<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Munteanu M</submitter><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Seventh Framework Programme</funding><pagination>877-89</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5113673</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>44(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Blood tests of liver injury are less well validated in non-alcoholic fatty liver disease (NAFLD) than in patients with chronic viral hepatitis.&lt;h4>Aims&lt;/h4>To improve the validation of three blood tests used in NAFLD patients, FibroTest for fibrosis staging, SteatoTest for steatosis grading and ActiTest for inflammation activity grading.&lt;h4>Methods&lt;/h4>We pre-included new NAFLD patients with biopsy and blood tests from a single-centre cohort (FibroFrance) and from the multicentre FLIP consortium. Contemporaneous biopsies were blindly assessed using the new steatosis, activity and fibrosis (SAF) score, which provides a reliable and reproducible diagnosis and grading/staging of the three elementary features of NAFLD (steatosis, inflammatory activity) and fibrosis with redu</pubmed_abstract><journal>Alimentary pharmacology &amp; therapeutics</journal><pubmed_title>Diagnostic performance of FibroTest, SteatoTest and ActiTest in patients with NAFLD using the SAF score as histological reference.</pubmed_title><pmcid>PMC5113673</pmcid><funding_grant_id>FP7/2007‐2013</funding_grant_id><funding_grant_id>CL-2013-01-002</funding_grant_id><funding_grant_id>HEALTH‐F2‐2009‐241762</funding_grant_id><funding_grant_id>MC_UU_12013/5</funding_grant_id><pubmed_authors>Sorensen T</pubmed_authors><pubmed_authors>Perlemuter G</pubmed_authors><pubmed_authors>Mercadier A</pubmed_authors><pubmed_authors>Gouw AS</pubmed_authors><pubmed_authors>Bellentani S</pubmed_authors><pubmed_authors>Castille JM</pubmed_authors><pubmed_authors>FLIP Consortium and the FibroFrance Group</pubmed_authors><pubmed_authors>Bruckert E</pubmed_authors><pubmed_authors>Munteanu M</pubmed_authors><pubmed_authors>Rosmorduc O</pubmed_authors><pubmed_authors>Varsat B</pubmed_authors><pubmed_authors>Marra F</pubmed_authors><pubmed_authors>Schirmacher P</pubmed_authors><pubmed_authors>Ngo Y</pubmed_authors><pubmed_authors>Deckmyn O</pubmed_authors><pubmed_authors>Ziol M</pubmed_authors><pubmed_authors>Hartemann A</pubmed_authors><pubmed_authors>Montani M</pubmed_authors><pubmed_authors>De Minicis S</pubmed_authors><pubmed_authors>David E</pubmed_authors><pubmed_authors>Perazzo H</pubmed_authors><pubmed_authors>Losi L</pubmed_authors><pubmed_authors>Wendum D</pubmed_authors><pubmed_authors>Romero Gomez M</pubmed_authors><pubmed_authors>Cabibi D</pubmed_authors><pubmed_authors>Trauner M</pubmed_authors><pubmed_authors>Giral P</pubmed_authors><pubmed_authors>Traussnig S</pubmed_authors><pubmed_authors>Bismuth FI</pubmed_authors><pubmed_authors>Pareja MJ</pubmed_authors><pubmed_authors>Thabut D</pubmed_authors><pubmed_authors>Tiniakos D</pubmed_authors><pubmed_authors>Lawlor D</pubmed_authors><pubmed_authors>Bugianesi E</pubmed_authors><pubmed_authors>Ratziu V</pubmed_authors><pubmed_authors>Moussalli J</pubmed_authors><pubmed_authors>Dufour JF</pubmed_authors><pubmed_authors>Wrba F</pubmed_authors><pubmed_authors>Poynard T</pubmed_authors><pubmed_authors>Langon T</pubmed_authors><pubmed_authors>Lebray P</pubmed_authors><pubmed_authors>Marchesini G</pubmed_authors><pubmed_authors>Burt AD</pubmed_authors><pubmed_authors>Anstee Q</pubmed_authors><pubmed_authors>Naveau S</pubmed_authors><pubmed_authors>Rudler M</pubmed_authors><pubmed_authors>Bedossa P</pubmed_authors><pubmed_authors>Lackner C</pubmed_authors><pubmed_authors>Jacqueminet S</pubmed_authors><pubmed_authors>Brain J</pubmed_authors><pubmed_authors>Tribelli C</pubmed_authors><pubmed_authors>Day C</pubmed_authors><pubmed_authors>Bury Y</pubmed_authors><pubmed_authors>Terracciano L</pubmed_authors><pubmed_authors>Oliveira C</pubmed_authors><pubmed_authors>Charlotte F</pubmed_authors><pubmed_authors>Calmus Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diagnostic performance of FibroTest, SteatoTest and ActiTest in patients with NAFLD using the SAF score as histological reference.</name><description>&lt;h4>Background&lt;/h4>Blood tests of liver injury are less well validated in non-alcoholic fatty liver disease (NAFLD) than in patients with chronic viral hepatitis.&lt;h4>Aims&lt;/h4>To improve the validation of three blood tests used in NAFLD patients, FibroTest for fibrosis staging, SteatoTest for steatosis grading and ActiTest for inflammation activity grading.&lt;h4>Methods&lt;/h4>We pre-included new NAFLD patients with biopsy and blood tests from a single-centre cohort (FibroFrance) and from the multicentre FLIP consortium. Contemporaneous biopsies were blindly assessed using the new steatosis, activity and fibrosis (SAF) score, which provides a reliable and reproducible diagnosis and grading/staging of the three elementary features of NAFLD (steatosis, inflammatory activity) and fibrosis with redu</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2026-05-29T20:29:55.143Z</modification><creation>2019-03-27T02:29:12Z</creation></dates><accession>S-EPMC5113673</accession><cross_references><pubmed>27549244</pubmed><doi>10.1111/apt.13770</doi></cross_references></HashMap>