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APOE and FABP2 Polymorphisms and History of Myocardial Infarction, Stroke, Diabetes, and Gallbladder Disease

机译:APOE和FABP2多态性与心肌梗塞,中风,糖尿病和胆囊疾病的病史

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Dysfunctional lipid metabolism plays a central role in pathogenesis of major chronic diseases, and genetic factors are important determinants of individual lipid profiles. We analyzed the associations of two well-established functional polymorphisms (FABP2A54T andAPOEisoforms) with past and family histories of 1492 population samples.FABP2-T54allele was associated with an increased risk of past history of myocardial infarction (odds ratio (OR) = 1.51). Likewise, the subjects withAPOE4, compared withE2andE3, had a significantly increased risk of past history myocardial infarction (OR = 1.89). The OR associated withAPOE4was specifically increased in women for past history of myocardial infarction but decreased for gallstone disease. Interactions between gender andAPOEisoforms were also significant or marginally significant for these two conditions.FABP2-T54allele may be a potential genetic marker for myocardial infarction, andAPOE4may exert sex-dependent effects on myocardial infarction and gallbladder disease.
机译:脂质代谢异常在主要慢性疾病的发病机理中起着核心作用,遗传因素是单个脂质谱的重要决定因素。我们分析了两种公认的功能性多态性(FABP2A54T和APOEisoforms)与1492人群样本的过去和家族史的关联.FABP2-T54等位基因与过去的心肌梗塞病史风险增加相关(比值比(OR)= 1.51)。同样,与E2和E3相比,患有APOE4的受试者罹患既往心肌梗塞的风险显着增加(OR = 1.89)。在过去的心肌梗塞病史中,女性与APOE4相关的OR特别升高,而胆结石疾病的OR降低。在这两种情况下,性别与APOE同工型之间的相互作用也很显着或略有显着性。FABP2-T54等位基因可能是心肌梗死的潜在遗传标志,而APOE4可能对心肌梗塞和胆囊疾病发挥性别依赖性。

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