首页> 外文期刊>ORL: Journal for oto-rhino-laryngology and its borderlands >Single Nucleotide Polymorphisms in Adiponectin Gene Are Not Directly Associated with Increased Risk of Obstructive Sleep Apnea Syndrome in a Chinese Han Population
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Single Nucleotide Polymorphisms in Adiponectin Gene Are Not Directly Associated with Increased Risk of Obstructive Sleep Apnea Syndrome in a Chinese Han Population

机译:脂联素基因中的单核苷酸多态性与中国汉族人群阻塞性睡眠呼吸暂停综合征的风险增加不直接相关

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Purpose: This study aims to test the possible correlation between single nucleotide polymorphisms (SNPs) in the adiponectin gene and increased risk of obstructive sleep apnea syndrome (OSAS) in a Chinese Han population. Materials and Methods: A total of 266 subjects were enrolled into the study to detect 9 SNPs in the adiponectin gene. Multivariate unconditional logistic regression analysis, adjusted for gender and age, was used to estimate the associations of these SNPs with OSAS risk. Results: No evidence of a direct association was observed between these SNPs and the risk of OSAS in the Chinese Han population. However, the stratified analysis also revealed a remarkable genotype difference for SNP rs6773957 between cases and controls in the overweight subgroup (p < 0.05). In addition, the allele or genotype distributions of rs12495941, rs182052, and rs16861205 had significant differences with regard to the severity of OSAS (p < 0.05). No differences were identified in the other subgroups. Conclusion: The current research demonstrated that the SNPs in the adiponectin gene did not represent susceptibility loci for OSAS in Chinese Han individuals overall. However, variants of rs6773957 have an association with OSAS in overweight individuals. In addition, polymorphisms of rs12495941, rs182052, and rs16861205 are associated with the severity of OSAS. (C) 2017 S. Karger AG, Basel
机译:目的:本研究旨在测试脂联素基因中单核苷酸多态性(SNP)的可能相关性,以及中国汉族人群中阻塞性睡眠呼吸暂停综合征(OSAS)的风险增加。材料和方法:共纳入研究中的266名受试者,以检测脂联素基因中的9个SNP。对性别和年龄调整的多变量无条件逻辑回归分析用于估计这些SNP与OSAS风险的关联。结果:这些SNP之间没有观察到直接关联的证据以及中国汉族人口中OSA的风险。然而,分层分析还揭示了超重亚组的病例和对照之间的SNP RS6773957的显着基因型差异(P <0.05)。此外,RS12495941,RS182052和RS16861205的等位基因或基因型分布在OSA的严重程度方面具有显着差异(P <0.05)。在其他亚组中没有发现差异。结论:目前的研究表明,脂联蛋白基因中的SNP在整体上的中国汉族人民中的OSAS易感性基因座。但是,RS6773957的变体与超重个体中的OSA有关。此外,RS12495941,RS182052和RS16861205的多态性与OSA的严重程度相关。 (c)2017年S. Karger AG,巴塞尔

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