PREDICTIVE VALUE FOR CELIAC-DISEASE OF ANTIBODIES TO GLIADIN, ENDOMYSIUM, AND JEJUNUM IN PATIENTS ATTENDING FOR JEJUNAL BIOPSY

被引:121
作者
MCMILLAN, SA [1 ]
HAUGHTON, DJ [1 ]
BIGGART, JD [1 ]
EDGAR, JD [1 ]
PORTER, KG [1 ]
MCNEILL, TA [1 ]
机构
[1] QUEENS UNIV BELFAST,BELFAST BT7 1NN,ANTRIM,NORTH IRELAND
关键词
D O I
10.1136/bmj.303.6811.1163
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - To investigate the extent to which the detection of antibodies to gliadin, endomysium, and jejunum predicts the eventual diagnosis of coeliac disease according to the revised ESPGAN diagnostic criteria in a group of patients in whom there is a high suspicion of coeliac disease. Design - Clinical assessment and laboratory analysis of patients with suspected coeliac disease. Setting - Gastroenterology department of teaching hospital. Patients - 96 adults with suspected coeliac disease attending for jejunal biopsy. Main outcome measures - Diagnosis of coeliac disease with the revised criteria of the European Society of Paediatric Gastroenterology and Nutrition in patients with and without antibodies associated with coeliac disease. Results - 28 patients had a clinical diagnosis of coeliac disease, seven of other gastrointestinal diseases, and 12 of miscellaneous diseases; 49 had no diagnosis. Gliadin IgA detected by ELISA was found in all patients with coeliac disease and none of those without, giving a sensitivity, specificity, positive and negative predictive values, and predictive efficiency of 100% for diagnosing coeliac disease within the group. Endomysial IgA was found in 25 (89%) patients with coeliac disease and jejunal IgA in 21 (75%); neither IgA was found in patients without coeliac disease. Conclusion - Detection of gliadin IgA by ELISA and to a lesser extent the endomysial IgA should allow better selection of patients for jejunal biopsy and thus make diagnosing coeliac disease simpler and more efficient.
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页码:1163 / 1165
页数:3
相关论文
共 20 条
[1]   A NEW LABORATORY KIT FOR ANTIGLIADIN IGA AT DIAGNOSIS AND FOLLOW-UP OF CHILDHOOD CELIAC-DISEASE [J].
ASCHER, H ;
LANNER, A ;
KRISTIANSSON, B .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1990, 10 (04) :443-450
[2]   IGG, IGA AND IGE GLIADIN ANTIBODY DETERMINATIONS AS SCREENING-TEST FOR UNTREATED CELIAC-DISEASE IN CHILDREN, A MULTICENTER STUDY [J].
BURGINWOLFF, A ;
BERGER, R ;
GAZE, H ;
HUBER, H ;
LENTZE, MJ ;
NUSSLE, D .
EUROPEAN JOURNAL OF PEDIATRICS, 1989, 148 (06) :496-502
[3]   IGA ANTI-ENDOMYSIUM ANTIBODY - A NEW IMMUNOLOGICAL MARKER OF DERMATITIS-HERPETIFORMIS AND CELIAC-DISEASE [J].
CHORZELSKI, TP ;
BEUTNER, EH ;
SULEJ, J ;
TCHORZEWSKA, H ;
JABLONSKA, S ;
KUMAR, V ;
KAPUSCINSKA, A .
BRITISH JOURNAL OF DERMATOLOGY, 1984, 111 (04) :395-402
[4]  
DIAS J, 1987, LANCET, V2, P157
[5]   IGA ISOTYPING OF ANTIGLIADIN ANTIBODIES - A POSSIBLE CLUE FOR A LESS INVASIVE DIAGNOSIS OF CELIAC-DISEASE [J].
ELEWAUT, A ;
DACREMONT, G ;
ROBBERECHT, E ;
LEROY, J ;
DEBAETS, MH .
CLINICA CHIMICA ACTA, 1989, 183 (03) :285-294
[6]  
GALLEN RS, 1986, MANUAL CLIN LABORATO, P966
[7]   PRESENCE OF IGA AND IGG ANTIGLIADIN ANTIBODIES IN HEALTHY-ADULTS AS MEASURED BY MICRO-ELISA - EFFECT OF VARIOUS CUTOFF LEVELS ON SPECIFICITY AND SENSITIVITY WHEN DIAGNOSING CELIAC-DISEASE [J].
GRODZINSKY, E ;
HED, J ;
LIEDEN, G ;
SJOGREN, F ;
STROM, M .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1990, 92 (02) :119-123
[8]   DIAGNOSIS OF CELIAC-DISEASE - TIME FOR A CHANGE [J].
GUANDALINI, S ;
VENTURA, A ;
ANSALDI, N ;
GIUNTA, AM ;
GRECO, L ;
LAZZARI, R ;
MASTELLA, G ;
RUBINO, A .
ARCHIVES OF DISEASE IN CHILDHOOD, 1989, 64 (09) :1320-1324
[9]   COMPARISON OF IGA-CLASS RETICULIN AND ENDOMYSIUM ANTIBODIES IN CELIAC-DISEASE AND DERMATITIS-HERPETIFORMIS [J].
HALLSTROM, O .
GUT, 1989, 30 (09) :1225-1232
[10]  
KARPATI S, 1990, LANCET, P1335