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The Association of Fasting Glucose Insulin and C-Peptide with 19-Year Incidence of Coronary Heart Disease in Older Japanese-American Men; the Honolulu Heart Program

机译:空腹血糖胰岛素和C肽与年长日裔美国人冠心病发病率19年的关系;檀香山心脏计划

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摘要

The role of fasting glucose, insulin levels, and C-peptide in coronary heart disease (CHD) in non-diabetic individuals remains uncertain. We examined the association between fasting glucose, insulin and C-peptide with the long-term incidence of CHD in Japanese-American men. In 1980–1982, from a random sample of the Honolulu Heart Program men (n = 1378), aged 61–81 years, data on several CHD and metabolic risk factors were obtained to examine the relation of fasting glucose, insulin and C-peptide to 19-year CHD incidence. Age-adjusted incidence of CHD increased with increasing quintiles of glucose, insulin and C-peptide. Age-adjusted CHD rates in the glucose quintiles were 11.9, 11.6, 14.4, 18.1 and 24.1 per 1000 person-years (trend p < 0.001). In individual Cox models (lowest quintiles of glucose, insulin and C-peptide as reference) the relative risks (95% confidence interval) of CHD incidence for the glucose quintiles adjusting for age, smoking, hypertension, cholesterol, physical activity, and body mass index, were 0.9 (0.6–1.4), 1.2 (0.8–1.8), 1.4 (0.9–2.2), and 1.7 (1.1–2.6), respectively (trend p = 0.004). Insulin and C-peptide were not significantly associated with CHD on multivariate analysis. Fasting glucose remained the only significant predictor of increased CHD risk (p = 0.003) in a model combining all 3 metabolic variables. In this cohort, only fasting glucose independently predicts long-term incidence of CHD. Age-adjusted insulin and C-peptide levels were associated with CHD incidence, but after adjustment for other risk factors, do not independently predict CHD.
机译:空腹血糖,胰岛素水平和C肽在非糖尿病个体中的冠心病(CHD)中的作用仍不确定。我们研究了日裔男性中空腹血糖,胰岛素和C肽与冠心病的长期发生之间的关系。在1980–1982年间,从檀香山心脏计划男性(n = 1378)(年龄为61–81岁)的随机样本中,获得了几种冠心病和代谢危险因素的数据,以检查空腹血糖,胰岛素和C肽之间的关系。至19年的冠心病发病率。年龄调整后的冠心病发病率随葡萄糖,胰岛素和C肽五分位数的增加而增加。葡萄糖五分位数的年龄校正后冠心病发生率分别为每1000人年11.9、11.6、14.4、18.1和24.1(趋势p <0.001)。在各个Cox模型中(以葡萄糖,胰岛素和C肽的最低五分位数为参考),针对葡萄糖五分位数的CHD发生率的相对风险(95%置信区间)针对年龄,吸烟,高血压,胆固醇,身体活动和体重进行了调整指数分别为0.9(0.6-1.4),1.2(0.8-1.8),1.4(0.9-2.2)和1.7(1.1-2.6)(趋势p = 0.004)。在多变量分析中,胰岛素和C肽与冠心病无显着相关性。空腹血糖仍然是合并所有3种代谢变量的模型中CHD风险增加的唯一重要预测因子(p = 0.003)。在这个队列中,只有空腹血糖才能独立预测CHD的长期发生率。年龄调整后的胰岛素和C肽水平与冠心病发生率相关,但在调整其他危险因素后,不能独立预测冠心病。

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