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首页> 外文期刊>Yonsei Medical Journal >A Novel Association between Lysyl Oxidase Gene Polymorphism and Intracranial Aneurysm in Koreans
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A Novel Association between Lysyl Oxidase Gene Polymorphism and Intracranial Aneurysm in Koreans

机译:赖氨酰氧化酶基因多态性与韩国颅内动脉瘤之间的新型关联。

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Purpose Lysyl oxidase ( LOX ) controls the cross-linking and maturation of elastin and collagen fibers. In this study, we investigated the association between LOX gene polymorphisms and intracranial aneurysm (IA) formation in a homogeneous Korean population. Materials and Methods This cross-sectional study involved 80 age-sex matched patients with IA and controls. Fisher's exact test was performed to analyze allelic associations between ten single nucleotide polymorphisms (SNPs) and IA, including 41 ruptured and 39 unruptured cases. Haplotype-specific associations were analyzed using the omnibus test estimating asymptotic chi-square statistics. Results Of ten SNPs, three SNPs (rs2303656, rs3900446, and rs763497) were significantly associated with IA ( p ?5]. Meanwhile, the A allele of rs2303656 showed a preventive effect against IA formation ( p =8.2×10?4). Seventeen of 247 haplotype structures showed a suggestive association with IA (asymptotic p ?5). However, there was no association between aneurysm rupture and the LOX gene. Conclusion This preliminary study indicated that LOX gene polymorphisms, such as rs2303656, rs3900446, and rs763497, may play crucial roles in IA formation in the Korean population. Our novel findings need to be validated in a large-scale independent population.
机译:目的赖氨酰氧化酶(LOX)控制弹性蛋白和胶原纤维的交联和成熟。在这项研究中,我们调查了韩国同质人群中LOX基因多态性与颅内动脉瘤(IA)形成之间的关联。材料和方法这项横断面研究涉及80位年龄匹配的IA和对照患者。 Fisher的精确检验用于分析十个单核苷酸多态性(SNP)与IA之间的等位基因关联,包括41例破裂和39例未破裂的病例。使用综合测试估计渐进卡方统计量,对单倍型特异性关联进行了分析。结果10个SNP中,有3个SNPs(rs2303656,rs3900446和rs763497)与IA显着相关(p?5 ),而rs2303656的A等位基因显示了对IA形成的预防作用(p = 8.2×10 ?4 )。247个单倍型结构中有17个提示与IA(渐近性p?5 )相关,但动脉瘤破裂与LOX基因之间没有关联。研究表明,LOX基因多态性(如rs2303656,rs3900446和rs763497)可能在朝鲜族人群IA形成中起关键作用,我们的新发现需要在大规模独立人群中进行验证。

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