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解旋酶C诱导干扰素结构域蛋白1基因多态性与江苏地区汉族人群多发性肌炎/皮肌炎的相关性研究 被引量:3

Association of interferon induced lielicase C domain 1 gene polymorphism and polymyositis/dermatomyosttis in Chinese Han patients from Jiangsu area
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摘要 目的探讨解旋酶C诱导干扰素结构域蛋白1基因(IFIH1)的单核苷酸多态性(SNP)rs1990760C〉T与江苏地区汉族PM/DM发病的相关性。方法共纳入183例PM/DM患者和400名健康对照。采用TaqmanMGB探针法对rs1990760进行基因分型;采用ELISA法检测抗黑色素瘤分化相关蛋白5(MDA5)抗体;基因型及等位基因的分布频率、Hardy-Weinberg平衡(HWE)采用r检验或Fisher确切概率法进行统计分析。结果各患者组和对照组IFIHI rs1990760。的基因型均符合HWE分布。T和C等位基因频率在PM/DM组(分别为20.8%和79.2%)、DM组(分别为20.9%和79.1%)、PM组(分别为20.5%和79.5%)和对照组(分别为18.0%和82.0%)之间的分布差异无统计学意义。在隐性模型(TT与CT+CC)和加性模型(TT与CC)中,PM/DM组TT基因型频率均显著高于对照组(6.6%与2.8%,x2值分别为4.8和4.54,P值均为0.03),DM合并间质性肺疾病(ILD)组TT基因型频率均显著高于对照组(8.3%与2.8%,x2值分别为4.84和4.41,P值分别为0.03和0.04)差异有统计学意义。在隐性模型(TT与CT+CC)中,PM未合并ILD组TT基因型频率显著高于对照组(9.8%与2.8%,x2=5.56,P=0.04),差异有统计学意义。抗MDA5阳性患者的rs1990760等位基因和基因型分布与对照组差异无统计学意义。结论IFIHI的rs1990760 TT基因型可能与江苏地区汉族PM/DM易感性相关,且其相关性可能因DM和PM患者是否合并ILD而有所不同。 Objective To explore the associations between interferon induced helicase C domain 1 (IFIH1) gene single nucleotide polymorphism (SNP) rs1990760 C 〉T and polymyositis/dermatomyositis (PM/DM) in Chinese Han patients from Jiangsu area. Methods A total of 183 PM/DM patients and 400 healthy controls were included. SNP typing was performed by Taqman MGB probe method. The ffxstfihutlons of genotypes and alleles and Hardy-Weinberg equilibrium (HWE) were examined by X2 tests or Fisher's exact tests. Results The distribution of IFIH1 rs1990760 genotypes 6f all patients group and the control group were consistent, with HWE. The frequencies of T and C alleles were not significantly different between the PM/DM group (20.8% and 79.2%, respectively), the DM group (20.9% and 79.1%. respectively), the PM group (20.5% and 79.5%, respectively) and control group (18.0% and 82.0%, respectively). In recessive model OT vs CT+ CC) and additive model (TT vs CC), the frequencies of TT genotype in PM/DM group (6.6% vs 2.8%;X2=4.8 and 4.54, respectively; both P=0.03) and in DM with interstitial lung disease OLD) group (8.30/0 vs 2.8%; ,12=4.84 and 4.41, respectively; P=0.03 and 0.04, respectively) were significantly higher than those in the control group.In recessive model(TT vs CT+CC), the frequency of TT genotype in PM without ILD group was significantly higher than that in the control group (9.8% vs 2.8%, X2=5.56, P=0.04). The genotype and allele distributions of rs1990760 were not significantly different between the anti-MDA5 positive group and control group. Conclusion The rs1990760 Tr genotype of IFIH1 gene may be associated with the susceptibility of PM/DM in Jiangsu Han Chinese population, and the associations may differ based on the ILD status.
出处 《中华风湿病学杂志》 CAS CSCD 北大核心 2016年第2期77-82,共6页 Chinese Journal of Rheumatology
基金 国家自然科学基金(81302556) 江苏省科技厅青年基金(BK20130087)
关键词 皮肌炎 解旋酶C诱导干扰素结构域蛋白1基因 多态性 单核苷酸 Dermatomyositis Interferon induced with helicase C domain 1 Polymorphism, single nucleotide
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