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The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease
BACKGROUND: Celiac disease (CD) is an immune mediated condition that leads to small bowel atrophy and improve with a gluten free diet (GFD). Extra-intestinal manifestations of CD include hypertransaminasemia. In this study, the effects of a GFD on hypertransaminasemia in patients with newly diagnose...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733038/ https://www.ncbi.nlm.nih.gov/pubmed/23930188 |
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author | Moghaddam, Mostafa Alavi Nejad, Mohammad Rostami Shalmani, Hamid Mohaghegh Rostami, Kamran Mojarad, Ehsan Nazemalhosseini Aldulaimi, David Zali, Mohammad Reza |
author_facet | Moghaddam, Mostafa Alavi Nejad, Mohammad Rostami Shalmani, Hamid Mohaghegh Rostami, Kamran Mojarad, Ehsan Nazemalhosseini Aldulaimi, David Zali, Mohammad Reza |
author_sort | Moghaddam, Mostafa Alavi |
collection | PubMed |
description | BACKGROUND: Celiac disease (CD) is an immune mediated condition that leads to small bowel atrophy and improve with a gluten free diet (GFD). Extra-intestinal manifestations of CD include hypertransaminasemia. In this study, the effects of a GFD on hypertransaminasemia in patients with newly diagnosed CD were studied. METHODS: Ninety eight new diagnosed consecutive patients with CD 40 males and 58 females) with mean age of 32 ± 17.1 were studied. All patients with CD were treated with a GFD. Patients with hypertransaminasemia, at diagnosis, had a cirrhosis screen performed. Patients with a negative cirrhosis screen were reviewed, 6 months after the introduction of a GFD, and serum levels of liver transaminases were measured again. RESULTS: Nine patients had hypertransaminasemia. One patient was Hepatitis B surface antigen positive and was excluded from this study. The 8 remaining patients had no obvious cause for the hypertransaminasemia. Mean (± SD) of baseline aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels were 42.6 ± 16.5 IU/L (range: 16-66 IU/L) and 69.3 ± 9.3 IU/L (range: 52-81 IU/L). Six months after treatment with a GFD, mean AST and ALT levels decreased to 24.5 ± 5.1 IU/L (range: 18-31 IU/L) (P: 0.04) and 24.6 ± 6 IU/L (range: 17-32 IU/L) (P: 0.01), respectively. In 7 patients the hypertransaminasemia, at diagnosis had resolved. CONCLUSIONS: This study provides further evidence that some patients with CD have a reversible hypertransaminasemia that resolves with a GFD. |
format | Online Article Text |
id | pubmed-3733038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37330382013-08-08 The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease Moghaddam, Mostafa Alavi Nejad, Mohammad Rostami Shalmani, Hamid Mohaghegh Rostami, Kamran Mojarad, Ehsan Nazemalhosseini Aldulaimi, David Zali, Mohammad Reza Int J Prev Med Original Article BACKGROUND: Celiac disease (CD) is an immune mediated condition that leads to small bowel atrophy and improve with a gluten free diet (GFD). Extra-intestinal manifestations of CD include hypertransaminasemia. In this study, the effects of a GFD on hypertransaminasemia in patients with newly diagnosed CD were studied. METHODS: Ninety eight new diagnosed consecutive patients with CD 40 males and 58 females) with mean age of 32 ± 17.1 were studied. All patients with CD were treated with a GFD. Patients with hypertransaminasemia, at diagnosis, had a cirrhosis screen performed. Patients with a negative cirrhosis screen were reviewed, 6 months after the introduction of a GFD, and serum levels of liver transaminases were measured again. RESULTS: Nine patients had hypertransaminasemia. One patient was Hepatitis B surface antigen positive and was excluded from this study. The 8 remaining patients had no obvious cause for the hypertransaminasemia. Mean (± SD) of baseline aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels were 42.6 ± 16.5 IU/L (range: 16-66 IU/L) and 69.3 ± 9.3 IU/L (range: 52-81 IU/L). Six months after treatment with a GFD, mean AST and ALT levels decreased to 24.5 ± 5.1 IU/L (range: 18-31 IU/L) (P: 0.04) and 24.6 ± 6 IU/L (range: 17-32 IU/L) (P: 0.01), respectively. In 7 patients the hypertransaminasemia, at diagnosis had resolved. CONCLUSIONS: This study provides further evidence that some patients with CD have a reversible hypertransaminasemia that resolves with a GFD. Medknow Publications & Media Pvt Ltd 2013-06 /pmc/articles/PMC3733038/ /pubmed/23930188 Text en Copyright: © International Journal of Preventive Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moghaddam, Mostafa Alavi Nejad, Mohammad Rostami Shalmani, Hamid Mohaghegh Rostami, Kamran Mojarad, Ehsan Nazemalhosseini Aldulaimi, David Zali, Mohammad Reza The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title | The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title_full | The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title_fullStr | The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title_full_unstemmed | The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title_short | The Effects of Gluten-Free Diet on Hypertransaminasemia in Patients with Celiac Disease |
title_sort | effects of gluten-free diet on hypertransaminasemia in patients with celiac disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733038/ https://www.ncbi.nlm.nih.gov/pubmed/23930188 |
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