Zhou Jian-Zhe, Li Jing-Jing, Hua Dong-Jin, Huang Si-Chao, Sun Qing-Qing, Huang Hua, Xin Xia-Fei, Cen Han
Department of Preventive Medicine, School of Medicine, Ningbo University, 818 Fenghua Road, 315211, Ningbo, Zhejiang, People's Republic of China.
Zhejiang Provincial Key Laboratory of Pathophysiology, School of Medicine, Ningbo University, 818 Fenghua Road, 315211, Ningbo, Zhejiang, People's Republic of China.
Inflamm Res. 2017 Jun;66(6):515-521. doi: 10.1007/s00011-017-1035-5. Epub 2017 Mar 17.
The purpose of our study was to examine whether the H19 rs2839698, rs217727, and HOX transcript antisense RNA (HOTAIR) rs12826786 polymorphisms were associated with genetic susceptibility to rheumatoid arthritis (RA) in a Chinese population.
A total of 777 participants were enrolled in this study, including 328 RA patients and 449 healthy controls. The H19 rs2839698, rs217727, and HOTAIR rs12826786 polymorphisms were detected by the ligase detection reaction-polymerase chain reaction (LDR-PCR) technology.
No significant difference in genotype distribution between RA patients and healthy controls was found (P = 0.38 for rs2839698; P = 0.79 for rs217727; P = 0.39 for rs12826786). The difference in allele frequencies between RA patients and controls was also non-significant (rs2839698 T versus C, P = 0.23, odds ratio (OR) = 1.15, 95% confidence interval (CI) = 0.92-1.43; rs217727 C versus T, P = 0.55, OR = 1.07, 95% CI = 0.87-1.32; and rs12826786 T versus C, P = 0.32, OR = 1.14, 95% CI = 0.88-1.47). We have also evaluated the relationships of above-mentioned polymorphisms with risk of RA under dominant model and recessive model, but non-significant evidence was found. No significant evidence was detected for the relationships of H19 rs2839698, rs217727, and HOTAIR rs12826786 polymorphisms with risk of different serotypes of RA.
Our results indicated that H19 rs2839698, rs217727, and HOTAIR rs12826786 polymorphisms might not be involved in the genetic background of RA in Chinese.
我们研究的目的是检测在中国人群中,H19基因的rs2839698、rs217727多态性以及HOX反义转录RNA(HOTAIR)基因的rs12826786多态性是否与类风湿关节炎(RA)的遗传易感性相关。
本研究共纳入777名参与者,包括328例RA患者和449名健康对照。采用连接酶检测反应-聚合酶链反应(LDR-PCR)技术检测H19基因的rs2839698、rs217727多态性以及HOTAIR基因的rs12826786多态性。
RA患者与健康对照之间的基因型分布无显著差异(rs2839698,P = 0.38;rs217727,P = 0.79;rs12826786,P = 0.39)。RA患者与对照之间的等位基因频率差异也无统计学意义(rs2839698,T对C,P = 0.23,优势比(OR)= 1.15,95%置信区间(CI)= 0.92 - 1.43;rs217727,C对T,P = 0.55,OR = 1.07,95% CI = 0.87 - 1.32;rs12826786,T对C,P = 0.32,OR = 1.14,95% CI = 0.88 - 1.47)。我们还评估了上述多态性在显性模型和隐性模型下与RA风险的关系,但未发现显著证据。未检测到H19基因的rs2839698、rs217727多态性以及HOTAIR基因的rs12826786多态性与不同血清型RA风险之间的显著关系。
我们的结果表明,H19基因的rs2839698、rs217727多态性以及HOTAIR基因的rs12826786多态性可能不参与中国人群RA的遗传背景。