Mayer E J, Newman B, Austin M A, Zhang D, Quesenberry C P, Edwards K, Selby J V
Department of Public Health Sciences, Bowman Gray School of Medicine, Wake Forest University, Winston Salem, NC 27157-1063, USA.
Am J Epidemiol. 1996 Feb 15;143(4):323-32. doi: 10.1093/oxfordjournals.aje.a008746.
Multiple factors may determine insulin resistance and the insulin resistance syndrome. The contributions of genes and environment to the distribution of fasting insulin levels and to the associations of fasting insulin with elements of the syndrome were evaluated in the second examination of the Kaiser Permanente Women Twins Study (Oakland, California, 1989-1990). Subjects included 556 white women (165 monozygous twin pairs, 113 dizygous pairs; 455 women with normal glucose tolerance, 75 with impaired glucose tolerance, and 26 with non-insulin-dependent diabetes by World Health Organization criteria). The intraclass correlation coefficients for log fasting insulin for monozygous and dizygous twin pairs were 0.64 and 0.40, respectively. After adjustment for age, behavioral factors, and body mass index, the estimated classic heritability was 0.53 (p = 0.003). Commingling analysis of fasting insulin indicated the presence of four distributions (p < 0.001), consistent with at least one, and perhaps two, genes influencing this trait. In an unmatched multiple regression model among women from monozygous twin pairs only, log fasting insulin was independently associated with body mass index (p < 0.0001), waist/hip ratio (p = 0.02), and glucose intolerance (p = 0.04), but not with triglycerides, high density lipoprotein cholesterol, or hypertension. After removal of genetic influences by analysis of monozygous intrapair differences, only body mass index (p < 0.0001) remained independently related to fasting insulin. The authors conclude that, in addition to significant genetic influences on fasting insulin, environmental or behavioral factors (particularly nongenetic variation in obesity) are important determinants of fasting insulin and the insulin resistance syndrome.
多种因素可能决定胰岛素抵抗和胰岛素抵抗综合征。在凯泽永久医疗集团女性双胞胎研究的第二次检查(1989 - 1990年,加利福尼亚州奥克兰)中,评估了基因和环境对空腹胰岛素水平分布以及空腹胰岛素与该综合征各要素之间关联的影响。研究对象包括556名白人女性(165对同卵双胞胎,113对异卵双胞胎;根据世界卫生组织标准,455名葡萄糖耐量正常的女性,75名葡萄糖耐量受损的女性,以及26名非胰岛素依赖型糖尿病女性)。同卵和异卵双胞胎对的空腹胰岛素对数的组内相关系数分别为0.64和0.40。在对年龄、行为因素和体重指数进行调整后,估计的经典遗传度为0.53(p = 0.003)。空腹胰岛素的混合分析表明存在四种分布(p < 0.001),这与至少一个,也许两个影响该性状的基因一致。在仅针对同卵双胞胎女性的非匹配多元回归模型中,空腹胰岛素对数与体重指数(p < 0.0001)、腰臀比(p = 0.02)和葡萄糖不耐受(p = 0.04)独立相关,但与甘油三酯、高密度脂蛋白胆固醇或高血压无关。通过分析同卵双胞胎对内差异去除遗传影响后,只有体重指数(p < 0.0001)仍与空腹胰岛素独立相关。作者得出结论,除了基因对空腹胰岛素有显著影响外,环境或行为因素(特别是肥胖的非遗传变异)是空腹胰岛素和胰岛素抵抗综合征的重要决定因素。