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Association between SNPs in miRNA-machinery genes and chronic hepatitis B in the Chinese Han population

机译:中国汉族人群miRNA机器基因中的SNP与慢性乙型肝炎的相关性

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Single nucleotide polymorphisms (SNPs) in miRNA-machinery genes can influence their generation and maturation, then expression and structure. To explore the relationship between three SNPs (rs3757 in DGCR8, rs636832 in AGO1, rs7813 in GEMIN4) in miRNA-machinery genes and chronic hepatitis B, we genotyped the SNPs by high resolution melting method (HRM) in a case-control study of 332 unrelated chronic hepatitis B patients and 352 unrelated healthy controls in Western China. Interestingly, the rs636832 was significantly associated with the susceptibility of CHB (genotype: AA/GA/GG: p = 0.010; allele: A/G: OR = 0.727, 95% CI = 0.575-0.920, p = 0.008). The minor allele A of rs636832 was significantly associated with a decreased risk of CHB. Additionally, the dominant model AG + GG vs. AA showed a risk of 1.442-fold (p = 0.018) with CHB. Further exploration for the association between rs636832 and HBV-DNA load in 329 cases showed no significant difference (genotype: p = 0.321; allele: p = 0.148). Neither did the association between rs636832 and the status of HBsAg and HbeAg (HBsAg: genotype p = 0.337, allele p = 0.436; HBeAg: genotype p = 0.861, allele p = 0.822). Our study first provided the evidence that rs636832 in AGO1 was associated with chronic HBV infection susceptibility in Chinese Han population. Further epidemiological and functional studies in larger populations are warranted to verify our results. (C) 2014 Elsevier B.V. All rights reserved.
机译:miRNA机械基因中的单核苷酸多态性(SNP)可以影响其生成和成熟,进而影响表达和结构。为了探讨miRNA机械基因中三个SNP(DGCR8中的rs3757,AGO1中的rs636832,GEMIN4中的rs7813)与慢性乙型肝炎之间的关系,我们在一项332例病例对照研究中,通过高分辨率熔解法(HRM)对SNPs进行了基因分型。西部地区与慢性乙型肝炎无关的患者和352名与健康无关的对照。有趣的是,rs636832与CHB的易感性显着相关(基因型:AA / GA / GG:p = 0.010;等位基因:A / G:OR = 0.727,95%CI = 0.575-0.920,p = 0.008)。 rs636832的次要等位基因A与CHB风险降低显着相关。此外,优势模型AG + GG与AA相比,CHB的风险为1.442倍(p = 0.018)。在329例病例中进一步研究rs636832与HBV-DNA负荷之间的相关性无显着差异(基因型:p = 0.321;等位基因:p = 0.148)。 rs636832与HBsAg和HbeAg的状态之间也没有关联(HBsAg:基因型p = 0.337,等位基因p = 0.436; HBeAg:基因型p = 0.861,等位基因p = 0.822)。我们的研究首次提供了证据,表明AGO1中的rs636832与中国汉族人群的慢性HBV感染易感性有关。有必要在更大的人群中进行进一步的流行病学和功能研究,以验证我们的结果。 (C)2014 Elsevier B.V.保留所有权利。

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