Putative Biomarkers of Environmental Enteric Disease Fail to Correlate in a Cross-Sectional Study in Two Study Sites in Sub-Saharan Africa.
Sub-Saharan Africa
alpha-1-antitrypsin
anemia
biomarker
calprotectin
citrulline
environmental enteric dysfunction
insulin-like growth factor
lactulose-mannitol test
stunted child growth
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
12 Aug 2022
12 Aug 2022
Historique:
received:
07
07
2022
revised:
07
08
2022
accepted:
10
08
2022
entrez:
26
8
2022
pubmed:
27
8
2022
medline:
30
8
2022
Statut:
epublish
Résumé
Environmental enteric dysfunction (EED) is an elusive, inflammatory syndrome of the small intestine thought to be associated with enterocyte loss and gut leakiness and lead to stunted child growth. To date, the gold standard for diagnosis is small intestine biopsy followed by histology. Several putative biomarkers for EED have been proposed and are widely used in the field. Here, we assessed in a cross-sectional study of children aged 2-5 years for a large set of biomarkers including markers of protein exudation (duodenal and fecal alpha-1-antitrypsin (AAT)), inflammation (duodenal and fecal calprotectin, duodenal, fecal and blood immunoglobulins, blood cytokines, C-reactive protein (CRP)), gut permeability (endocab, lactulose-mannitol ratio), enterocyte mass (citrulline) and general nutritional status (branched-chain amino acids (BCAA), insulin-like growth factor) in a group of 804 children in two Sub-Saharan countries. We correlated these markers with each other and with anemia in stunted and non-stunted children. AAT and calprotectin, CRP and citrulline and citrulline and BCAA correlated with each other. Furthermore, BCAA, citrulline, ferritin, fecal calprotectin and CRP levels were correlated with hemoglobin levels. Our results show that while several of the biomarkers are associated with anemia, there is little correlation between the different biomarkers. Better biomarkers and a better definition of EED are thus urgently needed.
Identifiants
pubmed: 36014817
pii: nu14163312
doi: 10.3390/nu14163312
pmc: PMC9412633
pii:
doi:
Substances chimiques
Biomarkers
0
Leukocyte L1 Antigen Complex
0
Citrulline
29VT07BGDA
C-Reactive Protein
9007-41-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Total Foundation
ID : 2014
Organisme : Bill and Melinda Gates Foundation
ID : OPP1204689
Organisme : Fondation Petram
ID : 2016
Organisme : Odyssey Re-Insurance company
ID : 2016
Organisme : Swiss National Science Foundation
ID : P2EZP3_152159
Pays : Switzerland
Organisme : Swiss National Science Foundation
ID : P300PA_177876
Pays : Switzerland
Organisme : Swiss National Science Foundation
ID : P3P3PA_17877
Pays : Switzerland
Organisme : Roux-Cantarini Fellowship
ID : 2016
Organisme : L'Oréal-UNESCO for Women in Science France Fellowship
ID : 22017
Organisme : Excellence Scholarship from the University of Basel (Forschungsfonds, 2019)
ID : 2019
Déclaration de conflit d'intérêts
The authors declare no conflict of interest.
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