Evaluation of Serum Calprotectin Levels in Patients with Inflammatory Bowel Disease.


Journal

The Kurume medical journal
ISSN: 1881-2090
Titre abrégé: Kurume Med J
Pays: Japan
ID NLM: 2985210R

Informations de publication

Date de publication:
15 Dec 2021
Historique:
pubmed: 26 10 2021
medline: 24 12 2021
entrez: 25 10 2021
Statut: ppublish

Résumé

Fecal calprotectin has been proposed as a useful biomarker of disease activity in inflammatory bowel disease (IBD). However, the role of calprotectin in systemic circulation is not well established. Thus, this study aimed to quantify serum calprotectin levels to identify a potential inflammatory marker for IBD. Ninety-eight patients with ulcerative colitis (UC) and 105 patients with Crohn's disease (CD) were prospectively enrolled and clinically scored. Ninety-two healthy, age-matched subjects served as controls. Blood samples from UC and CD patients and controls were analyzed for serum calprotectin levels and routine laboratory parameters. Disease activity was assessed by partial Mayo score and Harvey-Bradshaw index for UC and CD, respectively. Serum calprotectin levels were higher in CD and UC patients than in controls and were higher during active disease than during inactive disease in CD but not in UC. In UC, serum calprotectin levels were correlated with C-reactive protein (CRP) but not with other laboratory parameters or disease activity. In CD, serum calprotectin levels were positively correlated with disease activity, serum CRP, and platelet count. In UC and CD, serum calprotectin and CRP levels increased during the acute phase and decreased towards remission. Serum calprotectin is an inflammatory marker in IBD but might be more effective in evaluating patients with CD than those with UC. Further studies are needed to confirm these findings and to better determine the specific uses of serum calprotectin in routine practice.

Sections du résumé

BACKGROUND BACKGROUND
Fecal calprotectin has been proposed as a useful biomarker of disease activity in inflammatory bowel disease (IBD). However, the role of calprotectin in systemic circulation is not well established. Thus, this study aimed to quantify serum calprotectin levels to identify a potential inflammatory marker for IBD.
METHODS METHODS
Ninety-eight patients with ulcerative colitis (UC) and 105 patients with Crohn's disease (CD) were prospectively enrolled and clinically scored. Ninety-two healthy, age-matched subjects served as controls. Blood samples from UC and CD patients and controls were analyzed for serum calprotectin levels and routine laboratory parameters. Disease activity was assessed by partial Mayo score and Harvey-Bradshaw index for UC and CD, respectively.
RESULTS RESULTS
Serum calprotectin levels were higher in CD and UC patients than in controls and were higher during active disease than during inactive disease in CD but not in UC. In UC, serum calprotectin levels were correlated with C-reactive protein (CRP) but not with other laboratory parameters or disease activity. In CD, serum calprotectin levels were positively correlated with disease activity, serum CRP, and platelet count. In UC and CD, serum calprotectin and CRP levels increased during the acute phase and decreased towards remission.
CONCLUSIONS CONCLUSIONS
Serum calprotectin is an inflammatory marker in IBD but might be more effective in evaluating patients with CD than those with UC. Further studies are needed to confirm these findings and to better determine the specific uses of serum calprotectin in routine practice.

Identifiants

pubmed: 34690210
doi: 10.2739/kurumemedj.MS664009
doi:

Substances chimiques

Biomarkers 0
Leukocyte L1 Antigen Complex 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

209-215

Auteurs

Atsushi Mori (A)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Keiichi Mitsuyama (K)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.
Inflammatory Bowel Disease Center, Kurume University School of Medicine.

Ryosuke Sakemi (R)

Department of Gastroenterology, Tobata Kyoritsu Hospital.

Shinichiro Yoshioka (S)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Shuhei Fukunaga (S)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Kotaro Kuwaki (K)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Ryosuke Yamauchi (R)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Toshihiro Araki (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Tetsuhiro Yoshimura (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Hiroshi Yamasaki (H)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Kozo Tsuruta (K)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Taku Morita (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Sayo Yamasaki (S)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Osamu Tsuruta (O)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

Takuji Torimura (T)

Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine.

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Classifications MeSH