Elevated plasma cryofibrinogen in patients with active inflammatory bowel disease is morbigenous

• Published in: World journal of gastroenterology : WJG Vol. 12; no. 10; pp. 1621 - 1625
• Main Authors: Sawada, Koji, Takahashi, Ryouki, Saniabadi, Abbi R, Ohdo, Maiko, Shimoyama, Takashi
• Format: Journal Article
• Language: English
• Published: United States Department of Gastroenterology,Fujimoto, Hospital Medicine, Osaka and Department of Gastroenterology, Hyogo College of Medicine, Nishinomiya,Japan%Wakamoto Pharmaceuticals, Sagami Laboratory, Kanagawa, Japan%Japan Immunoresearch Laboratories.Takasaki, Japan%Department of Gastroenterology, Hyogo College of Medicine, Nishinomiya, Japan 14.03.2006; Baishideng Publishing Group Co., Limited
• Subjects: Adolescent; Adult; Antibodies - blood; Biomarkers - blood; Blood Sedimentation; C-Reactive Protein - metabolism; Chronic Disease; Cryoglobulins - metabolism; Female; Fibrinogen - metabolism; Fibrinogens, Abnormal - metabolism; Humans; Inflammatory Bowel Diseases - blood; Inflammatory Bowel Diseases - physiopathology; Male; Middle Aged; Rapid Communication; Trypsin Inhibitors - blood; 冷纤维蛋白原; 疾病炎症; 等离子体; 药物抗体; Inflammatory bowel disease; Acute colitis; Cryofibrinogen; Trypsin inhibitor; Trypsin inhibitor antibody
• DOI: 10.3748/wjg.v12.i10.1621
• ISSN: 1007-9327

AIM： To investigate the role of cryofibrinogen （CF） in active inflammatory bowel disease （IBD）. METHODS： CF was assayed in 284 subjects： 61 with active and 63 with inactive ulcerative colitis （UC）, 45 who had proctocolectomy, 35 with active and 20 with inactive Crohn＇s disease （CD）, 40 with other diseases and 20 healthy controls. Trypsin inhibitor （TI） and TI antibody （TI-Ab） were measured in plasma and CF complex by ELISA. RESULTS： CF in active UC was strikingly high compared with all other groups （x^2〈0.001）. Similarly, CF was significantly higher in active CD than in inactive CD or in controls （x^2〈0.01）. In UC, high CF and TI-Ab were associated with the need for operations. Further, high CF, CF/fibrinogen ratio, low TI and high TI-Ab in plasma were associated with disease activity or refractoriness to medication. Elevated CF was not associated with acute reactants like C-reactive protein and white blood cell counts except for erythrocyte sedimentation rate, suggesting that elevated CF was not a consequence of acute inflammation. CONCLUSION： Elevated CF in active IBD appears to be morbigenous. CF promotes IBD via two main mechanisms, quenching of TI （an anti-inflammatory substance） and impairing microvascular perfusion by forming protein aggregates. CF may also serve as a biomarker of chronic IBD. Additional studies are warranted to fully evaluate the role of CF in IBD and the outcome should contribute to a better understanding of the pathogenesis of IBD.