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Renal outcomes in adults with HBV, HIV and HBV/HIV coinfection after 3 years of antiviral therapy in urban Tanzania.

Authors :
Wu, En-Ling
Christian, Beatrice
Rivera, Adovich S
Fabian, Emanuel
Macha, Irene
Aris, Eric
Mpangala, Shida
Ulenga, Nzovu
Mugusi, Ferdinand
Murphy, Robert L
Hawkins, Claudia A
Source :
Journal of Antimicrobial Chemotherapy (JAC); Jan2024, Vol. 79 Issue 1, p36-45, 10p
Publication Year :
2024

Abstract

Background An enhanced understanding of renal outcomes in persons with chronic HBV, HIV, and HBV/HIV coinfection is needed to mitigate chronic kidney disease in regions where HBV and HIV are endemic. Objectives To investigate changes in estimated glomerular filtration rate (eGFR) in adults with HBV, HIV or HBV/HIV enrolled in a 3 year prospective cohort study of liver outcomes in Dar es Salaam, Tanzania and initiated on antiviral therapy. Methods We compared eGFR between and within groups over time using mixed-effects models. Results Four hundred and ninety-nine participants were included in the analysis (HBV: 164; HIV: 271; HBV/HIV: 64). Mean baseline eGFRs were 106.88, 106.03 and 107.18 mL/min/1.73 m<superscript>2</superscript>, respectively. From baseline to Year 3, mean eGFR declined by 4.3 mL/min/1.73 m<superscript>2</superscript> (95% CI −9.3 to 0.7) and 3.7 (−7.8 to 0.5) in participants with HBV and HIV, respectively, and increased by 5.1 (−4.7 to 14.9) in those with HBV/HIV. In multivariable models, participants with HBV had lower eGFRs compared with those with HIV or HBV/HIV and, after adjusting for HBV DNA level and hepatitis B e antigen (HBeAg) status, significantly lower eGFRs than those with HBV/HIV at all follow-up visits. Conclusions In this Tanzanian cohort, coinfection with HBV/HIV did not appear to exacerbate renal dysfunction compared with those with either infection alone. Although overall changes in eGFR were small, persons with HBV experienced lower eGFRs throughout follow-up despite their younger age and similar baseline values. Longer-term studies are needed to evaluate continuing changes in eGFR and contributions from infection duration and other comorbidities. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03057453
Volume :
79
Issue :
1
Database :
Complementary Index
Journal :
Journal of Antimicrobial Chemotherapy (JAC)
Publication Type :
Academic Journal
Accession number :
174559801
Full Text :
https://doi.org/10.1093/jac/dkad341