Prevalence of celiac disease in adult patients with refractory functional dyspepsia: value of routine duodenal biopsy

被引:27
作者
Giangreco, Emiliano [1 ]
D'agate, Cinzia [1 ]
Barbera, Carmelo [1 ]
Puzzo, Lidia [1 ]
Aprile, Giuseppe [1 ]
Naso, Pietro [1 ]
Bonanno, Giacomo [1 ]
Russo, Francesco Paolo [2 ]
Nicoletti, Alessandra [1 ]
Incarbone, Salvatore [1 ]
Trama, Giuseppe [1 ]
Russo, Antonio [1 ]
机构
[1] Univ Catania, Dept Surg, Gastroenterol & Endoscopy Unit, I-95125 Catania, Italy
[2] Univ Padua, Dept Surg & Gastroenterol Sci, Gastroenterol Sect, I-35100 Padua, Italy
关键词
Celiac disease; Endoscopy; Biopsy; Functional; Dyspepsia;
D O I
10.3748/wjg.14.6948
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the prevalence of celiac disease (CD) in adult patients referred to an open access gastroenterology clinic in the south of Italy and submitted to esophago-gastro-duodenoscopy (EGD) for evaluation of refractory functional dyspepsia. METHODS: Seven hundred and twenty six consecutive dyspeptic patients (282 male, 444 female; mean age 39.6 years, range 18-75 years) with unexplained prolonged dyspepsia were prospectively enrolled. Duodenal biopsies were taken and processed by standard staining. Histological evaluation was carried out according to the Marsh-Oberhuber criteria. RESULTS: The endoscopic findings were: normal in 61.2%, peptic lesions in 20.5%, malignancies in 0.5%, miscellaneous in 16.7%. CD was endoscopically diagnosed in 8 patients (1.1%), histologically in 15 patients (2%). The endoscopic features alone showed a sensitivity of 34.8% and specificity of 100%, with a positive predictive value (PPV) of 100% and a negative predictive value (NPP) of 97.9%. CONCLUSION: This prospective study showed that CD has a high prevalence (1:48) in adult dyspeptic patients and suggests the routine use of duodenal biopsy in this type of patient undergoing EGD. (C) 2008 The WIG Press. All rights reserved.
引用
收藏
页码:6948 / 6953
页数:6
相关论文
共 53 条
[1]
[Anonymous], 2004, NIH CONS DEV C CEL D
[2]
How good is zoom endoscopy for assessment of villous atrophy in coeliac disease? [J].
Badreldin, R ;
Barrett, P ;
Wooff, DA ;
Mansfield, J ;
Yiannakou, Y .
ENDOSCOPY, 2005, 37 (10) :994-998
[3]
Reevaluation of duodenal endoscopic markers in the diagnosis of celiac disease [J].
Bardella, MT ;
Minoli, G ;
Radaelli, F ;
Quatrini, M ;
Bianchi, PA ;
Conte, D .
GASTROINTESTINAL ENDOSCOPY, 2000, 51 (06) :714-716
[4]
Increased prevalence of celiac disease in patients with dyspepsia [J].
Bardella, MT ;
Minoli, G ;
Ravizza, D ;
Radaelli, F ;
Velio, P ;
Quatrini, M ;
Bianchi, PA ;
Conte, D .
ARCHIVES OF INTERNAL MEDICINE, 2000, 160 (10) :1489-1491
[5]
Coeliac disease in primary care: Evaluation of a case-finding strategy [J].
Berti, I. ;
Della Vedova, R. ;
Paduano, R. ;
Devetta, M. ;
Caradonna, M. ;
Villanacci, V. ;
Not, T. ;
Martelossi, S. ;
Tamburlini, G. ;
Ventura, A. .
DIGESTIVE AND LIVER DISEASE, 2006, 38 (07) :461-467
[6]
The clinical pattern of subclinical silent celiac disease: An analysis on 1026 consecutive cases [J].
Bottaro, G ;
Cataldo, F ;
Rotolo, N ;
Spina, M ;
Corazza, GR .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 1999, 94 (03) :691-696
[7]
Routine duodenal biopsies: is it time to change our minds? [J].
Brocchi, E ;
Bonora, M ;
Epifanio, G ;
Tomassetti, P ;
Biasco, G ;
Corinaldesi, R .
GASTROINTESTINAL ENDOSCOPY, 2004, 59 (02) :331-332
[8]
Endoscopic markers in adult coeliac disease [J].
Brocchi, E ;
Tomassetti, P ;
Misitano, B ;
Epifanio, G ;
Corinaldesi, R ;
Bonvicini, F ;
Gasbarrini, G ;
Corazza, G .
DIGESTIVE AND LIVER DISEASE, 2002, 34 (03) :177-182
[9]
No more biopsy in the diagnostic work-up of celiac disease [J].
Cammarota, G ;
Gasbarrini, A ;
Gasbarrini, G .
GASTROINTESTINAL ENDOSCOPY, 2005, 62 (01) :119-121
[10]
CELIAC-DISEASE IN THE YEAR 2000 - EXPLORING THE ICEBERG [J].
CATASSI, C ;
RATSCH, IM ;
FABIANI, E ;
ROSSINI, M ;
BORDICCHIA, F ;
CANDELA, F ;
COPPA, GV ;
GIORGI, PL .
LANCET, 1994, 343 (8891) :200-203