Serum leucine‐rich alpha‐2 glycoprotein and calprotectin in children with inflammatory bowel disease: A multicenter study in Japan

Author:

Yasuda Ryosuke1,Arai Katsuhiro2ORCID,Kudo Takahiro3ORCID,Nambu Ryusuke4ORCID,Aomatsu Tomoki5,Abe Naoki6,Kakiuchi Toshihiko7ORCID,Hashimoto Kunio8,Sogo Tsuyoshi9,Takahashi Michiko10,Etani Yuri11,Kato Ken1,Yamashita Yushiro1,Mitsuyama Keiichi1213,Mizuochi Tatsuki1ORCID

Affiliation:

1. Department of Pediatrics and Child Health Kurume University School of Medicine Kurume Japan

2. Division of Gastroenterology National Center for Child Health and Development Tokyo Japan

3. Department of Pediatrics Juntendo University Faculty of Medicine Tokyo Japan

4. Division of Gastroenterology and Hepatology Saitama Children's Medical Center Saitama Japan

5. Department of Pediatrics Osaka Medical and Pharmaceutical University Takatsuki Japan

6. Department of Infection and Immunology Aichi Children's Health and Medical Center Ohfu Japan

7. Department of Pediatrics, Faculty of Medicine Saga University Saga Japan

8. Department of Pediatrics Nagasaki University Graduate School of Biomedical Sciences Nagasaki Japan

9. Department of Pediatric Hepatology and Gastroenterology Saiseikai Yokohamashi Tobu Hospital Yokohama Japan

10. Department of Pediatrics Sapporo Kosei General Hospital Sapporo Japan

11. Department of Gastroenterology and Endocrinology Osaka Women's and Children's Hospital Osaka Japan

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

13. Inflammatory Bowel Disease Center, Department of Gastroenterology St. Mary's Hospital Kurume Japan

Abstract

AbstractBackground and AimSerum leucine‐rich alpha‐2 glycoprotein (LRG) and calprotectin have been studied as disease activity markers in adults with inflammatory bowel disease (IBD). We evaluated them in pediatric IBD patients.MethodsSubjects under 17 years old undergoing care at 11 Japanese pediatric centers were retrospectively assigned to 3 groups representing Crohn's disease (CD), ulcerative colitis (UC), and normal controls (NC) with irritable bowel syndrome or no illness. Serum LRG and calprotectin were measured using commercial enzyme‐linked immunosorbent assay kits.ResultsWe enrolled 173 subjects, including 74 with CD, 77 with UC, and 22 NC. Serum LRG concentrations in active CD (median, 200 μg/mL) were significantly greater than in remission (81 μg/mL; P < 0.001) or NC (69 μg/mL; P < 0.001). Serum calprotectin concentrations in active CD (2941 ng/mL) also were significantly greater than in remission (962 ng/mL; P < 0.05) or NC (872 ng/mL; P < 0.05). Serum LRG concentrations in active UC (134 μg/mL) were significantly greater than in remission (65 μg/mL; P < 0.01) but not significantly greater than in NC (69 μg/mL); serum calprotectin concentrations in active UC (1058 ng/mL) were not significantly different from those in remission (671 ng/mL) or NC (872 ng/mL). In receiver operating characteristic analyses of LRG, calprotectin, C‐reactive protein, and erythrocyte sedimentation rate for ability to distinguish active IBD from remission, CD and UC showed areas under receiver operating characteristic curves for LRG (0.77 and 0.70, respectively), exceeding those for calprotectin, C‐reactive protein, or erythrocyte sedimentation rate.ConclusionsIn pediatric IBD, serum LRG may better reflect disease activity than serum calprotectin, particularly in CD.

Publisher

Wiley

Subject

Gastroenterology,Hepatology

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