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Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)

ABTRACT: BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver diseases, ranging from pure steatosis to nonalcoholic steatohepatitis (NASH), and eventually to liver cirrhosis with its complications. Identifying advanced fibrosis in patients is crucial to evaluating p...

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Autores principales: Raszeja-Wyszomirska, Joanna, Szymanik, Barbara, Ławniczak, Małgorzata, Kajor, Maciej, Chwist, Alina, Milkiewicz, Piotr, Hartleb, Marek
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905324/
https://www.ncbi.nlm.nih.gov/pubmed/20584330
http://dx.doi.org/10.1186/1471-230X-10-67
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author Raszeja-Wyszomirska, Joanna
Szymanik, Barbara
Ławniczak, Małgorzata
Kajor, Maciej
Chwist, Alina
Milkiewicz, Piotr
Hartleb, Marek
author_facet Raszeja-Wyszomirska, Joanna
Szymanik, Barbara
Ławniczak, Małgorzata
Kajor, Maciej
Chwist, Alina
Milkiewicz, Piotr
Hartleb, Marek
author_sort Raszeja-Wyszomirska, Joanna
collection PubMed
description ABTRACT: BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver diseases, ranging from pure steatosis to nonalcoholic steatohepatitis (NASH), and eventually to liver cirrhosis with its complications. Identifying advanced fibrosis in patients is crucial to evaluating prognosis and possible therapeutic intervention. A novel, simple, and highly accurate scoring system called BARD, which identifies patients with NAFLD and without significant fibrosis, has been recently introduced and validated in North America..The aim of this study is to validate the BARD scoring system in a Polish cohort with NAFLD. METHODS: A group of 104 Caucasians with biopsy-proven NAFLD were included in this study. Fibrosis in liver biopsies was evaluated according to the Histological Scoring System for Nonalcoholic Fatty Liver Disease. The BARD scoring system was assessed according to Harrison et al.: BMI ≥ 28 = 1 point, AST/ALT ratio (AAR) ≥ 0.8 = 2 points, type 2 diabetes mellitus = 1point. RESULTS: Age over 50 and AAR over 0.8 showed, respectively, a moderate and strong association with advanced fibrosis. A BARD score of 2-4 points was associated with F3 or F4 stages of fibrosis with an odds ratio of 17.333 (95% Cl; 3,639 - 82.558) and negative predictive value of 97%. CONCLUSION: Our results demonstrate that the BARD scoring system has value in the non-invasive diagnosis of advanced fibrosis in NAFLD patients. The vast majority of patients with NAFLD would avoid liver biopsy if BARD was broadly introduced into the clinic.
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spelling pubmed-29053242010-07-17 Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD) Raszeja-Wyszomirska, Joanna Szymanik, Barbara Ławniczak, Małgorzata Kajor, Maciej Chwist, Alina Milkiewicz, Piotr Hartleb, Marek BMC Gastroenterol Research Article ABTRACT: BACKGROUND: Nonalcoholic fatty liver disease (NAFLD) includes a wide spectrum of liver diseases, ranging from pure steatosis to nonalcoholic steatohepatitis (NASH), and eventually to liver cirrhosis with its complications. Identifying advanced fibrosis in patients is crucial to evaluating prognosis and possible therapeutic intervention. A novel, simple, and highly accurate scoring system called BARD, which identifies patients with NAFLD and without significant fibrosis, has been recently introduced and validated in North America..The aim of this study is to validate the BARD scoring system in a Polish cohort with NAFLD. METHODS: A group of 104 Caucasians with biopsy-proven NAFLD were included in this study. Fibrosis in liver biopsies was evaluated according to the Histological Scoring System for Nonalcoholic Fatty Liver Disease. The BARD scoring system was assessed according to Harrison et al.: BMI ≥ 28 = 1 point, AST/ALT ratio (AAR) ≥ 0.8 = 2 points, type 2 diabetes mellitus = 1point. RESULTS: Age over 50 and AAR over 0.8 showed, respectively, a moderate and strong association with advanced fibrosis. A BARD score of 2-4 points was associated with F3 or F4 stages of fibrosis with an odds ratio of 17.333 (95% Cl; 3,639 - 82.558) and negative predictive value of 97%. CONCLUSION: Our results demonstrate that the BARD scoring system has value in the non-invasive diagnosis of advanced fibrosis in NAFLD patients. The vast majority of patients with NAFLD would avoid liver biopsy if BARD was broadly introduced into the clinic. BioMed Central 2010-06-28 /pmc/articles/PMC2905324/ /pubmed/20584330 http://dx.doi.org/10.1186/1471-230X-10-67 Text en Copyright ©2010 Raszeja-Wyszomirska et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Raszeja-Wyszomirska, Joanna
Szymanik, Barbara
Ławniczak, Małgorzata
Kajor, Maciej
Chwist, Alina
Milkiewicz, Piotr
Hartleb, Marek
Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title_full Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title_fullStr Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title_full_unstemmed Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title_short Validation of the BARD scoring system in Polish patients with nonalcoholic fatty liver disease (NAFLD)
title_sort validation of the bard scoring system in polish patients with nonalcoholic fatty liver disease (nafld)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2905324/
https://www.ncbi.nlm.nih.gov/pubmed/20584330
http://dx.doi.org/10.1186/1471-230X-10-67
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