HCV Co-Infection and Its Genotypic Distribution in HIV-Infected Patients in Nepalese Population

Author:

Sah Uday Kant1,Sah Anil Kumar2,Ansari Mehraj3,Chaudhary Priyanka4,Gupta Saurav5,Kumar Pawan1,Sah Jay Prakash67

Affiliation:

1. Department of Biochemistry, Singhania University, Pacheri Bari, Rajasthan 333515, India

2. Annapurna Research Center, Kathmandu 44600, Nepal

3. Shi-Gan International College of Science and Technology, Kathmandu 44600, Nepal

4. Patan Academy of Health Sciences, Lalitpur 44700, Nepal

5. Department of Neuroscience, The University of Alabama at Birmingham, Birmingham, AL 35294, USA

6. School of Health and Allied Sciences, Pokhara University, Pokhara-30, Kaski 33700, Nepal

7. Division of Molecular and Cellular Pathology, Department of Pathology, The University of Alabama at Birmingham, Birmingham, AL 35233, USA

Abstract

Hepatitis C Virus (HCV) co-infection and its genotypic distribution in people living with Human Immunodeficiency Virus (HIV) show global inconsistency. Therefore, the present study aimed to investigate the prevalence and genotypic distribution patterns of HCV, along with viral load, in people living with HIV. This cross-sectional study was conducted at SRL Diagnostics Nepal, Pvt. Ltd. in 203 HIV-seropositive patients attending the Tribhuvan University Teaching Hospital (TUTH), Maharajgunj, Kathmandu, Nepal from October 2021 to May 2022. The viral load and HCV genotypes were estimated from RNA extracted from the blood sample (plasma) of PLHIV by using a standard Q-PCR protocol. HCV infection was considered as a core variable, whereas covariates used for this study were duration of HIV infection, age, sex, and ART regimen. Out of total 203 PLHIV, the estimated prevalence of HCV co-infection was 115 (56.6%). Male gender was a unique characteristic associated with a high prevalence of HCV co-infection compared to females. The HCV viral load among PLHIV ranged from 34 to 3,000,000 IU/mL. Among HCV co-infected PLHIV, 56 (48.69%) had a low level of HCV viral load. Interestingly, only 3 (2.6%) patients had an HCV viral load higher than 3,000,000 IU/mL. Diverse HCV genotypes were found in the population, including genotypes 1, 1a, 3a, 5a, and 6. However, genotype 3 was the most prevalent HCV variant among HCV-co-infected PLHIV, with a distribution of 36 (61.1%) and viral load ranging from 34 to 3000 IU/mL. HCV co-infection is frequent in the Nepalese population of people living with HIV, particularly due to HCV genotypic variant 3. The findings of this study could be useful for the management and clearance of the HCV co-infection in PLHIV, aiming to provide a good quality of life.

Publisher

MDPI AG

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Immunology and Microbiology

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