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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >LDLR, ApoB and ApoE genes polymorphisms and classical risk factors in premature coronary artery disease
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LDLR, ApoB and ApoE genes polymorphisms and classical risk factors in premature coronary artery disease

机译:早发性冠心病的LDLR,ApoB和ApoE基因多态性和经典危险因素

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Lipoproteins play a central role in the development of atherosclerotic disease. So, with their ability to affect lipid levels, the LDLR, ApoB and ApoE polymorphisms could be one of the factors influencing development of atherosclerosis. This hypothesis has been tested in different populations with conflicting results. The purpose of the present study was to investigate the association between the LDLR, ApoB and ApoE genes polymorphisms with premature CAD (PCAD) in Egyptians. One hundred thirty-five patients of PCAD and one hundred thirty-two ages and sex matched control subjects were included in the study. LDLR and ApoB genes polymorphisms were analyzed by polymerase chain reaction (PCR). The ApoE genotypes were identified by multiplex amplification refractory mutation system (multi-AMRS). We found that LDLR A(+) A(+) genotype, ApoB X+ allele and ApoE E4 allele increased the risk of PCAD by 1.8, 2.1 and 12.1 respectively. The present study proved that smoking, metabolic syndrome, ApoB X+X+ genotype and ApoE E4 allele were independent risk factors for the development of PCAD. This is the first study investigate the association between low density lipoprotein receptor, apolipoprotein B and apolipoprotein E genes polymorphisms with PCAD and lipid levels in Egyptians and we concluded that the LDLR A(+)A(+) genotype, ApoB X+ allele and ApoE E4 allele may be associated with an increased risk for development of PCAD by elevated levels of total cholesterol (TC) and low density lipoprotein (LDLc). The coexistence of CAD risk factors with LDLR A(+)A(+) genotype, ApoB X+ allele and ApoE E4 allele may increase the risk of the development of PCAD in Egyptian patients. (C) 2016 Elsevier B.V. All rights reserved.
机译:脂蛋白在动脉粥样硬化疾病的发展中起着核心作用。因此,LDLR,ApoB和ApoE多态性具有影响脂质水平的能力,可能是影响动脉粥样硬化发展的因素之一。该假设已在不同人群中进行了检验,结果相互矛盾。本研究的目的是调查埃及人的LDLR,ApoB和ApoE基因多态性与早产CAD(PCAD)的关联。这项研究包括了135名PCAD患者和132名年龄与性别相匹配的对照组。通过聚合酶链反应(PCR)分析LDLR和ApoB基因多态性。通过多重扩增难治性突变系统(multi-AMRS)鉴定ApoE基因型。我们发现LDLR A(+)A(+)基因型,ApoB X +等位基因和ApoE E4等位基因分别使PCAD的风险增加1.8、2.1和12.1。本研究证明吸烟,代谢综合征,ApoB X + X +基因型和ApoE E4等位基因是发展PCAD的独立危险因素。这是首次研究埃及人低密度脂蛋白受体,载脂蛋白B和载脂蛋白E基因多态性与PCAD和血脂水平之间的关系,我们得出结论:LDLR A(+)A(+)基因型,ApoB X +等位基因和ApoE E4总胆固醇(TC)和低密度脂蛋白(LDLc)水平升高,等位基因可能与PCAD发生风险增加有关。 CAD危险因素与LDLR A(+)A(+)基因型,ApoB X +等位基因和ApoE E4等位基因共存可能增加埃及患者发生PCAD的风险。 (C)2016 Elsevier B.V.保留所有权利。

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