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多囊卵巢综合征中的新型脂肪因子WISP1和β-促胰岛素分泌素:与抗苗勒管激素水平、致动脉粥样硬化及代谢特征的关系

Novel adipokines WISP1 and betatrophin in PCOS: relationship to AMH levels, atherogenic and metabolic profile.

作者信息

Sahin Ersoy Gulcin, Altun Ensari Tugba, Vatansever Dogan, Emirdar Volkan, Cevik Ozge

机构信息

a Department of Obstetrics and Gynecology , Kartal Dr. Lutfi Kirdar Education and Research Hospital , Istanbul , Turkey.

b Department of Obstetrics and Gynecology , Etlik Zubeyde Hanim Women's Health Education and Research Hospital , Ankara , Turkey.

出版信息

Gynecol Endocrinol. 2017 Feb;33(2):119-123. doi: 10.1080/09513590.2016.1223286. Epub 2016 Sep 30.

Abstract

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-Müllerian hormone (AMH) levels, atherogenic profile and metabolic parameters Methods: 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.

摘要

目的

测定多囊卵巢综合征(PCOS)正常体重和肥胖女性中WISP1和β-促细胞生成素的水平,并评估它们与抗苗勒管激素(AMH)水平、动脉粥样硬化指标和代谢参数之间的关系。方法:在这项前瞻性横断面研究中,研究组由49名根据鹿特丹标准诊断为PCOS的正常体重女性和34名肥胖女性组成;36名正常体重和26名肥胖的年龄匹配、月经周期规律的非高雄激素血症女性。评估血清WISP1、β-促细胞生成素、胰岛素抵抗稳态模型评估(HOMA-IR)和AMH水平。对β-促细胞生成素、WISP1水平与AMH水平、代谢和动脉粥样硬化参数进行单因素和多因素分析。

结果

PCOS组血清WISP1和β-促细胞生成素值高于对照组。此外,肥胖PCOS亚组的血清WISP1和β-促细胞生成素水平高于正常体重和肥胖对照组亚组。多因素分析显示,体重指数、HOMA-IR、AMH独立且正向预测WISP1水平。血清β-促细胞生成素水平的变异性由同型半胱氨酸、HOMA-IR和雄烯二酮水平解释。

结论

WISP1和β-促细胞生成素可能在PCOS的发病机制中起关键作用。

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