Objectives: Positivity of both immumoglobulin A anti-tissue transglutaminase (TTG) and anti-endomysium antibodies (EMA) has a positive predictive value of nearly 100% for celiac disease (CD). The objective of the present study was to evaluate whether patients of any age, with high pretest probability of CD and high titre of anti-TTG and EMA positivity, have a high probability of intestinal damage and may not require the biopsy for final diagnosis.
Methods: A retrospective analysis of 412 consecutively referred patients, age range 10 months to 72 years, who underwent small-bowel biopsy for suspicion of CD and positivity to both anti-TTG and EMA, was performed at 4 Italian centers. Biopsies were evaluated independently by 2 pathologists using Marsh modified classification; in cases of dissimilar results, a third pathologist examined the biopsy. The final histological finding diagnosis was expressed as the prevalent or highest score assigned by the pathologist board.
Results: Three hundred ninety-six patients (96.1%) had histological findings consistent with CD (grade 2 and 3a, 3b, or 3c of modified Marsh classification). An anti-TTG ratio ≥7 was able to identify with the 3 assays used (Celikey, anti-TTG immumoglobulin A, EuTTG) all of the patients with significant mucosal damage (Marsh ≥2) independent of age and sex; specificity and positive predictive value were 100%. An anti-TTG ratio >20 was more specific (99.8%) for identification of patients with villous atrophy (Marsh 3 a, b, or c).
Conclusions: Patients with positivity of anti-TTG ≥7-fold cutoff, confirmed by positivity to EMA, have a high-degree probability of duodenal damage. In selected conditions, a duodenal biopsy may be avoided and a confirmed greatly positive anti-TTG result could be the basis to prescribe a gluten-free diet.
*Department of Laboratory Medicine, Biochemistry Laboratory, Riuniti Hospital, Bergamo
†Immunopathology and Allergology Unit, S. Maria della Misericordia Hospital, Udine
‡Department of Clinical Pathology, Buccheri La Ferla Hospital, Palermo
§Microbiology and Virology Laboratory, San Carlo Hospital, Milan
||Department of Laboratory Medicine, Pathological Anatomy, Riuniti Hospital, Bergamo
¶Department of Human Pathology, University of Palermo, Palermo
#Pathological Anatomy and Histology, San Carlo Hospital, Milan
**Pathological Anatomy, Santa Maria degli Angeli Hospital
††Departement of Laboratory Medicine, Allergy and Clinical Immunology, S. Maria degli Angeli Hospital, Pordenone, Italy.
Address correspondence and reprint requests to Maria G. Alessio, Largo Barozzi, 1 I-24123 Bergamo, Italy (e-mail: email@example.com).
Received 1 March, 2011
Accepted 16 December, 2011
The authors report no conflicts of interest.