Growth measurements in Ugandan children with sickle cell anaemia from a hydroxyurea (hydroxycarbamide) treatment trial relative to unaffected sibling controls

一项针对乌干达镰状细胞贫血患儿的羟基脲(羟基脲)治疗试验中患儿的生长测量结果,与未患病同胞对照组进行比较。

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Abstract

Children with sickle cell anaemia (SCA) in sub-Saharan Africa (SSA) frequently experience impaired growth. Hydroxyurea (hydroxycarbamide) improves growth in higher resourced countries, but its effects on growth and body composition have not been evaluated in SSA. In an open-label, single-arm, 30-month dose-escalated hydroxyurea trial in Ugandan children aged 3 to <10 years (N = 264, mean age 5.6 ± 1.7 years), participant anthropometrics were compared to non-SCA sibling controls using global age- and sex-normalized z-scores. Body composition was determined using bioelectrical impedance analysis (BIA), comparing their z-scores to those generated from the controls (N = 110). Prospectively, SCA growth parameters on hydroxyurea paralleled and correlated with haemoglobin levels but remained lower than controls for weight, height and body mass index for age. Notably, growth of the SCA participants enrolled at ages 3 to <5 years did not differ from controls; instead, all group differences were attributable to those enrolled at ages 5 to <10. Further analyses revealed that growth trajectories of SCA age-dependent weight and height improved from being significantly lower than controls at trial entry to similarity at completion. Fat-free mass improved, although it and the fat mass both remained lower than that of the controls. Findings suggest that hydroxyurea promotes healthier growth and may improve body composition in children with SCA in SSA; earlier treatment initiation had a greater impact.

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