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Journal of Family Medicine and Primary Care logoLink to Journal of Family Medicine and Primary Care
. 2022 May 14;11(5):1785–1788. doi: 10.4103/jfmpc.jfmpc_1261_21

Prevalence of hepatitis B and C virus infections and immunity among hemodialysis patients in the Mazandaran province, Northern Iran

Amin Darrudi 1, Melody Omrani Nava 2,, Ata Ebrahimi 1, Kosar Ghaffari 1, Kasra Ahmadi Moghaddam 1, Fatemeh Roozbeh 2
PMCID: PMC9254791  PMID: 35800504

ABSTRACT

Background:

Hemodialysis (HD) is one of the most common causes of blood-borne infections. In order to prevent viral hepatitis and confront with the virus on the next step, health providers specify infected patients by screening and vaccination. This study is designed to investigate the prevalence of Hepatitis B virus (HBV) and Hepatitis C virus (HCV) infections in HD patients in Mazandaran, Iran.

Methods:

The medical records of 216 patients referred to the hemodialysis centers were evaluated in this cross-sectional study between 2019 and 2020. The collected data was analyzed using t-test and Chi-square.

Results:

Among 216 patients, 106 cases were female (49.07%) and 110 subjects were male (50.9%). The mean age was 40.1 y/o in females and 50.9 y/o in the male patients. The study recorded nine HBs-Ag positive (prevalence: 0.06%) and 15 HCV-Ab positive (prevalence: 6.94%) patients. Also, the most common co-morbidities were diabetes and hypertension. It was observed that 13 patients from 34 patients with negative HBs-Ag (who had 10–100 U HBs-Ab in the first stage) experienced sudden drop in the antibody titration to less than 10 U (P < 0.05). From 50 HBs-Ag negative patients with HBs-Ab more than 100 U in the first stage, antibody titration of five patients was decreased to less than 10 U in the second stage (P < 0.05).

Conclusions:

The prevalence of HCV and HBV was low in HD patients in Mazandaran province. However, due to the large number of patients with non-protective HBs-Ab levels, there is a risk of an increased prevalence of the disease.

Keywords: HBs-Ab, HBV, HCV, hemodialysis, viral hepatitis

Introduction

Hemodialysis (HD) is considered as an alternative approach for purifying blood in patients with renal diseases, and especially in individuals with end-stage renal disease (ESRD).[1] Among the various complications related to HD, blood-borne infections have been attributed with challenges.[2] According to the reports, the prevalence of viral infections, particularly hepatitis viruses in individuals performing HD is higher in comparison to the general population. Additionally, subjects undergoing prolonged HD potentially have a higher risk of exposure with hepatitis B virus (HBV), hepatitis C virus (HCV), Human immunodeficiency virus (HIV), and other blood-borne complications.[3,4] According to estimations, over 240 million individuals are chronic carriers of HBV and over 780 thousand mortalities occur because of HBV.[5] Reports demonstrate an increasing frequency of ESRD in Iranian individuals.[2] Notwithstanding, a recent systematic review demonstrated that the national prevalence of HBV was between 2.1% and 18.2%.[6] Additionally, based on a 2008 systematic review, approximately 2.5% of Iranians were infected with HBV between 2001 and 2007, regardless of 94% of people being vaccinated for HBV in 2005.[7] In fact, reports estimate a 2.2% of Iranian general population being infected with HBV. Hence, Iran is classified as a country with a low-intermediate prevalence of HBV infection.[8]

HCV is also a blood-borne infection attributed to HD. Infection by HCV has been associated with liver diseases, and cirrhosis of liver at the intense stages, and cause significant rate of mortality among general population as well as those under HD.[9] Although a remarkable decline in the prevalence of HCV has been reported among Iranian individuals undergoing HD, it remains a subject of challenge and concern for health priorities. Reports indicate that 54,000 individuals are dead annually due to HCV infection.[9] Life expectancy of the HD subjects is under the impression of HCV infection.[10] According to studies, HCV infection led to 57.29, 59.92, and 66.45 (per 100 thousand individuals) disability-adjusted life years (DALYs), respectively, in 1990, 2000, and 2010 in the Asian-pacific countries. Nonetheless, a decreasing trend for death rates and DALYs were reported for the HCV-related cirrhosis. But, there was a promoting trend of DALYs and mortality for HCV-related acute hepatitis and liver cancer.[11] In relation to the developed countries, no consistent reports are available about the prevalence estimates of HCV infection in the individuals undergoing HD in the developing countries. According to the reports by systematic review on the national data, a 0.16% seroprevalence of HCV infection was estimated between 2001 and 2008. In addition, the prevalence of HCV infection in cases undergoing HD was 30%–90%.[12,13] Studies demonstrated that the seroprevalence of HCV infection in the subjects with HD in the Iranian population was 14.4% in 1999 and 4.5% in 2006, which reported a decreasing trend.[2,14] In a 2010 systematic review, the prevalence of HCV infection in the Iranian individuals under HD was reported to be 7.61%.[15] But, a 2017 systematic review and meta-analysis study indicated that the estimated pooled prevalence of HCV infection in the subjects undergoing HD was 11% (95% confidence interval [CI] = 10%–13%).[16]

Here in this study, we retrospectively evaluated the prevalence of HBV and HCV infections in the Mazandaran province, Iran during 2019–2020.

Study Subjects and Methods

This retrospective cross-sectional descriptive study was conducted on 261 subjects under HD referred to three dialysis centers in the Mazandaran province from 2019 to 2020. Baseline characteristics and demographic specifications of the study subjects including sex, age, weight, and duration under dialysis were recorded from the medical history of subjects. Among the inclusion criteria of the subjects were aging above 15 years, a duration of dialysis more than 6 months, and availability of data for hepatitis B surface antigen (HBS-Ag), hepatitis B surface antibody (HBS-Ab), and HCV-Ab. If the patients did not have complete data, they would be excluded from the study. The local ethical committee of Mazandaran University of Medical Sciences approved the protocol of this study.

Analysis of data was conducted using the Statistical Package for the Social Sciences (SPSS) version 23 software for windows (SPSS, Chicago, IL, USA). To compare scale variables, independent samples t-test was used. Chi-square test was exerted for the comparison of nominal variables. Data were presented as either mean ± standard deviation (SD) for scale variables or frequency (percentage) for the nominal variables. A P value less than 0.05 was considered as statistically significant [Table 1].

Table 1.

Descriptive Statistics

n Minimum Maximum Mean Std. deviation
AGE 216 26.00 95.00 62.2454 13.71911
Weight 213 33 113 68.19 15.020
Valid n (listwise) 213

Results

From the 1377 subjects available, we evaluated the medical records of 280 subjects under HD in the dialysis centers of Mazandaran province. Finally, 216 individuals met the inclusion criteria and were studied.

The study group comprised 110 (50.9%) males and 106 (49.1%) females. The mean age of subjects was 62.25 ± 13.71 years. The mean age was 40.1 ± 11.52 in females and 50.9 ± 9.43 in the male patients. Subjects had a mean weight of 68.19 ± 15.52 Kg. The most common co-morbidities were diabetes [138 subjects (63.8%)] and hypertension [96 subjects (44.4%)].

The study recorded nine cases with HBs-Ag positive (prevalence: 0.65%) and 15 subjects with HCV-Ab positive (prevalence: 6.94%). Overall, nine cases (37.5%) with positive hepatitis virus (either HBV or HCV) were females and 15 cases (62.5%) were males [Table 2].

Table 2.

Baseline data and demographic characteristics of the study subjects undergoing HD

Specification Total HBV HCV


HBs-Ag positive HBs-Ag negative HCV-Ab positive HCV-Ab negative
Age; Year 62.25±13.71 57.65±17.81 62.79±13.7 51±4.1 62.78±13.7
Sex; Male/Female 110 (50.9%)/106 (49.1%) 6/3 104/103 9/6 101/100
Weight; kg 68.19±15.52 63±4.6 68±15.5 59±3.3 68±15.5
Dialysis duration (month) 48±8 38±3 48±8 42±4 48±8
Co-morbidities 194 (89.8%) 9 207 15 201

HBV, Hepatitis B virus; HCV, Hepatitis C virus; HBs-Ag, Hepatitis B surface antigen; HCV-Ab, Hepatitis C virus antibody

The mean weight of non-hepatitis HD subjects [193 (89.4%)] was 68.25 ± 15.03 kg and that of hepatitis HD cases [23 (10.6%)] was 67.65 ± 15.23 kg. Hence, no significant difference was observed in the weight of HD cases with hepatitis and non-hepatitis individuals (P = 0.85). Additionally, age of non-hepatitis HD cases and hepatitis HD individuals was 62.79 ± 13.09 years and 57.65 ± 17.81 years, respectively, with no statistically significant difference (P = 0.85; Table 3).

Table 3.

Comparison of the weight and HD individuals with and without hepatitis

Status Number Mean Standard deviation P
Weight Non-hepatitis 193 (89.4%) 68.25 15.03 0.85
Hepatitis 23 (10.6%) 67.65 15.23
Age Non-hepatitis 193 (89.4%) 62.79 13.09 0.08
Hepatitis 23 (10.6%) 57.65 17.81

It was observed that 13 patients from 34 patients with negative HBs-Ag (who had 10–100 U HBs-Ab in the first stage) experienced sudden drop in the antibody titration to less than 10 U (P < 0.05). From 50 HBs-Ag negative patients with HBs-Ab more than 100 U in the first stage, antibody titration of five patients was decreased to less than 10 U in the second stage (P < 0.05; Table 4).

Table 4.

The immunization developed by HD subjects against HBV

Primary HBs-Ag

<10 U 10-100 U >100 U Sum
Secondary HBs-Ab
 <10 U 35 2 5 42
 10-100 U 12 19 5 36
 >100 U 3 13 20 36
 Sum 50 34 30 114

HBs-Ab, Hepatitis B surface antibody

Discussion

Viral infections, particularly HBV and HCV are considered as the critical complications in the individuals performing HD. The transmission of viruses and contamination of subjects undergoing HD stem primarily from the contamination of devices employed for performing hemodialysis because of an ineffectual sterilizing among the dialysis sessions.[17] In spite of availability of vaccine (for HBV), diagnostic tests, and preventive approaches developed by WHO, the risk of HBV and HCV infection during dialysis remain a challenging issue. Nonetheless, the HBV prevalence is lower than HCV.[18] The HBV prevalence was reported to be 2.53% in 2011, which stayed at a similar level over the course of following years.

In the Guilan province (which is in vicinity to the Mazandaran province), Mohtasham-Amiri et al. in 2003 reported that the prevalence of HCV was 24.8% in subjects with HD.[19] According to the reports by Alavian et al.[20] in 2003 performed in a hemodialysis unit in the Mazandaran province, the prevalence of HCV in cases undergoing HD was 12%. Five years later, Alavian et al.[15] in 2008 reported that the prevalence of HCV in cases undergoing HD was 11.8 in the Mazandaran province. Nonetheless, Hasanjani Roushan et al. in 2016 reported that the prevalence of HCV in the subjects under HD was 8.27% in the Mazandaran province, which indicates a decline in the prevalence of HCV among HD cases from the Mazandaran province.[21] However, our study revealed that the prevalence of HCV was even lower (6.94%) compared to the 2016 study (8.27%). This might be due to higher commitment to the hygiene recommendations by the medical staff and improvement in the sterilization of the devices used in the medical systems.

In 2007, it was reported that the prevalence of HBV in Iranian subjects with HD was 4.6%.[22] Mansour-Ghanaei et al.[23] reported that the prevalence of HBV in the subjects undergoing HD in the Guilan province was 3.06%. Hasanjani Roushan et al. reported that the prevalence of HBV in the subjects under HD was 2.1% in the Mazandaran province during 2012–2014.[21] Our study indicated that the HBs-Ag positivity was detected in 0.65% of subjects. Again, our investigation suggests decreased prevalence of HBV in the HD cases from 2.1% to 0.65% in 2012–2016[21] in the Mazandaran province. This might be due to higher commitment to increased number of vaccinated subjects and the hygiene recommendations by the medical staff and improvement in the sterilization of the devices employed in the medical systems. In addition, it appears that due to the geographical location of Mazandaran province and the long distance of some cities from the referral centers of this province, HBS-Ag positive patients living in the eastern and especially western cities of the province prefer to refer to neighboring provinces, which can falsely represent a lower prevalence of HBV.

It was observed that 13 patients from 34 patients with negative HBs-Ag (who had 10–100 U HBs-Ab in the first stage) experienced sudden drop in the antibody titration to less than 10 U. From 50 HBs-Ag negative patients with HBs-Ab more than 100 U in the first stage, antibody titration of five patients was decreased to less than 10 U in the second stage. This observation can be used to make decisions in vaccination schedules and in controlling the examinations of immunity level in the general population. Notwithstanding, further studies are needed to survey and estimate the etiology of decreased immunity in the non-respondents.

In consideration of all, our study demonstrates a decreasing trend of HBV and HCV infection in the cases under HD in the Mazandaran province over the course of the past years. Nonetheless, due to the large number of patients with non-protective HBs-Ab levels, there is a risk of an increased prevalence of the disease. The most common co-morbidities were diabetes and hypertension in our study subjects. Although it is unclear that the infection by HCV or HBV might contribute to the co-morbidities, further attempts are mandatory to decrease the rate of HD-associated complications and their related co-morbidities.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

  • 1.Kakar S, Burgart LJ, Batts KP, Garcia J, Jain D, Ferrell LD. Clinicopathologic features and survival in fibrolamellar carcinoma:Comparison with conventional hepatocellular carcinoma with and without cirrhosis. Mod Pathol. 2005;18:1417–23. doi: 10.1038/modpathol.3800449. [DOI] [PubMed] [Google Scholar]
  • 2.Alavian SM, Bagheri-Lankarani K, Mahdavi-Mazdeh M, Nourozi S. Hepatitis B and C in dialysis units in Iran:Changing the epidemiology. Hemodial Int. 2008;12:378–82. doi: 10.1111/j.1542-4758.2008.00284.x. [DOI] [PubMed] [Google Scholar]
  • 3.Karimabad MN, Hassanshahi G, Arababadi MK. Controversial report regarding seroprevalence of hepatitis B and C viruses among hemodialysis patients in kerman province, South-East Iran. Hepat Mon. 2013;13:e7046. doi: 10.5812/hepatmon.7046. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Sherbahn R. Spontaneous ruptured subcapsular liver hematoma associated with pregnancy. A case report. J Reprod Med. 1996;41:125–8. [PubMed] [Google Scholar]
  • 5.Eleftheriadis T, Liakopoulos V, Leivaditis K, Antoniadi G, Stefanidis I. Infections in hemodialysis:A concise review. Part II:Blood transmitted viral infections. Hippokratia. 2011;15:120–6. [PMC free article] [PubMed] [Google Scholar]
  • 6.Djalalinia S, Ghorbani NR, Tajbakhsh R, Modirian M, Abdar ZE, Gorabi AM, et al. Hepatitis B virus infection in Iranian hemodialysis patients:A systematic review and meta-analysis. Iran J Kidney Dis. 2018;12:1–9. [PubMed] [Google Scholar]
  • 7.Alavian SM, Hajarizadeh B, Ahmadzad-Asl M, Kabir A, Bagheri-Lankarani K. Hepatitis B Virus infection in Iran:A systematic review. Hepat Mon. 2008;8:281–94. [Google Scholar]
  • 8.Salehi-Vaziri M, Sadeghi F, Hashiani AA, Fesharaki MG, Alavian SM. Hepatitis B virus infection in the general population of Iran:An updated systematic review and meta-analysis. Hepat Mon. 2016;16:e35577. doi: 10.5812/hepatmon.35577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Shepard CW, Finelli L, Alter MJ. Global epidemiology of hepatitis C virus infection. Lancet Infect Dis. 2005;5:558–67. doi: 10.1016/S1473-3099(05)70216-4. [DOI] [PubMed] [Google Scholar]
  • 10.Taherkhani R, Farshadpour F. Epidemiology of hepatitis C virus in Iran. World J Gastroenterol. 2015;21:10790–810. doi: 10.3748/wjg.v21.i38.10790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.The 22nd conference of the Asian pacific association for the study of the liver:APASL 2012-Taipei, Taiwan-16-19 February. Hepatol Int. 2012;6:67–309. doi: 10.1007/s12072-011-9333-4. [DOI] [PubMed] [Google Scholar]
  • 12.Alavian SM, Ahmadzad-Asl M, Lankarani KB, Shahbabaie MA, Bahrami-Ahmadi A, Kabir A. Hepatitis C infection in the general population of Iran:A systematic review. Hepat Mon. 2009:9. [Google Scholar]
  • 13.Argaw B, Mihret A, Aseffa A, Tarekegne A, Hussen S, Wachamo D, et al. Sero-prevalence of hepatitis B virus markers and associated factors among children in Hawassa City, Southern Ethiopia. BMC Infect Dis. 2020;20:528. doi: 10.1186/s12879-020-05229-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Liang TJ. Current progress in development of hepatitis C virus vaccines. Nat Med. 2013;19:869–78. doi: 10.1038/nm.3183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Alavian S-M, Kabir A, Ahmadi AB, Lankarani KB, Shahbabaie MA, Ahmadzad-Asl M. Hepatitis C infection in hemodialysis patients in Iran:A systematic review. Hemodial Int. 2010;14:253–62. doi: 10.1111/j.1542-4758.2010.00437.x. [DOI] [PubMed] [Google Scholar]
  • 16.Ghorbani NR, Djalalinia S, Modirian M, Abdar ZE, Mansourian M, Gorabi AM, et al. Prevalence of hepatitis C infection in Iranian hemodialysis patients:An updated systematic review and meta-analysis. J Res Med Sci. 2017;22:123. doi: 10.4103/jrms.JRMS_223_17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Thongsawat S, Maneekarn N, Kuniholm MH, Pantip C, Thungsuputi A, Lumlertkul D, et al. Occult hepatitis C virus infection during an outbreak in a hemodialysis unit in Thailand. J Med Virol. 2008;80:808–15. doi: 10.1002/jmv.21126. [DOI] [PubMed] [Google Scholar]
  • 18.Khedmat H, Amini M, Ghamar-Chehreh ME, Agah S. Hepatitis C virus infection in dialysis patients. Saudi J Kidney Dis Transpl. 2014;25:1–8. doi: 10.4103/1319-2442.124455. [DOI] [PubMed] [Google Scholar]
  • 19.Mohtasham A.Z., Jaefari S.A., Toorchi R.M. Seroprevalence of hepatitis C and risk factors in hemodialysis patients in Guilan province, Iran. 2003 [Google Scholar]
  • 20.Alavian S, Ardeshiri A, Hajarizadeh B. Prevalence of HCV, HBV and HIV infections among hemophiliacs. Hakim Res J. 2003;6:45–51. [Google Scholar]
  • 21.Roushan, M.R.H., et al. Epidemiological aspects of hepatitis B and C and human immunodeficiency viruses among hemodialysis patients in Mazandaran Province, Iran. Nephro-urology monthly. 2016:8. doi: 10.5812/numonthly.37878. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Kheradpezhouh M, Taremi M, Gachkar L, Aghabozorgi S, Khoshbaten M. Presence and significance of transfusion-transmitted virus infection in Iranian patients on maintenance hemodialysis. J Microbiol Immunol Infect. 2007;40:106–11. [PubMed] [Google Scholar]
  • 23.Mansour-Ghanaei F, Sadeghi A, Mashhour MY, Joukar F, Besharati S, Roshan Z, et al. Prevalence of hepatitis B and C infection in hemodialysis patients of Rasht (Center of Guilan Province, Northern Part of Iran) Hepat Mon. 2009;9:45–9. [Google Scholar]

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