Abstract

BackgroundHIV infection exacerbates the prognosis of HCV infection, with a faster progression of hepatitis. Hepatic fibrosis is the major disruption of the hepatic tissue architecture characterized by anarchic deposition and excess of the extracellular matrix. The objective of this study was to evaluate hepatic fibrosis in HIV/HCV co-infected individuals as compared to HCV mono-infected.MethodsA total of 97 participants (mean age 60.2 ± 14.3 years and 0.76 male/female sex ratio) was enrolled in a study conducted in Yaoundé, Cameroon from November 2018 to January 2019. Liver fibrosis was assessed by the APRI score (Aspartate Aminotransferase or AST/Platelet Ratio Index) which identifies the stage of fibrosis as classified by the Metavir system (F0 to F4). CD4 counts and plasmatic HIV viral load of HIV/HCV co-infected individuals were determined and the correlation between hepatic fibrosis and immuno-virological status established. Statistical analysis was done using Microsoft Excel 2016 and EpiInfo7 software.ResultsA high proportion (63.6%) of HIV/HCV co-infected participants had an abnormal AST level: 73.6 ± 45.8 IU/L as compared to 58.5 ± 39.3 IU/L (59.3%) among HCV mono-infected participants. The frequency of thrombocytopenia was 63.6% with a mean platelet count of 137 ± 50 × 103 IU/L in HIV/HCV co-infected participants as compared to 176 ± 67 × 103 IU/L in HCV mono-infected participants (38.4%). The progression of hepatic fibrosis in participants with clinically significant fibrosis: F2, F3 and F4 was higher among HIV/HCV co-infected and the mean APRI score was 1.7 ± 1.4 versus 1 ± 0.8 among HCV mono-infected (26.7%). All participants (100%) with detectable HIV viral load had clinically significant fibrosis compared to 33.4% in those with undetectable HIV viral load (p = 0.55). Only 42.9% participants with CD4 > 500 cells/μL had clinically significant fibrosis (p = 0.72) while 100% participants with CD4 < 200 cells/μL had clinically significant fibrosis (p = 0.58).ConclusionsA high level of AST combined with thrombocytopenia (APRI score > 1.5) is an indicator of hepatic fibrosis in HIV/HCV co-infected individuals. Because of its non-invasive and less costly nature, the APRI score can be a suitable biomarker to monitor hepatic fibrosis in HIV/HCV co-infected individuals in resource constrained settings.

Highlights

  • Human Immunodeficiency Virus (HIV) infection exacerbates the prognosis of Hepatitis C Virus (HCV) infection, with a faster progression of hepatitis

  • In 2019, United Nations Acquired Immune Deficiency Syndrome (UNAIDS) estimated that 37.9 million people worldwide were living with HIV (PLWHIV) [1]

  • The objective of this study was to evaluate hepatic fibrosis in HIV/HCV coinfected participants as compared to HCV mono-infected using AST/Platelet Ratio Index (APRI) score; In addition, we evaluated the effect of HIV viremia and CD4 count on the occurrence of hepatic fibrosis in HIV/HCV co-infected participants

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Summary

Introduction

HIV infection exacerbates the prognosis of HCV infection, with a faster progression of hepatitis. The objective of this study was to evaluate hepatic fibrosis in HIV/HCV co-infected individuals as compared to HCV mono-infected. Hepatitis C Virus (HCV) and Human Immunodeficiency Virus (HIV) infections are serious public health problems worldwide due to their high prevalence. In 2019, UNAIDS estimated that 37.9 million people worldwide were living with HIV (PLWHIV) [1]. Africa is the second most endemic area for HCV after the Middle East with an estimated prevalence of 3.2% [4]. In a recent meta-analysis, approximately 2,278,400 individuals worldwide were co-infected with HIV/HCV, representing a prevalence of 6.1% of people infected with HIV [5]

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