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Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study
OBJECTIVE: To evaluate bone mass accrual and determine the influence of clinical, anthropometric, dietary and biochemical parameters on bone mass. METHODS: A cohort study including 35 prepubertal HIV-infected children, between 7 and 12 years, attended at a referral center. At time 1 (T1) and time 2...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425359/ https://www.ncbi.nlm.nih.gov/pubmed/26477385 http://dx.doi.org/10.1016/j.bjid.2015.08.010 |
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author | Palchetti, Cecília Zanin Szejnfeld, Vera Lúcia de Menezes Succi, Regina Célia Patin, Rose Vega Teixeira, Patrícia Fonseca Machado, Daisy Maria Oliveira, Fernanda Luisa Ceragioli |
author_facet | Palchetti, Cecília Zanin Szejnfeld, Vera Lúcia de Menezes Succi, Regina Célia Patin, Rose Vega Teixeira, Patrícia Fonseca Machado, Daisy Maria Oliveira, Fernanda Luisa Ceragioli |
author_sort | Palchetti, Cecília Zanin |
collection | PubMed |
description | OBJECTIVE: To evaluate bone mass accrual and determine the influence of clinical, anthropometric, dietary and biochemical parameters on bone mass. METHODS: A cohort study including 35 prepubertal HIV-infected children, between 7 and 12 years, attended at a referral center. At time 1 (T1) and time 2 (T2), patients were assessed according to clinical, anthropometric, dietary, biochemical parameters and bone mineral density (BMD). At T2, patients were divided into prepubertal and pubertal. RESULTS: Despite the increase in bone mass absolute values, there was no improvement in lumbar spine BMD (LSBMD) Z-score (p = 0.512) and worsening in total body BMD (TBMD) Z-score (p = 0.040). Pubertal patients (n = 19) showed higher bone mineral content (BMC) (p = 0.001), TBMD (p = 0.006) and LSBMD (p = 0.002) compared to prepubertal patients. After multivariate linear regression analysis, the predictors of bone mass in T1 were age, BMI and HA Z-scores for BMC; BMI Z-score, adequate serum magnesium concentration and dietary calcium intake for TBMD; adequate serum concentration of magnesium, BMI and HA Z-scores for LSBMD. In T2, age, total body fat and lean body mass (kg) for BMC; BMI Z-score and puberty for TBMD; dietary fat intake, BMI Z-score for BMD and puberty for LSBMD. CONCLUSION: HIV-infected children have compromised bone mass and the presence of puberty seems to provide suitability of these parameters. Adequate intake of calcium and fat appears to be protective for proper bone mass accumulation factor, as well as monitoring nutritional status and serum magnesium concentration. |
format | Online Article Text |
id | pubmed-9425359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94253592022-08-31 Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study Palchetti, Cecília Zanin Szejnfeld, Vera Lúcia de Menezes Succi, Regina Célia Patin, Rose Vega Teixeira, Patrícia Fonseca Machado, Daisy Maria Oliveira, Fernanda Luisa Ceragioli Braz J Infect Dis Original Article OBJECTIVE: To evaluate bone mass accrual and determine the influence of clinical, anthropometric, dietary and biochemical parameters on bone mass. METHODS: A cohort study including 35 prepubertal HIV-infected children, between 7 and 12 years, attended at a referral center. At time 1 (T1) and time 2 (T2), patients were assessed according to clinical, anthropometric, dietary, biochemical parameters and bone mineral density (BMD). At T2, patients were divided into prepubertal and pubertal. RESULTS: Despite the increase in bone mass absolute values, there was no improvement in lumbar spine BMD (LSBMD) Z-score (p = 0.512) and worsening in total body BMD (TBMD) Z-score (p = 0.040). Pubertal patients (n = 19) showed higher bone mineral content (BMC) (p = 0.001), TBMD (p = 0.006) and LSBMD (p = 0.002) compared to prepubertal patients. After multivariate linear regression analysis, the predictors of bone mass in T1 were age, BMI and HA Z-scores for BMC; BMI Z-score, adequate serum magnesium concentration and dietary calcium intake for TBMD; adequate serum concentration of magnesium, BMI and HA Z-scores for LSBMD. In T2, age, total body fat and lean body mass (kg) for BMC; BMI Z-score and puberty for TBMD; dietary fat intake, BMI Z-score for BMD and puberty for LSBMD. CONCLUSION: HIV-infected children have compromised bone mass and the presence of puberty seems to provide suitability of these parameters. Adequate intake of calcium and fat appears to be protective for proper bone mass accumulation factor, as well as monitoring nutritional status and serum magnesium concentration. Elsevier 2015-10-23 /pmc/articles/PMC9425359/ /pubmed/26477385 http://dx.doi.org/10.1016/j.bjid.2015.08.010 Text en © 2015 Elsevier Editora Ltda. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Palchetti, Cecília Zanin Szejnfeld, Vera Lúcia de Menezes Succi, Regina Célia Patin, Rose Vega Teixeira, Patrícia Fonseca Machado, Daisy Maria Oliveira, Fernanda Luisa Ceragioli Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title | Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title_full | Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title_fullStr | Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title_full_unstemmed | Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title_short | Impaired bone mineral accrual in prepubertal HIV-infected children: a cohort study |
title_sort | impaired bone mineral accrual in prepubertal hiv-infected children: a cohort study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9425359/ https://www.ncbi.nlm.nih.gov/pubmed/26477385 http://dx.doi.org/10.1016/j.bjid.2015.08.010 |
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