Szathmary E J
Hum Genet. 1987 Apr;75(4):368-72. doi: 10.1007/BF00284110.
The metabolically active form of vitamin D, 1,25-(OH)2D3, is involved in the regulation of insulin level. Because the serum group-specific component (Gc) binds vitamin D, it is worth knowing whether differences in basal insulin levels are associated with Gc genotype. Such differences would warrant further investigation to clarify whether selection maintains Gc polymorphism through differential risk of Gc genotypes to diseases that involve insulin. Blood samples were collected in a study designed to address issues in the etiology of non-insulin-dependent diabetes mellitus in Amerindians. Fasting insulin levels and Gc genotype (including subtypes of Gc1) were determined for 144 adult Dogrib Indians of the Northwest Territories, Canada. Hierarchical regression of log10 transformed fasting insulin on age and adiposity within each sex showed that age had no effect on insulin level, but adiposity as measured by the body mass index (BMI) had a very highly significant effect. Analysis of covariance of log10 fasting insulin by sex, by Gc genotype and with adjustment for the effects of the covariate, BMI, was very highly significant. All interaction terms in the model were nonsignificant. The only variable that had a significant effect after adjustment for the BMI was Gc genotype (F4,133 = 3.71; P = 0.007). Covariance analysis was repeated on a subset of the sample (124 people). The reduced data set excluded all individuals who had, on at least one occasion, abnormal response to oral glucose challenge [impaired glucose tolerance (IGT) or non-insulin-dependent diabetes mellitus (NIDDM]). Again, after correction for the effects of the BMI, only Gc genotype had a significant effect on fasting insulin level (F4,113 = 2.61; P = 0.040). Homozygotes for Gc 1F-1F had the lowest measures of fasting insulin.
维生素D的代谢活性形式1,25-(OH)₂D₃参与胰岛素水平的调节。由于血清组特异性成分(Gc)能结合维生素D,因此了解基础胰岛素水平的差异是否与Gc基因型相关是有意义的。这种差异值得进一步研究,以阐明选择是否通过Gc基因型对涉及胰岛素的疾病的不同风险来维持Gc多态性。在一项旨在解决美洲印第安人非胰岛素依赖型糖尿病病因问题的研究中采集了血样。对加拿大西北地区144名成年多格里布印第安人的空腹胰岛素水平和Gc基因型(包括Gc1的亚型)进行了测定。对每个性别中经log₁₀转换的空腹胰岛素与年龄和肥胖程度进行分层回归分析,结果显示年龄对胰岛素水平无影响,但用体重指数(BMI)衡量的肥胖程度有非常显著的影响。对经log₁₀转换的空腹胰岛素按性别、Gc基因型进行协方差分析,并对协变量BMI的影响进行校正,结果非常显著。模型中的所有交互项均无显著意义。在对BMI进行校正后,唯一有显著影响的变量是Gc基因型(F4,133 = 3.71;P = 0.007)。对样本的一个子集(124人)重复进行协方差分析。简化后的数据集排除了所有至少有一次口服葡萄糖耐量试验反应异常[糖耐量受损(IGT)或非胰岛素依赖型糖尿病(NIDDM)]的个体。同样,在对BMI的影响进行校正后,只有Gc基因型对空腹胰岛素水平有显著影响(F4,113 = 2.61;P = 0.040)。Gc 1F-1F纯合子的空腹胰岛素测量值最低。