Evidence map›Paper›PMID 39835685›Full record

ArticleClinical and translational gastroenterology2025

Neutrophil-to-Lymphocyte Ratio at Diagnosis Predicts Colonoscopic Activity in Pediatric Inflammatory Bowel Diseases.

Bishoi Aziz, Reza Belaghi, Hien Huynh, Kevan Jacobson, David R Mack, Colette Deslandres, Anthony Otley, Jennifer DeBruyn, Wael El-Matary, Eileen Crowley and 7 more

Abstract read
In one paragraph

Article in Clinical and translational gastroenterology, 2025. 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
–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

2 citing papers in PubMed.

  1. Article
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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

17 authors.

Bishoi AzizDepartment of Pediatrics, Division of Pediatric Gastroenterology and Nutrition, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-8762-753
Reza BelaghiChildren's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
Hien HuynhDepartment of Pediatrics, Division of Pediatric Gastroenterology and Nutrition, University of Alberta, Edmonton, Alberta, Canada.
Kevan JacobsonDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
David R MackChildren's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
Colette DeslandresDepartment of Pediatrics, University of Montreal, Montreal, Quebec, Canada.
Anthony OtleyDepartement of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada.
Jennifer DeBruynDepartment of Pediatrics, University of Calgary, Calgary, Alberta, Canada.
Wael El-MataryDepartment of Pediatrics, University of Manitoba, Winnipeg, Manitoba, Canada.
Eileen CrowleyDepartment of Pediatrics, Division of Pediatric Gastroenterology, Children's Hospital Western Ontario, Western University, London, Ontario, Canada.
Mary SherlockDepartment of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Jeffery CritchDepartment of Pediatrics, Memorial University, St. John's, Newfoundland and Labrador, Canada.
Najma AhmedDepartment of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.
Anne GriffithsDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Thomas WaltersDepartment of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Eytan WineDepartment of Pediatrics, Division of Pediatric Gastroenterology and Nutrition, University of Alberta, Edmonton, Alberta, Canada.ORCID 0000-0002-3458-4142
Canadian Children IBD Network

Funding

CH.I.L.D. Foundation
6 · The paper itself

Abstract

introductionNeutrophil-to-lymphocyte ratio (NLR) is a novel biomarker studied in several autoimmune diseases including inflammatory bowel disease (IBD) in adults but poorly characterized in pediatric IBD (pIBD). We aimed to primarily investigate the relationship between NLR and pIBD endoscopic disease severity. We also examined whether NLR predicted hospitalization, surgery, and therapy response by 52 weeks.

methodsWe used the Canadian Children IBD Network prospective inception cohort including patients < 18 years old with baseline data from 2013 to 2022. We excluded patients with concurrent diseases affecting NLR. Both Mayo endoscopic score (MES) and simple endoscopic scale for Crohn's disease (SES-CD) were dichotomized as low activity (quiescent-mild) and high activity (moderate-severe). For therapy responses, we examined year-1 steroid- and biologic-free remission. We used logistic regression for binary outcomes.

resultsA total of 580 patients with ulcerative colitis and 1,081 patients with CD were included. High NLR was associated with high-activity MES and SES-CD in both univariate and multivariable analyses (odds ratio = 1.45, 95% CI = 1.07-1.97, P value = 0.016; and odds ratio = 1.42, 95% CI = 1.04-1.94, P value = 0.026, respectively). We also calculated the best NLR cutoff point to predict MES (1.90, sensitivity = 68%, specificity = 67%, area under the curve [AUC] = 0.67, AUC 95% CI = 0.59-0.74) and SES-CD (2.50, sensitivity = 63%, specificity = 69%, AUC = 0.66, AUC 95% CI = 0.59-0.75) high activity. NLR did not predict therapy response in either ulcerative colitis or CD. DISCUSSION: Patients with pIBD with high baseline NLR are more probable to have worse endoscopic disease at diagnosis. This highlights NLR potential as a reliable noninvasive biomarker of disease activity. The predictive power of NLR is based mostly on neutrophils and the balance between neutrophils and lymphocytes.

Indexed as

Colitis, UlcerativeColonoscopyCrohn DiseaseLymphocytesNeutrophilsAdolescentBiomarkersCanadaChildFemaleHospitalizationHumansLeukocyte CountLymphocyte CountMalePredictive Value of TestsBiomarkersbiologic-free remissioncolonoscopic activityCrohn's diseasesteroid-free remissionulcerative colitis

Identifiers

PMID39835685
PMCPMC12020715

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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.