Rewers M, Kamboh M I, Hoag S, Shetterly S M, Ferrell R E, Hamman R F
Department of Preventive Medicine, University of Colorado, Denver 80262.
Diabetes. 1994 Dec;43(12):1485-9. doi: 10.2337/diab.43.12.1485.
Non-insulin-dependent diabetes mellitus (NIDDM) confers myocardial infarction (MI) risk unexplained by known factors. In 356 NIDDM patients and 1,087 people with normal glucose tolerance, we investigated the association between MI risk and polymorphism at codon 360 in the apolipoprotein A-IV (apoA-IV) gene. During 1984-1992, MI was diagnosed in 84 diabetic and in 106 nondiabetic people. The risk of MI did not differ by apoA-IV phenotype in nondiabetic people; however, in NIDDM patients, those with the apoA-IV 1-2 phenotype had 2.8 (95% confidence interval: 1.4-5.6) higher MI risk than those with the 1-1 phenotype, adjusting for age, gender, ethnicity, hypertension, smoking, body mass index, fat centrality, and low-density lipoprotein and high-density lipoprotein cholesterol. The risk of MI was particularly high in obese NIDDM patients with the apoA-IV 1-2 phenotype: 5.1 (2.4-11.2) times that in obese apoA-IV 1-1 NIDDM patients and 7.7 (3.6-16.7) times that in lean nondiabetic people. The effect of apoA-IV 1-2 did not appear to be a part of the insulin-resistance syndrome nor was it dependent on diabetes duration or control. One half of the excess MI risk in the diabetic population studied was explained by the apoA-IV 1-2 phenotype. These results indicate that approximately 17% of NIDDM patients have a high MI risk apoA-IV phenotype that is particularly deleterious in obese patients.
非胰岛素依赖型糖尿病(NIDDM)会带来已知因素无法解释的心肌梗死(MI)风险。在356例NIDDM患者和1087例糖耐量正常的人群中,我们研究了载脂蛋白A-IV(apoA-IV)基因第360位密码子多态性与MI风险之间的关联。在1984年至1992年期间,84例糖尿病患者和106例非糖尿病患者被诊断出患有MI。在非糖尿病患者中,MI风险在不同apoA-IV表型之间没有差异;然而,在NIDDM患者中,调整年龄、性别、种族、高血压、吸烟、体重指数、中心性肥胖以及低密度脂蛋白和高密度脂蛋白胆固醇后,具有apoA-IV 1-2表型的患者发生MI的风险比具有1-1表型的患者高2.8倍(95%置信区间:1.4-5.6)。具有apoA-IV 1-2表型的肥胖NIDDM患者发生MI的风险特别高:是肥胖apoA-IV 1-1 NIDDM患者的5.1倍(2.4-11.2),是瘦的非糖尿病患者的7.7倍(3.6-16.7)。apoA-IV 1-2的影响似乎不是胰岛素抵抗综合征的一部分,也不依赖于糖尿病病程或控制情况。在研究的糖尿病患者人群中,超过一半的额外MI风险可由apoA-IV 1-2表型解释。这些结果表明,约17%的NIDDM患者具有高MI风险的apoA-IV表型,这在肥胖患者中尤其有害。