University of Zambia School of Medicine.
Tropical Gastroenterology & Nutrition group, Lusaka, Zambia.
J Pediatr Gastroenterol Nutr. 2022 Apr 1;74(4):529-534. doi: 10.1097/MPG.0000000000003343. Epub 2021 Oct 28.
Stunting, the most common form of childhood undernutrition, is associated with environmental enteropathy (EE). Enteric infections are believed to play a role in the pathophysiology of EE and stunting though the exact mechanism remains undetermined. The FUT2 (secretor) and FUT3 (Lewis) genes have been shown to be associated with some symptomatic enteric infections in both children and adults. These genes are responsible for the presence of histo-blood group antigens (HBGAs) in various secretions and epithelial surfaces.We evaluated whether the secretor and Lewis status influences asymptomatic enteric infections and thus EE severity on duodenal biopsies of stunted children.
In this case-control study, we used saliva samples to determine the secretor and Lewis status of stunted children (cases, n = 113) enrolled in a nutritional rehabilitation program and from their well-nourished counterparts (controls, n = 42). Where available, saliva was also collected from the mothers. Baseline stool samples were used to detect asymptomatic enteropathogen carriage. Duodenal biopsies were collected from a subgroup of stunted children (n = 77) who had an upper gastrointestinal endoscopy done as part of the evaluation process for their non-response to nutritional therapy.
The proportion of secretors was similar between the cases and the controls (82% vs 81%, P = 0.81). The stunted children had significantly higher rates of carrying multiple enteropathogens, but this was not associated with their secretor status nor that of their mothers. The secretor status was also not associated with mucosal morphometry of duodenal biopsies.
This case-control analysis in Zambian children does not support the hypothesis that fucosylation status determines asymptomatic enteropathogen carriage in stunting.
发育迟缓是儿童中最常见的营养不良形式,与肠病相关。肠内感染被认为在肠病和发育迟缓的病理生理学中起作用,但确切机制尚不清楚。FUT2(分泌型)和 FUT3(Lewis)基因已被证明与儿童和成人的一些有症状的肠内感染有关。这些基因负责各种分泌物和上皮表面的组织血型抗原(HBGAs)的存在。我们评估了分泌型和 Lewis 状态是否会影响无症状的肠内感染,从而影响发育迟缓儿童十二指肠活检中的肠病严重程度。
在这项病例对照研究中,我们使用唾液样本来确定营养康复计划中发育迟缓儿童(病例,n=113)及其营养良好的对照组(n=42)的分泌型和 Lewis 状态。在有条件的情况下,还从母亲那里收集了唾液。基线粪便样本用于检测无症状的肠病原体携带情况。从接受上消化道内窥镜检查的发育迟缓儿童亚组(n=77)中收集十二指肠活检,作为对营养治疗无反应评估过程的一部分。
病例组和对照组之间分泌型的比例相似(82%比 81%,P=0.81)。发育迟缓儿童携带多种肠病原体的比例显著更高,但这与他们的分泌型状态或其母亲的分泌型状态无关。分泌型状态也与十二指肠活检的黏膜形态计量学无关。
这项赞比亚儿童的病例对照分析不支持 fucosylation 状态决定发育迟缓儿童无症状肠病原体携带的假设。