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Impaired beta-cell function in lean normotolerant former gestational diabetic women.

机译:瘦瘦的前妊娠糖尿病妇女的β细胞功能受损。

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BACKGROUND: Former gestational diabetes (fGDM) constitutes a risk condition for the development of Type 2 diabetes. Former gestational diabetes is often characterized by obesity and hyperglycaemia, which may be concomitant and independent risk factors. MATERIALS AND METHODS: To assess insulin sensitivity and beta-cell function in fGDM uncomplicated by obesity and hyperglycaemia, we studied 24 lean fGDM women and 23 control women matched for age (30.7 +/- 0.7 years, whole cohort), body mass index (22.2 +/- 0.3 kg m(-2)), and indistinguishable for plasma glucose both at fasting and at 120 min. Several insulin sensitivity and beta-cell function indices were computed: homeostasis model assessment insulin resistance index (HOMA-R), insulin sensitivity index derived from an oral glucose tolerance test (OGIS), insulinogenic index, other empirical indices of insulin secretion and beta-cell function, and indices obtained using a beta-cell model. RESULTS: Though the majority of indices, and in particular insulinsensitivity (HOMA-R: 1.35 +/- 0.13 vs. 1.65 +/- 0.14; OGIS: 492.7 +/- 6.3 vs. 496.4 +/- 9.4 mL min(-1) m(-2)), were not significantly different in the two groups, the beta-cell glucose sensitivity obtained by modelling analysis was lower in fGDM (108 +/- 14 vs. 165 +/- 22 pmol min(-1) m(-2) mM(-1), P = 0.031). CONCLUSIONS: Impairment of beta-cell glucose sensitivity may be an intrinsic risk factor in fGDM independently of obesity and hyperglycaemia. Furthermore, we have shown that modelling analysis, in contrast to the empirical parameters, may be able to detect early beta-cell alterations in fGDM women.
机译:背景:前妊娠糖尿病(fGDM)构成2型糖尿病发展的风险条件。前妊娠糖尿病通常以肥胖和高血糖症为特征,这可能是伴随和独立的危险因素。材料与方法:为了评估未伴有肥胖和高血糖的fGDM患者的胰岛素敏感性和β细胞功能,我们研究了24位瘦身的fGDM妇女和23名对照妇女,其年龄(30.7 +/- 0.7岁,整个队列),体重指数( 22.2 +/- 0.3 kg m(-2)),并且在禁食和120分钟时血浆葡萄糖均无法区分。计算了几种胰岛素敏感性和β细胞功能指数:稳态模型评估胰岛素抵抗指数(HOMA-R),源自口服葡萄糖耐量试验的胰岛素敏感性指数(OGIS),胰岛素生成指数,其他胰岛素分泌和β-内分泌的经验性指数细胞功能,以及使用β细胞模型获得的指标。结果:尽管大多数指标,尤其是胰岛素敏感性(HOMA-R:1.35 +/- 0.13 vs. 1.65 +/- 0.14; OGIS:492.7 +/- 6.3 vs.496.4 +/- 9.4 mL min(-1) m(-2)),两组间无显着差异,通过模型分析获得的β细胞葡萄糖敏感性在fGDM中较低(108 +/- 14 vs. 165 +/- 22 pmol min(-1)m (-2)mM(-1),P = 0.031)。结论:β-细胞葡萄糖敏感性受损可能是fGDM的固有危险因素,与肥胖和高血糖无关。此外,我们已经表明,与经验参数相比,建模分析可能能够检测fGDM妇女的早期β细胞改变。

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