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Clinical Chemistry 53: 2186-2192, 2007. First published September 27, 2007; 10.1373/clinchem.2006.081364
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(Clinical Chemistry. 2007;53:2186-2192.)
© 2007 American Association for Clinical Chemistry, Inc.


Clinical Immunology

Antibodies against Synthetic Deamidated Gliadin Peptides as Predictors of Celiac Disease: Prospective Assessment in an Adult Population with a High Pretest Probability of Disease

Sonia Niveloni1, Emilia Sugai1, Ana Cabanne1, Horacio Vazquez1, Julio Argonz1, Edgardo Smecuol1, María L. Moreno1, Fabio Nachman1, Roberto Mazure1, Zulema Kogan2, Juan C. Gomez3, Eduardo Mauriño1 and Julio C. Bai1,a

1 Department of Medicine, Hospital de Gastroenterología "Dr. Carlos Bonorino Udaondo", Buenos Aires, Argentina.
2 Pathology Service, Department of Medicine, Hospital de Gastroenterologiá, "Dr. Carlos Bonorino Udaondo", Buenos Aires, Argentina.
3 Unidad de Soporte Nutricional y Malabsorción, Hospital San Martín, La Plata, Argentina.

aAddress correspondence to this author at: Department of Medicine, Hospital de Gastroenterología "Carlos Bonorino Udaondo", Av. Caseros 2061, 1264 Buenos Aires, Argentina. Fax 54-11-4304-1018; e-mail jbai{at}intramed.net.

Background: Noninvasive serologic tests have shown high diagnostic accuracy for celiac disease (CD) in selected populations. Our aim was to determine prospectively the performance of CD-related serology in individuals undergoing intestinal biopsy because of clinical suspicion of small-bowel disorders.

Methods: We enrolled 141 unselected consecutive adult patients attending a small-bowel disease clinic. Patients underwent endoscopy and biopsy; serum samples were obtained at that time for measurements of anti–tissue transglutaminase (a-tTG), IgA and IgG anti–deamidated gliadin-related peptide (a-DGP), and IgA antiactin antibodies (AAAs). Characterization of patients was based on histological criteria (Marsh type II lesion or greater).

Results: The prevalence of CD was 42.5%. Sensitivity, specificity, and positive and negative predictive values were >90% for most assays. Diagnostic accuracy based on ROC curve analysis was similar for all assays [area under the curve (95% CI): 0.996 (0.967–0.998) for a-tTG, 0.995 (0.964–0.998) for IgA a-DGP, 0.989 (0.954–0.999) for IgG a-DGP, 0.996 (0.966–0.998) for blended conjugated of IgA + IgG a-DGP in a single assay, and 0.967 (0.922–0.990) for AAA]. The combinations of 2 tests, IgG a-DGP plus IgA a-tTG or the single blended conjugate detecting IgA + IgG a-DGP plus IgA a-tTG had 100% positive and negative predictive values if concentrations of both tests in either combination were above or below the cutoff.

Conclusions: In a population with high pretest probability, the newly developed a-DGP tests have diagnostic accuracy that is at least equivalent to that of established assays.




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