Han Zhihua, Heath Simon C, Shmulewitz Dvora, Li Wentian, Auerbach Steve B, Blundell Maude L, Lehner Thomas, Ott Jurg, Stoffel Markus, Friedman Jeffrey M, Breslow Jan L
Starr Center Human Genetics, Rockefeller University, New York, New York 10021, USA.
Am J Med Genet. 2002 Jul 1;110(3):234-42. doi: 10.1002/ajmg.10445.
Altered plasma levels of lipids and lipoproteins, obesity, hypertension, and diabetes are major risk factors for atherosclerotic cardiovascular disease. To identify genes that affect these traits and disorders, we looked for association between markers in candidate genes (apolipoprotein AII (apo AII), apolipoprotein AI-CIII-AIV gene cluster (apo AI-CIII-AIV), apolipoprotein E (apo E), cholesteryl ester transfer protein (CETP), cholesterol 7alpha-hydroxylase (CYP7a), hepatic lipase (HL), and microsomal triglyceride transfer protein (MTP)) and known risk factors (triglycerides (Tg), total cholesterol (TC), apolipoprotein AI (apo AI), apolipoprotein AII (apo AII), apolipoprotein B (apo B), body mass index (BMI), blood pressure (BP), leptin, and fasting blood sugar (FBS) levels.) A total of 1,102 individuals from the Pacific island of Kosrae were genotyped for the following markers: Apo AII/MspI, Apo CIII/SstI, Apo AI/XmnI, Apo E/HhaI, CETP/TaqIB, CYP7a/BsaI, HL/DraI, and MTP/HhpI. After testing for population stratification, family-based association analysis was carried out. Novel associations found were: 1) the apo AII/MspI with apo AI and BP levels, 2) the CYP7a/BsaI with apo AI and BMI levels. We also confirmed the following associations: 1) the apo AII/MspI with Tg level; 2) the apo CIII/SstI with Tg, TC, and apo B levels; 3) the Apo E/HhaI E2, E3, and E4 alleles with TC, apo AI, and apo B levels; and 4) the CETP/TaqIB with apo AI level. We further confirmed the connection between the apo AII gene and Tg level by a nonparametric linkage analysis. We therefore conclude that many of these candidate genes may play a significant role in susceptibility to heart disease.
血浆脂质和脂蛋白水平改变、肥胖、高血压及糖尿病是动脉粥样硬化性心血管疾病的主要危险因素。为了确定影响这些性状和疾病的基因,我们研究了候选基因(载脂蛋白AII(apo AII)、载脂蛋白AI-CIII-AIV基因簇(apo AI-CIII-AIV)、载脂蛋白E(apo E)、胆固醇酯转运蛋白(CETP)、胆固醇7α-羟化酶(CYP7a)、肝脂酶(HL)和微粒体甘油三酯转运蛋白(MTP))中的标记物与已知危险因素(甘油三酯(Tg)、总胆固醇(TC)、载脂蛋白AI(apo AI)、载脂蛋白AII(apo AII)、载脂蛋白B(apo B)、体重指数(BMI)、血压(BP)、瘦素和空腹血糖(FBS)水平)之间的关联。对来自太平洋科斯雷岛的1102名个体进行了以下标记物的基因分型:Apo AII/MspI、Apo CIII/SstI、Apo AI/XmnI、Apo E/HhaI、CETP/TaqIB、CYP7a/BsaI、HL/DraI和MTP/HhpI。在检测了人群分层后,进行了基于家系的关联分析。发现的新关联有:1)apo AII/MspI与apo AI和BP水平;2)CYP7a/BsaI与apo AI和BMI水平。我们还证实了以下关联:1)apo AII/MspI与Tg水平;2)apo CIII/SstI与Tg、TC和apo B水平;3)Apo E/HhaI的E2、E3和E4等位基因与TC、apo AI和apo B水平;4)CETP/TaqIB与apo AI水平。我们通过非参数连锁分析进一步证实了apo AII基因与Tg水平之间的联系。因此,我们得出结论,这些候选基因中的许多可能在心脏病易感性中起重要作用。