Lu Liang-Ping, Li Xing-Wang, Liu Ying, Sun Guo-Chang, Wang Xue-Ping, Zhu Xi-Lin, Hu Quan-You, Li Hui
Department of Epidemiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences; School of Basic Medicine, Peking Union Medical College, 5 Dongdan 3 Tiao, Beijing 100005, China.
World J Gastroenterol. 2004 Jun 15;10(12):1810-4. doi: 10.3748/wjg.v10.i12.1810.
To clarify whether -238G/A polymorphism of tumor necrosis factor-alpha (TNF-alpha) gene promoter region was associated with outcomes of hepatitis B virus (HBV) infection in Han population of northern China, and to analyze the gene-environment interaction between -238G/A polymorphism and cigarette smoking or alcohol consumption.
A case-control study was conducted to analyze the association of TNF-alpha gene promoter polymorphism with HBV infection outcomes. A total of 207 patients with chronic hepatitis B (HB) and 148 cases of self-limited HBV infection from Ditan Hospital and Shunyi District Hospital in Beijing, respectively were recruited. History of smoking and alcohol drinking was inquired by a questionnaire. The -238G/A polymorphism of TNF-alpha gene promoter was genotyped by polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP).
The frequencies of GG and GA genotypes were 98.07% and 1.93% in chronic HB patients and 93.24% and 6.76% in self-limited HBV infection individuals, respectively (chi(2)=5.30, P=0.02). The frequency of G allele was significantly higher in patients with chronic HB that in individuals with self-limited HBV infection (99.03% vs 96.62%, chi(2)=5.20, P=0.02). Only modestly increased risk of onset of chronic HB was found in smokers (OR=1.40, 95% CI: 0.87-2.28, P=0.14) and drinkers (OR=1.26, 95%CI: 0.78-2.05, P=0.32). There was a positive interaction between genotype GG and cigarette smoking with an interaction index (II) of 2.95, or alcohol consumption with an II of 1.64.
The -238G/A polymorphism of TNF-alpha gene promoter region is independently associated with different outcomes of HBV infection.
明确肿瘤坏死因子-α(TNF-α)基因启动子区域-238G/A多态性是否与中国北方汉族人群乙型肝炎病毒(HBV)感染的转归相关,并分析-238G/A多态性与吸烟或饮酒之间的基因-环境相互作用。
进行一项病例对照研究,以分析TNF-α基因启动子多态性与HBV感染转归的相关性。分别从北京地坛医院和顺义区医院招募了207例慢性乙型肝炎(CHB)患者和148例自限性HBV感染者。通过问卷调查询问吸烟和饮酒史。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对TNF-α基因启动子的-238G/A多态性进行基因分型。
慢性乙型肝炎患者中GG和GA基因型频率分别为98.07%和1.93%,自限性HBV感染者中分别为93.24%和6.76%(χ²=5.30,P=0.02)。慢性乙型肝炎患者中G等位基因频率显著高于自限性HBV感染者(99.03%对96.62%,χ²=5.20,P=0.02)。吸烟者(OR=1.40,95%CI:0.87-2.28,P=0.14)和饮酒者(OR=1.26,95%CI:0.78-2.05,P=0.32)发生慢性乙型肝炎的风险仅略有增加。基因型GG与吸烟之间存在正向相互作用,相互作用指数(II)为2.95,与饮酒之间存在正向相互作用,II为1.64。
TNF-α基因启动子区域-238G/A多态性与HBV感染的不同转归独立相关。