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首页> 外文期刊>The Lancet >Effect of a diabetic environment in utero on predisposition to type 2 diabetes.
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Effect of a diabetic environment in utero on predisposition to type 2 diabetes.

机译:子宫内糖尿病环境对2型糖尿病易感性的影响。

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BACKGROUND: Type 2 diabetes is affected by genetics and environmental factors. We aimed to assess the effect of an in-utero diabetic environment independently of the genetic background for type 2 diabetes. METHODS: We measured insulin sensitivity and insulin secretion in response to oral and intravenous glucose in 15 non-diabetic adult offspring of mothers with type 1 diabetes (exposed participants) and 16 offspring of type 1 diabetic fathers (controls). No participants had type 1 diabetes-associated autoantibodies. We also measured pancreatic polypeptide, a marker of parasympathetic drive to the pancreas. FINDINGS: There was no difference between the groups with respect to percent body fat and insulin sensitivity. Five of the 15 exposed participants, but none of the controls had impaired glucose tolerance (p=0.02). Early insulin secretion after an oral glucose tolerance test was lower in exposed participants than in controls: 8.6 IU/mmol (SD 5.4) in exposed participants with impaired glucose tolerance, 14.2 IU/mmol (6.5) in those with normal glucose tolerance and 17.7 IU/mmol (10.9) in controls (p=0.04). Mean insulin secretion rate during glucose infusion study was 4.7 pmol/kg per min (3.6) in people with impaired glucose tolerance, 5.5 pmol/kg per min (4.5) in exposed participants with normal glucose tolerance and 7.5 pmol/kg per min (6.1) in controls (p<0.0001). The area under the curve of pancreatic polypeptide 120 min after oral glucose ingestion was 1007 (429) in people with impaired glucose tolerance, 2829 (1701) in those with normal glucose tolerance, and 3224 (1352) in controls (p=0.04). INTERPRETATION: Exposure to a diabetic environment in utero is associated with increased occurrence of impaired glucose tolerance and a defective insulin secretory response in adult offspring, independent of genetic predisposition to type 2 diabetes. This insulin secretory defect could be related to low parasympathetic tone. Epidemiological studies are needed to confirm our observations before therapeuticstrategies can be devised.
机译:背景:2型糖尿病受遗传和环境因素的影响。我们旨在独立于2型糖尿病的遗传背景评估宫内糖尿病环境的影响。方法:我们测量了15位1型糖尿病母亲的非糖尿病成年后代(暴露的参与者)和16位1型糖尿病父亲的后代(对照)对口服和静脉葡萄糖反应的胰岛素敏感性和胰岛素分泌。没有参与者患有1型糖尿病相关的自身抗体。我们还测量了胰腺多肽,它是胰腺副交感神经驱动的标志物。结果:两组之间在体脂百分比和胰岛素敏感性方面没有差异。 15位暴露的参与者中有5位,但没有一个对照组的葡萄糖耐量受损(p = 0.02)。口服葡萄糖耐量测试后的早期胰岛素分泌低于暴露的参与者,低于对照组:葡萄糖耐量受损的暴露参与者为8.6 IU / mmol(SD 5.4),葡萄糖耐量正常和17.7 IU的参与者为14.2 IU / mmol(6.5)对照中为/ mmol(10.9)(p = 0.04)。在葡萄糖耐量受损的人群中,葡萄糖输注研究期间的平均胰岛素分泌率为4.7 pmol / kg / min(3.6),在葡萄糖耐量正常的暴露受试者中平均胰岛素分泌率为5.5 pmol / kg / min(4.5),每分钟7.5 pmol / kg(6.1) )(p <0.0001)。口服葡萄糖摄取后120分钟的胰多肽曲线下面积在葡萄糖耐量受损的人群中为1007(429),在葡萄糖耐量正常的人群中为2829(1701),而对照组为3224(1352)(p = 0.04)。解释:在子宫内暴露于糖尿病环境与成年后代中糖耐量降低的发生率增加和胰岛素分泌反应不良有关,而与2型糖尿病的遗传易感性无关。该胰岛素分泌缺陷可能与副交感神经张力低有关。在制定治疗策略之前,需要进行流行病学研究以证实我们的观察结果。

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