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

Authors :
Boyd, Anders
Kouamé, Menan Gerard
Houghtaling, Laura
Moh, Raoul
Gabillard, Delphine
Maylin, Sarah
Chekaraou, Mariama Abdou
Delaugerre, Constance
Anglaret, Xavier
Eholié, Serge Paul
Danel, Christine
Zoulim, Fabien
Lacombe, Karine
studies, on behalf of the ANRS 12136 Temprano and ANRS 12240 VarBVA
Source :
Transactions of the Royal Society of Tropical Medicine & Hygiene; Aug2019, Vol. 113 Issue 8, p437-445, 9p
Publication Year :
2019

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 log<subscript>10</subscript> 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00359203
Volume :
113
Issue :
8
Database :
Complementary Index
Journal :
Transactions of the Royal Society of Tropical Medicine & Hygiene
Publication Type :
Academic Journal
Accession number :
137748454
Full Text :
https://doi.org/10.1093/trstmh/trz021