Within-Stool and Within-Day Sample Variability of Fecal Calprotectin in Patients With Inflammatory Bowel Disease A Prospective Observational Study

被引:28
作者
Du, Lillian [1 ]
Foshaug, Rae [1 ]
Huang, Vivian W. [1 ]
Kroeker, Karen I. [1 ]
Dieleman, Levinus A. [1 ]
Halloran, Brendan P. [1 ]
Wong, Karen [1 ]
Fedorak, Richard N. [1 ]
机构
[1] Univ Alberta, Div Gastroenterol, Edmonton, AB, Canada
关键词
inflammatory bowel disease (IBD); fecal calprotectin (FC); stool biomarker; ACTIVE ULCERATIVE-COLITIS; QUALITY-OF-LIFE; COLONOSCOPIC PERFORATIONS; CROHNS-DISEASE; INTRAINDIVIDUAL VARIABILITY; INTESTINAL INFLAMMATION; CLINICAL UTILITY; DEEP REMISSION; LACTOFERRIN; MANAGEMENT;
D O I
10.1097/MCG.0000000000000776
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Goals: The use of fecal calprotectin (FC) as a stool biomarker for differentiating inflammatory bowel disease (IBD) from IBS has been well validated, and there is a strong correlation between FC and the presence of endoscopic inflammatory lesions. However, recent studies have demonstrated intraindividual sample variability in patients with IBD, possibly limiting the reliability of using a single sample for monitoring disease activity. Our aim was to assess the within-stool and within-day sample variability of FC concentrations in patients with IBD. Study: We examined a cross-sectional cohort of 50 adult IBD patients. Eligible patients were instructed to collect 3 samples from different parts of the stool from their first bowel movement of the day and 3 samples from each of up to 2 additional bowel movements within 24 hours. FC concentrations were measured by a rapid, quantitative point-of-care test using lateral flow technology (Quantum Blue). Descriptive statistics were used to assess FC variability within a single bowel movement and between different movements at different FC positivity cutoffs. Results: Within a single bowel movement, there was clinically significant sample variability ranging from 8% to 23% depending on the time of the day or on the FC positivity cutoff value. Between bowel movements, there was clinically significant sample variability ranging from 13% to 26% depending on the FC positivity cutoff. Conclusions: Considering a single FC sample, the first sample of the day with an FC positivity cutoff of 250 mu g/g provided the most reliable indication of disease activity.
引用
收藏
页码:235 / 240
页数:6
相关论文
共 45 条
[1]   Fecal Markers: Calprotectin and Lactoferrin [J].
Abraham, Bincy P. ;
Kane, Sunanda .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2012, 41 (02) :483-+
[2]   Fecal calprotectin use in inflammatory bowel disease and beyond: A mini-review [J].
Alibrahim, Bashaar ;
Aljasser, Mohammed I. ;
Salh, Baljinder .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2015, 29 (03) :157-163
[3]   Colonoscopic perforations [J].
Araghizadeh, FY ;
Timmcke, AE ;
Opelka, FG ;
Hicks, TC ;
Beck, DE .
DISEASES OF THE COLON & RECTUM, 2001, 44 (05) :713-716
[4]   Clinicians' guide to the use of fecal calprotectin to identify and monitor disease activity in inflammatory bowel disease [J].
Bressler, Brian ;
Panaccione, Remo ;
Fedorak, Richard N. ;
Seidman, Ernest G. .
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2015, 29 (07) :369-372
[5]  
Buhlmann, AB IBDOC SIT
[6]   Monitoring of Therapy for Inflammatory Bowel Disease [J].
Burri, Emanuel ;
Beglinger, Christoph ;
Lehmann, Frank Serge .
DIGESTION, 2012, 86 :1-5
[7]   High Within-day Variability of Fecal Calprotectin Levels in Patients with Active Ulcerative Colitis: What Is the Best Timing for Stool Sampling? [J].
Calafat, Margalida ;
Cabre, Eduard ;
Manosa, Miriam ;
Lobaton, Triana ;
Marin, Laura ;
Domenech, Eugeni .
INFLAMMATORY BOWEL DISEASES, 2015, 21 (05) :1072-1076
[8]  
Cobb WS, 2004, AM SURGEON, V70, P750
[9]   Epidemiology and Natural History of Inflammatory Bowel Diseases [J].
Cosnes, Jacques ;
Gower-Rousseau, Corinne ;
Seksik, Philippe ;
Cortot, Antoine .
GASTROENTEROLOGY, 2011, 140 (06) :1785-U118
[10]   Role of faecal calprotectin as non-invasive marker of intestinal inflammation [J].
Costa, F ;
Mumolo, MG ;
Bellini, M ;
Romano, MR ;
Ceccarelli, L ;
Arpe, P ;
Sterpi, C ;
Marchi, S ;
Maltinti, G .
DIGESTIVE AND LIVER DISEASE, 2003, 35 (09) :642-647