Evidence map›Paper›PMID 41701698›Full record

ArticlePLOS global public health2026

Longitudinal changes in bone mineral density among children living with HIV over 96 weeks following switch to second-line antiretroviral therapy in Uganda.

Eva Natukunda, Erisa Mwaka, Alexander J Szubert, Alasdair Bamford, Katja Doerholt, Centurio Wandera, Spencer Byaruhanga, Esther Nambi, Diana M Gibb, Victor Musiime and 2 more

Abstract read
In one paragraph

Article in PLOS global public health, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

12 authors.

Eva NatukundaDepartment of Paediatrics, Joint Clinical Research Centre, Kampala, Uganda.ORCID https://orcid.org/0000-0002-2944-5412
Erisa MwakaDepartment of Anatomy, College of Health Sciences, Makerere University, Kampala, Uganda.ORCID https://orcid.org/0000-0003-1672-9608
Alexander J SzubertMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.
Alasdair BamfordMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.
Katja DoerholtMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-5105-0970
Centurio WanderaDepartment of Paediatrics, Joint Clinical Research Centre, Kampala, Uganda.ORCID https://orcid.org/0009-0009-7529-0552
Spencer ByaruhangaDepartment of Paediatrics, Joint Clinical Research Centre, Kampala, Uganda.ORCID https://orcid.org/0009-0008-1538-0014
Esther NambiDepartment of Paediatrics, Joint Clinical Research Centre, Kampala, Uganda.
Diana M GibbMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.
Victor MusiimeDepartment of Paediatrics, Joint Clinical Research Centre, Kampala, Uganda.ORCID https://orcid.org/0000-0001-7472-9054
Philippa MusokeDepartment of Paediatrics and Child Health, College of Health Sciences, Makerere University, Kampala, Uganda.
Ann Sarah WalkerMedical Research Council Clinical Trials Unit at University College London, London, United Kingdom.ORCID https://orcid.org/0000-0002-0412-8509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term impact of antiretroviral therapy (ART) on bone health in children living with HIV (CLWH) remains uncertain. We aimed to determine associations of change in bone mineral density (BMD) among CLWH in Uganda in a 2-year prospective sub-study in the CHAPAS-4 randomized trial (ISRCTN22964075). CLWH aged 3-15 years switched to second-line ART including tenofovir alafenamide fumarate-emtricitabine (TAF/FTC) or standard-of-care (SOC) (abacavir (ABC) or zidovudine (ZDV) with dolutegravir (DTG), atazanavir/ritonavir (ATV/r), darunavir/ritonavir (DRV/r) or lopinavir/ritonavir (LPV/r). BMD was assessed by dual-energy X-ray absorptiometry (DXA) at baseline, weeks 48 and 96 and bone turnover markers measured at baseline, week 24, 48, and 96. Robust regression analysis determined associations of BMD and bone turnover markers through week 96. Of 196 participants,167 contributed BMD measurements. Median (IQR) age was 9.9(7.0,12.3) years, 47% male, median (IQR) CD4 T-cell count 797(537,1140) cells/µl and mean (SD) viral load (log10 copies/ml) 4.3(0.8). Change in Procollagen type I N-terminal propeptide (PINP), C-terminal telopeptide of type I collagen (CTX) and height-adjusted (HA) BMD were similar between TAF/FTC and SOC. Greater declines in total-body-less-head (TBLH) BMD were associated with higher baseline TBLH (HA) BMD (Coef. -0.30,95% CI: -0.46, -0.15], p < 0.001) and first-line nevirapine (NVP) exposure (-0.25,95% CI: -0.43, -0.06, p = 0.009). Smaller TBLH HA BMD declines were associated with higher baseline fat-mass (0.06, 95% CI:0.01, 0.11, p = 0.021), higher lumbar spine (LS) HA BMD (0.17, 95% CI:0.03, 0.31, p = 0.015), DRV/r (0.46, p < 0.001,95% CI:0.21,0.71), DTG (0.26, p = 0.041,95% CI:0.01,0.51) or ATV/r (0.28, p = 0.026, 95% CI: 0.03, 0.52) use compared with LPV/r. Smaller declines in TBLH BMD were associated with higher baseline fat mass, higher LS HA BMD, and use of DRV/r, DTG, or ATV/r compared with LPV/r. These findings emphasize the importance of ART selection and body composition in supporting bone health among CLWH.

Identifiers

PMID41701698
PMCPMC12912597

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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.