Evidence map›Paper›PMID 40839595›Full record

ArticlePloS one2025

Correlation of fecal calprotectin levels with the detection of treatable enteric pathogens in children with severe acute diarrheal disease in Botswana.

Muhammad Rehan, Elspeth MacBain, M Sharif Shajib, Margaret Mokomane, Kwana Lechiile, Tonya Arscott-Mills, Andrew P Steenhoff, Loeto Mazhani, Cheryl Main, Marek Smieja and 3 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Muhammad RehanDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.
Elspeth MacBainDepartment of Pediatrics, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0009-0009-4097-2641
M Sharif ShajibDepartment of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.
Margaret MokomaneFaculty of Health Sciences, School of Allied Health Professions, University of Botswana, Gaborone, Botswana.
Kwana LechiileBotswana-UPenn Partnership, Gaborone, Botswana.
Tonya Arscott-MillsBotswana-UPenn Partnership, Gaborone, Botswana.ORCID https://orcid.org/0000-0002-7873-9871
Andrew P SteenhoffDepartment of Pediatrics, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0001-9002-8207
Loeto MazhaniDepartment of Pediatric and Adolescent Health, University of Botswana, Gaborone, Botswana.
Cheryl MainDepartment of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.
Marek SmiejaDepartment of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.
Waliul I KhanDepartment of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, Ontario, Canada.
David M GoldfarbDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID https://orcid.org/0000-0003-0835-9504
Jeffrey M PernicaDepartment of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.ORCID https://orcid.org/0000-0002-4380-5402

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diarrheal disease is a leading cause of death among young children globally. Current guidelines recommend supportive treatment of acute diarrhea and using antimicrobials only with presence of blood in the stool. Select enteric pathogens, including Shigella, commonly cause disease in high-burden settings; targeted treatment of these pathogens could decrease morbidity and mortality. In settings with limited access to microbiological testing, practical diagnostics are needed to differentiate treatable causes of pediatric diarrhea. Evolving evidence suggests fecal calprotectin (fCal) could help differentiate viral and bacterial gastroenteritis. This study describes a post hoc analysis of stool samples prospectively collected from children hospitalized with severe acute diarrheal disease in Botswana. Specimens were characterized using multiplex PCR panels for selected enteropathogens and assayed for fCal. Stool samples from 312 participants were tested. Samples positive for Shigella had significantly higher fCal than samples positive for rotavirus. Stools that were negative for all assayed pathogens had higher fCal values than expected using standard normative values for healthy children in higher-income settings. Given the prevalence of Shigella and rotavirus infections in young children globally, fCal may be a useful aid to identify children with acute diarrhea for whom antimicrobials could provide benefit and potentially reduce growth failure and mortality.

Indexed as

DiarrheaFecesLeukocyte L1 Antigen ComplexAcute DiseaseBotswanaChildChild, PreschoolDysentery, BacillaryFemaleGastroenteritisHumansInfantMaleProspective StudiesRotavirusRotavirus InfectionsLeukocyte L1 Antigen Complex

Identifiers

PMID40839595
PMCPMC12370036

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Registered trials

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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.