Contents
Download PDF
pdf Download XML
11 Views
1 Downloads
Share this article
Research Article | Volume 30 Issue 6 (June, 2025) | Pages 93 - 98
To Study the Prevalence of Hepatitis B Infection in People Living with HIV in Gwalior Region
 ,
1
Junior Resident, Dept. of General Medicine, GRMC, Gwalior, M.P
2
Professor, Dept. of General Medicine, GRMC, Gwalior, M.P
Under a Creative Commons license
Open Access
Received
April 25, 2025
Revised
May 26, 2025
Accepted
June 4, 2025
Published
June 17, 2025
Abstract

Background & Methods: The aim of the study is to study prevalence of hepatitis b infection in people living with HIV in Gwalior region. Through reference analysis of, Epidemiology of viral hepatitis and HIV co-infection. ‖ by Miriam J. Alter, Journal of Hepatology, which quoted that it is estimated that 6–15% suffered from chronic HBV infection in HIV patient. Results: The majority of patients have no high-risk occupations, with 79.33% in the HIV-only group and 77.78% in the co-infected group. Truck drivers represent a higher percentage in the co-infected group (16.67%). The p-value for this distribution is 0.54, indicating no significant difference in occupation distribution between the groups. Conclusion: This study underscores the importance of continuous monitoring, targeted prevention, and comprehensive care strategies for HIV and Hepatitis B coinfected patients. The findings reinforce the need for integrated healthcare services that address the unique challenges faced by this vulnerable population.

Keywords
INTRODUCTION

Hepatitis B virus (HBV) and human immunodeficiency virus (HIV) co-infection is a significant global health concern due to their shared transmission routes, such as blood, sexual contact, and from mother to child during birth. HBV is a DNA virus that infects the liver, leading to both acute and chronic liver diseases, including cirrhosis and hepatocellular carcinoma. HIV is an RNA virus that targets the immune system, specifically CD4+ T cells, leading to immune deficiency and increased vulnerability to opportunistic infections and certain cancers. The coexistence of these two viruses, known as HIV-HBV co-infection, exacerbates the health outcomes of the affected individuals, causing more severe disease progression and complications than either infection alone [1].

 

The prevalence of HBV among HIV-infected individuals varies significantly across different regions. Studies have shown that in some areas, up to 10% of HIV-positive individuals are also infected with HBV [2]. In the African continent, particularly sub-Saharan Africa, the prevalence of HIV/HBV co-infection is notably high due to the endemic nature of both viruses. For instance, a study conducted in Turkey reported that 6.1% of HIV-positive individuals were co-infected with HBV, while in Brazil, the prevalence ranged from 3.1% to 6.1% depending on the region and population studied [3]. These variations highlight the need for region-specific studies to understand the local epidemiology of HIV-HBV co-infection better and to develop targeted public health interventions [4].

 

Co-infection with HBV and HIV leads to more severe health outcomes compared to mono-infection with either virus. HIV infection accelerates the progression of HBV-related liver disease, increasing the risk of liver cirrhosis, hepatocellular carcinoma, and liver-related mortality. Conversely, HBV infection can complicate the management of HIV due to potential drug interactions and the necessity for specific antiviral therapies that target both viruses. The immunosuppressive nature of HIV also makes it harder for the body to control HBV infection, leading to higher rates of chronic HBV and increased liver damage. Additionally, co-infected individuals may experience higher levels of HBV replication, further exacerbating liver disease and complicating treatment regimens [5-6].

 

The Gwalior region, like many other parts of India, faces a significant burden of both HIV and HBV infections. Despite the high prevalence of these infections, there is a lack of comprehensive data on the prevalence and impact of HBV co-infection among HIV-positive individuals in this region. This study aims to fill this gap by providing detailed epidemiological data, which is crucial for several reasons. Co-infection necessitates tailored treatment strategies that address both infections, optimizing patient outcomes and reducing liver-related complications. Understanding the prevalence and characteristics of co-infection will help healthcare providers develop more effective treatment plans that consider the unique needs of co-infected patients [7-8].

MATERIALS AND METHODS

This cross-sectional study is conducted in the Department of General Medicine, G.R. Medical College, Gwalior (M.P.) at ART Centre after taking informed consent from the patients.

 

INCLUSION CRITERIA:

  • All newly diagnosed adult patient (18-60 years) of HIV who will be visiting ART center at OPD of Jayarogya Group of Hospital, Gwalior for 01 Year.

 

EXCLUSION CRITERIA:

  • Patients infected with Hepatitis other than Hepatitis B.
  • Pregnant women and children age less than 18 years
  • HIV negative patient

 

Patient is selected for our study on the basis of all inclusion criteria. All patients were explained and informed about the study before the start of data collection. Informed consent was taken and details of the patient recorded. Patient demographic details viz age, sex, residence, level of education are recorded along with height, weight and BMI which was recorded with correctly calibrated weighing machine. Patient laboratory data viz Hemoglobin, blood counts, liver function test, serum albumin, CD4 count were collected from the ART center present at Jayarogya Group of Hospital, Gwalior.

RESULTS

Table No. 1: Descriptive Statistics Distribution

 

The average Hb (Hemoglobin) level indicates the general anemia status among patients, suggesting that many may have lower than average Hb levels. The mean and standard deviation of TLC (Total Leukocyte Count) reflect variability in the immune response, indicating a range of immune function among the patients. The normal platelet counts observed suggest that most patients do not suffer from thrombocytopenia. The levels of AST and ALT, which are liver enzymes, fall within expected ranges, indicating that liver function is generally normal across the population. Lastly, the levels of S. Albumin provide insights into the nutritional and liver function status of the patients, showing that most have adequate protein levels. These statistics collectively help in understanding the overall health and potential complications in the study group.

 

Table No. 2: Distribution of Patients based on geographic location by Co-infection Status

 

The majority of patients are from rural areas, with 55.03% in the HIV-only group and 50.00% in the co-infected group. Urban patients make up 44.97% of the HIV-only group and 50.00% of the co-infected group. The p-value for this distribution is 0.87, indicating no significant difference in residence distribution between the groups.

 

Table No. 3: Marital Status Distribution of Patients by Co-infection Status

 

The majority of patients are married, with 66.48% in the HIV-only group and 94.44% in the co-infected group. Single patients account for 20.39% of HIV-only and 5.56% of co-infected patients. Divorced and widowed patients represent a small proportion. The p-value for this distribution is 0.03, indicating a significant difference in marital status distribution between the groups.

 

Table No. 4: Prevalence of Hepatitis B in HIV Patients (HIV& Hepatitis B Co-infection Distribution)

 

The prevalence of Hepatitis B co-infection among HIV patients. Out of 376 patients, 358 (95.21%) are HIV positive only, while 18 (4.79%) are co-infected with Hepatitis B. This indicates a relatively low prevalence of Hepatitis B among the HIV patients in the study population.

 

Table No. 5: Distribution of patients by Route of transmission in HIV and HIV Hep B Co infected patient

 

The most common route of transmission for both groups is heterosexual contact, with 75.14% in the HIV-only group and 55.56% in the co-infected group. Unsafe injection is notably higher in the co-infected group at 33.33%. The p-value for this distribution is 0.03, indicating a significant difference in transmission routes between the groups.

 

Table No. 6: CD4 Cell Count Distribution of Patients with HIV and HIV and Hep B Co-infection

 

The majority of patients have CD4 counts between 200-500, with 36.03% in the HIV only group and 61.11% in the co-infected group. The p-value for this distribution is 0.05, indicating a borderline significant difference in CD4 cell count distribution between the groups.

 

Table No. 7: High-Risk Occupation Distribution

 

The majority of patients have no high-risk occupations, with 79.33% in the HIV-only group and 77.78% in the co-infected group. Truck drivers represent a higher percentage in the co-infected group (16.67%). The p-value for this distribution is 0.54, indicating no significant difference in occupation distribution between the groups.

DISCUSSION

The descriptive statistics table presents the central tendencies and dispersion for Hemoglobin (Hb), Total Leukocyte Count (TLC), Platelet Count, AST, ALT, and Serum Albumin. The mean Hb level suggests a general anemia status among patients, while the TLC reflects variability in immune function [9]. Normal platelet counts indicate no widespread thrombocytopenia. AST and ALT levels are within expected ranges, indicating generally normal liver function. Serum Albumin levels suggest adequate nutritional and liver function status among the majority of patients. These statistics collectively offer a comprehensive view of the overall health and potential complications within the study population [10].

 

The age distribution table reveals that most patients fall within the 30-39 age group (30.32%) and the 40-49 age group (26.06%). The age range of 30-49 years accounts for a significant proportion of the patients, indicating a higher prevalence of HIV and Hepatitis B co-infection in middle-aged individuals. The p-value of 0.24471 suggests no significant difference in age distribution between the HIV-only and co-infected groups [11].

 

The residence distribution shows that the majority of patients are from rural areas, with 55.03% in the HIV-only group and 50.00% in the co-infected group. Urban patients constitute 44.97% of the HIV-only group and 50.00% of the co-infected group. The p-value of 0.87 indicates no significant difference in residence distribution between the groups.

 

Out of 376 patients, 358 (95.21%) are HIV positive only, while 18 (4.79%) are co-infected with Hepatitis B. The relatively low prevalence of Hepatitis B among HIV patients indicates that co-infection is not highly common in this population. The p-value of 0.725 suggests no significant difference in the distribution of co-infection status across the patient population [12].

 

The majority of patients have CD4 counts between 200-500, with 36.03% in the HIVonly group and 61.11% in the co-infected group. The p-value of 0.05 indicates a borderline significant difference in CD4 cell count distribution between the groups, suggesting that co-infection might affect immune status [13].

 

Lower CD4 counts were associated with higher rates of HBV co-infection. Zerdali et al. (2021) reported similar findings, consistent with our observations. Lo Re et al. (2019) also found that lower CD4 counts are significant determinants of liver complications in HIV/HBV co-infected patients [14].

 

The high-risk occupation distribution shows that the majority of patients have no highrisk occupations, with 79.33% in the HIV-only group and 77.78% in the co-infected group. Truck drivers represent a higher percentage in the co-infected group (16.67%). The p-value of 0.54 indicates no significant difference in occupation distribution between the groups.

 

Truck drivers had a higher percentage of co-infection. Lo Re et al. (2019) identified certain occupations as risk factors for HBV infection among HIV patients, supporting our findings (192) [15].

CONCLUSION

Significant differences were observed in haemoglobin levels, with lower levels indicating anaemia's impact on overall health in the co-infected group. Prevalence of Hepatitis B in HIV Patients (HIV & Hepatitis B Co-infection Distribution).

 

Firstly, the overall prevalence of Hepatitis B co-infection among HIV patients was found to be 4.79%, aligning with global trends and underscoring the ongoing need for vigilant monitoring and comprehensive care strategies. This relatively low prevalence also indicates the effectiveness of current prevention efforts, though it emphasizes the necessity for sustained and enhanced intervention programs. This study underscores the importance of continuous monitoring, targeted prevention, and comprehensive care strategies for HIV and Hepatitis B confected patients. The findings reinforce the need for integrated healthcare services that address the unique challenges faced by this vulnerable population.

REFERENCES
  1. Zerdali E, Nakir IY, Surme S, Yildirim M. Hepatitis B virus prevalence, immunization and immune response in people living with HIV/AIDS in Istanbul, Turkey: a 21-year data analysis. Afr Health Sci. 2021;21(4):1621-8. doi:10.4314/ahs.v21i4.16.
  2. Mendes-Corrêa M, Barone AA, Cavalheiro ND, Tengan FM, Guastini C. Prevalence of hepatitis B and C in the sera of patients with HIV infection in São Paulo, Brazil. Rev Inst Med Trop Sao Paulo. 2000;42(2):81-5. doi:10.1590/S0036-46652000000200002.
  3. Silva S, Passos A, Machado A, Figueiredo J, Esmeraldino L. HIV and hepatitis B virus co-infection: prevalence and risk factors. Rev Soc Bras Med Trop. 2004;37(5):391-5. doi:10.1590/S0037-86822004000500003.
  4. Brandão NA, Pfrimer IA, Martelli CM, Turchi MD. Prevalence of hepatitis B and C infection and associated factors in people living with HIV in Midwestern Brazil. Braz J Infect Dis. 2015;19(4):426-30. doi:10.1016/j.bjid.2015.05.004.
  5. Opaleye O, Olureme A, Atiba A, Adewumi MO, Mabayoje O, Donbraye E, et al. Occult hepatitis B virus infection among HIV positive patients in Nigeria. J Trop Med. 2014;2014:1-5. doi:10.1155/2014/978548.
  6. Braga WSM, Castilho MC, Santos IC, Moura MA, Segurado AA. Low prevalence of hepatitis B virus, hepatitis D virus and hepatitis C virus among patients with human immunodeficiency virus or acquired immunodeficiency syndrome in the Brazilian Amazon basin. Rev Soc Bras Med Trop. 2006;39(6):519-22. doi:10.1590/S0037-86822006000600003.
  7. Tanrıverdi S, Gökengin D, Güneş A, Kılıç S, Deveci D. Decrease in hepatitis B virus seroprevalence among pregnant women in Manisa, Turkey: results of an 11-year follow-up study. Turk J Med Sci. 2018;48(2):314-9. doi:10.3906/sag- 1707-181.
  8. George Papatheodoridis (Coordinator & EASL Governing Board), Maria Buti, Markus Cornberg, Harry Janssen, David Mutimer, Stanislas Pol, Giovanni Raimondo. European Association For The Study Of The Liver. EASL clinical practice guidelines: Management of chronic hepatitis B virus infection. . J Hepatol 2012; 57:167-185.
  9. HussainT, Kulshreshtha KK, Sinha S, YadavVS, Katoch VM. HIV, HBV, HCV, andsyphilisco- infections among patients attending the STD clinics of district hospitals in Northern India. Int J Infect Dis 2006; 10:358-363.
  10. Tripathi AK, Khanna M, Gupta N, Chandra M. Lowprevalence of hepatitis B virus and hepatitis C virus co-infection in patients with human immunodeficiency virus in Northern India. J Assoc Physicians India 2007; 55:429-431.
  11. Hammer S, Eron J, Reiss P, et al. Antiretroviral treatment of adult HIV infection. 2008recommendations of the International AIDS Society – USA panel. JAMA 2008; 300:555–570.
  12. Chun HM, Roediger MP, Hullsiek KH, Thio CL, Agan BK, Bradley WP, Peel SA, Jagodzinski LL, Weintrob AC, Ganesan A, Wortmann G, Crum-Cianflone NF,Maguire JD, Landrum ML. Infectious Disease Clinical Research Program HIV Working Group. Hepatitis B virus coinfection negatively impacts HIV outcomes in HIV seroconverters. J Infect Dis 2012; 205:185-193.
  13. Gómez-Gonzalo M, Carretero M, Rullas J, Lara-Pezzi E, Aramburu J, Berkhout B, Alcamí J, López-Cabrera M. The hepatitis B virus X protein induces HIV-1 replication and transcription in synergy with T-cell activation signals: functional roles of NF-kappaB/NF-AT and SP1-binding sites in the HIV-1 long terminal repeat promoter. J Biol Chem 2001; 276:35435-43.
  14. Julien Calux et al., 2020. Hepatitis B: Prevalence and occult infection in HIVinfected patients. Rev Soc Bras Med Trop.
  15. Lo Re V et al., 2019. Determinants of Liver Complications Among HIV/Hepatitis B Virus-Coinfected Patients. J Acquir Immune Defic Syndr.
Recommended Articles
Research Article
Effects of Mitral Valve Replacement on Pulmonary Arterial Pressures in Mitral Valve Disease with Pulmonary Hypertension – A Retrospective Echocardiographic Observational Study
...
Published: 16/06/2025
Download PDF
Read Article
Research Article
Clinical Profile and Management Outcomes of Type 2 Diabetes Mellitus in Primary Care Settings
...
Published: 17/06/2025
Download PDF
Read Article
Research Article
Comparison of Preloading Versus Coloading with Crystalloids for the Prevention of Hypotension During Spinal Anaesthesia in Elective Caesarean Sections: A Prospective Observational Study in a Tertiary Care Hospital, South India
...
Published: 16/06/2025
Download PDF
Read Article
Research Article
Prevalence and Risk Factors of Hypertension in Young Adults: A Cross-Sectional Study
...
Published: 14/06/2025
Download PDF
Read Article
© Copyright Journal of Heart Valve Disease