# Prevalence and predictors of kidney dysfunction among people living with HIV in Tanzania

**Authors:** Daniel Msilanga, Elizabeth Msangi, Elliot Koranteng Tannor, Elliot Koranteng Tannor, Elliot Koranteng Tannor

PMC · DOI: 10.1371/journal.pgph.0005011 · PLOS Global Public Health · 2025-08-01

## TL;DR

This study finds that kidney dysfunction is common among HIV patients in Tanzania, especially those with comorbidities like hypertension, and highlights the need for better screening.

## Contribution

The study provides updated, context-specific data on kidney dysfunction prevalence and predictors among PLHIV in urban Tanzania.

## Key findings

- The prevalence of kidney dysfunction among PLHIV was 15.6%.
- Comorbid conditions were the only independent predictor of kidney dysfunction.
- Only 5.3% of participants with reduced eGFR had a prior kidney disease diagnosis.

## Abstract

As people living with HIV (PLHIV) in sub-Saharan Africa live longer due to widespread access to antiretroviral therapy (ART), the burden of non-communicable diseases, including kidney dysfunction (KD) has increased. Existing studies in Tanzania show varying prevalence and inconsistent predictors of KD, highlighting the need for updated, context-specific data. We conducted a cross-sectional sub-analysis of data from a larger study assessing point-of-care creatinine testing. PLHIV aged ≥18 years attending the HIV clinic at Temeke Regional Referral Hospital (TRRH) in Dar es Salaam from 5th January to 30th March 2025 consented to participate were included. Renal function was assessed using serum creatinine measured via the Jaffé method, and eGFR was calculated using the CKD-EPI 2021 equation. Kidney dysfunction was defined as eGFR < 60 mL/min/1.73 m². Logistic regression was used to identify predictors. Ethical approval was obtained from National Institute for Medical Research (NIMR) under reference number NIMR/HQ/R.8a/Vol.IX/4695. Among 358 participants, the majority were female (66.2%) and aged ≥45 years (62.3%). The prevalence of KD was 15.6% with 24.6% reporting at least one comorbid condition. In multivariable analysis, the presence of comorbidities was the only independent predictor of KD (aOR: 3.93; 95% CI: 1.85–8.36; p < 0.001). Only 5.3% of participants with reduced eGFR had a prior diagnosis of kidney disease. Kidney dysfunction is a significant but underdiagnosed comorbidity among PLHIV in urban Tanzania. Comorbid conditions, especially hypertension, are major contributors to reduced kidney function and integrating non-communicable disease screening and management into HIV care is needed to enable earlier detection and improve long-term renal outcomes.

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, ACSM3 (acyl-CoA synthetase medium chain family member 3) [NCBI Gene 6296] {aka SA, SAH}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** KD (MESH:D007674), dehydration (MESH:D003681), diabetes (MESH:D003920), HIV (MESH:D015658), CKD (MESH:D051436), NCD (MESH:D000073296), obese (MESH:D009765), Hypertension (MESH:D006973), PLHIV (MESH:C000719191), acute kidney injury (MESH:D058186), opportunistic infections (MESH:D009894), -communicable diseases (MESH:D003141), overweight (MESH:D050177), reduced kidney function (MESH:D007680), cardiovascular, liver, and kidney diseases (MESH:D002318), UACR (OMIM:194470), Proteinuria (MESH:D011507)
- **Chemicals:** PGPH-D-25-00958 (-), Creatinine (MESH:D003404), D (MESH:D003903), TDF (MESH:D000068698), Alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12316212/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12316212/full.md

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Source: https://tomesphere.com/paper/PMC12316212