Prediction of intestinal histological lesions in paediatric patients with coeliac disease

被引:0
作者
Sierra Salinas, C. [1 ]
Blasco Alonso, J. [1 ]
Navas Lopez, V. M. [1 ]
Vicioso, M. I. [2 ]
Serrano Nieto, J. [1 ]
Weil Lara, B. [3 ]
Alfageme Perez de las Vacas, D. [1 ]
Barco Galvez, A. [1 ]
机构
[1] Hosp Maternoinfantil Carlos Haya, Unidad Gastroenterol Hepatol & Nutr Infantil, Malaga, Spain
[2] Hosp Maternoinfantil Carlos Haya, Serv Lab Clin Pediat, Malaga, Spain
[3] Hosp Maternoinfantil Carlos Haya, Serv Anat Patol, Malaga, Spain
来源
ANALES DE PEDIATRIA | 2011年 / 74卷 / 04期
关键词
Coeliac disease; Tissue transglutaminase; Antiendomysial; Intestinal biopsy; TISSUE TRANSGLUTAMINASE; PREVALENCE; ANTIBODIES; DIAGNOSIS; CHILDREN;
D O I
10.1016/j.anpedi.2010.09.025
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Introduction: Serological markers are of great interest in coeliac disease (CD), although intestinal biopsy is still the gold standard for establishing the diagnosis. Tissue transglutaminase IgA antibodies (AATGt-IgA) and antiendomysial antibodies IgA (AAE-IgA) are closely correlated to intestinal damage observed in biopsies. Villous atrophy (Marsh 3) plays a major role in CD diagnosis. Marsh 2 stage (crypt hyperplasia) as a CD marker is still under debate. Objective: To ascertain an AATGt-IgA level that corresponds to a positive predictive value (PPV) of 100% for a histological CD diagnosis. Material and methods: A series of 120 patients younger than 14 years, non-IgA deficient, who underwent an intestinal biopsy and were positive for both serological markers (AATGt-IgA and AAE-IgA). For AATGt-IgA, according to the manufacturer's recommendations, a value greater than 161U/mL is considered as a positive value. The PPV of AATGt was determined for different cut-off points. Results: The histological findings distribution is directly correlated to the AATGt-IgA cut-off point. When the cut-off point is set above 7.5-10.6 times the commercial reference value, there is a 2.1% of Marsh 2 lessions and 93.4% of Marsh 3; above 10.6 times the reference value, all biopsies where Marsh 3 (100%). The PPV that considers Marsh 3 is (93.4%). The PPV, for considering Marsh 3 is low (55%) when AATGt-IgA serology is positive with levels between 16 and 67 IU/ml (1-4.2 times the cut-off point) and a higher value (92%) for concentrations between 68 and 118 IU/ml (4.3-7.4 times) and for cases with 69-170 IU/ml (7.5-10.6 times); above 170 IU/ml (> 10.6 times) PPV is 100%. Conclusion: The use of values higher than the recommended cut-off point must logically improve specificity and PPV. In 31.6% patients positive for AATGt-IgA and AAE-IgA (38/120) it would have been possible to diagnose the disease without intestinal biopsy as of the PPV was 100%. It is not possible to standardise results as there are different commercial kits with variable cut-off points, so we must be cautious when setting recommendations based on AATGt-IgA. (C) 2010 Asociacion Espanola de Pediatria. Published by Elsevier Espana, S.L. All rights reserved.
引用
收藏
页码:226 / 231
页数:6
相关论文
共 22 条
[1]   Can tissue transglutaminase antibody titers replace small-bowel biopsy to diagnose celiac disease in select pediatric populations? [J].
Barker, CC ;
Mitton, C ;
Jevon, G ;
Mock, T .
PEDIATRICS, 2005, 115 (05) :1341-1346
[2]   Prospective population screening for Celiac disease:: High prevalence in the first 3 years of life [J].
Castaño, L ;
Blarduni, E ;
Ortiz, L ;
Núñez, J ;
Bilbao, JR ;
Rica, I ;
Martul, P ;
Vitoria, JC .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2004, 39 (01) :80-84
[3]   Detection of celiac disease in primary care: A multicenter case-finding study in north america [J].
Catassi, Carlo ;
Kryszak, Deborah ;
Louis-Jacques, Otto ;
Duerksen, Donald R. ;
Hill, Ivor ;
Crowe, Sheila E. ;
Brown, Andrew R. ;
Procaccini, Nicholas J. ;
Wonderly, Brigid A. ;
Hartley, Paul ;
Moreci, James ;
Bennett, Nathan ;
Horvath, Karoly ;
Burk, Margaret ;
Fasano, Alessio .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (07) :1454-1460
[4]   Celiac Disease Diagnosis: Simple Rules Are Better Than Complicated Algorithms [J].
Catassi, Carlo ;
Fasano, Alessio .
AMERICAN JOURNAL OF MEDICINE, 2010, 123 (08) :691-693
[5]  
Coeliac Disease, 2009, COEL DIS REC ASS COE
[6]   Clinical value of immunoglobulin A antitransglutaminase assay in the diagnosis of celiac disease [J].
Diamanti, Antonella ;
Colistro, Franco ;
Calce, Angelica ;
Devito, Rita ;
Ferretti, Francesca ;
Minozzi, Antonio ;
Santoni, Alexandra ;
Castro, Massimo .
PEDIATRICS, 2006, 118 (06) :E1696-E1700
[7]   Correlation of duodenal histology with tissue transglutaminase and endomysial antibody levels in pediatric celiac disease [J].
Donaldson, Matthew R. ;
Firth, Sean D. ;
Wimpee, Holly ;
Leiferman, Kristin M. ;
Zone, John J. ;
Horsley, Wyatt ;
O'Gorman, Molly A. ;
Jackson, W. Daniel ;
Neuhausen, Susan L. ;
Hull, Christopher M. ;
Book, Linda S. .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2007, 5 (05) :567-573
[8]   Guideline for the diagnosis and treatment of celiac disease in children: Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition [J].
Hill, ID ;
Dirks, MH ;
Liptak, GS ;
Colletti, RB ;
Fasano, A ;
Guandalini, S ;
Hoffenberg, EJ ;
Horvath, K ;
Murray, JA ;
Pivor, M ;
Seidman, EG .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2005, 40 (01) :1-19
[9]   A prospective study of the incidence of childhood celiac disease [J].
Hoffenberg, EJ ;
MacKenzie, T ;
Barriga, KJ ;
Eisenbarth, GS ;
Bao, F ;
Haas, JE ;
Erlich, H ;
Bugawan, TL ;
Sokol, RJ ;
Taki, I ;
Norris, JM ;
Rewers, M .
JOURNAL OF PEDIATRICS, 2003, 143 (03) :308-314
[10]   Diagnosing Mild Enteropathy Celiac Disease: A Randomized, Controlled Clinical Study [J].
Kurppa, Kalle ;
Collin, Pekka ;
Viljamaa, Mervi ;
Haimila, Katri ;
Saavalainen, Paivi ;
Partanen, Jukka ;
Laurila, Kaija ;
Huhtala, Heini ;
Paasikivi, Kaija ;
Maki, Markku ;
Kaukinen, Katri .
GASTROENTEROLOGY, 2009, 136 (03) :816-823