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[微小RNA-149的单核苷酸多态性与类风湿关节炎易感性]

[Single nucleotide polymorphism of miR-149 and susceptibility of rheumatoid arthritis].

作者信息

Xiao Mingyuan, Ma Yi, Chen Xingguo, Kuang Bohai

机构信息

Department of Genetics, Basic Medical College of Nanchang University, Nanchang 330006, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2015 May;40(5):495-8. doi: 10.11817/j.issn.1672-7347.2015.05.006.

DOI:10.11817/j.issn.1672-7347.2015.05.006
PMID:26032077
Abstract

OBJECTIVE

To investigate the association between microRNA (miR)-149 polymorphism and susceptibility to rheumatoid arthritis (RA ), as well as the clinical characteristics in patients with RA .

METHODS

A total of 200 RA patients and 120 healthy controls were recruited from Department of Rheumatology and Immunology of Nanjing First Hospital. After obtaining the informed consent, we collected 2 mL of anti-coagulated venous blood samples from all studied subjects to isolate the whole blood genomic DNA, and the clinical data were collected as well. Single nucleotide polymorphisms of miR-149 rs22928323 were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Correlation between single nucleotide polymorphisms and clinical features were compared.

RESULTS

The frequencies of TT, TC and CC for rs22928323 of miR-149 were 25.3%, 51.1% and 23.6% or 18.3%, 20.0% and 61.7% in the patients or the healthy controls, respectively. The onset risk of allele C in RA patients was increased compared with allele T [OR=1.38, 95% CI (1.01-1.75), P=0.023]. There were no significant difference in rheumatoid factor, blood urine nitrogen, antikeratin antibody, and other clinical characteristics among the 3 genotypes in RA patients (P>0.05).

CONCLUSION

SNP rs22928323 in miR-149 is correlated with RA in the east of Chinese Han population, whereas there is no correlation between miR-149 polymorphism and clinical characteristics in patients with RA.

摘要

目的

探讨微小RNA(miR)-149基因多态性与类风湿关节炎(RA)易感性的关系以及RA患者的临床特征。

方法

从南京第一医院风湿免疫科招募200例RA患者和120例健康对照者。在获得知情同意后,采集所有研究对象2 mL抗凝静脉血样本以分离全血基因组DNA,并收集临床资料。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测miR-149 rs22928323的单核苷酸多态性。比较单核苷酸多态性与临床特征之间的相关性。

结果

miR-149 rs22928323的TT、TC和CC基因型频率在患者中分别为25.3%、51.1%和23.6%,在健康对照者中分别为18.3%、20.0%和61.7%。RA患者中C等位基因的发病风险高于T等位基因[比值比(OR)=1.38,95%可信区间(CI)(1.01-1.75),P=0.023]。RA患者的3种基因型在类风湿因子、血尿素氮、抗角蛋白抗体及其他临床特征方面差异无统计学意义(P>0.05)。

结论

在中国东部汉族人群中,miR-149基因的单核苷酸多态性rs22928323与RA相关,而miR-149基因多态性与RA患者的临床特征无关。

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