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Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis
BACKGROUND: Limited data are available regarding the role of magnetic resonance imaging (MRI), particularly the new generation 3 Tesla technology, and especially diffusion-weighted imaging (DWI) in predicting liver fibrosis. The aim of our pilot study was to assess the clinical performance of the ap...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hellenic Society of Gastroenterology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289984/ https://www.ncbi.nlm.nih.gov/pubmed/25608776 |
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author | Papalavrentios, Lavrentios Sinakos, Emmanouil Chourmouzi, Danai Hytiroglou, Prodromos Drevelegas, Konstantinos Constantinides, Manos Drevelegas, Antonios Talwalkar, Jayant Akriviadis, Evangelos |
author_facet | Papalavrentios, Lavrentios Sinakos, Emmanouil Chourmouzi, Danai Hytiroglou, Prodromos Drevelegas, Konstantinos Constantinides, Manos Drevelegas, Antonios Talwalkar, Jayant Akriviadis, Evangelos |
author_sort | Papalavrentios, Lavrentios |
collection | PubMed |
description | BACKGROUND: Limited data are available regarding the role of magnetic resonance imaging (MRI), particularly the new generation 3 Tesla technology, and especially diffusion-weighted imaging (DWI) in predicting liver fibrosis. The aim of our pilot study was to assess the clinical performance of the apparent diffusion coefficient (ADC) of liver parenchyma for the assessment of liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). METHODS: 18 patients with biopsy-proven NAFLD underwent DWI with 3 Tesla MRI. DWI was performed with single-shot echo-planar technique at b values of 0-500 and 0-1000 s/mm(2). ADC was measured in four locations in the liver and the mean ADC value was used for analysis. Staging of fibrosis was performed according to the METAVIR system. RESULTS: The median age of patients was 52 years (range 23-73). The distribution of patients in different fibrosis stages was: 0 (n=1), 1 (n=7), 2 (n=1), 3 (n=5), 4 (n=4). Fibrosis stage was poorly associated with ADC at b value of 0-500 s/mm(2) (r= -0.30, P=0.27). However it was significantly associated with ADC at b value of 0-1000 s/mm(2) (r= -0.57, P=0.01). For this b value (0-1000 s/mm(2)) the area under receiver-operating characteristic curve was 0.93 for fibrosis stage ≥3 and the optimal ADC cut-off value was 1.16 ×10(-3) mm(2)/s. CONCLUSION: 3 Tesla DWI can possibly predict the presence of advanced fibrosis in patients with NAFLD. |
format | Online Article Text |
id | pubmed-4289984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hellenic Society of Gastroenterology |
record_format | MEDLINE/PubMed |
spelling | pubmed-42899842015-01-21 Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis Papalavrentios, Lavrentios Sinakos, Emmanouil Chourmouzi, Danai Hytiroglou, Prodromos Drevelegas, Konstantinos Constantinides, Manos Drevelegas, Antonios Talwalkar, Jayant Akriviadis, Evangelos Ann Gastroenterol Original Article BACKGROUND: Limited data are available regarding the role of magnetic resonance imaging (MRI), particularly the new generation 3 Tesla technology, and especially diffusion-weighted imaging (DWI) in predicting liver fibrosis. The aim of our pilot study was to assess the clinical performance of the apparent diffusion coefficient (ADC) of liver parenchyma for the assessment of liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). METHODS: 18 patients with biopsy-proven NAFLD underwent DWI with 3 Tesla MRI. DWI was performed with single-shot echo-planar technique at b values of 0-500 and 0-1000 s/mm(2). ADC was measured in four locations in the liver and the mean ADC value was used for analysis. Staging of fibrosis was performed according to the METAVIR system. RESULTS: The median age of patients was 52 years (range 23-73). The distribution of patients in different fibrosis stages was: 0 (n=1), 1 (n=7), 2 (n=1), 3 (n=5), 4 (n=4). Fibrosis stage was poorly associated with ADC at b value of 0-500 s/mm(2) (r= -0.30, P=0.27). However it was significantly associated with ADC at b value of 0-1000 s/mm(2) (r= -0.57, P=0.01). For this b value (0-1000 s/mm(2)) the area under receiver-operating characteristic curve was 0.93 for fibrosis stage ≥3 and the optimal ADC cut-off value was 1.16 ×10(-3) mm(2)/s. CONCLUSION: 3 Tesla DWI can possibly predict the presence of advanced fibrosis in patients with NAFLD. Hellenic Society of Gastroenterology 2015 /pmc/articles/PMC4289984/ /pubmed/25608776 Text en Copyright: © Hellenic Society of Gastroenterology 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 Papalavrentios, Lavrentios Sinakos, Emmanouil Chourmouzi, Danai Hytiroglou, Prodromos Drevelegas, Konstantinos Constantinides, Manos Drevelegas, Antonios Talwalkar, Jayant Akriviadis, Evangelos Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title | Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title_full | Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title_fullStr | Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title_full_unstemmed | Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title_short | Value of 3 Tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
title_sort | value of 3 tesla diffusion-weighted magnetic resonance imaging for assessing liver fibrosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289984/ https://www.ncbi.nlm.nih.gov/pubmed/25608776 |
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