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Changes in insulin sensitivity during leptin replacement therapy in leptin-deficient patients

机译:瘦素缺乏症患者瘦素替代疗法期间胰岛素敏感性的变化

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摘要

Leptin replacement rescues the phenotype of morbid obesity and hypogonadism in leptin-deficient adults. However, leptin's effects on insulin resistance are not well understood. Our objective was to evaluate the effects of leptin on insulin resistance. Three leptin-deficient adults (male, 32 yr old, BMI 23.5 kg/m2; female, 42 yr old, BMI 25.1 kg/m2; female, 46 yr old, BMI 31.7 kg/m2) with a missense mutation of the leptin gene were evaluated during treatment with recombinant methionyl human leptin (r-metHuLeptin). Insulin resistance was determined by euglycemic hyperinsulinemic clamps and by oral glucose tolerance tests (OGTTs), whereas patients were on r-metHuLeptin and after treatment was interrupted for 2–4 wk in the 4th, 5th, and 6th years of treatment. At baseline, all patients had normal insulin levels, C-peptide, and homeostatic model assessment of insulin resistance index, except for one female diagnosed with type 2 diabetes. The glucose infusion rate was significantly lower with r-metHuLeptin (12.03 ± 3.27 vs. 8.16 ± 2.77 mg·kg−1·min−1, P = 0.0016) but did not differ in the 4th, 5th, and 6th years of treatment when all results were analyzed by a mixed model [F(,) = 0.57 and P = 0.5951]. The female patient with type 2 diabetes became euglycemic after treatment with r-metHuLeptin and subsequent weight loss. The OGTT suggested that two patients showed decreased insulin resistance while off treatment. During an off-leptin OGTT, one of the patients developed a moderate hypoglycemic reaction attributed to increased posthepatic insulin delivery and sensitivity. We conclude that, in leptin-deficient adults, the interruption of r-metHuLeptin decreases insulin resistance in the context of rapid weight gain. Our results suggest that hyperleptinemia may contribute to mediate the increased insulin resistance of obesity.
机译:瘦素替代可以挽救缺乏瘦素的成年人的病态肥胖和性腺功能减退的表型。然而,瘦蛋白对胰岛素抵抗的作用尚不十分清楚。我们的目的是评估瘦素对胰岛素抵抗的影响。三个瘦素缺乏症的成年人(男性,32岁,BMI 23.5 kg / m 2 ;女性,42岁,BMI 25.1 kg / m 2 ;女性,46岁在重组甲硫氨酰人瘦素(r-metHuLeptin)治疗期间,对年龄为31.7 kg / m 2 的BMI进行了评估。胰岛素抵抗是通过正常血糖高胰岛素钳夹和口服葡萄糖耐量试验(OGTT)来确定的,而患者使用r-metHuLeptin并在治疗的第4、5和6年中中断治疗后2-4周。在基线时,除一名女性被诊断患有2型糖尿病外,所有患者的胰岛素水平,C肽水平均正常,并且胰岛素抵抗指数的稳态模型评估。 r-metHuLeptin的葡萄糖输注率显着降低(12.03±3.27 vs. 8.16±2.77 mg·kg -1 ·min -1 ,P = 0.0016),但确实当通过混合模型[F(,)= 0.57和P = 0.5951]分析所有结果时,在治疗的第4年,第5年和第6年没有差异。 2型糖尿病女性患者经r-metHuLeptin治疗后体重减轻,血糖正常。 OGTT建议两名患者在停药时胰岛素抵抗降低。在瘦素OGTT期间,其中一名患者出现中度降血糖反应,这归因于肝后胰岛素传递和敏感性增加。我们得出的结论是,在瘦素缺乏的成年人中,r-metHuLeptin的中断会在体重快速增加的情况下降低胰岛素抵抗。我们的结果表明,高瘦素血症可能有助于介导肥胖症胰岛素抵抗的增加。

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