Genetic variants in IL33 and IL1RL1 genes confer susceptibility to HBV-related liver cirrhosis in Chinese Han population

被引:5
|
作者
Ma, Ning [1 ]
Xu, Mengyuan [2 ]
Dong, Yi [3 ]
Yu, Fengxue [4 ]
Zhang, Xiaolin [2 ]
Gao, Xia [2 ]
Meng, Yanxin [5 ]
Gao, Ping [1 ]
Zhou, Jin [1 ]
Yuan, Meina [1 ]
Mi, Yingjun [1 ]
Qi, Sufen [1 ]
Li, Lu [1 ]
Liu, Dianwu [2 ]
Liu, Wenxuan [2 ]
Yang, Lei [2 ]
机构
[1] Hebei Med Univ, Sch Publ Hlth, Dept Social Med & Hlth Care Management, Hebei Key Lab Environm & Human Hlth, Shijiazhuang 050017, Hebei, Peoples R China
[2] Hebei Med Univ, Sch Publ Hlth, Dept Epidemiol & Stat, Hebei Key Lab Environm & Human Hlth, Shijiazhuang 050017, Hebei, Peoples R China
[3] Hebei Med Univ, Dept Sch Basic Med Sci, Shijiazhuang 050017, Hebei, Peoples R China
[4] Hebei Med Univ, Hosp 2, Div Gastroenterol, Hebei Key Lab Gastroenterol, Shijiazhuang 050017, Hebei, Peoples R China
[5] Fourth Hosp Shijiazhuang, Antenatal Diag Ctr, Shijiazhuang 050017, Hebei, Peoples R China
关键词
HBV; Polymorphism; Liver cirrhosis; IL33; IL1RL1; IL-33; GENE; INTERLEUKIN-33; POLYMORPHISMS; ASSOCIATION; FIBROSIS;
D O I
10.1016/j.meegid.2021.104983
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Introduction: Previous studies indicate that the IL-33/ST2 pathway is involved in hepatitis B virus (HBV) -related liver diseases. This study aimed to determine the relationship between genetic variants in IL-33/ST2 pathway with susceptibility to liver cirrhosis. Materials and methods: A total of 2632 Han Chinese samples met the inclusion and exclusion criteria, including 840 negative controls (NeC), 691 chronic hepatitis B (CHB), 680 HBV-related liver cirrhosis (LC) and 421 HBV-related hepatocellular carcinoma (HCC) (without LC) patients. Four polymorphisms (IL33-rs4742170, rs1048274, rs10975519 and IL1RL1-rs1041973) were selected and genotyping was performed. All statistical analyses were performed by SPSS21.0, mainly using the Hardy-Weinberg equilibrium test, Pearson chi-square, unconditional Logistic regression and haplotype analysis. Results: After adjusting for age, sex, smoking and drinking, significant associations were observed between IL33-rs4742170, rs1048274 and rs10975519 polymorphisms with LC risk. NeC with IL33-rs4742170 CC genotype was 1.80 times more likely to develop LC compared with TT genotype, while NeC with rs10975519(TC + CC) genotype was 1.32 times more likely to develop LC when compared with the TT genotype. CHB cases with rs4742170 (CC + TC) genotype had 1.30 times higher susceptibility to develop LC compared with the TT genotype. The IL33-rs1048274G allele occurred more frequently in the LC group compared with the HCC group in codominant model (AG/AA: P = 0.001, OR =1.66, 95%CI =1.22-2.25; GG/AA: P = 0.018, OR =1.54, 95% CI =1.08-2.20). The IL33 haplotype CG conformed by rs10975519C and rs1048274G was more frequent in the LC group than in the NeC group and CHB group. Moreover, the IL33 haplotype CCG conformed by rs4742170C, rs10975519C and rs1048274G was found to be more frequent in the LC group than the HCC group. However, there was no association between IL1RL1-rs1041973 and LC risk. Conclusion: Our findings demonstrate the association between genetic variants in IL33 with susceptibility to liver cirrhosis. IL33-rs4742170C, rs1048274G and rs10975519C could serve as biomarkers of LC.
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页数:8
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