Kidney dysfunction in adults living with HIV and HBV: a 10-year retrospective cohort study across seven Asia-Pacific countries

dc.contributor.authorVu T.T.
dc.contributor.authorRupasinghe D.
dc.contributor.authorNguyen D.T.H.
dc.contributor.authorChoi J.Y.
dc.contributor.authorKiertiburanakul S.
dc.contributor.authorKumarasamy N.
dc.contributor.authorKhusuwan S.
dc.contributor.authorKhol V.
dc.contributor.authorKetut Agus Somia I.
dc.contributor.authorLee M.P.
dc.contributor.authorPujari S.
dc.contributor.authorAvihingsanon A.
dc.contributor.authorDo C.D.
dc.contributor.authorRoss J.
dc.contributor.authorJiamsakul A.
dc.contributor.correspondenceVu T.T.
dc.contributor.otherMahidol University
dc.date.accessioned2026-02-10T18:26:49Z
dc.date.available2026-02-10T18:26:49Z
dc.date.issued2025-12-12
dc.description.abstractBACKGROUND: This study investigated kidney dysfunction among people with HIV (PWH), comparing those with and without hepatitis B virus (HBV) co-infection. We further identified predictors of kidney dysfunction in PWH with HBV. METHODS: Adult PWH in the TREAT Asia Observational Database-Low Intensity TransfEr cohort, who were on antiretroviral therapy, with follow-up after 2010 were included. HBV co-infection was defined by positive hepatitis B surface antigen. Kidney dysfunction was determined as a single estimated glomerular filtration rate < 60mL/min/1.73m2. Kaplan-Meier curves were used to evaluate cumulative incidence of kidney dysfunction, and we used Cox proportional hazards model to analyze factors associated with kidney dysfunction in PWH with HBV. RESULTS: Among 23,415 participants (median age = 37 years; interquartile range [IQR]: 31-43), most were male (62.2%), from lower-middle income countries (67.1%), and reported heterosexual HIV transmission (79.3%). The median follow-up time was 5.41 years (IQR: 2.05-8.67). The majority were prescribed NRTI + NNRTI (83.6%), and 4.9% had HBV co-infection. Overall, 8.0% had kidney dysfunction, with a higher proportion among PWH with HBV than those without HBV (14.8% vs. 7.6%, p < 0.001). Most cases of kidney dysfunction were stage III (84.2%). Factors associated with kidney dysfunction in PWH with HBV included older age (≥ 50 years: Hazard ratio [HR] = 6.45, 95%CI: 2.31, 18.04) compared to 18-29 years, higher income country (upper-middle income: HR = 1.78, 95%CI: 1.16, 2.74) compared to lower-middle income, low platelet counts (< 150 × 109/L: HR = 2.82, 95%CI: 1.85, 4.31) compared to normal platelets, and ART regimens (NRTI + NNRTI: HR = 0.43, 95%CI: 0.27, 0.70; NRTI + PI: HR = 0.60, 95%CI: 0.36, 1.01) compared to NRTI + INSTI. Higher CD4 counts (200-349 cells/µL: HR = 0.53, 95%CI: 0.31, 0.93; 350-499 cells/µL: HR = 0.45, 95%CI: 0.26, 0.79; ≥500 cells/µL: HR = 0.33, 95%CI: 0.20, 0.56) compared to < 200 cells/µL were associated with lower risk of renal dysfunction. There was no significant difference in kidney dysfunction between those on TDF and TAF (HR = 0.55, 95%CI: 0.25, 1.23). CONCLUSIONS: A high prevalence of kidney dysfunction was observed among PWH with HBV co-infection in the Asia-Pacific. Renal screening and monitoring should prioritize PWH with HBV with older age, low platelets and CD4 counts in low-resource settings.
dc.identifier.citationAIDS Research and Therapy Vol.23 No.1 (2025) , 14
dc.identifier.doi10.1186/s12981-025-00831-8
dc.identifier.eissn17426405
dc.identifier.pmid41388558
dc.identifier.scopus2-s2.0-105029099687
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114939
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.subjectImmunology and Microbiology
dc.titleKidney dysfunction in adults living with HIV and HBV: a 10-year retrospective cohort study across seven Asia-Pacific countries
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105029099687&origin=inward
oaire.citation.issue1
oaire.citation.titleAIDS Research and Therapy
oaire.citation.volume23
oairecerif.author.affiliationThe City University of New York
oairecerif.author.affiliationYonsei University College of Medicine
oairecerif.author.affiliationThe Kirby Institute
oairecerif.author.affiliationUniversitas Udayana
oairecerif.author.affiliationFaculty of Medicine Ramathibodi Hospital, Mahidol University
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University
oairecerif.author.affiliationQueen Elizabeth Hospital Hong Kong
oairecerif.author.affiliationBach Mai Hospital
oairecerif.author.affiliationThe HIV Netherlands Australia Thailand Research Collaboration
oairecerif.author.affiliationVHS Medical Centre India
oairecerif.author.affiliationInstitute of Infectious Diseases
oairecerif.author.affiliationamfAR - The Foundation for AIDS Research
oairecerif.author.affiliationNational Centre for HIV/AIDS
oairecerif.author.affiliationNational Hospital for Tropical Diseases
oairecerif.author.affiliationChiangrai Prachanukroh Hospital

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