Lu LP, Li XW, Liu Y, Sun GC, Wang XP, Zhu XL, Hu QY, Li H. Association of -238G/A polymorphism of tumor necrosis factor-alpha gene promoter region with outcomes of hepatitis B virus infection in Chinese Han population. World J Gastroenterol 2004; 10(12): 1810-1814 [PMID: 15188512 DOI: 10.3748/wjg.v10.i12.1810]
Corresponding Author of This Article
Hui Li, 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. lihui99360@sohu.com
Article-Type of This Article
Brief Reports
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Gastroenterol. Jun 15, 2004; 10(12): 1810-1814 Published online Jun 15, 2004. doi: 10.3748/wjg.v10.i12.1810
Association of -238G/A polymorphism of tumor necrosis factor-alpha gene promoter region with outcomes of hepatitis B virus infection in Chinese Han population
Liang-Ping Lu, Hui Li, Department of Epidemiology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences; School of Basic Medicine, Peking Union Medical College, Beijing 100005, China
Xing-Wang Li, Department of Internal Medicine, Ditan Hospital, Beijing 100011, China
Xue-Ping Wang, Department of Clinical Laboratory, Ditan Hospital, Beijing 100011, China
Ying Liu, Xi-Lin Zhu, National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences; School of Basic Medicine, Peking Union Medical College, Beijing 100005, China
Guo-Chang Sun, Quan-You Hu, Department of Clinical Laboratory, Shunyi District Hospital, Beijing 101300, China
ORCID number: $[AuthorORCIDs]
Author contributions: All authors contributed equally to the work.
Supported by the Research Fund for the Doctoral Training Program from the Ministry of Education, No.2000002340 and Beijing Municipal Government Commission for Science & Technology, No. H020920020590
Correspondence to: Hui Li, 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. lihui99360@sohu.com
Telephone: +86-10-65296971 Fax: +86-10-65225752
Received: November 22, 2003 Revised: December 9, 2003 Accepted: December 16, 2003 Published online: June 15, 2004
Abstract
AIM: To clarify whether -238G/A polymorphism of tumor necrosis factor-α (TNF-α) 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.
METHODS: A case-control study was conducted to analyze the association of TNF-α 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-α gene promoter was genotyped by polymerase chain reaction-restricted fragment length polymorphism (PCR-RFLP).
RESULTS: 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 (χ2 = 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%, χ2 = 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.
CONCLUSION: The -238G/A polymorphism of TNF-α gene promoter region is independently associated with different outcomes of HBV infection.
Key Words: $[Keywords]
Citation: Lu LP, Li XW, Liu Y, Sun GC, Wang XP, Zhu XL, Hu QY, Li H. Association of -238G/A polymorphism of tumor necrosis factor-alpha gene promoter region with outcomes of hepatitis B virus infection in Chinese Han population. World J Gastroenterol 2004; 10(12): 1810-1814
Human beings are susceptible to HBV. HBV infection in adults is usually clinically inapparent, and the virus is cleared after infection. Only about 5%-10% of them become persistently infected and develop chronic liver disease with varied severity[1], which could not be explained completely by the virus itself and environmental factors. Progress of HBV infection might be affected by host genetic susceptibility[2].
Since HBV is not cytolytic for hepatocytes, and hepatocellular injuries caused by HBV infection are predominantly immune-mediated[3-6]. Immune attacks by host against HBV are mainly mediated by a cellular reaction. Cytokines produced by immune cells, such as TNF-α, might play a role in immune pathogenesis of HBV infection.
TNF-α is secreted by macrophages, monocytes, neutrophils, T-cells and NK-cells following the stimulus by bacterial lipopolysaccharides and shows a broad spectrum of biological activities, causing cytolysis and cytostasis in many tumor cell lines in vitro. Several lines of evidence suggest the importance of TNF-α in HBV. Patients with acute and chronic hepatitis B have an elevated plasma concentration of TNF-α[7,8]. Some individual differences in cytokine production may be related to genetic components, and certain polymorphism alleles may be associated with higher or lower levels of TNF-α production, which has been ascribed to polymorphisms within the regulatory regions of cytokine genes[9-14].
There were some studies about the association of TNF-α gene promoter polymorphism with progress of the disease[13,15], but ethnic difference could lead to different results. The aim of the present study was to investigate whether the TNF-α promoter polymorphism at position -238 was associated with outcomes of HBV infection in Han people of northern China.
MATERIALS AND METHODS
Study design
Case-control study was used to analyze the association between the polymorphism at position -238 of TNF-α gene promoter and outcomes of HBV infection, as well as the interaction between the gene and smoking or alcohol drinking.
Subjects
The clinical diagnosis for all subjects in this study was based on references[16,17]. Two hundred and seven patients with chronic HB from Ditan Hospital in Beijing, China during November 2001 to August 2002 were recruited, with inclusion criteria as follows: hepatitis B surface antigen (HBsAg) seropositive, anti-HBs antibodies (anti-HBs) seronegative, abnormally elevated serum alanine aminotransferase level, and duration of chronic HB ≥ 2 years. One hundred and forty-eight subjects with self-limited HBV infection were from Shunyi District Hospital in Beijing, China during the same period, with inclusion criteria as positive for both anti-HBs and anti-HBc antibodies only, definitely negative for HBsAg, normal liver function tests, and no history of HBV vaccination. All subjects were Chinese Han people and they were recruited with their informed consent for genetic analysis. Venous blood was drawn from all subjects after an overnight fasting. Serum was separated immediately to detect ALT and blood corpuscles were stored at -70 °C to extract DNA and analyze genotypes.
Serological tests
Enzyme-linked immunoadsorbent assay (ELISA) was used for detection of serum HBsAg, anti-HBs, and anti-HBc (IMX; Abbott Diagnostics, North Chicago, IL).
Analysis of TNF-α gene promoter polymorphism
Genomic DNAs were obtained from peripheral blood leukocytes by standard phenol-chloroform extraction[18]. The -238G/A polymorphism in the promoter region of TNF-α gene was detected by PCR-RFLP as described by Miyazoe et al[19]. A 152-bp fragment was amplified using primers (5’: 5’AGAAG ACCCCCCTCGGAACC3’ and 3’: 5’ATCTGGAGGAAGCG GTAGTG3’). Amplification was performed in a Perkin Elmer thermocycler (2700; Applied Biosystems, Foster City, CA) with 50 ng of genomic DNA, 20 pmol/L of each primer, 200 μmol/L each dNTP, 1.5 mmol/L MgCl2, standard polymerase chain reaction (PCR) buffer and 1U Taq polymerase (Shanghai Biocolor) to 25 μL reaction system. PCR procedure was as follows: predenaturation at 94 °C for 2 min, followed by 30 cycles of denaturation at 94 °C for 1 min, annealing at 59 °C for 1 min and extension at 72 °C for 1 min, with a final extension at 72 °C for 5 min to terminate the reaction. After amplification, 10 μL PCR product was digested with restriction endonuclease (Msp-I 3U, Takara Bio Cor Dalian) at 37 °C for 5 h after addition of appropriate incubation buffer and ddH2O to 20 μL. The digestion products were separated on 3% agarose gel and visualized directly under UV light with ethidium bromide staining. One base-exchange substitution from A to G position at position -238 created the Msp-I restriction site, resulting in 20-bp and 132-bp fragments with Msp-I digestion, where -238A allele could not create the Msp-I restriction site, which resulted in an 152-bp fragment.
Cigarette smoking and alcohol consumption
Cigarette smoking and alcohol consumption of the subjects were assessed by their self-report in a questionnaire.
Evaluation of the interaction
The gene-environment interaction was defined according to Rothman et al[20], with a formula to estimate interaction index (II) = OR11/OR01×OR10. II > 1 was defined as positive, and II < 1 as negative.
Statistical analysis
The frequencies of TNF-α promoter region alleles and genotypes were estimated. The Hardy-Weinberg equilibrium and frequencies of the alleles and genotypes between two groups were compared by χ2 tests with two-tailed P values[21]. Odds ratios and their 95% confidence intervals were also calculated as measures of association of the polymorphism with outcomes of HBV infection. All the statistical procedures were performed with SAS version 6.12.
RESULTS
Characteristics of subjects
The main characteristics of study subjects are summarized in Table 1. The average age of the patients with chronic HB and subjects with self-limited HBV infection was 40.06 (40.06 ± 14.55) and 37.75 (37.75 ± 13.35) years, respectively, without significant difference (t = 1.53, P = 0.40). The number of men was more in the group of patients with chronic HB that in the group of subjects with self-limited HBV infection (χ2 = 36.54, P < 0.01). The proportion of married subjects was also different between the two groups (χ2 = 6.29, P = 0.01), whereas their education level was not statistically different (χ2 = 5.66, P = 0.06).
Association of -238G/A polymorphism of TNF-α promoter and behavior factors with outcomes of HBV infection
The distribution of genotype frequencies in patients with chronic HB and subjects with self-limited HBV infection was coincident with Hardy-Weinberg equilibrium (χ2 = 0.02, P = 0.89; χ2 = 0.02, P = 0.89).
The genotype distribution and allele frequencies of the -238 polymorphism in both groups are shown in Table 2. The homozygous AA genotype was not found in the study. Two hundred and three (98.07%) patients with chronic HB had GG genotype, significantly increased as compared with subjects with self-limited HBV infection (χ2 = 5.30, P = 0.02). The frequency of G allele in patients with chronic HB was significantly higher than that in subjects with self-limited HBV infection (99.03% vs 96.62%, χ2 = 5.20, P = 0.02).
Table 2 Genotype and allele frequencies in subjects with chronic HB and self-limited HBV infection.
The frequency of exposure to cigarette smoking or alcohol consumption in patients with chronic HB was significantly higher than that in subjects with self-limited HBV infection (OR > 1), but there was no significant difference between the two groups (χ2 = 2.13, P = 0.14 and χ2 = 0.99, P = 0.32).( Table 3)
Table 3 Association of behavior factors with risk of chronic HB.
Characteristics
Chronic HB (%)
Self-limited HBV infection (%)
OR (95%CI)
P
Cigarette smoking
1.40 (0.87, 2.28)
0.14
Yes
74 (35.75)
42 (28.38)
No
133 (64.25)
106 (71.62)
Alcohol consumption
1.26 (0.78, 2.05)
0.32
Yes
69 (33.33)
42 (28.38)
No
138 (66.67)
106 (71.62)
Multivariate unconditional logistic regression model was used to analyze the association of outcomes of HBV infection with age, sex, cigarette smoking, alcohol consumption and genotypes. It indicated that genotype GG was independently associated with chronic HB after the other factors were controlled (Table 4).
Table 4 Multivariate logistic regression analysis for determinants of chronic HB.
Variable
β
χ2
P
OR
95%CI
Intercept
-0.5076
7.2203
0.0072
—
—
Sex (Male = 1, Female = 0)
1.4088
35.1138
< 0.0001
4.091
2.567–6.519
-238G/A (GG = 1, GA = 0)
1.4183
5.1467
0.0233
4.132
1.212–14.085
Gene-environmental interaction
As GG genotype was defined as positive exposure in this study, the results of gene-environmental interaction analysis between GG genotype and smoking or alcohol drinking are shown in Table 5, Table 6. The odds ratios for smoking exposure alone and GG genotype alone were 0.50 (P = 1.00) and 2.60 (P = 0.19), respectively, whereas the odds ratio for combination of smoking and GG genotype was 3.84 (P = 0.07) in a synergic pattern (II = 3.84/ 0.50×2.60 = 2.95). The odds ratio was 0.78 (P = 1.00) for alcohol consumption alone and 3.18 (P = 0.11) for GG genotype alone, respectively, and their combined odds ratio was 4.07 (P = 0.05), indicating an effect of interaction between them (II = 4.07/0.78×3.18 = 1.64).
Table 5 Case-control analysis for interaction between ciga-rette smoking and GG genotype.
It is estimated that HBV is present in about 130 million chronic carriers, accounting for 10% of Chinese population[22]. HBV infection can result in acute hepatitis, HBV carriage, chronic hepatitis, liver cirrhosis, even primary hepatocellular carcinoma. One reason of broad spectrum of HBV infection could be attributed to the interaction of genetic and environmental factors. The majority of human genetic studies on HBV infection focused on human leucocyte antigen (HLA) in recent years[23-27]. Several pro-inflammatory cytokines such as interleukin-2 and interferon-γ and TNF-α, have been identified to participate in the process of viral clearance and host immune response to HBV[28,29]. In addition, TNF-α/TNF-α receptor system has an important role in the pathogenesis of liver damage and viral clearance[30].
TNF-α is a principal mediator of inflammation and cellular immune response regulated both transcriptionally and posttranscriptionally[31] . In the past years -238G/A polymorphism in a putative regulation box of the TNF-α gene promoter region has been identified. Genetic polymorphisms in the regulatory regions of various cytokine genes could influence the amount of cytokines produced in response to inflammatory stimuli.
In our study, chronic HB patients and self-limited HBV infection individuals (the same as the patients recovered from HB in other studies) were recruited to examine the TNF-α promoter polymorphism at position -238. The results demonstrated that 98.07% of the patients carried genotype GG, significantly higher than the frequency in those with self-limited infection, suggesting that genotype GG could increase the risk of chronic HB and was different from the report of Hohler[32]. Fifty-three (75%) of 71 subjects with chronic HB were homozygous in TNF-α G/G, lower than the frequency of those with self-limited HBV infection (94%). Ethnic difference could play a certain role in these conflicting results, because the results from several studies suggested that the distribution of TNF promoter polymorphisms in the study subjects was different from those with other racial origins[7,32,33].
The difference in genotype and allele frequency between patients with chronic HB and subjects with self-limited HB infection in our study suggested that GG genotype might have no advantage to antigen presenting, but further study would be needed to demonstrate its significance as a susceptible gene. This difference may be due to the fact that the TNF-α promoter polymorphism at position -238, likely serving as a marker, was in linkage disequilibrium with neighboring genes encoding HLA or other undefined genes, thus possibly influencing the outcomes of diseases.
Some studies suggested that the TNFA-A allele falling within a putative Y regulation box of the TNF-α promoter, was associated with increased TNF-α expression[34-36], which was inconsistent with other studies[37-40]. It is necessary to carry out the experimental study to confirm the causality between the -238G/A polymorphism of TNF-α promoter gene and the outcome of HBV infection, based on the population study.
The gene of TNF-α is located in the HLA class III region in the short arm of chromosome 6. Some single nucleotide polymorphism (SNP) loci have been found in the promoter region of TNF-α gene. It is speculated that these loci would be in linkage disequilibrium with other unknown mutations or HLA genes. It is important to further demonstrate the association of their constructed haplotypes with outcomes of HBV infection.
Epidemiological findings indicated that alcohol consumption and viral hepatitis could act synergistically to promote the development and progression of liver disease. Patients with viral hepatitis and alcohol consumption accelerated their liver injury with a higher risk of liver cirrhosis and primary hepatocellular carcinoma than those with viral hepatitis alone or alcohol consumption alone[41,42]. Wang[43] reported cigarette smoking and alcohol consumption were independently associated with elevated ALT levels among anti-HCV-seropositive individuals. Our study showed cigarette smoking and alcohol consumption might be risk factors of chronic HB (OR > 1), but further study is needed due to lack of evidence that could reveal statistically significant differences between groups of chronic HB and self-limited HBV infection.
The analysis of gene-environmental interaction in this study showed there was a synergic effect between GG genotype and cigarette smoking or alcohol consumption. The very wide confidence interval was due to only one subject who smoked or drank without GG genotype in patient group, which needs a larger sample size to be confirmed.
In summary, different outcomes of HBV infection are independently associated with TNF-α promoter polymorphism at position -238, and there might be a synergic effect between TNF-α promoter gene and cigarette smoking or alcohol consumption in the development of chronic HB.
ACKNOWLEDGMENT
The authors thank Drs.Yi-Fan Chen, Xiu-Yun Ma, Min-Ying Mu, Hao-Dong Cai, Yun-Zhong Wu, Qing-Hua Dong, Zhi-Hai Cheng, Jie Xu from Ditan Hospital and Drs. Guo-Hua Yan, Xiu-Ling Wang, Yi-Liu from Shunyi District Hospital for data and sample collection.
Wang FS. Current status and prospects of studies on human genetic alleles associated with hepatitis B virus infection.World J Gastroenterol. 2003;9:641-644.
[PubMed] [DOI][Cited in This Article: ]
Bozkaya H, Bozdayi M, Türkyilmaz R, Sarioglu M, Cetinkaya H, Cinar K, Köse K, Yurdaydin C, Uzunalimoglu O. Circulating IL-2, IL-10 and TNF-alpha in chronic hepatitis B: their relations to HBeAg status and the activity of liver disease.Hepatogastroenterology. 2000;47:1675-1679.
[PubMed] [DOI][Cited in This Article: ]
Sleijffers A, Yucesoy B, Kashon M, Garssen J, De Gruijl FR, Boland GJ, Van Hattum J, Luster MI, Van Loveren H. Cytokine polymorphisms play a role in susceptibility to ultraviolet B-induced modulation of immune responses after hepatitis B vaccination.J Immunol. 2003;170:3423-3428.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 53][Cited by in F6Publishing: 49][Article Influence: 2.3][Reference Citation Analysis (0)]
Jazrawi SF, Zaman A, Muhammad Z, Rabkin JM, Corless CL, Olyaei A, Biggs A, Ham J, Chou S, Rosen HR. Tumor necrosis factor-alpha promoter polymorphisms and the risk of rejection after liver transplantation: a case control analysis of 210 donor-recipient pairs.Liver Transpl. 2003;9:377-382.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 18][Cited by in F6Publishing: 20][Article Influence: 1.0][Reference Citation Analysis (0)]
McCusker SM, Curran MD, Dynan KB, McCullagh CD, Urquhart DD, Middleton D, Patterson CC, McIlroy SP, Passmore AP. Association between polymorphism in regulatory region of gene encoding tumour necrosis factor alpha and risk of Alzheimer's disease and vascular dementia: a case-control study.Lancet. 2001;357:436-439.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 137][Cited by in F6Publishing: 147][Article Influence: 6.4][Reference Citation Analysis (0)]
Shibue T, Tsuchiya N, Komata T, Matsushita M, Shiota M, Ohashi J, Wakui M, Matsuta K, Tokunaga K. Tumor necrosis factor α 5'-flanking region, tumor necrosis factor receptor II, and HLA-DRB1 polymorphisms in Japanese patients with rheumatoid arthritis.Arthritis Rheum. 2000;43:753-757.
[PubMed] [DOI][Cited in This Article: ][Cited by in F6Publishing: 1][Reference Citation Analysis (0)]
The branch of infectious diseases, parasitology and hepatology of Chinese Medical Association. The strategy of prevention and cure in viral hepatitis.Zhonghua Chuanranbing Zazhi. 2001;19:56-62.
[PubMed] [DOI][Cited in This Article: ]
Rothman KJ, Greenland S. ed. Interactions between Causes. Mod-ern Epidemiology, 2nd ed, Boston:.Lippincott Williams Wilkins. 1998;311-326.
[PubMed] [DOI][Cited in This Article: ]
Jiang SD, Lv BZ. ed. Mathematical and Statistical Methods in Medical Genetics. 1st ed. Beijing:.Science Publishing House. 1998;10-11.
[PubMed] [DOI][Cited in This Article: ]
Diepolder HM, Jung MC, Keller E, Schraut W, Gerlach JT, Grüner N, Zachoval R, Hoffmann RM, Schirren CA, Scholz S. A vigorous virus-specific CD4+ T cell response may contribute to the association of HLA-DR13 with viral clearance in hepatitis B.Clin Exp Immunol. 1998;113:244-251.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 59][Cited by in F6Publishing: 66][Article Influence: 2.5][Reference Citation Analysis (0)]
González-Amaro R, García-Monzón C, García-Buey L, Moreno-Otero R, Alonso JL, Yagüe E, Pivel JP, López-Cabrera M, Fernández-Ruiz E, Sánchez-Madrid F. Induction of tumor necrosis factor alpha production by human hepatocytes in chronic viral hepatitis.J Exp Med. 1994;179:841-848.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 205][Cited by in F6Publishing: 223][Article Influence: 7.4][Reference Citation Analysis (0)]
Drouet C, Shakhov AN, Jongeneel CV. Enhancers and transcription factors controlling the inducibility of the tumor necrosis factor-alpha promoter in primary macrophages.J Immunol. 1991;147:1694-1700.
[PubMed] [DOI][Cited in This Article: ]
Kaijzel EL, van Krugten MV, Brinkman BM, Huizinga TW, van der Straaten T, Hazes JM, Ziegler-Heitbrock HW, Nedospasov SA, Breedveld FC, Verweij CL. Functional analysis of a human tumor necrosis factor alpha (TNF-alpha) promoter polymorphism related to joint damage in rheumatoid arthritis.Mol Med. 1998;4:724-733.
[PubMed] [DOI][Cited in This Article: ]
Huizinga TW, Westendorp RG, Bollen EL, Keijsers V, Brinkman BM, Langermans JA, Breedveld FC, Verweij CL, van de Gaer L, Dams L. TNF-alpha promoter polymorphisms, production and susceptibility to multiple sclerosis in different groups of patients.J Neuroimmunol. 1997;72:149-153.
[PubMed] [DOI][Cited in This Article: ][Cited by in Crossref: 159][Cited by in F6Publishing: 170][Article Influence: 6.3][Reference Citation Analysis (0)]
