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Reference values of fecal calgranulin C (S100A12) in school aged children and adolescents

  • Anke Heida ORCID logo , Anneke C. Muller Kobold , Lucie Wagenmakers , Koos van de Belt and Patrick F. van Rheenen EMAIL logo
Published/Copyright: July 14, 2017

Abstract

Background:

Calgranulin C (S100A12) is an emerging marker of inflammation. It is exclusively released by activated neutrophils which makes this marker potentially more specific for inflammatory bowel disease (IBD) compared to established stool markers including calprotectin and lactoferrin. We aimed to establish a reference value for S100A12 in healthy children and investigated whether S100A12 levels can discriminate children with IBD from healthy controls.

Methods:

In a prospective community-based reference interval study we collected 122 stool samples from healthy children aged 5–19 years. Additionally, feces samples of 41 children with suspected IBD (who were later confirmed by endoscopy to have IBD) were collected. Levels of S100A12 were measured with a sandwich enzyme-linked immunosorbent assay (ELISA) (Inflamark®). The limit of detection was 0.22 μg/g.

Results:

The upper reference limit in healthy children was 0.75 μg/g (90% confidence interval: 0.30–1.40). Median S100A12 levels were significantly higher in patients with IBD (8.00 μg/g [interquartile range (IQR) 2.5–11.6] compared to healthy controls [0.22 μg/g (IQR<0.22); p<0.001]). The best cutoff point based on receiver operating characteristic curve was 0.33 μg/g (sensitivity 93%; specificity 97%).

Conclusions:

Children and teenagers with newly diagnosed IBD have significantly higher S100A12 results compared to healthy individuals. We demonstrate that fecal S100A12 shows diagnostic promise under ideal testing conditions. Future studies need to address whether S100A12 can discriminate children with IBD from non-organic disease in a prospective cohort with chronic gastrointestinal complaints, and how S100A12 performs in comparison with established stool markers.


Article note:

An interim analysis of this study was orally presented at the ESPGHAN Annual Meeting in Athens in 2016.



Corresponding author: Patrick F. van Rheenen, MD, PhD, Department of Pediatric Gastroenterology, University Medical Center Groningen, University of Groningen, Internal Code CA 31, PO Box 30001, 9700 RB Groningen, The Netherlands, Phone: +31 30 3614147

Acknowledgments

We would like to thank Hanna van Rheenen (a student from Werkman Stadslyceum Groningen) for enthusing her fellow students to send in a stool sample, and all volunteers (and parents) who sent in a stool sample.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This study was supported by CisBio Bioassay, Codolet, France (developer and producer of Inflamark®). Trial registry: Clinical trials.gov NCT02588222.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplemental Material:

The online version of this article (https://doi.org/10.1515/cclm-2017-0152) offers supplementary material, available to authorized users.


Received: 2017-2-22
Accepted: 2017-4-25
Published Online: 2017-7-14
Published in Print: 2017-11-27

©2018 Walter de Gruyter GmbH, Berlin/Boston

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