Evidence map›Paper›PMID 39068422›Full record

ArticleBMC pediatrics2024

The impact of HIV infection on skeletal maturity in peripubertal children in Zimbabwe: a cross-sectional study.

Farirayi Kowo-Nyakoko, Celia L Gregson, Leo D Westbury, Tafadzwa Madanhire, Amaka C Offiah, Lisa K Micklesfield, Rashida Abbas Ferrand, Andrea M Rehman, Kate A Ward

Abstract read
In one paragraph

Article in BMC pediatrics, 2024. 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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Farirayi Kowo-NyakokoMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK. F.Nyakoko@soton.ac.uk.
Celia L GregsonMusculoskeletal Research Unit, Bristol Medical School, University of Bristol, Bristol, UK.
Leo D WestburyMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.
Tafadzwa MadanhireThe Health Research Unit Zimbabwe, Biomedical Research and Training Institute, 10, Seagrave Road, Avondale, Zimbabwe.
Amaka C OffiahDivision of Clinical Medicine, University of Sheffield, Sheffield, UK.
Lisa K MicklesfieldSAMRC/Wits Developmental Pathways for Health Research Unit, Department of Paediatrics, School of Clinical Medicine, University of the Witwatersrand, Johannesburg, South Africa.
Rashida Abbas FerrandThe Health Research Unit Zimbabwe, Biomedical Research and Training Institute, 10, Seagrave Road, Avondale, Zimbabwe.
Andrea M RehmanMRC International Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK.
Kate A WardMRC Lifecourse Epidemiology Centre, University of Southampton, Southampton, UK.

Funding

University of Southampton Global Challenges Research Fund and Faculty of Medicine, and part-funding from UK Medical Research Council Program . U105960371Wellcome Trust 206316_Z_17_Z
6 · The paper itself

Abstract

introductionHIV infection and its treatment compromises skeletal development (growth and maturation). Skeletal maturity is assessed as bone age (BA) on hand and wrist radiographs. BA younger than chronological age (CA) indicates delayed development. We conducted a cross-sectional study to determine differences between BA and CA (i.e., skeletal maturity deviation [SMD]), and risk factors associated with SMD in peripubertal children with and without HIV established on antiretroviral therapy (ART) including use of tenofovir disoproxil fumarate (TDF).

methodsChildren with HIV taking ART for at least two years and a comparison group of HIV-negative children, aged 8-16 years and frequency-matched by age and sex, were recruited from HIV clinics and local schools in the same catchment area, in Harare, Zimbabwe. BA was assessed from non-dominant hand-wrist radiographs using the Tanner Whitehouse 3 method. Negative SMD values correspond to delayed development, i.e., BA younger than CA. Multivariable linear regression models determined factors associated with SMD overall, and in children with HIV.

resultsIn total, 534 participants (54% males) were included; by design CA was similar in males and females, whether living with or without HIV. Mean (SD) SMD was more negative in CWH than in HIV-negative children in both males [-1.4(1.4) vs. -0.4(1.1) years] and females [-1.1(1.3) vs. -0.0(1.2) years]. HIV infection and weight-for-age Z-score<-2 were associated with more negative SMD in both males and females after adjusting for socio-economic status, orphanhood, pubertal stage, and calcium intake. Age at ART initiation was associated with SMD in both males and females with those starting ART later more delayed: starting ART aged 4-8 years 1.14 (-1.84, -0.43), or over 8 years 1.47 (-2.30, -0.65) (p-value for trend < 0.001). Similar non-significant trends were seen in males. TDF exposure TDF exposure whether < 4years or ≥ 4 years was not associated with delayed development.

conclusionPerinatally-acquired HIV infection and being underweight were independently associated with delayed skeletal maturation in both males and females. Starting ART later was independently associated with skeletal maturation delay in CWH. Given the known effects of delayed development on later health, it is important to find interventions to ensure healthy weight gain through early years and in CWH to initiate ART as early as possible.

Indexed as

Age Determination by SkeletonHIV InfectionsAdolescentAnti-HIV AgentsBone DevelopmentCase-Control StudiesChildCross-Sectional StudiesFemaleHumansMaleRisk FactorsTenofovirZimbabweAnti-HIV AgentsTenofovirAdolescenceAfricaBone ageChildrenHIVPuberty

Identifiers

PMID39068422
PMCPMC11282653

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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.