Interleukin-10 Gene Promoter Polymorphism and Susceptibility to Liver Cirrhosis
被引:10
作者:
Jin, Xue-yuan
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机构:
Chinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Chinese PLA Med Sch, Beijing, Peoples R China
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Jin, Xue-yuan
[1
,2
,3
]
Wang, Ya-qing
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机构:
305 Mil Hosp, Dept Gastroenterol, Beijing, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Wang, Ya-qing
[4
]
Yan, Tao
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机构:
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Yan, Tao
[3
]
Wang, Jianjun
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机构:
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Wang, Jianjun
[3
]
Qing, Song
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机构:
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Qing, Song
[3
]
Ding, Ning
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机构:
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Ding, Ning
[3
]
Tian, Hong
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机构:
302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Tian, Hong
[3
]
Zhao, Ping
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302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R ChinaChinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
Zhao, Ping
[3
]
机构:
[1] Chinese Peoples Liberat Army Gen Hosp, Beijing, Peoples R China
[2] Chinese PLA Med Sch, Beijing, Peoples R China
[3] 302 Mil Hosp, Int Ctr Liver Dis Treatment, Beijing 100039, Peoples R China
[4] 305 Mil Hosp, Dept Gastroenterol, Beijing, Peoples R China
Background/Aims: Liver cirrhosis is the end-stage of various liver diseases, which has a poor prognosis and determined by deterioration of hepatic functional capacity and consecutive development of hepatic complications. We investigated the role of IL-10-592 A/C, IL-10-819 C/T and IL-10-1082 A/G gene polymorphisms on the development of liver cirrhosis. Methodology: A 1:2 matched case-control study was conducted, including 266 patients from 302 Military Hospital. Genotyping of IL-10-592 A/C, IL-10-819 C/T and IL-10-1082 A/G were performed in a 384-well plate format on the Sequenom MassARRAY platform. Results: Multivariate regression analyses showed that subjects carrying the IL-10-592 CC variant had a significant increased risk of liver cirrhosis (OR: 1.83, 95% CI: 1.10-3.03), and IL-10-592 A/C showed a significant increased risk in recessive model (OR: 1.97, 95% CI: 1.15-3.45). We found those carrying IL-10-592 CC genotype had a heavy increased risk of liver cirrhosis in those with positive chronic hepatitis B, with an OR (95% CI) of 2.46 (1.35-4.42), and a significant interaction was observed between the IL-10-592 A/C genotype and chronic hepatitis B infection (P = 0.036). Those carrying IL-10-819 C/T and IL-10-1082 A/G variants had non-significant increased risk of liver cirrhosis. Conclusions: Our study demonstrates that IL-10-592A/C gene polymorphism would enhance the risk for liver cirrhosis, and this gene variant has interaction with chronic hepatitis B infection in Asian population.