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同卵双胞胎研究:无证据表明胰岛素分泌或敏感性的基因决定改变易导致1型糖尿病。

No evidence for genetically determined alteration in insulin secretion or sensitivity predisposing to type 1 diabetes: a study of identical twins.

作者信息

Hawa Mohammed I, Bonfanti Riccardo, Valeri Christina, Delli Castelli Michela, Beyan Huriya, Leslie R David G

机构信息

St. Bartholomew's Hospital, West Smithfield, London EC1A 7BE, U.K.

出版信息

Diabetes Care. 2005 Jun;28(6):1415-8. doi: 10.2337/diacare.28.6.1415.

Abstract

OBJECTIVE

To determine whether inherited changes in insulin secretion or sensitivity could predispose to type 1 diabetes, we studied identical twins of type 1 diabetic patients.

RESEARCH DESIGN AND METHODS

We studied prospectively a consecutive series of 27 identical twins of patients with type 1 diabetes who were initially nondiabetic, as well as 14 control subjects, over a period of 18 years. Of these 27 twins, 15 remain nondiabetic (now estimated at low disease risk) and 12 developed diabetes (pre-diabetic twins). Subjects were tested when not diabetic on at least two occasions with an intravenous glucose tolerance test (IVGTT), and we estimated insulin secretion as first-phase insulin response (FPIR), glucose clearance (K(g)), and insulin sensitivity both by homeostasis model assessment of insulin resistance (HOMA-IR) and relative to insulin response by the basal HOMA-IR-to-FPIR ratio.

RESULTS

Twins now at low risk and control subjects had similar fasting blood glucose and insulin levels, FPIR, K(g), HOMA-IR, and HOMA-IR-to-FPIR ratio. In contrast, pre-diabetic twins compared with control twins had higher fasting insulin levels (10.3 +/- 6.0 vs. 4.6 +/- 4.0 mIU/ml), lower FPIR (245 +/- 129 vs. 796 +/- 622 mIU . ml(-1) . 10 min(-1)), lower K(g) (1.5 +/- 0.6 vs. 2.6 +/- 0.8% per min), and higher HOMA-IR-to-FPIR ratio (0.007 +/- 0.005 vs. 0.001 +/- 0.0009) (all P < 0.01).

CONCLUSIONS

These observations in low-risk nondiabetic identical twins failed to identify a familial alteration in either insulin secretion or sensitivity predisposing to type 1 diabetes.

摘要

目的

为了确定胰岛素分泌或敏感性的遗传变化是否会导致1型糖尿病,我们对1型糖尿病患者的同卵双胞胎进行了研究。

研究设计与方法

我们前瞻性地研究了27对1型糖尿病患者的同卵双胞胎(最初均无糖尿病)以及14名对照受试者,研究时长为18年。在这27对双胞胎中,15人仍未患糖尿病(目前估计疾病风险较低),12人患上了糖尿病(糖尿病前期双胞胎)。受试者在未患糖尿病时至少接受过两次静脉葡萄糖耐量试验(IVGTT)测试,我们通过第一阶段胰岛素反应(FPIR)、葡萄糖清除率(K(g))来评估胰岛素分泌,并通过胰岛素抵抗的稳态模型评估(HOMA-IR)以及基础HOMA-IR与FPIR比值相对于胰岛素反应来评估胰岛素敏感性。

结果

目前处于低风险的双胞胎和对照受试者的空腹血糖和胰岛素水平、FPIR、K(g)、HOMA-IR以及HOMA-IR与FPIR比值相似。相比之下,糖尿病前期双胞胎与对照双胞胎相比,空腹胰岛素水平更高(10.3±6.0对4.6±4.0 mIU/ml),FPIR更低(245±129对796±622 mIU·ml⁻¹·10 min⁻¹),K(g)更低(1.5±0.6对2.6±0.8%每分钟),HOMA-IR与FPIR比值更高(0.007±0.005对0.001±0.0009)(所有P<0.01)。

结论

在低风险非糖尿病同卵双胞胎中的这些观察结果未能发现胰岛素分泌或敏感性方面的家族性改变会导致1型糖尿病。

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