May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?

<i>Background and Objective</i>: Pediatric guidelines on celiac disease (CD) state that children with anti-transglutaminase antibodies (TGAs) >×10 upper limit of normal (ULN) may avoid endoscopy and biopsy. We aimed to evaluate whether these criteria may be suitable for villous atroph...

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Autores principales: Giuseppe Losurdo, Milena Di Leo, Edoardo Santamato, Antonio Giangaspero, Maria Rendina, Carmelo Luigiano, Enzo Ierardi, Alfredo Di Leo
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/42f70ef61b0f4b49b4560908650bb4ee
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spelling oai:doaj.org-article:42f70ef61b0f4b49b4560908650bb4ee2021-11-25T18:18:37ZMay Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?10.3390/medicina571112121648-91441010-660Xhttps://doaj.org/article/42f70ef61b0f4b49b4560908650bb4ee2021-11-01T00:00:00Zhttps://www.mdpi.com/1648-9144/57/11/1212https://doaj.org/toc/1010-660Xhttps://doaj.org/toc/1648-9144<i>Background and Objective</i>: Pediatric guidelines on celiac disease (CD) state that children with anti-transglutaminase antibodies (TGAs) >×10 upper limit of normal (ULN) may avoid endoscopy and biopsy. We aimed to evaluate whether these criteria may be suitable for villous atrophy diagnosis in CD adults. <i>Materials and Methods</i>: We retrospectively enrolled patients with CD aged >18 years. TGAs were expressed as xULN. Duodenal lesions were classified as atrophic or non-atrophic according to Marsh-Oberhuber. Fisher’s exact and <i>t</i>-test were used for variables comparison. Receiver operating characteristics (ROC) curve analysis was performed with estimation of area under the curve (AUC), sensitivity, specificity, and positive and negative predictive value (PPV/NPV). <i>Results:</i> One hundred and twenty-one patients were recruited. Sixty patients (49.6%) had TGA >×10 ULN, and 93 (76.8%) had villous atrophy. The cut-off of >×10 ULN had sensitivity = 53.7%, specificity = 64.3%, PPV = 83.3%, and NPV = 29.5% to predict atrophy. Therefore, considering pediatric criteria, in 50 (41.3%) patients, biopsy could have been avoided. Patient subgroup with atrophy had higher TGA levels despite being not significant (37.2 ± 15.3 vs. 8.0 ± 1.3 ULN, <i>p</i> = 0.06). In adults, a slightly better diagnostic performance was obtained using a cut-off of TGA >×6.2 ULN (sensitivity = 57.1%, specificity = 65.6%, and AUC = 0.62). <i>Conclusions:</i> Despite our confirmation that villous atrophy is linked to high TGA levels, CD and atrophy diagnosis based only on serology is not reliable in adults.Giuseppe LosurdoMilena Di LeoEdoardo SantamatoAntonio GiangasperoMaria RendinaCarmelo LuigianoEnzo IerardiAlfredo Di LeoMDPI AGarticleceliac diseaseserologyvillous atrophyserologyanti-transglutaminaseadultsMedicine (General)R5-920ENMedicina, Vol 57, Iss 1212, p 1212 (2021)
institution DOAJ
collection DOAJ
language EN
topic celiac disease
serology
villous atrophy
serology
anti-transglutaminase
adults
Medicine (General)
R5-920
spellingShingle celiac disease
serology
villous atrophy
serology
anti-transglutaminase
adults
Medicine (General)
R5-920
Giuseppe Losurdo
Milena Di Leo
Edoardo Santamato
Antonio Giangaspero
Maria Rendina
Carmelo Luigiano
Enzo Ierardi
Alfredo Di Leo
May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
description <i>Background and Objective</i>: Pediatric guidelines on celiac disease (CD) state that children with anti-transglutaminase antibodies (TGAs) >×10 upper limit of normal (ULN) may avoid endoscopy and biopsy. We aimed to evaluate whether these criteria may be suitable for villous atrophy diagnosis in CD adults. <i>Materials and Methods</i>: We retrospectively enrolled patients with CD aged >18 years. TGAs were expressed as xULN. Duodenal lesions were classified as atrophic or non-atrophic according to Marsh-Oberhuber. Fisher’s exact and <i>t</i>-test were used for variables comparison. Receiver operating characteristics (ROC) curve analysis was performed with estimation of area under the curve (AUC), sensitivity, specificity, and positive and negative predictive value (PPV/NPV). <i>Results:</i> One hundred and twenty-one patients were recruited. Sixty patients (49.6%) had TGA >×10 ULN, and 93 (76.8%) had villous atrophy. The cut-off of >×10 ULN had sensitivity = 53.7%, specificity = 64.3%, PPV = 83.3%, and NPV = 29.5% to predict atrophy. Therefore, considering pediatric criteria, in 50 (41.3%) patients, biopsy could have been avoided. Patient subgroup with atrophy had higher TGA levels despite being not significant (37.2 ± 15.3 vs. 8.0 ± 1.3 ULN, <i>p</i> = 0.06). In adults, a slightly better diagnostic performance was obtained using a cut-off of TGA >×6.2 ULN (sensitivity = 57.1%, specificity = 65.6%, and AUC = 0.62). <i>Conclusions:</i> Despite our confirmation that villous atrophy is linked to high TGA levels, CD and atrophy diagnosis based only on serology is not reliable in adults.
format article
author Giuseppe Losurdo
Milena Di Leo
Edoardo Santamato
Antonio Giangaspero
Maria Rendina
Carmelo Luigiano
Enzo Ierardi
Alfredo Di Leo
author_facet Giuseppe Losurdo
Milena Di Leo
Edoardo Santamato
Antonio Giangaspero
Maria Rendina
Carmelo Luigiano
Enzo Ierardi
Alfredo Di Leo
author_sort Giuseppe Losurdo
title May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
title_short May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
title_full May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
title_fullStr May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
title_full_unstemmed May Antitransglutaminase Levels Predict Severity of Duodenal Lesions in Adults with Celiac Disease?
title_sort may antitransglutaminase levels predict severity of duodenal lesions in adults with celiac disease?
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/42f70ef61b0f4b49b4560908650bb4ee
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