妊娠期糖尿病肥胖妇女妊娠早期血清分泌卷曲相关蛋白4、分泌卷曲相关蛋白5和趋化素的浓度

IF 2.4 Q3 ENDOCRINOLOGY & METABOLISM
R. Beernink, J. Schuitemaker, M. Faas, L. Poston, S. White
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引用次数: 0

摘要

背景:本研究的目的是评估在肥胖队列中,妊娠早期分泌卷曲相关蛋白4 (sFRP4)、分泌卷曲相关蛋白5 (sFRP5)和趋化素血清浓度是否与妊娠期糖尿病(GDM)的发生有关。在以往的研究中,在正常和超重女性中,sFRP4和趋化素的升高以及sFRP5浓度的降低与GDM的发生有关。方法:在本探索性病例对照研究中,采用ELISA法检测50例发生GDM的肥胖妇女和100例无并发症的对照妊娠的血清sFRP4、sFRP5和趋化素浓度。血清样本采集于15+ 0-18 +6周孕龄之间,根据已知与GDM发生的先验关联,选择体重指数(BMI)和母亲年龄进行多变量分析调整。结果:在该肥胖队列中(中位BMI为35.7 kg/m2, IQR为33.2-40.3 kg/m2),生化指标与GDM无相关性:sFRP5比值比(OR) 0.44(95%可信区间(CI) 0.01-23.18, p = 0.687), sFRP4比值比(OR) 0.55 (95% CI 0.09-3.52, p = 0.528), chemerin比值比(OR) 3.47 (95% CI 0.05-227.72, p = 0.560)。BMI和母亲年龄的调整对这种关联没有影响。这些指标与胰岛素抵抗(HOMA2-IR)均无显著相关性。结论:在肥胖孕妇队列中,未发现sFRP4、sFRP5或趋化素浓度与GDM的发生相关。相关性的缺失可能表明这些蛋白在肥胖女性GDM的病理生理中发挥的生物学作用较小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Pregnancy Serum Concentration of Secreted Frizzled-Related Protein 4, Secreted Frizzled-Related Protein 5, and Chemerin in Obese Women Who Develop Gestational Diabetes Mellitus
Background: The aim of this study was to evaluate whether secreted frizzled-related protein 4 (sFRP4), secreted frizzled-related protein 5 (sFRP5), and chemerin serum concentrations in early pregnancy are associated with the development of gestational diabetes mellitus (GDM) in an obese cohort. In previous studies, increased sFRP4 and chemerin, and decreased sFRP5 concentrations were associated with the development of GDM in normal and overweight women. Methods: In this exploratory case control study, sFRP4, sFRP5, and chemerin serum concentrations were determined by ELISA in 50 obese women who developed GDM and 100 uncomplicated control pregnancies. Serum samples were obtained between 15+0–18+6 weeks’ gestational age and based on a priori known associations with the development of GDM, body mass index (BMI) and maternal age were selected for adjustment in multivariate analyses. Results: In this obese cohort (median BMI 35.7 kg/m2, IQR 33.2–40.3 kg/m2), the biochemical markers showed no association with GDM: sFRP5 odds ratio (OR) 0.44 (95% confidence interval (CI) 0.01–23.18, p = 0.687), sFRP4 OR 0.55 (95% CI 0.09–3.52, p = 0.528), and chemerin OR 3.47 (95% CI 0.05–227.72, p = 0.560). Adjustment for BMI and maternal age did not influence the association. None of the markers were significantly correlated with insulin resistance (HOMA2-IR). Conclusion: No association was found between sFRP4, sFRP5, or chemerin concentration and the development of GDM in a cohort of obese pregnant women. The absence of the association may indicate that these proteins play a lesser biological role in the pathophysiology of GDM in obese women.
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