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. 2022 Oct 15;11(20):6086.
doi: 10.3390/jcm11206086.

Evaluation of Fecal Calprotectin, Serum C-Reactive Protein, Erythrocyte Sedimentation Rate, Seromucoid and Procalcitonin in the Diagnostics and Monitoring of Crohn's Disease in Children

Affiliations

Evaluation of Fecal Calprotectin, Serum C-Reactive Protein, Erythrocyte Sedimentation Rate, Seromucoid and Procalcitonin in the Diagnostics and Monitoring of Crohn's Disease in Children

Katarzyna Akutko et al. J Clin Med. .

Abstract

Background: The development of diagnostic and monitoring algorithms for Crohn’s disease based on non-invasive methods is of particular importance in children and is the subject of many studies. Objectives: Evaluate the usefulness of fecal calprotectin, serum C-reactive protein, erythrocyte sedimentation rate, seromucoid and procalcitonin in the differential diagnosis of non-inflammatory gastrointestinal tract diseases and Crohn’s disease in children and their usefulness in determining the phenotype of Crohn’s disease. Material and methods: Forty-seven children with non-inflammatory gastrointestinal tract diseases and fifty-four with Crohn’s disease were enrolled. Clinical and endoscopic activity was evaluated based on the Pediatric Crohn’s Disease Activity Index (PCDAI) and the Simple Endoscopic Score for Crohn’s Disease (SES-CD). Results: Fecal calprotectin, C-reactive protein, erythrocyte sedimentation rate and seromucoid were significantly higher in children with Crohn’s disease than in controls (p < 0.001). Fecal calprotectin correlated with clinical and endoscopic activity according to the Pediatric Crohn’s Disease Activity Index (r = 0.338; p = 0.012) and the Simple Endoscopic Score for Crohn’s Disease (r = 0.428; p = 0.001). Non-invasive biomarkers did not correlate with the location and clinical manifestation of Crohn’s disease. Conclusions: Fecal calprotectin, C-reactive protein, erythrocyte sedimentation rate and seromucoid are useful in the differentiation of Crohn’s disease from non-inflammatory gastrointestinal tract diseases in children and in monitoring the clinical course of Crohn’s disease, but not in evaluating activity and phenotype of the disease.

Keywords: activity; biomarkers; diagnosis; monitoring; non-invasive.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Correlation between (a) fecal calprotectin (FC), (b) C-reactive protein (CRP), (c) erythrocyte sedimentation rate (ESR), (d) seromucoid (AAG) and clinical activity according to the Pediatric Crohn’s Disease Activity Index (PCDAI) in children with Crohn’s disease.
Figure 2
Figure 2
Correlation between (a) fecal calprotectin (FC), (b) C-reactive protein (CRP), (c) erythrocyte sedimentation rate (ESR), (d) seromucoid (AAG) and endoscopic activity according to the Simple Endoscopic Score for Crohn’s Disease (SES-CD) in children with Crohn’s disease.
Figure 3
Figure 3
Receiver operator characteristic (ROC) curve for serum and fecal biomarkers: fecal calprotectin (FC) (a), C-reactive protein (CRP) (b), erythrocyte sedimentation rate (ESR) (c), seromucoid (AAG) (d) and procalcitonin (PCT) (e) in the differentiation of Crohn’s disease in children with non-inflammatory diseases of the gastrointestinal tract.

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References

    1. Setty M., Russell G.H., Bousvaros A. Clinical manifestations of Crohn disease in children and adolescents. In: Hoppin A.G., Post T.W., editors. UpToDate: Industry-Leading Clinical Decision Support. UpToDate; Waltham, MA, USA: 2016. [(accessed on 1 December 2016)]. Available online: http://www.uptodate.com/home.
    1. Gomollón F., Dignass A., Annese V., Tilg H., Van Assche G., Lindsay J.O., Peyrin-Biroulet L., Cullen G.J., Daperno M., Kucharzik T., et al. 3rd European Evidence-based Consensus on the Diagnosis and Management of Crohn’s Disease 2016: Part 1: Diagnosis and Medical Management. J. Crohns Colitis. 2017;11:3–25. doi: 10.1093/ecco-jcc/jjw168. - DOI - PubMed
    1. Schoepfer A., Dehlavi M., Fournier N., Safroneeva E., Straumann A., Pittet V., Peyrin-Biroulet L., Michetti P., Rogler G., Vavricka S., et al. Diagnostic delay in Crohn’s disease is associated with a complicated disease course and increased operation rate. Am. J. Gastroenterol. 2013;108:1744–1753. doi: 10.1038/ajg.2013.248. - DOI - PubMed
    1. Ruemmele F., Veres G., Kolho K., Griffiths A., Levine A., Escher J., Amil Dias J., Barabino A., Braegger C.P., Bronskyet J., et al. Consensus guidelines of ECCO/ESPGHAN on the medical management of pediatric Crohn’s disease. J. Crohns Colitis. 2014;8:1179–1207. doi: 10.1016/j.crohns.2014.04.005. - DOI - PubMed
    1. Levine A., Griffiths A., Markowitz J., Wilson D., Turner D., Russell R., Fell J., Ruemmele F.M., Walters T., Sherlock M., et al. Pediatric modification of the Montreal classification for inflammatory bowel disease: The Paris classification. Inflamm. Bowel. Dis. 2011;17:1314–1321. doi: 10.1002/ibd.21493. - DOI - PubMed