Ying Ying, Chen Yong, Li Zhen, Huang Haiyan, Gong Qiongyao
Department of Rheumatology, Ningbo No. 2 Hospital, Ningbo University School of Medicine, Zhejiang, China.
Rheumatol Int. 2017 Apr;37(4):571-578. doi: 10.1007/s00296-017-3669-6. Epub 2017 Feb 27.
The purpose of this study was to investigate the relationship between P2RX7 gene single nucleotide polymorphisms and primary gout and hyperuricemia in a Chinese Han male population. The genetic distributions of the single nucleotide polymorphisms (SNPs) rs2230911, rs208294, rs435309, rs28360447, rs1718119, rs28360457, and rs3751143 in P2RX7 were detected in 293 primary gout patients, 187 hyperuricemia patients and 269 controls using SNaPshot technology. Statistical analyses were implemented using SPSS version 20.0. The genetic distributions of each group were tested for Hardy-Weinberg equilibrium (HWE). T test, analysis of variance, rank sum test and Chi-square test were measured to assess differences in clinical data and polymorphisms among groups. Logistic regression was used to assess susceptibility to disease with odds ratios (ORs) and 95% confidence intervals (95% CIs). SHEsis software was used to calculate linkage disequilibrium blocks and haplotype association risk. P < .05 was regarded as statistically significant. Three SNPs (rs2230911, rs208294 and rs435309) did not deviate significantly from HWE (P > .05). In the comparison between primary gout and control, the frequencies of rs2230911 genotypes were significantly different (P = .002), and allele G was associated with a higher risk of primary gout than allele C [OR (95% CI) = 1.755 (1.278, 2.410), P < .001]. There was also a higher risk of primary gout in genotype (CG + GG) compared with genotype CC [OR (95% CI) = 1.876 (1.303, 2.701), P = .001]. However, no significant difference in allelic or genotypic frequency was observed between primary gout patients and hyperuricemia patients (P > .0167). Similarly, there were no obvious differences in the other two polymorphisms among the three groups (P > .05). Our results reveal that P2RX7 rs2230911 may be associated with primary gout risk in a Chinese Han male population and allele G may be a susceptibility factor for primary gout.
本研究旨在探讨P2RX7基因单核苷酸多态性与中国汉族男性人群原发性痛风及高尿酸血症之间的关系。采用SNaPshot技术检测了293例原发性痛风患者、187例高尿酸血症患者和269例对照者中P2RX7基因单核苷酸多态性(SNP)rs2230911、rs208294、rs435309、rs28360447、rs1718119、rs28360457和rs3751143的基因分布。使用SPSS 20.0版进行统计分析。对每组的基因分布进行Hardy-Weinberg平衡(HWE)检验。采用t检验、方差分析、秩和检验和卡方检验来评估各组临床数据和多态性的差异。使用逻辑回归分析以比值比(OR)和95%置信区间(95%CI)评估疾病易感性。使用SHEsis软件计算连锁不平衡块和单倍型关联风险。P < 0.05被认为具有统计学意义。三个SNP(rs2230911、rs208294和rs435309)与HWE无显著偏差(P > 0.05)。在原发性痛风患者与对照组的比较中,rs2230911基因型频率存在显著差异(P = 0.002),等位基因G比等位基因C与原发性痛风风险更高相关[OR(95%CI)= 1.755(1.278,2.410),P < 0.001]。与基因型CC相比,基因型(CG + GG)患原发性痛风的风险也更高[OR(95%CI)= 1.876(1.303,2.701),P = 0.001]。然而,原发性痛风患者与高尿酸血症患者之间的等位基因或基因型频率无显著差异(P > 0.0167)。同样,三组中其他两个多态性也无明显差异(P > 0.05)。我们的结果表明,P2RX7 rs2230911可能与中国汉族男性人群原发性痛风风险相关,等位基因G可能是原发性痛风的一个易感因素。