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. 2019 May;114(5):746-757.
doi: 10.1038/s41395-018-0409-9.

Spectrum of Liver Disease in Hepatitis B Virus (HBV) Patients Co-infected with Human Immunodeficiency Virus (HIV): Results of the HBV-HIV Cohort Study

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Spectrum of Liver Disease in Hepatitis B Virus (HBV) Patients Co-infected with Human Immunodeficiency Virus (HIV): Results of the HBV-HIV Cohort Study

Richard K Sterling et al. Am J Gastroenterol. 2019 May.

Abstract

Background: Because most HBV/HIV co-infected patients on combination antiretroviral therapy (cART) have suppressed HBV DNA and normal liver enzymes, the histologic spectrum of liver disease in HBV/HIV coinfection is poorly defined. To address this gap in knowledge, we conducted a prospective study to comprehensively characterize liver disease severity assessed by liver biopsy in a well-defined cohort of HBV/HIV patients in North America receiving cART.

Methods: Adult HIV/HBsAg positive patients on stable cART were recruited. Demographic, clinical, serological, and virological data were collected. Liver histology was assessed by a central pathology committee. The association of demographic, clinical, serologic, and virologic characteristics with liver histology was assessed using logistic regression.

Results: In this cross-sectional analysis, the mean age of the cohort (N = 139) was 49 years; 92% were male, 51% were non-Hispanic black, 7% had at-risk alcohol use with a median duration of infections of 14 years. The median ALT was 28 IU/L and CD4 count was 568 cells/mm. Almost all (99%) were on cART. Three-fourths (75%) had undetectable HIV RNA (<20 copies/mL). HBeAg was positive in 62%, HBV DNA was below the limit of quantification (<20 IU/mL) in 57% and <1000 IU/ mL in 80%; 7% had incomplete viral suppression (HBV DNA ≥1000 IU/mL and HIV RNA <20 copies/mL). Liver histology (available in n = 114) showed significant periportal, lobular, and portal inflammation (scores ≥2) in 14%, 31%, and 22% respectively. Over a third (37%) had significant fibrosis (Ishak stage ≥2); 24% had advanced fibrosis (Ishak stage ≥3). Higher ALT (adjusted OR 1.19 per 10 IU/L; 95% CI [1.01, 1.41]; p = 0.03) and lower platelet count (adjusted OR 0.81 per 20,000 mm; 95% CI [0.67-0.97]; p = 0.02) but not HBV DNA were independently associated with advanced fibrosis.

Conclusions: In this cohort of patients with HBV/HIV coinfection receiving long-term cART with viral suppression, we observed significant fibrosis in more than one-third of patients.

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Conflict of interest statement

Conflicts of interest: Richard K. Sterling: Gilead, AbbVie, Merck, Roche, Pfizer, and Baxter. Abdus S. Wahed: none. Wendy C. King: none. David K. Kleiner: none. Mandana Khalili: Gilead, Intercept Pharmaceuticals, and AbbVie. Mark Sulkowski: Gilead (consultant, research support). Raymond T. Chung: Gilead, BMS, Janssen, AbbVie, Boehringer, and Merck. Mamta Jain: Gilead, Janssen, Merck, and GSK. Mauricio Lisker-Melman: Abbvie, Gilead, Merck, and Simply Speaking. David K. Wong: Gilead, BMS, Vertex, and Boehringer. Marc Ghany: none

Figures

Figure 1.
Figure 1.
Flow of patients from screening to enrollment
Figure 2.
Figure 2.
Histology: proportion grade of Ishak Inflammation (portal, peri-portal, lobular)
Figure 3.
Figure 3.
Histology fibrosis (Ishak 0–6)

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