Evidence map›Paper›PMID 36096405›Full record

ArticleThe American journal of tropical medicine and hygiene2022

Enteropathy Markers in Early Life Were Associated with Adipokine, Apolipoprotein, and Cytokine Profiles Consistent with an Adverse Cardiometabolic Disease Risk Profile Later in Childhood in a Peruvian Birth Cohort.

Josh M Colston, Yen Ting Chen, Patrick Hinson, Nhat-Lan H Nguyen, Pablo Peñataro Yori, Maribel Paredes Olortegui, Dixner Rengifo Trigoso, Mery Siguas Salas, Richard L Guerrant, Ruthly François and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 37% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

11 authors at 4 institutions in 3 countries.

Josh M ColstonDivision of Infectious Diseases and International Health, University of Virginia School of Medicine, Charlottesville, Virginia.
Yen Ting ChenDepartment of Emergency Medicine, Chi-Mei Medical Center, Tainan, Taiwan.
Patrick HinsonCollege of Arts and Sciences, University of Virginia, Charlottesville, Virginia.
Nhat-Lan H NguyenCollege of Arts and Sciences, University of Virginia, Charlottesville, Virginia.
Pablo Peñataro YoriDivision of Infectious Diseases and International Health, University of Virginia School of Medicine, Charlottesville, Virginia.
Maribel Paredes OlorteguiAsociación Benéfica Prisma, Unidad de Investigaciones Biomédicas, Iquitos, Peru.
Dixner Rengifo TrigosoAsociación Benéfica Prisma, Unidad de Investigaciones Biomédicas, Iquitos, Peru.
Mery Siguas SalasAsociación Benéfica Prisma, Unidad de Investigaciones Biomédicas, Iquitos, Peru.
Richard L GuerrantDivision of Infectious Diseases and International Health, University of Virginia School of Medicine, Charlottesville, Virginia.
Ruthly FrançoisSchool of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Margaret N KosekDivision of Infectious Diseases and International Health, University of Virginia School of Medicine, Charlottesville, Virginia.
University of Virginia · USPrisma · PEChi Mei Medical Center · TWUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome is a cluster of risk factors for cardiovascular disease afflicting more than 1 billion people worldwide and is increasingly being identified in younger age groups and in socioeconomically disadvantaged settings in the global south. Enteropathogen exposure and environmental enteropathy in infancy may contribute to metabolic syndrome by disrupting the metabolic profile in a way that is detectable in cardiometabolic markers later in childhood. A total of 217 subjects previously enrolled in a birth cohort in Amazonian Peru were monitored annually from ages 2 to 5 years. A total of 197 blood samples collected in later childhood were analyzed for 37 cardiometabolic biomarkers, including adipokines, apolipoproteins, cytokines, which were matched to extant early-life markers of enteropathy ascertained between birth and 2 years. Multivariate and multivariable regression models were fitted to test for associations, adjusting for confounders. Fecal and urinary markers of intestinal permeability and inflammation (myeloperoxidase, lactulose, and mannitol) measured in infancy were associated with later serum concentrations of soluble CD40-ligand, a proinflammatory cytokine correlated with adverse metabolic outcomes. Fecal myeloperoxidase was also associated with later levels of omentin-1. Enteric protozoa exposure showed stronger associations with later cardiometabolic markers than viruses, bacteria, and overall diarrheal episodes. Early-life enteropathy markers were associated with altered adipokine, apolipoprotein, and cytokine profiles later in childhood consistent with an adverse cardiometabolic disease risk profile in this cohort. Markers of intestinal permeability and inflammation measured in urine (lactulose, mannitol) and stool (myeloperoxidase, protozoal infections) during infancy may predict metabolic syndrome in adulthood.

Indexed as

Cardiovascular DiseasesIntestinal DiseasesMetabolic SyndromeAdipokinesApolipoproteinsBiomarkersBirth CohortChild, PreschoolCytokinesHumansInflammationLactuloseLigandsMannitolPeroxidasePeruAdipokinesApolipoproteinsBiomarkersCytokinesLactuloseLigandsMannitolPeroxidase

Identifiers

PMID36096405
PMCPMC9651527
OpenAlexW4295279698

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.