Department of Pediatrics, University of Minnesota School of Medicine, Minneapolis, MN, USA.
Department of Paediatrics and Child Health, Makerere University College of Health Sciences, Kampala, Uganda.
Am J Clin Nutr. 2020 May 1;111(5):1059-1067. doi: 10.1093/ajcn/nqaa004.
WHO guidelines recommend concurrent iron and antimalarial treatment in children with malaria and iron deficiency, but iron may not be well absorbed or utilized during a malaria episode.
We aimed to determine whether starting iron 28 d after antimalarial treatment in children with severe malaria and iron deficiency would improve iron status and lower malaria risk.
We conducted a randomized clinical trial on the effect of immediate compared with delayed iron treatment in Ugandan children 18 mo-5 y of age with 2 forms of severe malaria: cerebral malaria (CM; n = 79) or severe malarial anemia (SMA; n = 77). Asymptomatic community children (CC; n = 83) were enrolled as a comparison group. Children with iron deficiency, defined as zinc protoporphyrin (ZPP) ≥ 80 µmol/mol heme, were randomly assigned to receive a 3-mo course of daily oral ferrous sulfate (2 mg · kg-1 · d-1) either concurrently with antimalarial treatment (immediate arm) or 28 d after receiving antimalarial treatment (delayed arm). Children were followed for 12 mo.
All children with CM or SMA, and 35 (42.2%) CC, were iron-deficient and were randomly assigned to immediate or delayed iron treatment. Immediate compared with delayed iron had no effect in any of the 3 study groups on the primary study outcomes (hemoglobin concentration and prevalence of ZPP ≥ 80 µmol/mol heme at 6 mo, malaria incidence over 12 mo). However, after 12 mo, children with SMA in the delayed compared with the immediate arm had a lower prevalence of iron deficiency defined by ZPP (29.4% compared with 65.6%, P = 0.006), a lower mean concentration of soluble transferrin receptor (6.1 compared with 7.8 mg/L, P = 0.03), and showed a trend toward fewer episodes of severe malaria (incidence rate ratio: 0.39; 95% CI: 0.14, 1.12).
In children with SMA, delayed iron treatment did not increase hemoglobin concentration, but did improve long-term iron status over 12 mo without affecting malaria incidence.This trial was registered at clinicaltrials.gov as NCT01093989.
世界卫生组织指南建议在患有疟疾和缺铁的儿童中同时进行铁和抗疟治疗,但在疟疾发作期间,铁可能无法被很好地吸收或利用。
我们旨在确定在患有严重疟疾和缺铁的儿童中,在抗疟治疗后 28 天开始补铁是否会改善铁状态并降低疟疾风险。
我们在乌干达开展了一项随机临床试验,比较了即时与延迟补铁对 2 种严重疟疾(脑型疟疾 [CM];n=79 和严重疟疾性贫血 [SMA];n=77)患儿及无症状社区儿童(CC;n=83)的影响。缺铁定义为锌原卟啉(ZPP)≥80µmol/mol 血红素,患有缺铁的儿童被随机分为 3 组,分别接受为期 3 个月的每日口服硫酸亚铁(2mg·kg-1·d-1)治疗:同时接受抗疟治疗(即刻组)或在接受抗疟治疗后 28 天(延迟组)开始治疗。儿童接受为期 12 个月的随访。
所有患有 CM 或 SMA 的儿童以及 35 名(42.2%)CC 儿童均患有缺铁,他们被随机分为即刻或延迟补铁组。在 3 个研究组中,与延迟补铁相比,即刻补铁对主要研究结局(6 个月时血红蛋白浓度和 ZPP≥80µmol/mol 血红素的患病率,12 个月时疟疾发生率)均无影响。然而,在 12 个月时,与即刻补铁组相比,延迟补铁组 SMA 患儿的缺铁患病率较低(29.4%比 65.6%,P=0.006),可溶性转铁蛋白受体浓度较低(6.1 比 7.8mg/L,P=0.03),严重疟疾发作次数也有减少的趋势(发病率比:0.39;95%CI:0.14,1.12)。
在患有 SMA 的儿童中,延迟补铁并未增加血红蛋白浓度,但在 12 个月内改善了长期铁状态,而不会影响疟疾发病率。本试验在 clinicaltrials.gov 注册,编号为 NCT01093989。