Wang Mengjun, Liu Qiuli, Liu Chunhua
Department of Urology, Liaocheng People's Hospital, Liaocheng, Shandong 252000, P.R. China.
Department of Infectious Disease, Liaocheng People's Hospital, Liaocheng, Shandong 252000, P.R. China.
Exp Ther Med. 2018 Oct;16(4):3055-3059. doi: 10.3892/etm.2018.6558. Epub 2018 Aug 1.
Correlation of C-C chemokine receptor type 5 (CCR5) and NACHT, LRR and PYD domain-containing protein 3 (NLRP3) gene polymorphisms with renal damage due to hepatitis C virus (HCV)-related cryoglobulinemia were investigated. The 1:1 matched case-control study design was adopted, 171 patients with renal damage due to HCV-related cryoglobulinemia were selected as the case group, and 171 patients without renal damage were selected as the control group. Polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) analysis was used to detect the polymorphisms of locus rs1799987A/G in CCR5 gene and locus rs35829419A/C in NLRP3 gene of 171 pairs of HCV patients. SPSS 20.0 software was used for logistic regression analysis, and genetics package of the R programming language for Hardy-Weinberg equilibrium test. The frequencies of locus rs1799987A/G in CCR5 gene in the case group were 48.0 and 52.0%, while those in the control group were 47.9 and 52.1%; the frequencies of locus rs35829419A/C in NLRP3 gene were 55.8 and 44.2%, while those in the control group were 55.3 and 44.7%. The results of logistic regression analysis showed that the distribution of CCR5 gene polymorphism in the case group was statistically different from that in the control group (P<0.05), which had a statistical correlation with the renal damage due to HCV-related cryoglobulinemia (P<0.05). At rs1799987, GG genotype was compared with AA genotype, and AG genotype was compared with AA genotype; the results showed that the renal damage due to HCV-related cryoglobulinemia was not decreased [odds ratio (OR) = 0.91, 95% confidence interval (95% CI): 0.47-1.54; OR = 0.89, 95% CI: 0.49-1.31]. The negative analysis model of the GG genotype reduced the risk of renal damage due to HCV-related cryoglobulinemia remarkably (OR = 0.62, 95% CI: 0.39-0.98). Rs1799987A/G and gene polymorphism of CCR5 may be associated with renal damage due to HCV-related cryoglobulinemia, and the carriage of G allele may lower the incidence rate of the disease, while rs35829419A/C in NLRP3 has no correlation with renal damage due to HCV-related cryoglobulinemia.
研究了C-C趋化因子受体5(CCR5)和含NACHT、LRR和PYD结构域蛋白3(NLRP3)基因多态性与丙型肝炎病毒(HCV)相关冷球蛋白血症所致肾损害的相关性。采用1:1匹配的病例对照研究设计,选取171例HCV相关冷球蛋白血症所致肾损害患者作为病例组,选取171例无肾损害患者作为对照组。采用聚合酶链反应和限制性片段长度多态性(PCR-RFLP)分析检测171对HCV患者CCR5基因rs1799987A/G位点和NLRP3基因rs35829419A/C位点的多态性。应用SPSS 20.0软件进行逻辑回归分析,应用R编程语言的遗传软件包进行Hardy-Weinberg平衡检验。病例组CCR5基因rs1799987A/G位点频率分别为48.0%和52.0%,对照组分别为47.9%和52.1%;NLRP3基因rs35829419A/C位点频率分别为55.8%和44.2%,对照组分别为55.3%和44.7%。逻辑回归分析结果显示,病例组CCR5基因多态性分布与对照组差异有统计学意义(P<0.05),与HCV相关冷球蛋白血症所致肾损害有统计学相关性(P<0.05)。在rs1799987位点,GG基因型与AA基因型比较,AG基因型与AA基因型比较;结果显示,HCV相关冷球蛋白血症所致肾损害未降低[比值比(OR)=0.91,95%置信区间(95%CI):0.47-1.54;OR = 0.89,95%CI:0.49-1.31]。GG基因型的阴性分析模型显著降低了HCV相关冷球蛋白血症所致肾损害的风险(OR = 0.62,95%CI:0.39-0.98)。CCR5基因的rs1799987A/G多态性可能与HCV相关冷球蛋白血症所致肾损害有关,携带G等位基因可能降低该病的发病率,而NLRP3基因的rs35829419A/C与HCV相关冷球蛋白血症所致肾损害无相关性。