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. 2009 Oct 14;15(38):4775-80.
doi: 10.3748/wjg.15.4775.

Duodenal biopsy may be avoided when high transglutaminase antibody titers are present

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Duodenal biopsy may be avoided when high transglutaminase antibody titers are present

Santiago Vivas et al. World J Gastroenterol. .

Abstract

Aim: To evaluate the predictive value of tissue transglutaminase (tTG) antibodies for villous atrophy in adult and pediatric populations to determine if duodenal biopsy can be avoided.

Methods: A total of 324 patients with celiac disease (CD; 97 children and 227 adults) were recruited prospectively at two tertiary centers. Human IgA class anti-tTG antibody measurement and upper gastrointestinal endoscopy were performed at diagnosis. A second biopsy was performed in 40 asymptomatic adults on a gluten-free diet (GFD) and with normal tTG levels.

Results: Adults showed less severe histopathology (26% vs 63%, P < 0.0001) and lower tTG antibody titers than children. Levels of tTG antibody correlated with Marsh type in both populations (r = 0.661, P < 0.0001). Multiple logistic regression revealed that only tTG antibody was an independent predictor for Marsh type 3 lesions, but clinical presentation type and age were not. A cut-off point of 30 U tTG antibody yielded the highest area under the receiver operating characteristic curve (0.854). Based on the predictive value of this cut-off point, up to 95% of children and 53% of adults would be correctly diagnosed without biopsy. Despite GFDs and decreased tTG antibody levels, 25% of the adults did not recover from villous atrophy during the second year after diagnosis.

Conclusion: Strongly positive tTG antibody titers might be sufficient for CD diagnosis in children. However, duodenal biopsy cannot be avoided in adults because disease presentation and monitoring are different.

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Figures

Figure 1
Figure 1
Serum tTG antibody level vs patient age. An inverse relationship was observed for the levels of serum tTG antibody with increasing patient age.
Figure 2
Figure 2
Histopathological differences between children and adults according to Marsh classification.
Figure 3
Figure 3
Serum tTG antibody levels vs Marsh classification. tTG IgA was significantly correlated with Marsh type.
Figure 4
Figure 4
ROC showing the maximum area under the curve for Marsh type 3 histology at cut-off point of 30 U tTG antibody.
Figure 5
Figure 5
Follow-up of adult patients with an initial Marsh type 3 biopsy. Repeated biopsy showed persistent atrophy in 25% of the cases.

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