TY - JOUR
T1 - Histopathology underlying environmental enteric dysfunction in a cohort study of undernourished children in Bangladesh, Pakistan, and Zambia compared with United States children
AU - EEDBI Consortium
AU - Kelly, Paul
AU - VanBuskirk, Kelley
AU - Coomes, David
AU - Mouksassi, Samer
AU - Smith, Gerald
AU - Jamil, Zehra
AU - Hossain, Md Shabab
AU - Syed, Sana
AU - Marie, Chelsea
AU - Tarr, Phillip I.
AU - Sullivan, Peter B.
AU - Petri, William A.
AU - Denno, Donna M.
AU - Ahmed, Tahmeed
AU - Mahfuz, Mustafa
AU - Ali, S. Asad
AU - Moore, Sean R.
AU - Ndao, I. Malick
AU - Tearney, Guillermo J.
AU - Ömer H Yilmaz, H Yilmaz
AU - Raghavan, Shyam S.
AU - Moskaluk, Christopher A.
AU - Liu, Ta Chiang
AU - Ahmed, Kumail
AU - Ahmed, Sheraz
AU - Alam, Md Ashraful
AU - Begum, S. M.Khodeza Nahar
AU - Besa, Ellen
AU - Chandwe, Kanta
AU - Chipunza, Miyoba
AU - Das, Subhasish
AU - Denson, Lee A.
AU - Fahim, Shah Mohammad
AU - Gazi, Md Amran
AU - Hasan, Md Mehedi
AU - Hotwani, Aneeta
AU - Iqbal, Junaid
AU - Iqbal, Najeeha Talat
AU - Jakhro, Sadaf
AU - Kabir, Furqan
AU - Lawrence, Sarah
AU - Mann, Barbara J.
AU - Mazumder, Ramendra Nath
AU - Memon, Waheeda
AU - Morgan, Brooks
AU - Mudenda, Victor
AU - Mulenga, Chola
AU - Mweetwa, Monica
AU - Qureshi, Abdul Khalique
AU - Sadiq, Kamran
N1 - Publisher Copyright:
© 2024 The Author(s)
PY - 2024/9
Y1 - 2024/9
N2 - Background: Environmental enteric dysfunction (EED) is an asymptomatic intestinal disorder associated with growth impairment, delayed neurocognitive development, and impaired oral vaccine responses. Objectives: 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. Methods: 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. Results: 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. Conclusions: 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.
AB - Background: Environmental enteric dysfunction (EED) is an asymptomatic intestinal disorder associated with growth impairment, delayed neurocognitive development, and impaired oral vaccine responses. Objectives: 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. Methods: 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. Results: 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. Conclusions: 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.
KW - child health
KW - crypts
KW - enteropathy
KW - global health
KW - goblet cells
KW - intestine
KW - malnutrition
KW - Paneth cells
KW - stunting
KW - villi
UR - http://www.scopus.com/inward/record.url?scp=85203992304&partnerID=8YFLogxK
U2 - 10.1016/j.ajcnut.2024.02.028
DO - 10.1016/j.ajcnut.2024.02.028
M3 - Article
AN - SCOPUS:85203992304
SN - 0002-9165
VL - 120
SP - S15-S30
JO - American Journal of Clinical Nutrition
JF - American Journal of Clinical Nutrition
ER -