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

Author:

Wu En-Ling12ORCID,Christian Beatrice3,Rivera Adovich S45ORCID,Fabian Emanuel3,Macha Irene3,Aris Eric3,Mpangala Shida3,Ulenga Nzovu3,Mugusi Ferdinand3,Murphy Robert L16ORCID,Hawkins Claudia A16

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Northwestern University Feinberg School of Medicine , Chicago, IL , USA

2. Section of Infectious Diseases and Global Health, Department of Medicine, University of Chicago , Chicago, IL , USA

3. Management and Development for Health , Dar es Salaam , Tanzania

4. Institute for Public Health and Medicine, Northwestern University Feinberg School of Medicine , Chicago, IL , USA

5. Division of Epidemiologic Research, Department of Research and Evaluation , Kaiser Permanente Southern California, Pasadena, CA , USA

6. Havey Institute for Global Health, Northwestern University Feinberg School of Medicine , Chicago, IL , USA

Abstract

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 m2, respectively. From baseline to Year 3, mean eGFR declined by 4.3 mL/min/1.73 m2 (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.

Funder

National Institute of National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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