SstI、RFLP和高血压是意大利南部男性冠状动脉外粥样硬化的危险因素

Artery Pub Date : 1994-01-01
A Pujia, A Gnasso, D Siclari, A Dominijanni, A Zingone, O Marasco, E Mele, C Cortese, A Colonna, P L Mattioli
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摘要

本研究旨在探讨ApoAI-CIII-AIV基因簇SstI多态性与经典冠心病危险因素和冠状动脉外粥样硬化之间的可能关联。126名男性受试者接受颈动脉和股动脉超声多普勒检查、冠心病危险因素评估和SstI基因分型。在有或没有冠状动脉外病变的受试者中,罕见SsI等位基因的频率分别为12.1%和6.7%,与冠心病危险因素分布的差异无关。40例有高血压,34例有常见等位基因纯合,6例有罕见等位基因存在。其中,10例(29%)和5例(83%)分别患有冠状动脉外粥样硬化。此外,该罕见等位基因纯合子的受试者表现出血脂异常和高血压和/或高脂血症家族史阳性。这些发现表明ApoAI-CIII-AIV基因复合物在脂质代谢和血压调节中可能发挥作用,并可能有助于识别高血压患者中易于发生冠状动脉外粥样硬化的受试者。
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SstI RFLP and hypertension as risk factors for extracoronary atherosclerosis in a male population of southern Italy.

The present study was designed to investigate on possible association between SstI polymorphism in the ApoAI-CIII-AIV gene cluster, classical coronary heart disease risk factors and extracoronary atherosclerosis. One hundred and twenty six male subjects were enrolled and underwent echo-Doppler examination of carotid and femoral arteries, coronary heart disease risk factors assessment and SstI genotyping. The frequency of the rare SsI allele was 12.1% and 6.7% in subjects with or without extracoronary lesions respectively and was not associated with differences in the distribution of coronary heart disease risk factors. Forty subjects had hypertension, 34 homozygous for the frequent allele and 6 with presence of the rare allele. Among these, 10 subjects (29%) and 5 subjects (83%), respectively, had extracoronary atherosclerosis. Furthermore, subjects homozygous for the rare allele exhibited lipid abnormalities and a family history positive for hypertension and/or hyperlipidemia. These findings suggest a possible role for the ApoAI-CIII-AIV gene complex in both lipid metabolism and blood pressure regulation and could be of help to identify, within hypertensives, those subjects prone to extracoronary atherosclerosis.

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