Fecal calprotectin concentration is increased in children with celiac disease: relation with histopathological findings

被引:32
作者
Balamtekin, Necati [1 ]
Baysoy, Gokhan [3 ]
Uslu, Nuray [3 ]
Orhan, Diclehan [2 ]
Akcoren, Zuhal [3 ]
Ozen, Hasan [3 ]
Gurakan, Figen [3 ]
Saltik-Temizel, Inci Nur [3 ]
Yuce, Aysel [3 ]
机构
[1] GATA, Dept Pediat Gastroenterol Hepatol & Nutr, Ankara, Turkey
[2] Hacettepe Univ, Sch Med, Dept Pathol, Ankara, Turkey
[3] Hacettepe Univ, Sch Med, Dept Pediat Gastroenterol Hepatol & Nutr, Ankara, Turkey
关键词
Celiac disease; children; fecal calprotectin; INFLAMMATORY-BOWEL-DISEASE; BLOOD LEUKOCYTES; CROHNS-DISEASE; NEUTROPHIL; DIAGNOSIS; MARKER; CRP;
D O I
10.4318/tjg.2012.0366
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/aims: The aim of this study was to compare the fecal calprotectin concentration in children with newly diagnosed celiac disease, children with celiac disease strictly adhering to a gluten-free diet and healthy controls. We also tried to correlate the fecal calprotectin concentration with the clinical presentation, degree of neutrophilic infiltration and the severity of histopathological injury (Marsh grade) in the small bowel mucosa. Material and Methods: The study included three groups: children with untreated celiac disease, children with treated celiac disease, and healthy controls. Moreover, we obtained a second fecal sample from nine newly diagnosed children when their endomysial antibody became negative after gluten-free diet. Results: Fecal calprotectin concentrations were significantly higher in newly diagnosed celiac patients (n=31) compared to patients on gluten-free diet (n=33) and healthy controls (n=34) (117.2 yg/g (3.2-306) vs. 3.7 mu g/g (0.5-58.2) and 9.6 mu g/g (1-70), respectively, p<0.001). Patients presenting with gastrointestinal symptoms had higher fecal calprotectin concentration compared to the patients presenting with non-gastrointestinal symptoms [142.8 (12.2-306) vs. 79.7 (3.2-243.2) respectively, p=0.04]. Nine newly diagnosed patients gave a second fecal sample after starting gluten-free diet when endomysial antibody became negative. Their fecal calprotectin concentration had decreased from 113.7 mu g/g (8.7-295.2) to 4.2, mu g/g (0.5-20.7) (p<0.01). Conclusions: Increased fecal calprotectin concentration can be used as a non-invasive marker that might aid in the diagnosis of celiac disease, especially in patients with gastrointestinal presentation. Fecal calprotectin concentration returns to normal on a strict gluten-free diet. Fecal calprotectin may be used as a marker of diet adherence and improvement in gastrointestinal inflammation in children with celiac disease. Additionally, it may be used for the differentiation of celiac disease from functional disorders of the gastrointestinal system.
引用
收藏
页码:503 / 508
页数:6
相关论文
共 27 条
[1]   Faecal calprotectin: a marker of inflammation throughout the intestinal tract [J].
Aadland, E ;
Fagerhol, MK .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2002, 14 (08) :823-825
[2]   Fecal Calprotectin Levels and Serological Responses to Microbial Antigens Among Children and Adolescents with Inflammatory Bowel Disease [J].
Ashorn, Sara ;
Honkanen, Teemu ;
Kolho, Kaija-Leena ;
Ashorn, Merja ;
Vaelineva, Tuuli ;
Wei, Bo ;
Braun, Jonathan ;
Rantala, Immo ;
Luukkaala, Tiina ;
Iltanen, Sari .
INFLAMMATORY BOWEL DISEASES, 2009, 15 (02) :199-205
[3]   Faecal calprotectin in children with chronic gastrointestinal symptoms [J].
Bremner, A ;
Roked, S ;
Robinson, R ;
Phillips, I ;
Beattie, M .
ACTA PAEDIATRICA, 2005, 94 (12) :1855-1858
[4]   Faecal calprotectin as reliable non-invasive marker to assess the severity of mucosal inflammation in children with inflammatory bowel disease [J].
Canani, R. Berni ;
Terrin, G. ;
Rapacciuolo, L. ;
Miele, E. ;
Siani, M. C. ;
Puzone, C. ;
Cosenza, L. ;
Staiano, A. ;
Troncone, R. .
DIGESTIVE AND LIVER DISEASE, 2008, 40 (07) :547-553
[5]   Diagnostic value of faecal calprotectin in paediatric gastroenterology clinical practice [J].
Canani, RB ;
Rapacciuolo, L ;
Romano, MT ;
de Horatio, LT ;
Terrin, G ;
Manguso, F ;
Cirillo, P ;
Paparo, F ;
Troncone, R .
DIGESTIVE AND LIVER DISEASE, 2004, 36 (07) :467-470
[6]   Validation and clinical significance of a new calprotectin rapid test for the diagnosis of gastrointestinal diseases [J].
Damms, A. ;
Bischoff, S. C. .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2008, 23 (10) :985-992
[7]   MORPHOMETRIC ANALYSIS OF SMALL INTESTINAL-MUCOSA .2. DETERMINATION OF LAMINA PROPRIA VOLUMES - PLASMA-CELL AND NEUTROPHIL POPULATIONS WITHIN CONTROL AND CELIAC-DISEASE MUCOSAE [J].
DHESI, I ;
MARSH, MN ;
KELLY, C ;
CROWE, P .
VIRCHOWS ARCHIV A-PATHOLOGICAL ANATOMY AND HISTOPATHOLOGY, 1984, 403 (02) :173-180
[8]   Classification and grading of gastritis - The updated Sydney System [J].
Dixon, MF ;
Genta, RM ;
Yardley, JH ;
Correa, P ;
Batts, KP ;
Dahms, BB ;
Filipe, MI ;
Haggitt, RC ;
Haot, J ;
Hui, PK ;
Lechago, J ;
Lewin, K ;
Offerhaus, JA ;
Price, AB ;
Riddell, RH ;
Sipponen, P ;
Solcia, E ;
Watanabe, H .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (10) :1161-1181
[9]  
Ertekin V, 2010, J CLIN GASTROENTEROL, V44, P544, DOI [10.1097/MCG.0b013e3181cadbco, 10.1097/MCG.0b013e3181cadbc0]
[10]   Fecal Calprotectin and Lactoferrin for the Prediction of Inflammatory Bowel Disease Relapse [J].
Gisbert, Javier P. ;
Bermejo, Fernando ;
Perez-Calle, Jose-Lazaro ;
Taxonera, Carlos ;
Vera, Isabel ;
McNicholl, Adrian G. ;
Algaba, Alicia ;
Lopez, Pilar ;
Lopez-Palacios, Natalia ;
Calvo, Marta ;
Gonzalez-Lama, Yago ;
Carneros, Jose-Antonio ;
Velasco, Marta ;
Mate, Jose .
INFLAMMATORY BOWEL DISEASES, 2009, 15 (08) :1190-1198