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机构地区:[1]首都医科大学附属北京同仁医院急诊科,北京100730
出 处:《世界急危重病医学杂志》2006年第4期1352-1355,共4页internationl journal of emergency and critical care medicine
基 金:北京市同仁科研基金资助项目
摘 要:目的研究脂肪酸结合蛋白基因(FABP2)编码区exon2第54位密码子的多态性与冠心病的相关性。方法采用随机化同期平行病例一对照试验,冠心病组86例,正常对照组90例。应用聚合酶链反应(PCR)技术检测176例样本FABP2基因Hae—Ⅱ酶切位点的多态性。结果(1)样本人群的FABP2基因编码区exon2第54位密码子存在Hae—Ⅱ酶切位点.可产生多态性片段:野生型FABP2Ala54/Ala54;杂合变异型FABP2Ala54/Thr54;纯合变异型Thr54/Thr54。(2)冠心病组变异型FABP2Ala54/Trhr54及Thr54/Thr54基因型频率显著高于正常对照组(P=0.017)。(3)与野生型基因携带者相比,冠心病组FABP2Ala54/Thr54及Thr54/Thr54基因携带者的OR值为2.16(95%CI,1.03—3.54)结论(1)所研究的样本人群存在FABP2基因多态性;(2)FABP2基因多态性可能是涉及冠心病发生的遗传易感因素。(3)FABP2基因多态性可能是冠心病患者脂质代谢异常的影响因素之一。Objective To investigate the association between the polymorphism of codon-54 of the fatty acid binding protein gene(FABP2) and patients with coronary heart disease. Methods The Ala54Thr variation of FABP2 was detected by PCR and Hae-Ⅱ digestion in 176 Chinese subjects, including 86 cases of coronary heart disease and 90 cases of normal controls. Results (1) The polymorphism restriction site of codon-54 of FABP2 gene results in the substitution of threonine(Thr) for alanine(Ala). (2) The frequence of genotype Ala54/Thr54 and Thr54/Thr54 significiantly increased in the coronary heart disease as compared with that in healthy subjects (P=-0.017). (3) The odds ratio of FABP2 genotype AlaS4/ Thr54 and Thr54/Thr54 for the patients with coronary heart disease was 2.16 (95% confidence intervals is 1.03-3.54). Conclusion ( 1 )The sample is in existence of FABP2 polymorphism. (2)FABP2 gene polymorphism seems to be significantly associated with coronary heart disease. (3)FABP2 polymorphism may have a certain contribution to the abnormity of lipoprotein metabolism in coronary heart disease individuals.
分 类 号:R541.4[医药卫生—心血管疾病]
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