多囊卵巢综合征患者血清midkine水平与胰岛素抵抗和肥胖的关系

Fatma Beyazıt, Fatih Kamış, E. Pek, Y. Beyazıt
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引用次数: 1

摘要

目的:多囊卵巢综合征(PCOS)被认为是一种亚临床炎症状态,循环促炎细胞因子水平升高。Midkine是一种多效性肝素结合神经营养因子,具有促炎特性,越来越多的证据表明Midkine在炎症中的重要作用。本研究旨在探讨midkine是否在多囊卵巢综合征的发生发展中起作用及其与肥胖和胰岛素抵抗(IR)的关系。材料和方法:在这项比较横断面研究中,招募了56名多囊卵巢综合征(PCOS)女性和36名年龄和体重指数(BMI)匹配的绝经期无毛女性作为对照组。对两个研究组进行常规和特异性(midkine)实验室分析和IR测量。结果:PCOS患者与对照组血清midkine水平差异无统计学意义(P = 0.412)。根据BMI水平将PCOS患者进一步分为两个亚组。与正常体重PCOS患者相比,超重PCOS患者血清midkine水平升高(P = 0.044)。虽然PCOS伴IR(稳态模型评估-IR≥2.5)的妇女血清midkine水平有上升趋势,但这种升高无统计学意义(P = 0.301)。结论:肥胖对midkine水平的积极影响支持了midkine可能从脂肪细胞释放的观点。IR可能在这一机制中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of serum midkine levels with insulin resistance and obesity in patients with polycystic ovarian syndrome
Objectives: Polycystic ovarian syndrome (PCOS) is thought to be a subclinical inflammatory state with increased levels of circulating pro-inflammatory cytokines. Midkine is a pleiotropic heparin-binding neurotrophic factor with pro-inflammatory properties, and growing evidence has shown a substantial effect of midkine in inflammation. This study aimed to test whether midkine has a role in PCOS development and its relation to obesity and insulin resistance (IR). Materials and Methods: In this comparative cross-sectional study, 56 women with PCOS and 36 eumenorrheic nonhirsute, age- and body mass index (BMI)-matched women as the control group were recruited. Routine and specific (midkine) laboratory analysis and IR measurements were applied to both the study groups. Results: There were no statistically significant difference between PCOS patients and controls with regard to serum midkine levels (P = 0.412). PCOS patients were further divided into two subgroups according to BMI levels. Serum midkine levels were found to be increased in overweight PCOS patients compared with normal-weight PCOS patients (P = 0.044). Although an increasing trend was observed in respect to serum midkine levels in PCOS women with IR (Homeostatic Model Assessment-IR ≥2.5), this elevation was not statistically significant (P = 0.301). Conclusions: The positive effect of obesity on midkine levels supports the idea that midkine is probably released from adipocyte cells. IR possibly has an important role in this mechanism.
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