Literature DB >> 25157002

Hydroxyurea and growth in young children with sickle cell disease.

Sohail Rana1, Patricia E Houston2, Winfred C Wang3, Rathi V Iyer4, Jonathan Goldsmith5, James F Casella6, Caroline K Reed2, Zora R Rogers7, Myron A Waclawiw5, Bruce Thompson8.   

Abstract

BACKGROUND: Growth impairment is a known complication of sickle cell disease. Effects of hydroxyurea (HU) on growth in very young children are not known.
METHODS: Height, weight, BMI, and head circumference (HC) were compared with World Health Organization (WHO) standards in BABY HUG, a multicenter, randomized, double-blinded, placebo-controlled 2-year clinical trial of HU in 193 children 9 to 18 months of age. Anthropometric data were closely monitored and converted to z scores by using WHO standardized algorithms for descriptive analyses. The treatment and placebo groups were compared longitudinally by using a mixed model analysis.
RESULTS: At entry, the z scores of BABY HUG children were higher than WHO norms. After 2 years of HU or placebo treatment, there were no significant differences between the groups, except for the mean HC z scores at study exit (HU: +0.8 versus placebo: +1.0, P = .05). Baseline z scores were the best predictors of z scores at study exit. The absolute neutrophil count, absolute reticulocyte count, and total white blood cell count had significant negative correlations with growth measures.
CONCLUSIONS: Both groups had normal or near normal anthropometric measures during the study. The HC z scores at study entry and exit were slightly greater than WHO norms. Higher baseline white blood cell count, absolute reticulocyte count, and absolute neutrophil count were associated with poorer growth. The significance of the slightly lower HC in the treatment group at study exit is not clear. Trends toward normalization of weight and height and effects on HC will be monitored in ongoing BABY HUG follow-up studies.
Copyright © 2014 by the American Academy of Pediatrics.

Entities:  

Keywords:  BMI; children; growth; head circumference; height; hydroxyurea; sickle cell disease; weight

Mesh:

Substances:

Year:  2014        PMID: 25157002      PMCID: PMC4144002          DOI: 10.1542/peds.2014-0917

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  41 in total

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3.  Prediction of adverse outcomes in children with sickle cell disease.

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4.  Adequacy of dietary intake declines with age in children with sickle cell disease.

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8.  Delayed adolescent growth in homozygous sickle cell disease.

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Review 3.  Current Standards of Care and Long Term Outcomes for Thalassemia and Sickle Cell Disease.

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Review 6.  Novel insights in the management of sickle cell disease in childhood.

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8.  Effect of Sickle Cell Anemia Therapies on the Natural History of Growth and Puberty Patterns.

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Review 9.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

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Review 10.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

Authors:  Sarah J Nevitt; Ashley P Jones; Jo Howard
Journal:  Cochrane Database Syst Rev       Date:  2017-04-20
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