首页> 外文期刊>Gynecological endocrinology: the official journal of the International Society of Gynecological Endocrinology >Novel adipokines WISP1 and betatrophin in PCOS: relationship to AMH levels, atherogenic and metabolic profile
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Novel adipokines WISP1 and betatrophin in PCOS: relationship to AMH levels, atherogenic and metabolic profile

机译:新型adipokines isp1和bettrophin在pcos:与AMH水平,闭塞和代谢剖面的关系

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摘要

Objective: To determine the levels of WISP1 and betatrophin in normal weight and obese women with polycystic ovary syndrome (PCOS) and to assess their relationship with anti-Mullerian hormone (AMH) levels, atherogenic profile and metabolic parametersMethods: In this prospective cross-sectional study, the study group was composed of 49 normal weighed and 34 obese women with PCOS diagnosed based on the Rotterdam criteria; 36 normal weight and 26 obese age matched non-hyperandrogenemic women with regular menstrual cycle. Serum WISP1, betatrophin, homeostasis model assessment of insulin resistance (HOMA-IR) and AMH levels were evaluated. Univariate and multivariate analyses were performed between betatrophin, WISP1 levels and AMH levels, metabolic and atherogenic parameters.Results: Serum WISP1 and betatrophin values were elevated in the PCOS group than in the control group. Moreover, serum WISP1 and betatrophin levels were higher in the obese PCOS subgroup than in normal weight and obese control subgroups. Multivariate analyses revealed that Body mass index, HOMA-IR, AMH independently and positively predicted WISP1 levels. Serum betatrophin level variability was explained by homocysteine, HOMA-IR and androstenedione levels.Conclusion: WISP1 and betatrophin may play a key role on the pathogenesis of PCOS.
机译:目的:确定具有多囊卵巢综合征(PCOS)的正常体重和肥胖妇女的Wisp1和Bettrophin水平,并评估其与抗Mullerian激素(AMH)水平的关系,体育概况和代谢参数方法:在这一前瞻性横截面中研究,研究组由49名正常称重和34名肥胖妇女组成,具有基于鹿特丹标准的PCOS; 36正常体重和26岁的肥胖年龄与常规月经周期的非高糖尿病女性相匹配。评估血清Wisp1,Bettrophin,稳态胰岛素抵抗(HOMA-IR)和AMH水平的稳态模型评估。在Bettrophin,Wisp1水平和AMH水平,代谢和致动脉粥样菌的嗜血蛋白,代谢和致动脉发生参数之间进行单变量和多变量分析。结果:PCOS组在PCOS组中升高而不是对照组。此外,肥胖的PCOS亚组中血清碱度碱度水平高于正常重量和肥胖对照亚组。多变量分析显示,体重指数,HOMA-IR,AMH独立和积极地预测WISP1水平。血清BetroTrophy型可变性是通过同型半胱氨酸,HOMA-IR和Androstenione水平解释的。结论:Wisp1和Bettrophin可能在PCOS发病机制中发挥关键作用。

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