Tang Ling-yan, Wang Jie, Yu Rong-bin, Su Jing, Xu Ke, Peng Zhi-hang, Deng Xiao-zhao, Ding Wei-liang, Ge Zhi-jun, Zhang Yun
Department of Epidemiology and Biostatistics, Nanjing Medical University, Nanjing 210029, China.
Zhonghua Liu Xing Bing Xue Za Zhi. 2012 Sep;33(9):898-902.
To explore the relationship between interleukin (IL)-10 gene polymorphisms and the susceptibility or the outcomes of HCV infection among high-risk populations in Jiangsu province.
IL-10 gene SNPs were detected in 1555 subjects including 264 self-limited HCV infections. 371 persistent HCV infections and 920 healthy controls were selected through Taqman-MGB.
After adjusted for cofounders as sex, age and high-risk population, data from logistic regression analysis showed that the distribution of IL-10 genotypes among the controls, spontaneous clearances and those with persistent infections did not show much differences.
from further stratified analysis showed that, at the position of -819T/C, when compared with TT genotype, TC genotype had a significantly increasing chance of self-limited HCV infection among middle-aged, females and paid blood doners (adjusted OR values and 95%CI were: 2.160, 1.163 - 4.011; 1.693, 1.066 - 2.688 and 4.084, 1.743 - 9.570). It also had a lower risk of progressing to persistent HCV infection among those paid blood doners (the adjusted OR values and 95%CI were: 0.312, 0.130 - 0.747). CC genotype had a higher chance of self-limited HCV infection among people underwent blood dialysis (the adjusted OR values and 95%CI were: 2.120, 1.071 - 4.197).
also showed a decreased risk of progressing to persistent infection among paid blood doners (the adjusted OR values and 95%CI were: 0.156, 0.043 - 0.566). At the position of -592A/C, when compared to AA genotype, the AC genotype had a significantly increasing chance of self-limited HCV infection among middle-aged, females and paid blood doners (the adjusted OR values and 95%CI were: 2.176, 1.173 - 4.037; 1.659, 1.055 - 2.607; 3.704, 1.625 - 8.443) but had an increased risk of persistent HCV infection among females (the adjusted OR values and 95%CI were: 1.525, 1.017 - 2.286). AC genotype showed an increased opportunity to progress to HCV persistent infection among drug users (the adjusted OR values and 95%CI were: 1.845, 1.122 - 3.034) but had a reduced risk of progressing to HCV persistent infection among paid blood doners (the adjusted OR values and 95%CI were: 0.361, 0.155 - 0.841). CC genotype had an increased opportunity to self-limited HCV infection as well as having a decreased risk of progressing to persistent infection among paid blood doners (the adjusted OR values and 95%CI were: 3.125, 1.016 - 9.605; 0.218, 0.063 - 0.748). At the position of -1082A/G, AG/GG genotypes had an increased chance of self-limited infection among blood doners (the adjusted OR values and 95%CI were: 3.780, 1.620 - 8.820).
IL-10-819T/C, -592A/C, -1082A/G SNPs might be related with the susceptibility and the outcomes of HCV infection among populations at high risk.
探讨白细胞介素(IL)-10基因多态性与江苏省高危人群丙型肝炎病毒(HCV)感染易感性及感染结局之间的关系。
通过Taqman-MGB技术在1555名受试者中检测IL-10基因单核苷酸多态性(SNP),其中包括264例自限性HCV感染、371例持续性HCV感染以及920例健康对照。
在对性别、年龄和高危人群等混杂因素进行校正后,逻辑回归分析数据显示,对照组、自发清除组和持续性感染组中IL-10基因型的分布没有显著差异。
进一步分层分析结果显示,在-819T/C位点,与TT基因型相比,TC基因型在中年、女性和有偿献血者中自限性HCV感染的几率显著增加(校正后的比值比(OR)值及95%可信区间(CI)分别为:2.160,1.163 - 4.011;1.693,1.066 - 2.688;4.084,1.743 - 9.570)。在有偿献血者中,其进展为持续性HCV感染的风险也较低(校正后的OR值及95%CI分别为:0.312,0.130 - 0.747)。CC基因型在接受血液透析的人群中自限性HCV感染的几率较高(校正后的OR值及95%CI分别为:2.120,1.071 - 4.197)。
结果还显示,在有偿献血者中进展为持续性感染的风险也降低(校正后的OR值及95%CI分别为:0.156,0.043 - 0.566)。在-592A/C位点,与AA基因型相比,AC基因型在中年、女性和有偿献血者中自限性HCV感染的几率显著增加(校正后的OR值及95%CI分别为:2.176,1.173 - 4.037;1.659,1.055 - 2.607;3.704,1.625 - 8.443),但在女性中持续性HCV感染的风险增加(校正后的OR值及95%CI分别为:1.525,1.017 - 2.286)。AC基因型在吸毒者中进展为HCV持续性感染的机会增加(校正后的OR值及95%CI分别为:1.845,1.122 - 3.034),但在有偿献血者中进展为HCV持续性感染的风险降低(校正后的OR值及95%CI分别为:0.361,0.155 - 0.841)。CC基因型在有偿献血者中自限性HCV感染的机会增加,同时进展为持续性感染的风险降低(校正后的OR值及95%CI分别为:3.125,1.016 - 9.605;0.218,0.063 - 0.748)。在-1082A/G位点,AG/GG基因型在献血者中自限性感染的几率增加(校正后的OR值及95%CI分别为:3.780,1.620 - 8.820)。
IL-10基因-819T/C、-592A/C、-1082A/G位点的SNP可能与高危人群HCV感染的易感性及感染结局有关。