Blizard Institute, Barts & The London School of Medicine, Queen Mary University of London, London, United Kingdom.
Department of Global Health, University of Washington School of Public Health, Seattle, WA, United States.
Am J Clin Nutr. 2024 Sep;120 Suppl 1:S15-S30. doi: 10.1016/j.ajcnut.2024.02.028.
Environmental enteric dysfunction (EED) is an asymptomatic intestinal disorder associated with growth impairment, delayed neurocognitive development, and impaired oral vaccine responses.
We set out to develop and validate a histopathologic scoring system on duodenal biopsies from a cohort study of children with growth failure in Bangladesh, Pakistan, and Zambia ("EED") with reference to biopsies from United States children with no clinically reported histologic pathology (referred to hereafter as "normal") or celiac disease.
Five gastrointestinal pathologists evaluated 745 hematoxylin and eosin slide images from 291 children with EED (mean age: 1.6 y) and 66 United States children (mean age: 6.8 y). Histomorphologic features (i.e., villus/crypt architecture, goblet cells, epithelial and lamina propria acute/chronic inflammation, Brunner's glands, Paneth cells, epithelial detachment, enterocyte injury, and foveolar metaplasia) were used to score each histopathologic slide. Generalized estimating equations were used to determine differences between EED, normal, and celiac disease, and receiver operating characteristic curves were used to assess predictive value.
Biopsies from the duodenal bulb showed higher intramucosal Brunner's gland scores and lower intraepithelial lymphocyte scores than from the second or third parts of the duodenum (D2/3), so only D2/3 were included in the final analysis. Although 7 parameters differed significantly between EED and normal biopsies in regression models, only 5 (blunted villus architecture, increased intraepithelial lymphocytosis, goblet cell depletion, Paneth cell depletion, and reduced intramucosal Brunner's glands) were required to create a total score percentage (TSP-5) that correctly identified EED against normal biopsies (AUC: 0.992; 95% CI: 0.983, 0.998). Geographic comparisons showed more severe goblet cell depletion in Bangladesh and more marked intraepithelial lymphocytosis in Pakistan.
This scoring system involving 5 histologic parameters demonstrates very high discrimination between EED and normal biopsies, indicating that this scoring system can be applied with confidence to studies of intestinal biopsies in EED.
肠病相关营养素吸收不良(EED)是一种无症状的肠道功能紊乱,与生长发育迟缓、神经认知发育迟缓以及口服疫苗应答受损有关。
我们旨在开发和验证一种组织病理学评分系统,该系统基于孟加拉国、巴基斯坦和赞比亚生长迟缓儿童队列研究中的十二指肠活检(简称“EED”),并参考美国无临床报告组织病理学(以下简称“正常”)或乳糜泻的儿童活检。
5 位胃肠病理学家评估了 291 例 EED 儿童(平均年龄:1.6 岁)和 66 例美国儿童(平均年龄:6.8 岁)的 745 张苏木精-伊红幻灯片图像。采用绒毛/隐窝结构、杯状细胞、上皮和固有层急性/慢性炎症、Brunner 腺、Paneth 细胞、上皮脱落、肠细胞损伤和滤泡性化生等组织形态学特征对每个组织病理学幻灯片进行评分。采用广义估计方程确定 EED、正常和乳糜泻之间的差异,并采用受试者工作特征曲线评估预测值。
十二指肠球部活检的黏膜内 Brunner 腺评分较高,上皮内淋巴细胞评分较低,而十二指肠的第二或第三部分(D2/3)则较低,因此最终分析仅包括 D2/3。虽然在回归模型中,EED 与正常活检之间有 7 个参数存在显著差异,但仅需要 5 个参数(绒毛结构变钝、上皮内淋巴细胞增多、杯状细胞缺失、Paneth 细胞缺失和黏膜内 Brunner 腺减少)即可创建正确识别 EED 与正常活检的总评分百分比(TSP-5)(AUC:0.992;95%CI:0.983,0.998)。地理比较显示,孟加拉国的杯状细胞缺失更严重,巴基斯坦的上皮内淋巴细胞增多更明显。
该评分系统涉及 5 个组织学参数,在 EED 与正常活检之间具有非常高的区分度,表明该评分系统可以有信心地应用于 EED 肠活检研究。