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A Case-Control Study between Gene Polymorphisms of Polyunsaturated Fatty Acid Metabolic Rate-Limiting Enzymes and Acute Coronary Syndrome in Chinese Han Population

机译:中国汉族汉族多不饱和脂肪酸代谢率限制酶及急性冠状动脉综合征的基因多态性案例研究

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The purpose of this study is to analyze the relationship between the polymorphisms of fatty acid desaturase 1 (FADS1), fatty acid desaturase 2 (FADS2), and elongation of very long-chain fatty acids-like 2 (ELOVL2) and acute coronary syndrome (ACS) in Chinese Han population. Therefore, we selected three single nucleotide polymorphisms (SNPs) from these candidate genes and genotyped them using PCR-based restriction fragment length polymorphism analysis in 249 ACS patients and 240 non-ACS subjects, as were Han Chinese ancestry. The results showed that rsl74556 in the FADS1 gene is found to be in allelic association (P = 0.003) and genotypic association (P = 0.036) with ACS. The frequencies of rsl74556 minor allele (T) in case group were obviously higher than in control group. The trans-phase gene-gene interaction analysis showed that the combined genotype of rsl74556 (T/T) and rs3756963 (T/T) was associated with ACS (P = 0.031). And the results suggest that, for rsl74556 C>T, the CT/TT genotypes were more likely to lead in ACS in subjects with hypertension after correction of all risk factors (OR = 4.236, 95% CI, 2.216-7.126). These findings suggest that the polymorphisms of rsl74556 in the FADSl gene are very likely to be associated with ACS in Chinese Han population, especially in subjects with hypertension.
机译:本研究的目的是分析脂肪酸去饱和酶1(FADS1),脂肪酸去饱和酶2(FADS2)的多态性之间的关系,以及非常长链脂肪酸样2(ELOVL2)和急性冠状动脉综合征的伸长率(中国汉族人口的ACS。因此,我们从这些候选基因中选择了三种单核苷酸多态性(SNP),并在249例ACS患者和240名非ACS受试者中使用基于PCR的限制性片段长度多态性分析进行基因分型。结果表明,FADS1基因中的RSL74556被发现是等位基因关联(P = 0.003)和基因型关联(P = 0.036),具有AC。案例组中RSL74556次要等位基因(T)的频率明显高于对照组。反相基因 - 基因相互作用分析表明,RSL74556(T / T)和RS3756963(T / T)的组合基因型与ACS相关(P = 0.031)。结果表明,对于RSL74556 C> T,CT / TT基因型更可能在校正所有风险因素(或= 4.236,95%CI,2.216-7.126)后在具有高血压的受试者中引入AC。这些发现表明,FADSL基因中的RSL74556的多态性非常可能与中国汉族人群中的AC相关,特别是在具有高血压的受试者中。

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