Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri; Department of Paediatrics and Child Health, University of Malawi College of Medicine, Blantyre, Malawi.
Clin Gastroenterol Hepatol. 2014 Sep;12(9):1507-13.e1. doi: 10.1016/j.cgh.2014.01.024. Epub 2014 Jan 22.
BACKGROUND & AIMS: Environmental enteropathy (EE) is a subclinical condition among children in the developing world, characterized by T-cell infiltration of the small-bowel mucosa and diffuse villous atrophy. EE leads to macronutrient and micronutrient malabsorption and stunting, with a resultant increased risk for infection and reduced cognitive development. We tested the hypothesis that zinc and albendazole treatments would reduce the severity of EE in rural African children.
In a randomized, double-blind, placebo-controlled trial in rural southern Malawi, asymptomatic children, 1 to 3 years old and at high risk for EE, received either a single dose of albendazole, a 14-day course of 20 mg zinc sulfate, or a placebo. Subjects were given the dual-sugar absorption test, and the ratio of lactulose to mannitol (L:M) in urine was used to determine the severity of EE at baseline and 34 days after completion of the assigned regimen. The primary outcome was the change in the L:M.
A complete set of urine samples was obtained from 222 of 234 children enrolled and analyzed. The mean baseline L:M was 0.32 ± 0.18 among all children and did not differ among groups (normal L:M range, <0.12). At the end of the study, the L:M ratio had increased more in the placebo group (0.12 ± 0.31) than in the zinc group (0.03 ± 0.20; P < .03) or the albendazole group (0.04 ± 0.22; P < .04).
Treatment with zinc or albendazole protects against a significant increase in the L:M ratio, a biomarker for EE, in asymptomatic rural Malawian children. These findings could provide insight into the etiology and pathogenesis of EE. Clinicaltrials.gov Number: NCT01440608.
环境肠病(EE)是发展中国家儿童的一种亚临床病症,其特征为 T 细胞浸润小肠黏膜和弥漫性绒毛萎缩。EE 导致宏量营养素和微量营养素吸收不良和发育迟缓,从而增加感染风险和降低认知发育。我们检验了以下假设,即锌和阿苯达唑治疗将减轻非洲农村儿童 EE 的严重程度。
在马拉维南部农村的一项随机、双盲、安慰剂对照试验中,无症状、1 至 3 岁且 EE 风险高的儿童接受单次阿苯达唑治疗、14 天 20 毫克硫酸锌疗程或安慰剂。给受试者进行双重糖吸收试验,尿中乳果糖与甘露醇(L:M)的比值用于在基线和完成指定方案后 34 天确定 EE 的严重程度。主要结局是 L:M 的变化。
234 名入组儿童中,222 名获得了完整的尿液样本并进行了分析。所有儿童的平均基线 L:M 为 0.32 ± 0.18,各组之间无差异(正常 L:M 范围,<0.12)。研究结束时,安慰剂组的 L:M 比值增加较多(0.12 ± 0.31),锌组(0.03 ± 0.20;P<.03)或阿苯达唑组(0.04 ± 0.22;P<.04)增加较少。
锌或阿苯达唑治疗可防止无症状马拉维农村儿童的 L:M 比值显著增加,L:M 比值是 EE 的生物标志物。这些发现可以深入了解 EE 的病因和发病机制。临床试验编号:NCT01440608。