Changes in peripheral quantitative computed tomography measured bone density, size and strength in Zimbabwean children with and without HIV over one year: a cohort study.

Analysis/quantification of bone Diseases and disorders of/related to bone Epidemiology

Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: England
ID NLM: 8610640

Informations de publication

Date de publication:
16 Oct 2024
Historique:
received: 23 05 2023
revised: 16 09 2024
accepted: 15 10 2024
medline: 16 10 2024
pubmed: 16 10 2024
entrez: 16 10 2024
Statut: aheadofprint

Résumé

Understanding bone accrual in adolescents may inform approaches to improve skeletal health and reduce adult fracture risk. We investigated the effect of HIV on bone mineral accrual assessed by peripheral Quantitative Computed tomography (pQCT). Children with HIV (CWH) on ART for ≥2 years, and children without HIV (CWOH), aged 8-16 years (n = 609), had tibial pQCT scans at 0 and 12 months. Linear regression estimated sex stratified differences in change (∆) and mean pQCT bone density (trabecular and cortical), size (total cross-sectional area [CSA]) and strength (SSI) between CWH and CWOH, adjusting for socio-economic status (SES) and orphanhood and incorporating an interaction term for baseline pubertal status (Tanner 1-2[pre/early] vs 3-5[mid/late]). Structural equation modelling tested whether baseline height-for-age-Z-scores (HAZ) mediate the effect of HIV on ∆bone outcomes. CWH were more likely than CWOH to be orphans (44% vs 7%), of lower SES (43% vs 27%) and be stunted (30% vs 8%); but similar in age. At baseline and follow up, CWH had lower trabecular density, CSA and SSI than CWOH. After adjustment, bone density and strength increased similarly in CWH and CWOH. CWH in mid/late puberty at baseline had greater 12 months increases in CSA than CWOH, particularly males (mean difference [31.3(95%CI:-3.1, 65.6) mm2 in mid/late puberty vs. -2.04(-23.8, 19.7) mm2 in pre/early puberty; interaction P-value = 0.013]. HAZ mediated the effect of HIV on ∆bone outcomes only in females as follows: indirect pathways from HIV to ∆trabecular density [-1.85(-3.5, -0.2) mg/cm3], ∆cortical density [-2.01(-3.9, -0.01) mg/cm3], ∆CSA [-2.59(-4.7, -0.5) mm] and ∆SSI [-18.36(-29.6, -7.2) mm3]. In conclusion, CWH show bone deficits at follow up. Investigations of bone mineral accrual earlier in life and post-puberty to peak bone mass are needed. We measured bone density, bone size and bone strength at 0 and 12 months in 609, 8-16 year old children living with (CWH) and children living without HIV (CWOH). CWH were more likely to be orphans, to be of a lower socio-economic status, to be shorter and to have lower bone density, size and strength than CWOH who are of the same age. After 12 months, there were persistent bone deficits in CWH, despite that CWH who were in their mid/late puberty (especially males) showed greater increases in bone size than CWOH. Investigations of bone accrual in early life and beyond puberty are necessary.

Autres résumés

Type: plain-language-summary (eng)
We measured bone density, bone size and bone strength at 0 and 12 months in 609, 8-16 year old children living with (CWH) and children living without HIV (CWOH). CWH were more likely to be orphans, to be of a lower socio-economic status, to be shorter and to have lower bone density, size and strength than CWOH who are of the same age. After 12 months, there were persistent bone deficits in CWH, despite that CWH who were in their mid/late puberty (especially males) showed greater increases in bone size than CWOH. Investigations of bone accrual in early life and beyond puberty are necessary.

Identifiants

pubmed: 39413242
pii: 7824248
doi: 10.1093/jbmr/zjae169
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research.

Auteurs

Cynthia Kahari (C)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.
Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.

Celia L Gregson (CL)

Musculoskeletal Research Unit, Bristol Medical School, University of Bristol, Bristol, United Kingdom.

Mícheál Ó Breasail (MÓ)

Department of Medicine, School of Clinical Sciences, Faculty of Medicine, Monash Medical Centre, Nursing and Health Sciences, Monash University, Clayton, VIC, Australia.
Population Health Sciences, Bristol Medical School, 1-5 Whiteladies Road, Bristol, BS8 1NU.

Ruramayi Rukuni (R)

The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.
Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Tafadzwa Madanhire (T)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.

Victoria Simms (V)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.

Joseph Chipanga (J)

The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.

Lynda Stranix-Chibanda (L)

Child and Adolescent Health Unit, University of Zimbabwe Faculty of Medicine and Health Sciences, Harare, Zimbabwe.

Lisa K Micklesfield (LK)

South African Medical Research Council/Wits Developmental Pathways for Health Research Unit (DPHRU), Department of Paediatrics, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Rashida A Ferrand (RA)

The Health Research Unit (THRU-ZIM), Biomedical Research and Training Institute, Harare, Zimbabwe.
Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Kate A Ward (KA)

MRC Lifecourse Epidemiology Centre, University of Southampton, Southampton, United Kingdom.
MRC The Gambia Unit at LSHTM, London, UK/ The Gambia.

Andrea M Rehman (AM)

Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Classifications MeSH