Hong Eun Pyo, Jeon Jin Pyeong, Kim Sung Eun, Yang Jin Seo, Choi Hyuk Jai, Kang Suk Hyung, Cho Yong Jun
Department of Medical Genetics, Hallym University College of Medicine, Chuncheon, Korea.
Department of Neurosurgery, Hallym University College of Medicine, Chuncheon, Korea.
Yonsei Med J. 2017 Sep;58(5):1006-1011. doi: 10.3349/ymj.2017.58.5.1006.
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.
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.
Of ten SNPs, three SNPs (rs2303656, rs3900446, and rs763497) were significantly associated with IA (p<0.01). The C allele of rs3900446 was significantly related to increased IA risk with a significant threshold [odds ratio (OR)=20.15, p=4.8×10⁻⁵]. 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<0.001). Of ten SNP haplotype combinations, the CG combination of rs3900446 and rs763497 reached Bonferroni-adjusted significant threshold in IA patients (minor haplotype frequency=0.113, asymptotic p=1.3×10⁻⁵). However, there was no association between aneurysm rupture and the LOX gene.
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.
赖氨酰氧化酶(LOX)控制弹性蛋白和胶原纤维的交联与成熟。在本研究中,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。
这项横断面研究纳入了80例年龄和性别匹配的IA患者及对照。采用Fisher精确检验分析10个单核苷酸多态性(SNP)与IA之间的等位基因关联,包括41例破裂型和39例未破裂型病例。使用估计渐近卡方统计量的综合检验分析单倍型特异性关联。
在10个SNP中,3个SNP(rs2303656、rs3900446和rs763497)与IA显著相关(p<0.01)。rs3900446的C等位基因与IA风险增加显著相关,具有显著阈值[比值比(OR)=20.15,p=4.8×10⁻⁵]。同时,rs2303656的A等位基因对IA形成具有预防作用(p=8.2×10⁻⁴)。247种单倍型结构中的17种与IA存在提示性关联(渐近p<0.001)。在10种SNP单倍型组合中,rs3900446和rs763497的CG组合在IA患者中达到Bonferroni校正的显著阈值(次要单倍型频率=0.113,渐近p=1.3×10⁻⁵)。然而,动脉瘤破裂与LOX基因之间无关联。
这项初步研究表明,rs2303656、rs3900446和rs763497等LOX基因多态性可能在韩国人群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。