Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease

<p>Abstract</p> <p>Background</p> <p>Liver biopsy is considered the gold standard for assessing histologic lesions of non-alcoholic fatty liver disease (NAFLD). The aim was to develop and validate a new biomarker of non alcoholic steato hepatitis (NASH) the NashTest (NT...

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Main Authors: Thabut Dominique, Tahiri Mohamed, Bonyhay Luninita, Massard Julien, Munteanu Mona, Imbert-Bismut Françoise, Messous Djamila, Charlotte Frederic, Ratziu Vlad, Poynard Thierry, Cadranel Jean, Le Bail Brigitte, de Ledinghen Victor
Format: Article
Language:English
Published: BMC 2006-11-01
Series:BMC Gastroenterology
Online Access:http://www.biomedcentral.com/1471-230X/6/34
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spelling doaj-e22e24ebaf9f4db19f111ff670e8ab262020-11-25T03:57:33ZengBMCBMC Gastroenterology1471-230X2006-11-01613410.1186/1471-230X-6-34Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver diseaseThabut DominiqueTahiri MohamedBonyhay LuninitaMassard JulienMunteanu MonaImbert-Bismut FrançoiseMessous DjamilaCharlotte FredericRatziu VladPoynard ThierryCadranel JeanLe Bail Brigittede Ledinghen Victor<p>Abstract</p> <p>Background</p> <p>Liver biopsy is considered the gold standard for assessing histologic lesions of non-alcoholic fatty liver disease (NAFLD). The aim was to develop and validate a new biomarker of non alcoholic steato hepatitis (NASH) the NashTest (NT) in patients with NAFLD.</p> <p>Methods</p> <p>160 patients with NAFLD were prospectively included in a training group, 97 were included in a multicenter validation group and 383 controls. Histological diagnoses used Kleiner et al's scoring system, with 3 classes for NASH: "Not NASH", "Borderline", "NASH"). The area under the ROC curves (AUROC), sensitivity (Se), specificity (Sp), and positive and negative predictive values (PPV, NPV) were assessed.</p> <p>Results</p> <p>NT was developed using patented algorithms combining 13 parameters: age, sex, height, weight, and serum levels of triglycerides, cholesterol, alpha2macroglobulin, apolipoprotein A1, haptoglobin, gamma-glutamyl-transpeptidase, transaminases ALT, AST, and total bilirubin. AUROCs of NT for the diagnosis of NASH in the training and validation groups were, respectively, 0.79 (95%CI 0.69–0.86) and 0.79 (95%CI 0.67–0.87; P = 0.94); for the diagnosis of borderline NASH they were: 0.69 (95%CI 0.60–0.77) and 0.69 (95%CI 0.57–0.78; P = 0.98) and for the diagnosis of no NASH, 0.77 (95%CI 0.68–0.84) and 0.83 (95%CI 0.67–0.90; P = 0.34). When the two groups were pooled together the NashTest Sp for NASH = 94% (PPV = 66%), and Se = 33% (NPV = 81%); for borderline NASH or NASH Sp = 50% (PPV = 74%) and Se = 88% (NPV = 72%).</p> <p>Conclusion</p> <p>In patients with non-alcoholic fatty liver disease, NashTest, a simple and non-invasive biomarker reliably predicts the presence or absence of NASH.</p> http://www.biomedcentral.com/1471-230X/6/34
collection DOAJ
language English
format Article
sources DOAJ
author Thabut Dominique
Tahiri Mohamed
Bonyhay Luninita
Massard Julien
Munteanu Mona
Imbert-Bismut Françoise
Messous Djamila
Charlotte Frederic
Ratziu Vlad
Poynard Thierry
Cadranel Jean
Le Bail Brigitte
de Ledinghen Victor
spellingShingle Thabut Dominique
Tahiri Mohamed
Bonyhay Luninita
Massard Julien
Munteanu Mona
Imbert-Bismut Françoise
Messous Djamila
Charlotte Frederic
Ratziu Vlad
Poynard Thierry
Cadranel Jean
Le Bail Brigitte
de Ledinghen Victor
Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
BMC Gastroenterology
author_facet Thabut Dominique
Tahiri Mohamed
Bonyhay Luninita
Massard Julien
Munteanu Mona
Imbert-Bismut Françoise
Messous Djamila
Charlotte Frederic
Ratziu Vlad
Poynard Thierry
Cadranel Jean
Le Bail Brigitte
de Ledinghen Victor
author_sort Thabut Dominique
title Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
title_short Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
title_full Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
title_fullStr Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
title_full_unstemmed Diagnostic value of biochemical markers (NashTest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
title_sort diagnostic value of biochemical markers (nashtest) for the prediction of non alcoholo steato hepatitis in patients with non-alcoholic fatty liver disease
publisher BMC
series BMC Gastroenterology
issn 1471-230X
publishDate 2006-11-01
description <p>Abstract</p> <p>Background</p> <p>Liver biopsy is considered the gold standard for assessing histologic lesions of non-alcoholic fatty liver disease (NAFLD). The aim was to develop and validate a new biomarker of non alcoholic steato hepatitis (NASH) the NashTest (NT) in patients with NAFLD.</p> <p>Methods</p> <p>160 patients with NAFLD were prospectively included in a training group, 97 were included in a multicenter validation group and 383 controls. Histological diagnoses used Kleiner et al's scoring system, with 3 classes for NASH: "Not NASH", "Borderline", "NASH"). The area under the ROC curves (AUROC), sensitivity (Se), specificity (Sp), and positive and negative predictive values (PPV, NPV) were assessed.</p> <p>Results</p> <p>NT was developed using patented algorithms combining 13 parameters: age, sex, height, weight, and serum levels of triglycerides, cholesterol, alpha2macroglobulin, apolipoprotein A1, haptoglobin, gamma-glutamyl-transpeptidase, transaminases ALT, AST, and total bilirubin. AUROCs of NT for the diagnosis of NASH in the training and validation groups were, respectively, 0.79 (95%CI 0.69–0.86) and 0.79 (95%CI 0.67–0.87; P = 0.94); for the diagnosis of borderline NASH they were: 0.69 (95%CI 0.60–0.77) and 0.69 (95%CI 0.57–0.78; P = 0.98) and for the diagnosis of no NASH, 0.77 (95%CI 0.68–0.84) and 0.83 (95%CI 0.67–0.90; P = 0.34). When the two groups were pooled together the NashTest Sp for NASH = 94% (PPV = 66%), and Se = 33% (NPV = 81%); for borderline NASH or NASH Sp = 50% (PPV = 74%) and Se = 88% (NPV = 72%).</p> <p>Conclusion</p> <p>In patients with non-alcoholic fatty liver disease, NashTest, a simple and non-invasive biomarker reliably predicts the presence or absence of NASH.</p>
url http://www.biomedcentral.com/1471-230X/6/34
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