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Shift of Glucose Peak Time During Oral Glucose Tolerance Test is Associated with Changes in Insulin Secretion and Insulin Sensitivity After Therapy with Antidiabetic Drugs in Patients with Type?2 Diabetes

机译:口服葡萄糖耐量检测期间的葡萄糖峰值时间与患者患者患者患者患者2糖尿病患者治疗后的胰岛素分泌和胰岛素敏感性的变化有关

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IntroductionDelay in peak blood glucose during an oral glucose tolerance test (OGTT) predicts declining β-cell function and poor ability to regulate glucose metabolism. Glucose peak time has not been used as a comparative indicator of the improvement in islet function after treatment with exenatide, insulin, or oral antidiabetic drugs (OADs). We evaluated the efficacy of three types of antidiabetic drugs on the basis of blood glucose peak time in patients with non-newly diagnosed type?2 diabetes.MethodsThe data from 100 patients with diabetes who completed two OGTTs within 6?months were collected. Thirty-seven of them with type?2 diabetes were treated with Humalog Mix25, 28 patients with OADs (metformin, acarbose, and gliclazide), and 35 patients with exenatide.ResultsGlycated hemoglobin improved in all three groups after treatment ( P ?0.05). Subcutaneous adipose tissue ( P ?0.01) and visceral adipose tissue ( P ?0.0001) significantly decreased in the exenatide group. The insulinogenic index (IGI) ( P =?0.01) and IGI?×?oral glucose insulin sensitivity (OGIS) ( P =?0.01) improved in the exenatide group only. Homeostatic assessment of β-cell function (HOMA-β) and OGIS were greater in the exenatide and OAD groups than in the Humalog Mix25 group (all P ?0.05). A shift to an earlier peak was observed in 57.1%, 35.7%, and 27.0% of patients in the exenatide, OAD, and Humalog Mix25 groups, respectively ( P =?0.029). OGIS (odds ratio [OR] 0.54, 95% confidence interval [CI] 0.33–0.89, P =?0.026) and IGI?×?OGIS (OR 1.72, 95% CI 0.44–6.68, P =?0.012) were independently related to shifts in glucose peak time.ConclusionExenatide, Humalog Mix25, and OADs improved glycemic metabolism. However, exenatide exhibited superior efficacy in shifting blood glucose peak time to an earlier point, while it improved insulin secretion and insulin sensitivity. Hence, the shift of glucose peak time may be considered an indicator for the evaluation of the effect of hypoglycemic drugs.
机译:在口服葡萄糖耐量试验期间(OGTT)期间峰血糖中的引入预测β细胞功能下降和调节葡萄糖代谢的差。葡萄糖峰值时间未被用作用艾森司,胰岛素或口服抗糖尿病药物(OADS)治疗后胰岛功能改善的对比指标。我们在非新诊断的型糖尿病患者血糖峰值时间的基础上评估了三种抗糖尿病药物的功效。收集了100名糖尿病患者的10例糖尿病患者的数据。收集了6个月内的糖尿病患者。其中三十七种患有2型糖尿病治疗28例OADS(二甲双胍,氨基糖和神经脂醇)和艾塞那肽的35名患者治疗。治疗后,所有三组血红蛋白的血红蛋白得到改善(P <0.05 )。皮下脂肪组织(P&LT; 0.01)和内脏脂肪组织(P <0.0001)显着降低。胰岛素原指数(IgI)(p = 0.01)和IgI?×ααααααααααα-α×0℃(P =β01)仅在杂交组中改善。 β-细胞功能(HOMA-β)和OAD的稳态评估在eXenatide和OAD组中比Humalog Mix25组(所有P& 0.05)。在57.1%,35.7%和27.0%的患者中分别观察到早期峰的转变分别观察到exenatide,OAD和Humalog混合25组的57.1%,35.7%和27.0%(p = 0.029)。 OGIS(差距[或] 0.54,95%置信区间[CI] 0.33-0.89,P = 0.026)和IgI?×ααα×ogis(或1.72,95%CI 0.44-6.68,P = 0.012)是独立相关的转向葡萄糖峰时。合并份子,Humalog Mix25和OADS改善血糖新陈代谢。然而,艾塞那肽在将血糖峰值时间转移到较早点的卓越效果,而它改善了胰岛素分泌和胰岛素敏感性。因此,葡萄糖峰时间的变化可以被认为是评估降血糖药物的影响的指示。

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