种型都能够抵消胰岛素抵抗的下游后果。然而,虽然DCI在主要在非卵巢组织上培养胰岛素活性,但MI主要通过调节葡萄糖代谢和FSH信号传导卵巢对卵巢进行特异性效果。此外,MI还可以通过非胰岛素依赖性途径调节类固醇代谢来改善卵巢功能。由于DCI和MI活性可能涉及不同的生物机制,通过将MI和DCI与其生理等离子体相对量(40:1)的比率组合,可以根据多标核设计来协同整合。 MI Plus DCI的新实验和临床证据证明了这种综合方法的适用性,并提供了有希望的结果。进一步的研究需要彻底调查分子机制并确认此类初步数据。

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