Evidence map›Paper›PMID 33668048›Full record

ArticleThe American journal of clinical nutrition2021

Biomarkers of environmental enteric dysfunction are differently associated with recovery and growth among children with moderate acute malnutrition in Sierra Leone.

Akriti Singh, Shibani Ghosh, Honorine Ward, Mark J Manary, Beatrice L Rogers, Irwin H Rosenberg

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Article in The American journal of clinical nutrition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Akriti SinghFriedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA.
Shibani GhoshFriedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA.ORCID 0000-0001-5893-6774
Honorine WardTufts Medical Center and Tufts University School of Medicine, Boston, MA, USA.
Mark J ManaryDepartment of Pediatrics, Washington University, St Louis, MO, USA.
Beatrice L RogersFriedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA.
Irwin H RosenbergFriedman School of Nutrition Science and Policy, Tufts University, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnvironmental enteric dysfunction (EED) may influence growth during and recovery from moderate acute malnutrition (MAM), however, biomarkers to assess these relations have yet to be identified.

objectivesThe objectives of this study were to: 1) develop a score for EED based on host fecal mRNA transcripts, 2) compare biomarkers of EED with each other, and 3) examine associations between the EED biomarkers and recovery from MAM and growth outcomes.

methodsIn a cohort of 520 Sierra Leonean MAM children, biomarkers of EED included the lactulose: mannitol (L: M) test, 15 host fecal mRNA transcripts, and host fecal proteins [α-1-antitrypsin (AAT), myeloperoxidase (MPO), neopterin (NEO)]. Anthropometry data were also collected and z scores were computed for length-for-age (LAZ) and weight-for-length (WLZ). Recovery from MAM was defined as midupper arm circumference ≥12.5 cm. Factor analysis was used to identify EED scores using the mRNA transcripts, and mixed effects regression was conducted to test for associations.

resultsThe 15 host fecal mRNA transcripts were clustered into 3 scores: gut inflammation (GI) score, gut structure (GS) score, and gut defense (GD) score. We found agreement between certain inflammation markers (GI score and MPO), and permeability markers (GS score and AAT; AAT and the L: M excretion ratio). Antimicrobial gut defense (GD score) was inversely associated with percent lactulose excreted, a measure of intestinal permeability. LAZ (β: -0.08; 95% CI: -0.14, -0.02) and WLZ (β: -0.03; 95% CI: -0.06, -0.01) were negatively associated with GI score. A high GD score (β: 0.36; 95% CI: 0.08, 0.64) and low AAT (β: -1.35; 95% CI: -2.35, -0.36) were associated with recovery from MAM.

conclusionsScores derived from host fecal mRNA transcript variably correlated with the L: M test and host fecal proteins. Markers of intestinal inflammation, permeability, and defense were associated with growth outcomes and recovery from MAM.

Indexed as

Child DevelopmentBiomarkersChildChild Nutrition DisordersFecesHumansInflammationIntestinal DiseasesPermeabilityRNA, MessengerSierra LeoneBiomarkersRNA, Messengerbiomarkersenvironmental enteric dysfunctionfecal host mRNA transcriptsfecal host proteinsgrowth outcomesintestinal antimicrobial defenseintestinal inflammationintestinal permeabilitylactulose: mannitol testSierra Leone

Identifiers

PMID33668048
PMCPMC8243924

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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.