Global Child Health Group, Emma Children's Hospital, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Department of Paediatrics and Child Health, Queen Elizabeth Central Hospital, Blantyre, Malawi.
Sci Rep. 2019 Feb 19;9(1):2304. doi: 10.1038/s41598-019-38690-9.
Intestinal pathology in children with complicated severe acute malnutrition (SAM) persists despite standard management. Given the similarity with intestinal pathology in non-IgE mediated gastrointestinal food allergy and Crohn's disease, we tested whether therapeutic feeds effective in treating these conditions may benefit children with complicated SAM. After initial clinical stabilisation, 95 children aged 6-23 months admitted at Queen Elizabeth Central Hospital, Blantyre, Malawi between January 1 and December 31, 2016 were allocated randomly to either standard feeds, an elemental feed or a polymeric feed for 14 days. Change in faecal calprotectin as a marker of intestinal inflammation and the primary outcome was similar in each arm: elemental vs. standard 4.1 μg/mg stool/day (95% CI, -29.9, 38.15; P = 0.81) and polymeric vs. standard 10 (-23.96, 43.91; P = 0.56). Biomarkers of intestinal and systemic inflammation and mucosal integrity were highly abnormal in most children at baseline and abnormal values persisted in all three arms. The enteropathy in complicated SAM did not respond to either standard feeds or alternative therapeutic feeds administered for up to 14 days. A better understanding of the pathogenesis of the gut pathology in complicated SAM is an urgent priority to inform the development of improved therapeutic interventions.
尽管采用了标准治疗方法,患有复杂严重急性营养不良 (SAM) 的儿童的肠道病理学仍持续存在。鉴于其与非 IgE 介导的胃肠道食物过敏和克罗恩病的肠道病理学相似,我们测试了治疗这些疾病的治疗性喂养是否可能使患有复杂 SAM 的儿童受益。在最初的临床稳定后,2016 年 1 月 1 日至 12 月 31 日期间,马拉维伊丽莎白女王中央医院收治的 95 名年龄在 6-23 个月之间的儿童被随机分配到标准喂养组、元素喂养组或聚合喂养组,接受 14 天的治疗。粪便钙卫蛋白作为肠道炎症标志物的变化和主要结果在每个组中均相似:元素喂养组与标准喂养组相比为 4.1μg/mg 粪便/天(95%CI,-29.9,38.15;P=0.81),聚合喂养组与标准喂养组相比为 10μg/mg 粪便/天(-23.96,43.91;P=0.56)。大多数儿童在基线时的肠道和全身炎症以及黏膜完整性的生物标志物高度异常,所有三组的异常值均持续存在。在接受标准喂养或替代治疗性喂养最多 14 天的治疗后,复杂 SAM 中的肠病并未得到缓解。迫切需要更好地了解复杂 SAM 中肠道病理学的发病机制,以告知改善治疗干预措施的开发。