Skip to main content
Hepatitis Monthly logoLink to Hepatitis Monthly
. 2011 Apr 1;11(4):273–277.

Hepatitis B seromarkers, hepatitis C antibody, and risk behaviors in married couples, a bordered province of western Thailand

Hepatitis B seromarkers, hepatitis C antibody, and risk behaviors

Pipat Luksamijarulkul 1,*, Pittaya Piroonamornpun 2, Somporn Kantharadussadee Triamchaisri 3
PMCID: PMC3206700  PMID: 22087153

Abstract

Background

Married couples constitute a target group for reducing the risk of infections with hepatitis B virus (HBV) and hepatitis C virus (HCV).

Objectives

This study attempted to assess HBV seromarkers, anti-HCV-positive rates, and risk behaviors among married couples in a bordered province of western Thailand.

Materials and Methods

A cross-sectional study of 114 married couples aged 15-44 years was performed. Approximately 25-30 married couples were randomly selected from 4 districts in a province of western Thailand. All study participants who participated voluntarily were interviewed using structured questionnaires. Their blood specimens were collected to screen for HBV seromarkers (HBsAg, anti-HBs, and anti-HBc) and anti-HCV.

Results

Approximately 21.1% of husbands and 2.6% of wives had a history of extramarital sex without using a condom; 18.4% of husbands and 4.4% of wives had tattoos; and 18.4% and 3.5%, respectively, consumed alcohol regularly. Additionally, 4.4% of husbands and 2.6% of wives had a history of sexual contact before marriage. In the serological study, 10.5% of husbands and 5.3% of wives were HBsAg-positive, and 1.8% of husbands and 0.9% of wives were anti-HCV-positive. Among HBsAg-positive subjects, 15/18 had spouses who were positive for any HBV marker, and 1 had a spouse who was HBsAg- and anti-HBc positive. Three participants were positive for anti-HCV (2 males and 1 female). One anti-HCV-positive male had a history of regular alcohol consumption and extramarital sex without a condom, and another had a history of intravenous drug use. The anti-HCV-positive female had a history of sexual contact before marriage.

Conclusions

This study found high percentages of risk behaviors and HBsAg positivity among married couples in a bordered province of western Thailand, especially in husbands. These findings support the evidence of HCV transmission via sexual contact and intravenous drug use.

Keywords: HCV antibodies, Risk behaviors, Sex, Spouses

Background

Sexually transmitted and bloodborne infections, especially hepatitis B virus (HBV) and hepatitis C virus (HCV), are significant public health problems in many countries, including Thailand [1][2][3][4][5][6]. There are more than 350 million HBsAg carriers worldwide and 170 million HCV-infected individuals [1][2][3][4].

The complications from HCV and HBV infections are serious. Approximately 10% to 40% will develop chronic hepatitis and experience gradual progression to liver cirrhosis and hepatocellular carcinoma (HCC) [2][3][7][8]. If HCV patients are also infected with HBV or HIV, they will develop HCC and liver cirrhosis more quickly than those who are infected with HCV alone. Additionally, HCV infection may contribute to faster progression of HIV infection [9][10][11][12][13]. The incidence of HCC and cirrhosis is nearly 6.5 to 11 times higher among HIV-coinfected patients than those without HIV coinfection [10]. HBV is transmitted parenterally and by sexual contact, whereas the principal route of HCV transmission is parenteral [2][3][4][14][15][16].

In Thailand, drug users (IDUs) and female sex workers (FSWs) are the groups at highest risk of HBV and HCV infection [14][15][17]. The spouses of IDUs and clients of FSWs have an higher chance of acquiring HBV and/or HCV if they do not use condoms at each sexual encounter. If infected, these groups can transmit the infections to the general population.

Previous studies have demonstrated sexual transmission of HBV and HCV among spouses [16][18][19]. Such infections can affect their neonates and siblings from intrafamilial transmission [20][21][22]. Married couples constitute a target group for reducing the risk of these infections. Kanchanaburi province is a bordered province in western Thailand. Risk behaviors towards sexually transmitted and blood-borne infections probably tended increase due to the high migration rate of unskilled workers from a bordered country.

Objectives

A study of HBV seromarkers, antibodies to HCV, and risk behaviors among married couples in this province is valuable for the epidemiological surveillance and development of a special intervention program for this target group.

Materials and Methods

Study design and study participants

We performed a cross-sectional study between October 2004 and June 2005 of 114 married couples aged 15-44 years. Approximately 25-30 married couples, who participated voluntarily, were randomly selected from 4 districts in Kanchanaburi province, a bordered province in western Thailand. All participants, who had no history of HBV vaccination, were interviewed using structured questionnaires. Information on their socio-demographic characteristics and risk behaviors toward HBV and HCV infections was included. Blood specimens were collected to screen for HBV seromarkers (HBsAg, anti-HBs, and anti-HBc) and anti-HCV. Before the interviews and blood screening, the participants received the study information, after which they filled out informed consent forms. This study protocol was approved by the Ethics Committee of Mahidol University.

Methods for screening blood

Blood specimens were screened for HBV seromarkers and anti-HCV using immunochromatography and immunocomb ELISA kits (ABBOTT EIA and Pacific Biotech and Organics Immunocomb II, Bangkok, Thailand) with 96% to 100% sensitivity and specificity for HBV seromarkers compared with EIA and more than 99% sensitivity and specificity for anti-HCV. For samples to have been considered HBsAg- or anti-HCV-positive, the immunochromatography and EIAmust have had to be positive.

Data analysis

Data from interviews and blood screening were analyzed using SPSS for Windows, version 7.5, and expressed using descriptive statistics, including percentage, mean, and standard deviation. To analyze the homogeneity of the distribution of variables between 2 groups, we used the chi-square test. A critical level of p = 0.05 was considered to indicate statistical significance.

Results

Sociodemographic characteristics in the study couples

Of 114 married couples, 40.4% of husbands and 12.3% of wives were aged above 30 years. The mean age ± standard deviation was 28.2 ± 6.2 years for husbands and 22.1 ± 5.9 years for wives. Approximately 26.3% of husbands and 18.4% of wives had completed secondary education, and 3.5% and 1.8%, respectively, completed vocational education and undergraduate study. Most of participants had low incomes (< 10,000 baht/month). The distributions by age, occupation, and income differed significantly between husbands and wives (p < 0.001). The details are presented in Table 1.

Table 1. Sociodemographic characteristics of study couples (No. = 114 couples).

Sociodemographic Characteristics Husbands [No. (%)] Wives [No. (%)] p-value x(2)-test
Age (years)
≤ 20 2 (1.75) 19 (16.7) < 0.001  a
21– 30 66 (57.9) 81 (71.1)
≥ 31 46 (40.4) 14 (12.3)
Mean ± SD of Age 28.2 ± 6.2 22.1±5.9
Education
Primary level 39 (34.2) 54 (47.4) 0.109
Secondary level 45 (39.5) 39 (34.2)
Vocational/undergraduate 30 (26.3) 21 (18.4)
Occupation
Government officer 4 (3.5) 2 (1.8) < 0.001 a
Private business 21 (18.4) 18 (15.8)
Laborer 48 (42.1) 40 (35.2)
Agricultures 39 (34.2) 26 (22.8)
Housewives/Unemployed 2 (1.8) 28 (24.6)
Income (Baht/mon)
≤ 5000 33 (28.9) 70 (61.4) < 0.001  a
5001-10000 56 (49.1) 27 (23.6)
≥ 10001 20 (17.5) 17 (14.9)

a Statistical significance at α = 0.05

Risk behavior toward HBV and HCV infection

Among the study couples, 21.1% of husbands and 2.6% of wives had a history of extramarital sex without a condom. Approximately 18.4% of husbands and 4.4% of wives had tattoos, and 18.4% and 3.5%, respectively, had a history of regular alcohol consumption. Further, 4.4% of husbands and 2.6% of wives had a history of sexual contact before marriage. Study husbands had a significantly higher percentage of risk behaviors than studied wives (p = 0.018). The details are shown in Table 2.

Table 2. Risk behaviors toward HBV and HCV infection among study couples.

Risk Behaviors Husbands (No.=114) No. (%) Wives (No.=114) No. %
History of receiving blood and/or hemodialysis 6 (5.3) 8 (7.0)
History of jaundice 12 (10.5) 8 (7.0)
History of tattooing 21 (18.4) 5 (4.4)
History of intravenous drug use 1 (0.9) 0 (0.0)
History of regular alcohol consumption 21 (18.4) 4 (3.5)
History of STDs in the previous year 9 (7.9) 1 (0.9)
History of extramarital sexual relations without a condom in the previous year 24 (21.1) 3 (2.6)
History of sexual contact before marriage 5 (4.4) 3 (2.6)
p-value from x(2)-test 0.018 a

a Statistical significance at α = 0.05

Prevalence of HBV seromarkers and anti-HCV

Of the 114 studied couples, 53.5% of husbands and 46.5% of wives were positive for HBV markers. Approximately 10.5% of husbands and 5.3% of wives were HBsAg-positive, and 1.8% of husbands and 0.9% of wives were anti-HCV-positive. Study husbands had relatively higher overall HBV markers and HBsAg-positive and anti-HCV rates than study wives (p = 0.354), Table 3. Among 18 HBsAg-positive subjects, 15 had spouses who were positive for any HBV marker, and 1 had an HBsAg- and anti-HBc-positive spouse (Table 4). In addition, 3 participants were positive for anti-HCV (2 males and 1 female). Of the 2 anti-HCV positive males, 1 had consumed alcohol regularly and had a history of extramarital sex without a condom, and the other had a history of intravenous drug use. The anti-HCV positive female had a history of sexual contact before marriage and no history of other risk behaviors (Table 3).

Table 3. Prevalence of HBV seromarkers and anti-HCV among study couples.

Variables Numberof tested HBV Seromarker positive Anti-HCV positive
HBsAg , Anti-HBc Anti-HBs, Anti-HBc Anti-HBc only Any HBV markers
Married status
Husband 114 12 (10.5) 31 (27.2) 18 (15.8) 61 (53.5) a 2 (1.8)b
Wife 114 6 (5.3) 27 (23.7) 20 (17.5) 53 (46.5) a 1 (0.9) c
Total 228 18 (7.9) 58 (25.4) 38 (16.7) 114 (50.0) 3 (1.3)

a p-value from x(2)-test = 0.354

b One had regular alcohol consumption and a history of extramarital sex without a condom, and the other had a history of intravenous drug use.

c Had a history of sexual contact before marriage and no history of other risk behaviors

Table 4. Characteristics of 18 HBsAg-positive subjects and HBV seromarker status in their spouses.

Serial Number Titer of HBsAgin subjects Gender Duration of marriage (mon) HBV Seromarkers of married couple
1 < 1:80 Female 32 Negative
2 < 1:80 Female 59 Anti-HBs + Anti-HBc
3 1:80 Male 30 Anti-HBs + Anti-HBc
4 1:80 Female 51 Anti-HBs + Anti-HBc
5 1:80 Female 36 Negative
6 1:80 Male 37 Negative
7 1:320 Male 12 Anti-HBc only
8 1:320 Male 18 Anti-HBs + Anti-HBc
9 1:640 Male 41 Anti-HBs + Anti-HBc
10 1:640 Male 52 Anti-HBs + Anti-HBc
11 1:640 Male 52 Anti-HBs + Anti-HBc
12 1:1280 Female 60 HBsAg + Anti-HBc
13 1:1280 Male 24 Anti-HBc only
14 1:2560 Female 48 Anti-HBc only
15 1:2560 Male 59 Anti-HBc only
16 1:5120 Male 48 Anti-HBs + Anti-HBc
17 a 1:5120 Male 60 HBsAg + Anti-HBc
18 1:10240 Male 54 Anti-HBc only

a Both husband and wife were positive for HBsAg and anti-HBc

Discussion

Both sexual and parenteral routes are the predominant modes of HBV transmission. In adults, this transmission is primariily person-to-person, via sexual contact. The spouses of HBV carriers can acquire the virus from them and spread it to others [3][4][5][19]. In contrast, the major route of HCV transmission is parenteral [2][14][15][18]. This study identified a wife who was positive for anti-HCV and had a history of sexual contact before marriage and no other risk behaviorsand 1 of 2 positive anti-HCV husbands who had a history of extramarital sex without a condom; the other had a history of intravenous drug use. These findings demonstra the sexual transmission of HCV. Both HBV and HCV infections can affect neonates and siblings from intrafamilial transmission [20][21][22].

This study of married couples in a bordered province of western Thailand observed a high percentage of important risk behaviors, such as a history of extramarital sex without a condom (21.1% of husbands and 2.6% of wives), regular alcohol consumption (18.4% of husbands and 3.5% of wives), tattoos (18.4% of husbands and 4.4% of wives), and a history of sexual contact before marriage (4.4% of husbands and 2.6% of wives). Tattoos, extramarital sexual relations, and sexual contact are known risk factors for HBV infection [3][16][19][23]. Alcohol consumption is an indirect risk behavior for HBV infection, because after consumption, the subject is more prone to have extramarital sexual relations without the use of a condom [23]. Intravenous drug use is an important risk factor of HCV and HBV infection [1][2][4][15][16][17][19][20].

Males had a relatively higher percentage of risk behaviors than female, consistent with several studies [3][23][24][25]. Additionally, the HBsAg-positive rate in study husbands (10.5%) was relatively higher than in other studies in the Thai population (4.3-6.1%), whereas anti-HCV positivity was similar to other reports [4][24][25]. However, false positives for anti-HCV can occur in a low-risk group; thus, the anti-HCV results in this study were confirmed by 2 screens-immunochromatography and EIA. To reduce these risk behaviors, integrated preventive measures, including premarital counseling, life skill education, and a 100% condom use policy, should be implemented. Additionally, HBV vaccination in this target group is urged to prevent HBV infection.

Acknowledgments

The authors gratefully acknowledge the health care personnel of thestudy areas and also wish to extend our deep appreciation to all participants. Finally, we would like to thank the China Medical Board (CMB), Faculty of Public Health, Mahidol University for partial support of this publication.

Footnotes

Implication for health policy/practice/research/medical education: Due to high percentages of risk behaviors and HBsAg positivity among married couples in a bordered province of western Thailand, an integrated intervention of life skill education, a 100% condom use policy and HBV vaccination should be implemented in premarital counseling clinics in this group

Please cite this paper as: Luksamijarulkul P, Piroonamornpun P, Triamchaisri SK. Hepatitis B seromarkers, hepatitis C antibody and risk behaviors in married couples, a bordered province of western Thailand. Hepat Mon. 2011;11(4):273-277.

Financial support: This study is partially supported by Faculty of Graduate Studies, Mahidol University

Conflict of interest: We declare that we have no conflict of interest.

References

  • 1.Amini S, Mahmoodi Farahani Majd, Abadi M, Alavian SM, Joulaie M, Ahmadipour MH. Distribution of hepatitis C virus genotype in Iran: a population-based MHstudy. Hepat Mon. 2009;9(2):95–102. [Google Scholar]
  • 2.Cohen J. The scientific challenge of hepatitis C. Science. 1999;285(5424):26–30. doi: 10.1126/science.285.5424.26. [DOI] [PubMed] [Google Scholar]
  • 3.Lavanchy D. Hepatitis B virus epidemiology, disease burden, treatment, and current and emerging prevention and control measures. J Viral Hepat. 2004;11(2):97–107. doi: 10.1046/j.1365-2893.2003.00487.x. [DOI] [PubMed] [Google Scholar]
  • 4.Luksamijarulkul P, Kaepan W, Klamphakorn S. Hepatitis B virus sero-markers, hepatitis C virus antibody and risk behaviors among middle age and older Thai males. Southeast Asian J Trop Med Public Health. 2007;38(1):45–52. [PubMed] [Google Scholar]
  • 5.Russi JC, Serra M, Vinoles J, Perez MT, Ruchansky D, Alonso G, Sanchez JL, Russell KL, Montano SM, Negrete M, Weissenbacher M. Sexual transmission of hepatitis B virus, hepatitis C virus, and human immunodeficiency virus type 1 infections among male transvestite comercial sex workers in Montevideo, Uruguay. Am J Trop Med Hyg. 2003;68(6):716–20. [PubMed] [Google Scholar]
  • 6.Rosenberg SD, Goodman LA, Osher FC, Swartz MS, Essock SM, Butterfield MI, Constantine NT, Wolford GL, Salyers MP. Prevalence of HIV, hepatitis B, and hepatitis C in people with severe mental illness. Am J Public Health. 2001;91(1):31–7. doi: 10.2105/ajph.91.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Chen DS, Kuo GC, Sung JL, Lai MY, Sheu JC, Chen PJ, Yang PM, Hsu HM, Chang MH, Chen C, et al . Hepatitis C virus infection in an area hyperendemic for hepatitis B and chronic liver disease: the Taiwan experience. J Infect Dis. 1990;162(4):817–22. doi: 10.1093/infdis/162.4.817. [DOI] [PubMed] [Google Scholar]
  • 8.Custer B, Sullivan SD, Hazlet TK, Iloeje U, Veenstra DL, Kowdley KV. Global epidemiology of hepatitis B virus. J Clin Gastroenterol. 2004;38(10 Suppl 3):S158–68. doi: 10.1097/00004836-200411003-00008. [DOI] [PubMed] [Google Scholar]
  • 9.Fuster D, Planas R, Muga R, Ballesteros AL, Santos J, Tor J, Sirera G, Guardiola H, Salas A, Cabré E, Ojanguren I, Barluenga E, Rey-Joly C, Clotet B, Tural C. Advanced liver fibrosis in HIV/HCV-coinfected patients on antiretroviral therapy. AIDS Res Hum Retroviruses. 2004;20(12):1293–7. doi: 10.1089/aid.2004.20.1293. [DOI] [PubMed] [Google Scholar]
  • 10.Giordano TP, Kramer JR, Souchek J, Richardson P, El-Serag HB. Cirrhosis and hepatocellular carcinoma in HIV-infected veterans with and without the hepatitis C virus: a cohort study, 1992-2001. Arch Intern Med. 2004;164(21):2349–54. doi: 10.1001/archinte.164.21.2349. [DOI] [PubMed] [Google Scholar]
  • 11.Schiavini M, Angeli E, Mainini A, Zerbi P, Duca PG, Gubertini G, Vago L, Fociani P, Giorgi R, Cargnel A. Risk factors for fibrosis progression in HIV/HCV coinfected patients from a retrospective analysisof liver biopsies in 1985-2002. HIV Med. 2006;7(5):331–7. doi: 10.1111/j.1468-1293.2006.00384.x. [DOI] [PubMed] [Google Scholar]
  • 12.van Asten L, Prins M. Infection with concurrent multiple hepatitis C virus genotypes is associated with faster HIV disease progression. AIDS. 2004;18(17):2319–24. doi: 10.1097/00002030-200411190-00013. [DOI] [PubMed] [Google Scholar]
  • 13.Alter MJ. Epidemiology of viral hepatitis and HIV co-infection. J Hepatol. 2006;44(1 Suppl):S6–9. doi: 10.1016/j.jhep.2005.11.004. [DOI] [PubMed] [Google Scholar]
  • 14.Luksamijarulkul P, Deangbubpha A. Hepatitis C antibody prevalence and risk factors of some female sex workers in Thailand. Southeast Asian J Trop Med Public Health. 1997;28(3):507–12. [PubMed] [Google Scholar]
  • 15.Luksamijarulkul P, Triamchaisri SK. Relationship between antibodies to hepatitis C virus and human immunodeficiency virus among Thai selected groups. Hepat Mon. 2009;9(1):66–9. [Google Scholar]
  • 16.Feldman JG, Minkoff H, Landesman S, Dehovitz J. Heterosexual transmission of hepatitis C, hepatitis B, and HIV-1 in a sample of inner city women. Sex Transm Dis. 2000;27(6):338–42. doi: 10.1097/00007435-200007000-00007. [DOI] [PubMed] [Google Scholar]
  • 17.Luksamijarulkul P, Plucktaweesak S. High hepatitis C seroprevalence in Thai intravenous drug abusers and qualitative risk analysis. Southeast Asian J Trop Med Public Health. 1996;27(4):654–8. [PubMed] [Google Scholar]
  • 18.Hershow RC, Kalish LA, Sha B, Till M, Cohen M. Hepatitis C virus infection in Chicago women with or at risk for HIV infection: evidence for sexual transmission. Sex Transm Dis. 1998;25(10):527–32. doi: 10.1097/00007435-199811000-00006. [DOI] [PubMed] [Google Scholar]
  • 19.Luksamijarulkul P, Mooktaragosa A, Luksamijarulkul S. Risk factors for hepatitis B surface antigen positivity among pregnant women. J Med Assoc Thai. 2002;85(3):283–8. [PubMed] [Google Scholar]
  • 20.Ko YC, Li SC, Yen YY, Yeh SM, Hsieh CC. Horizontal transmission of hepatitis B virus from siblings and intramuscular injection among preschool children in a familial cohort. Am J Epidemiol. 1991;133(10):1015–23. doi: 10.1093/oxfordjournals.aje.a115810. [DOI] [PubMed] [Google Scholar]
  • 21.Assateerawatt A, Suvatte V, Tanphaichitr VS. Long term efficacy of hepatitis B immunoprophylaxis in neonates at risk: using different vaccine and schedule. J Med Assoc Thai. 1992;75(6):328–36. [PubMed] [Google Scholar]
  • 22.Papaevangelou V, Pollack H, Rochford G, Kokka R, Hou Z, Chernoff D, Hanna B, Krasinski k, Borkowsky W. Increased transmission of vertical hepatitis C virus (HCV) infection to human immunodeficiency virus (HIV)-infected infants of HIV- and HCV-coinfected women. J Infect Dis. 1998;178(4):1047–52. doi: 10.1086/515668. [DOI] [PubMed] [Google Scholar]
  • 23.Gilson RJ, de Ruiter A, Waite J, Ross E, Loveday C, Howell DR. Hepatitis B virus infection in patients attending a genitourinary medicine clinic: risk factors and vaccine coverage. Sex Transm Infect. 1998;74(2):110–5. doi: 10.1136/sti.74.2.110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Luksamijarulkul P, Thammata N, Tiloklurs M. Seroprevalence of hepatitis B, hepatitis C and human immunodeficiency virus among blood donors, Phitsanulok Regional Blood Center, Thailand. Southeast Asian J Trop Med Public Health. 2002;33(2):272–9. [PubMed] [Google Scholar]
  • 25.Luksamijarulkul P, Drph ST, Triamchaisri S. Risk behaviors and life skills towards sexually transmitted and blood-borne infections among Thai married couples. J Med Assoc Thai. 2007;90(5):962–70. [PubMed] [Google Scholar]

Articles from Hepatitis Monthly are provided here courtesy of Brieflands

RESOURCES