Impaired Bone Architecture in Peripubertal Children With HIV, Despite Treatment With Antiretroviral Therapy: A Cross-Sectional Study From Zimbabwe.
Impaired Bone Architecture in Peripubertal Children With HIV, Despite Treatment With Antiretroviral Therapy: A Cross-Sectional Study From Zimbabwe.
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DOI:
10.1002/jbmr.4752
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发表时间:
2023-03
影响因子:
6.2
通讯作者:
Gregson, Celia L.
中科院分区:
文献类型:
--
作者:
Mukwasi-Kahari, Cynthia;Rehman, Andrea M.;Breasail, Micheal O.;Rukuni, Ruramayi;Madanhire, Tafadzwa;Chipanga, Joseph;Stranix-Chibanda, Lynda;Micklesfield, Lisa K.;Ferrand, Rashida A.;Ward, Kate A.;Gregson, Celia L.
HIV infection has multi-system adverse effects in children including on the growing skeleton. We aimed to determine the association between chronic HIV infection and bone architecture (density, size, strength) in peripubertal children. We conducted a cross-sectional study of children aged 8–16 years with HIV (CWH) on antiretroviral therapy (ART), and children without HIV (CWOH) recruited from schools, frequency matched for age strata and sex. Outcomes, measured by tibial peripheral Quantitative Computed Tomography (pQCT), included 4% trabecular and 38% cortical volumetric bone mineral density (vBMD), 4% and 38% cross-sectional area (CSA), and 38% stress-strain index (SSI). Multivariable linear regression tested associations between HIV status and outcomes, stratified by sex and puberty (Tanner 1–2 vs. 3–5), adjusting for age, height, fat mass, physical activity, socio-economic and orphanhood statuses. We recruited 303 CWH and 306 CWOH; 50% female. Whilst CWH were similar in age to CWOH (overall mean±SD 12.4±2.5years), more were pre-pubertal (i.e Tanner 1; 41% vs. 23%). Median age at ART initiation was four (IQR 2–7) years, whilst median ART duration was eight (IQR 6–10) years. CWH were more often stunted (height-for-age Z-score<−2), than those without HIV (33% vs 7%). Both male and female CWH in later puberty had lower trabecular vBMD, CSA (4% and 38%) and SSI than those without HIV, whilst cortical density was similar. Adjustment explained some of these differences; however, deficits in bone size persisted in CWH in later puberty (HIV*puberty interaction p=0.035[males; 4% CSA] and p=0.029[females; 38% CSA]). Similarly, puberty further worsened the inverse association between HIV and bone strength (SSI) in both males (interaction p=0.008) and females (interaction p=0.004). Despite long-term ART, we identified deficits in predicted bone strength in those living with HIV, which were more overt in the later stages of puberty. This is concerning as this may translate to higher fracture risk later in life.
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影响因子:
4
作者:
Hamill, M. M.;Ward, K. A.;Pettifor, J. M.;Norris, S. A.;Prentice, A.
通讯作者:
Prentice, A.
影响因子:
2.5
作者:
Jain, Rajesh K.;Vokes, Tamara
通讯作者:
Vokes, Tamara
影响因子:
4
作者:
Hernandez, CJ;Beaupré, GS;Carter, DR
通讯作者:
Carter, DR
DOI:
10.1177/2325957414531621
发表时间:
2014-11-01
影响因子:
--
作者:
Joel, Dipesalema R;Mabikwa, Vincent;Ahmed, Syed Faisal
通讯作者:
Ahmed, Syed Faisal
影响因子:
4.1
作者:
Gregson, Celia L.;Hartley, April;Ferrand, Rashida A.
通讯作者:
Ferrand, Rashida A.