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Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease

Non-alcoholic fatty liver disease (NAFLD) can be detected in up to 33.6% of inflammatory bowel disease (IBD) patients, often in absence of metabolic risk factors. Nevertheless, most of previous studies on such issue were conducted within the IBD population only. The primary aim of this study was to...

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Autores principales: Sartini, Alessandro, Gitto, Stefano, Bianchini, Marcello, Verga, Maria Chiara, Di Girolamo, Maria, Bertani, Angela, Del Buono, Mariagrazia, Schepis, Filippo, Lei, Barbara, De Maria, Nicola, Villa, Erica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833704/
https://www.ncbi.nlm.nih.gov/pubmed/29367619
http://dx.doi.org/10.1038/s41419-017-0124-2
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author Sartini, Alessandro
Gitto, Stefano
Bianchini, Marcello
Verga, Maria Chiara
Di Girolamo, Maria
Bertani, Angela
Del Buono, Mariagrazia
Schepis, Filippo
Lei, Barbara
De Maria, Nicola
Villa, Erica
author_facet Sartini, Alessandro
Gitto, Stefano
Bianchini, Marcello
Verga, Maria Chiara
Di Girolamo, Maria
Bertani, Angela
Del Buono, Mariagrazia
Schepis, Filippo
Lei, Barbara
De Maria, Nicola
Villa, Erica
author_sort Sartini, Alessandro
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) can be detected in up to 33.6% of inflammatory bowel disease (IBD) patients, often in absence of metabolic risk factors. Nevertheless, most of previous studies on such issue were conducted within the IBD population only. The primary aim of this study was to compare clinical and metabolic features of NAFLD in patients with and without IBD (w/o IBD) and to identify specific NAFLD phenotypes within the IBD population. Among 223 NAFLD patients, 78 patients with IBD were younger compared to 145 without (w/o) IBD, were less likely to have altered liver enzymes, had lower mean body weight, smaller waist circumference and lower body mass index (BMI); at the same time, MetS was more prevalent among patients w/o IBD (56.6 vs. 23.1%, p < 0.001). Within IBD population, patients with severe IBD showed more often severe steatosis (S3) at ultrasound (US) (32.1 vs. 16.6%, p = 0.01), compared to mild-to-moderate disease. Independent risk factors for S3 US steatosis in IBD patients at the multivariate logistic regression analysis were: more than 1 IBD relapse per year during disease history (OR 17.3, 95% CI 3.6–84), surgery for IBD (OR 15.1, 95% CI 3.1–73.7) and more extensive intestinal involvement (OR 19.4, 95% CI 3.4–110.9); the ongoing anti-Tumor Necrosis Factor alpha (antiTNFα) therapy was the only independent factor which protect toward the presence of altered liver enzymes (OR 0.15, 95% CI 0–0.8, p = 0.02). In conclusion, NAFLD in IBD patients is different from that in patients w/o IBD, who seem to develop different NAFLD phenotypes according to intestinal disease clinical course. More severe IBD seem to predict the presence of more severe steatosis. Therapy with antiTNFα antibodies could prevent alteration of liver enzymes in such population.
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spelling pubmed-58337042018-03-05 Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease Sartini, Alessandro Gitto, Stefano Bianchini, Marcello Verga, Maria Chiara Di Girolamo, Maria Bertani, Angela Del Buono, Mariagrazia Schepis, Filippo Lei, Barbara De Maria, Nicola Villa, Erica Cell Death Dis Article Non-alcoholic fatty liver disease (NAFLD) can be detected in up to 33.6% of inflammatory bowel disease (IBD) patients, often in absence of metabolic risk factors. Nevertheless, most of previous studies on such issue were conducted within the IBD population only. The primary aim of this study was to compare clinical and metabolic features of NAFLD in patients with and without IBD (w/o IBD) and to identify specific NAFLD phenotypes within the IBD population. Among 223 NAFLD patients, 78 patients with IBD were younger compared to 145 without (w/o) IBD, were less likely to have altered liver enzymes, had lower mean body weight, smaller waist circumference and lower body mass index (BMI); at the same time, MetS was more prevalent among patients w/o IBD (56.6 vs. 23.1%, p < 0.001). Within IBD population, patients with severe IBD showed more often severe steatosis (S3) at ultrasound (US) (32.1 vs. 16.6%, p = 0.01), compared to mild-to-moderate disease. Independent risk factors for S3 US steatosis in IBD patients at the multivariate logistic regression analysis were: more than 1 IBD relapse per year during disease history (OR 17.3, 95% CI 3.6–84), surgery for IBD (OR 15.1, 95% CI 3.1–73.7) and more extensive intestinal involvement (OR 19.4, 95% CI 3.4–110.9); the ongoing anti-Tumor Necrosis Factor alpha (antiTNFα) therapy was the only independent factor which protect toward the presence of altered liver enzymes (OR 0.15, 95% CI 0–0.8, p = 0.02). In conclusion, NAFLD in IBD patients is different from that in patients w/o IBD, who seem to develop different NAFLD phenotypes according to intestinal disease clinical course. More severe IBD seem to predict the presence of more severe steatosis. Therapy with antiTNFα antibodies could prevent alteration of liver enzymes in such population. Nature Publishing Group UK 2018-01-24 /pmc/articles/PMC5833704/ /pubmed/29367619 http://dx.doi.org/10.1038/s41419-017-0124-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sartini, Alessandro
Gitto, Stefano
Bianchini, Marcello
Verga, Maria Chiara
Di Girolamo, Maria
Bertani, Angela
Del Buono, Mariagrazia
Schepis, Filippo
Lei, Barbara
De Maria, Nicola
Villa, Erica
Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title_full Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title_fullStr Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title_full_unstemmed Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title_short Non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
title_sort non-alcoholic fatty liver disease phenotypes in patients with inflammatory bowel disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833704/
https://www.ncbi.nlm.nih.gov/pubmed/29367619
http://dx.doi.org/10.1038/s41419-017-0124-2
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