Hepatitis B virus activity in untreated hepatitis B e antigen–negative human immunodeficiency virus–hepatitis B virus co-infected patients from sub-Saharan Africa

Author:

Boyd Anders1,Kouamé Menan Gerard2,Houghtaling Laura3,Moh Raoul245,Gabillard Delphine67,Maylin Sarah89,Abdou Chekaraou Mariama10,Delaugerre Constance8911,Anglaret Xavier267,Eholié Serge Paul245,Danel Christine267,Zoulim Fabien10,Lacombe Karine112,

Affiliation:

1. INSERM, Sorbonne Université, Institut Pierre Louis d’Épidémiologie et de Santé Publique, Paris, France

2. Programme PAC-CI, ANRS Research Site, Treichville University Hospital, Abidjan, Côte d’Ivoire

3. Division of Epidemiology & Community Health, University of Minnesota, Minneapolis, MN, USA

4. Department of Infectious and Tropical Diseases, Treichville University Teaching Hospital, Abidjan, Côte d’Ivoire

5. Medical School, University Felix Houphouet Boigny, Abidjan, Côte d’Ivoire

6. INSERM, U1219, Epidémiologie-Biostatistique, Bordeaux, France

7. University of Bordeaux, Bordeaux, France

8. Laboratoire de Virologie, Hôpital Saint-Louis, AP-HP, Paris, France

9. Université Paris-Diderot, Paris, France

10. Centre de Recherche sur le Cancer de Lyon, INSERM, Unité 1052, CNRS, UMR 5286, Lyon, France

11. INSERM U941, Paris, France

12. Department of Infectious and Tropical Diseases, Saint-Antoine Hospital, AP-HP, Paris, France

Abstract

Abstract Background In human immunodeficiency virus (HIV) and hepatitis B virus (HBV) co-infected patients from sub-Saharan Africa with hepatitis B e antigen (HBeAg)-negative status, data are limited on the evolution of HBV activity when antiretroviral treatment (ART) is absent. Methods A total of 43 HBeAg-negative co-infected patients not indicated for ART (per concomitant World Health Organization recommendations) were followed during participation in a randomized controlled trial in Côte d’Ivoire. Chronic HBeAg-negative phases were classified at yearly visits and defined as ‘infection’ (HBV DNA ≤10 000 copies/mL and normal alanine aminotransferase [ALT]) or ‘hepatitis’ (HBV DNA >10 000 copies/mL and/or above normal ALT). Dispersion in HBV DNA and ALT levels during follow-up was assessed using interquartile range (IQR) regression. Results During a median 25 months (IQR 19–31), 17 (40%) patients consistently had ‘infection’, 5 (12%) consistently had ‘hepatitis’ and 21 (48%) fluctuated between phases. Wider dispersion in HBV DNA over time was associated with higher baseline HIV RNA (p=0.02) and higher baseline HBV DNA levels (p=0.008), while wider dispersion in ALT was associated with higher baseline HIV RNA (p<0.001), higher baseline ALT levels (p=0.02) and baseline hepatitis surface antigen >4.0 log10 IU/mL (p=0.02). Conclusions HBV activity is common with HBeAg-negative status, whose variation is partly linked to HIV replication. Fluctuations in disease phase make it difficult to assess the risk of morbidity and mortality after ART initiation.

Funder

French Agence Nationale de Recherches sur le SIDA et les hépatites virales

ANRS

Sidaction

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Medicine,Parasitology

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