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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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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