Enterocyte actin autoantibody detection: a new diagnostic tool in celiac disease diagnosis: results of a multicenter study

Am J Gastroenterol. 2004 Aug;99(8):1551-6. doi: 10.1111/j.1572-0241.2004.30296.x.

Abstract

Objectives: This study describes a new method to detect autoantibodies against actin filaments (AAA) as a serological marker of intestinal villous atrophy (IVA) in celiac disease (CD), and reports the results of an Italian double-blind multicenter study.

Methods: IgA-AAA were analyzed by immunofluorescence using a newly developed method based on intestinal epithelial cells cultured in presence of colchicine. IgA-AAA were blindly evaluated prospectively in 223 antiendomysial antibody (AEA) and/or antitransglutaminase antibody (TGA) positive subjects and in 78 AEA and TGA negative subjects. IgA-AAA positive patients underwent an intestinal biopsy to confirm the diagnosis. Moreover, IgA-AAA were retrospectively investigated in 84 biopsy-proven CD patients and in 2,000 new consecutively collected serum samples from AEA and TGA negative nonbiopsied subjects.

Results: IgA-AAA were positive in 98.2% of the CD patients with flat mucosa, in 89% with subtotal villous atrophy, and in 30% with partial villous atrophy. IgA-AAA were present in none of the AEA and TGA negative nonbiopsied controls. In AEA and/or TGA positive CD patients IgA-AAA positivity significantly correlated with IVA (p < 0.000 in the prospective study, p = 0.005 in the retrospective study). In the prospective study, the values of sensitivity, specificity, the positive predictive value, the negative predictive value, and the efficiency of the IgA-AAA test to identify patients with IVA were, respectively, 83.9%, 95.1%, 97.8%, 69.2%, and 87.0%. Furthermore, a significant correlation (p < 0.0001) was found between the IgA-AAA serum titre and the degree of IVA (rs 0.56).

Conclusions: The results of this multicenter study show that the new method for IgA-AAA detection could represent a practical diagnostic tool in AEA and/or TGA positive subjects, which would be especially useful when IVA shows a patchy distribution, when the histological picture is difficult to interpret, or when a biopsy could represent a life-threatening risk.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / immunology*
  • Actins / metabolism
  • Adolescent
  • Adult
  • Aged
  • Autoantibodies / blood*
  • Biomarkers / blood
  • Biopsy
  • Celiac Disease / diagnosis*
  • Celiac Disease / pathology
  • Cells, Cultured
  • Child
  • Child, Preschool
  • Double-Blind Method
  • Enterocytes / metabolism*
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Immunoglobulin A / blood
  • Infant
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Middle Aged
  • Predictive Value of Tests
  • Prospective Studies
  • Retrospective Studies
  • Sensitivity and Specificity
  • Transglutaminases / immunology

Substances

  • Actins
  • Autoantibodies
  • Biomarkers
  • Immunoglobulin A
  • Transglutaminases