首页> 美国卫生研究院文献>American Journal of Human Genetics >Association of the insulin-receptor variant Met-985 with hyperglycemia and non-insulin-dependent diabetes mellitus in the Netherlands: a population-based study.
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Association of the insulin-receptor variant Met-985 with hyperglycemia and non-insulin-dependent diabetes mellitus in the Netherlands: a population-based study.

机译:在荷兰胰岛素受体变体Met-985与高血糖和非胰岛素依赖型糖尿病的关联:一项基于人群的研究。

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摘要

One of the characteristics of non-insulin-dependent diabetes mellitus (NIDDM) is the presence of insulin resistance. Most NIDDM patients have a normal sequence of the insulin receptor, indicating that, if insulin-receptor mutations contribute to the development of NIDDM, they will be present only in a minor fraction of the NIDDM population. The goal of the present study was to examine whether insulin-receptor mutations contribute to the development of NIDDM. We examined 161 individuals with NIDDM and 538 healthy controls from the population-based Rotterdam study for the presence of mutations in the insulin-receptor gene by SSCP. A heterozygous mutation changing valine-985 into methionine was detected in 5.6% of diabetic subjects and in 1.3% of individuals with normal oral glucose tolerance test. Adjusted for age, gender, and body-mass index, this revealed a relative risk for diabetes of 4.49 (95% confidence interval 1.59-12.25) for Met-985 carriers. When the total study group was analyzed, the prevalence of the mutation increased with increasing serum glucose levels (test for trend P < .005). We conclude that the Met-985 insulin-receptor variant associates with hyperglycemia and represents a risk factor for NIDDM.
机译:非胰岛素依赖型糖尿病(NIDDM)的特征之一是存在胰岛素抵抗。大多数NIDDM患者具有正常的胰岛素受体序列,这表明,如果胰岛素受体突变有助于NIDDM的发展,那么他们只会出现在NIDDM人群的一小部分。本研究的目的是检查胰岛素受体突变是否有助于NIDDM的发展。我们从基于人群的鹿特丹研究中检查了161名NIDDM个体和538名健康对照,以研究SSCP胰岛素受体基因中突变的存在。在5.6%的糖尿病患者和1.3%正常口服葡萄糖耐量试验的个体中检测到了将缬氨酸-985变为蛋氨酸的杂合突变。对年龄,性别和身体质量指数进行调整后,得出Met-985携带者患糖尿病的相对风险为4.49(95%置信区间1.59-12.25)。当对整个研究组进行分析时,突变的发生率随血清葡萄糖水平的升高而增加(趋势P <.005的检验)。我们得出的结论是,Met-985胰岛素受体变体与高血糖症相关,并且是NIDDM的危险因素。

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