Evidence map›Paper›PMID 41606521›Full record

ArticleBMC infectious diseases2026

Renal function during tenofovir‑based antiretroviral therapy among people living with HIV in Lilongwe, Malawi: findings from the prospective LighTen cohort study.

Melani R Mahanani, Florian Neuhann, Ethel Rambiki, Angelina Nhlema, Hannock Tweya, Myo Chit, Jane Chiwoko, Thom Chaweza, Claudia Wallrauch, Tom Heller and 3 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Melani R MahananiHeidelberg Institute of Global Health, Heidelberg University Hospital, 69120, Im Neuenheimer Feld 130.3, Heidelberg, Germany. melani.mahanani@uni-heidelberg.de.ORCID http://orcid.org/0000-0003-3391-934X
Florian NeuhannHeidelberg Institute of Global Health, Heidelberg University Hospital, 69120, Im Neuenheimer Feld 130.3, Heidelberg, Germany.ORCID http://orcid.org/0000-0001-5944-1597
Ethel RambikiLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.ORCID http://orcid.org/0000-0001-9742-5707
Angelina NhlemaLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.
Hannock TweyaInternational Training and Education Center for Health (I-TECH), Lilongwe, Malawi.ORCID http://orcid.org/0000-0002-8247-1273
Myo ChitHeidelberg Institute of Global Health, Heidelberg University Hospital, 69120, Im Neuenheimer Feld 130.3, Heidelberg, Germany.ORCID http://orcid.org/0009-0004-8711-8008
Jane ChiwokoLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.
Thom ChawezaLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.
Claudia WallrauchLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.ORCID http://orcid.org/0009-0008-9180-0850
Tom HellerLighthouse Clinic, Kamuzu Central Hospital, Lilongwe, Malawi.ORCID http://orcid.org/0009-0008-4626-0592
Volker WinklerHeidelberg Institute of Global Health, Heidelberg University Hospital, 69120, Im Neuenheimer Feld 130.3, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-9974-1145
Gerd FätkenheuerDivision of Infectious Diseases, Department I of Internal Medicine, Faculty of Medicine, University of Cologne, University Hospital Cologne, Cologne, Germany.
Hans-Michael SteffenClinic for Gastroenterology and Hepatology, Faculty of Medicine, University of Cologne, University Hospital Cologne, Cologne, Germany.ORCID http://orcid.org/0000-0001-6562-3549

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMost first-line antiretroviral therapy (ART) regimes in Sub-Saharan Africa contain tenofovir disoproxil fumarate (TDF) which has a nephrotoxic potential. Baseline renal function assessment is not feasible in many settings and therefore not required prior to starting ART according to Malawian guidelines. We assessed renal function over 36 months in people living with HIV (PLHIV) starting TDF-based ART at Lighthouse Clinic, Lilongwe, Malawi.

methodsData on demographics, medical history, laboratory values, WHO stage, and anthropometric measures were collected at study entry and during visits at 1, 3, 6 months, and every 6 months until month 36. The main outcome of the study was renal function, defined by the estimated glomerular filtration rate (eGFR) calculated using the CKD-EPI equation. Descriptive statistics and multivariable linear regression analysis were performed.

resultsA baseline creatinine value was available for 1,430 PLHIV (57% female, mean age ± SD 36.0 ± 9.3 years). Of these, 443 PLHIV (62% female) were observed until month 36. Factors associated with changes in eGFR over time included baseline log-transformed eGFR (coefficient = −0.787; p < 0.001), MAP at baseline, and initial WHO clinical HIV stage. The overall trend in eGFR categories indicated a shift towards lower classes.

conclusionsIn this large cohort of PLHIV, TDF did not result in a decline in eGFR. Indeed, an unexpected trend of improved renal function was observed. Even though findings need to be interpreted with caution due to considerable attrition, our results suggest TDF can be administered safely in resource-limited settings where ART decisions are frequently made without pre-treatment renal assessment.

Indexed as

Anti-HIV AgentsHIV InfectionsKidneyTenofovirAdultAntiretroviral Therapy, Highly ActiveFemaleGlomerular Filtration RateHumansKidney Function TestsMalawiMaleMiddle AgedProspective StudiesAnti-HIV AgentsTenofovirAntiretroviral therapyGlomerular filtration rateHIVRenal function

Identifiers

PMID41606521
PMCPMC12924523

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.