Evidence map›Paper›PMID 31331393›Full record

ArticleBMC pediatrics2019

Study of Environmental Enteropathy and Malnutrition (SEEM) in Pakistan: protocols for biopsy based biomarker discovery and validation.

Najeeha T Iqbal, Sana Syed, Kamran Sadiq, Marium N Khan, Junaid Iqbal, Jennie Z Ma, Fayaz Umrani, Sheraz Ahmed, Elizabeth A Maier, Lee A Denson and 15 more

2 registry-linked trialsOpen access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03588013 nacompletednot on this map

Study of Environmental Enteropathy and Malnutrition in Pakistan

TypeinterventionalSponsorAga Khan UniversityRan2016 to 2019Enrolled416ConditionsMalnutrition, Child, Enteropathy, Vaccine Response Impaired, StuntingArmsNutritional education, Ready to Use Therapeutic Food, Upper gastrointestinal endoscopy with biopsy
NCT07225153 narecruitingnot on this mapstarted 2025, after this paper: background citation

Goat Milk-Derived Formula Alternatives vs. Undiluted Goat Milk in Babies Unable to Exclusively Breastfeed: Analysis of Growth Metrics and Biological Markers

TypeinterventionalSponsorAga Khan UniversityRan2025 to 2026Enrolled15ConditionsMalnutrition (Calorie), Infant Nutrition Disorder, Growth Flatering, Gut MicrobiomeArmsGMDFA, Undiluted Goat Milk
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

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  9. Nutrient dataset development via FAO/INFOODS approach for infant nutritional survey in rural Matiari, Pakistan.Journal of food composition and analysis : an official publication of the United Nations University, International Network of Food Data Systems · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 2 countries.

Najeeha T IqbalDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Sana SyedDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Kamran SadiqDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Marium N KhanDepartment of Pediatrics, University of Virginia, Charlottesville, VA, USA.
Junaid IqbalDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Jennie Z MaDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA, USA.
Fayaz UmraniDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Sheraz AhmedDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Elizabeth A MaierDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Lee A DensonDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Yael HabermanDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Monica M McNealDivision of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Kenneth D R SetchellClinical Mass Spectrometry, Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Xueheng ZhaoClinical Mass Spectrometry, Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Shahida QureshiDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Lanlan ShenDepartment of Pediatrics, Baylor College of Medicine, USDA/ARS Children's Nutrition Research Center, Houston, TX, USA.
Christopher A MoskalukDepartment of Pathology, University of Virginia, Charlottesville, VA, USA.
Ta-Chiang LiuDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA.
Omer YilmazDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Donald E BrownData Science Institute, University of Virginia, Charlottesville, VA, USA.
Michael J BarrattCenter for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
Vanderlene L KungCenter for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
Jeffrey I GordonCenter for Genome Sciences and Systems Biology, Washington University School of Medicine, St. Louis, MO, USA.
Sean R MooreDepartment of Pediatrics, University of Virginia, Charlottesville, VA, USA. sean.moore@virginia.edu.
S Asad AliDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan. asad.ali@aku.edu.
Aga Khan University · PKCincinnati Children's Hospital Medical Center · USUniversity of Virginia · USWashington University in St. Louis · USChildren's Nutrition Research Center at Baylor College of Medicine · USHarvard University · US

Funding

Stem Cell/Organoid and Genome Editing CoreP30DK078392 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI Theresa Alenghat · 2007 to 2026
$24.4M
Organoids as a Model System for Studying Gastrointestinal DiseaseU19AI116491 · NIAID · UNIVERSITY OF CINCINNATI · PI WEISS, ALISON A., WELLS, JAMES M · 2015 to 2019
$4.6M
Microbiota, Inflammation and Environmental Enteric Dysfunction (MiEED)K43TW010697 · FIC · AGA KHAN UNIVERSITY (PAKISTAN) · PI IQBAL, NAJEEHA TALAT · 2017 to 2019
$185k
FIC NIH HHS K43 TW010697NIAID NIH HHS U19 AI116491NIDDK NIH HHS P30 DK078392
6 · The paper itself

Abstract

backgroundEnvironmental Enteropathy (EE), characterized by alterations in intestinal structure, function, and immune activation, is believed to be an important contributor to childhood undernutrition and its associated morbidities, including stunting. Half of all global deaths in children < 5 years are attributable to under-nutrition, making the study of EE an area of critical priority.

methodsCommunity based intervention study, divided into two sub-studies, 1) Longitudinal analyses and 2) Biopsy studies for identification of EE features via omics analyses. Birth cohorts in Matiari, Pakistan established: moderately or severely malnourished (weight for height Z score (WHZ) < - 2) children, and well-nourished (WHZ > 0) children. Blood, urine, and fecal samples, for evaluation of potential biomarkers, will be collected at various time points from all participants (longitudinal analyses). Participants will receive appropriate educational and nutritional interventions; non-responders will undergo further evaluation to determine eligibility for further workup, including upper gastrointestinal endoscopy. Histopathological changes in duodenal biopsies will be compared with duodenal biopsies obtained from USA controls who have celiac disease, Crohn's disease, or who were found to have normal histopathology. RNA-Seq will be employed to characterize mucosal gene expression across groups. Duodenal biopsies, luminal aspirates from the duodenum, and fecal samples will be analyzed to define microbial community composition (omic analyses). The relationship between histopathology, mucosal gene expression, and community configuration will be assessed using a variety of bioinformatic tools to gain better understanding of disease pathogenesis and to identify mechanism-based biomarkers. Ethical review committees at all collaborating institutions have approved this study. All results will be made available to the scientific community. DISCUSSION: Operational and ethical constraints for safely obtaining intestinal biopsies from children in resource-poor settings have led to a paucity of human tissue-based investigations to understand and reverse EE in vulnerable populations. Furthermore, EE biomarkers have rarely been correlated with gold standard histopathological confirmation. The Study of Environmental Enteropathy and Malnutrition (SEEM) is designed to better understand the pathophysiology, predictors, biomarkers, and potential management strategies of EE to inform strategies to eradicate this debilitating pathology and accelerate progress towards the 2030 Sustainable Development Goals.

trial registrationRetrospectively registered; clinicaltrials.gov ID NCT03588013 .

Indexed as

BiomarkersBiopsyCeliac DiseaseDuodenumFemaleGrowthGrowth DisordersHumansInfantInfant, NewbornInfant Nutrition DisordersMaleMalnutritionNutritional StatusPakistanResearch DesignBiomarkersChildhood undernutritionDuodenal biopsiesEndoscopyEnvironmental enteropathyGut barrier functionLow- middle income countriesMucosal gene expressionSmall intestinal microbiota

Identifiers

PMID31331393
PMCPMC6643315
OpenAlexW2963513660

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.