<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Valenti L</submitter><funding>Ministero della Salute</funding><funding>Fondazione IRCCS Ca&amp;apos; Granda Ospedale Maggiore Policlinico</funding><funding>European Commission</funding><funding>Gilead Sciences</funding><pagination>867-877</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8948549</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(4)</volume><pubmed_abstract>The aim of this study was to examine the impact of features of dysmetabolism on liver disease severity, evolution, and clinical outcomes in a real-life cohort of patients treated with direct acting antivirals for chronic hepatitis C virus (HCV) infection. To this end, we considered 7,007 patients treated between 2014 and 2018, 65.3% with advanced fibrosis, of whom 97.7% achieved viral eradication (NAVIGATORE-Lombardia registry). In a subset (n = 748), liver stiffness measurement (LSM) was available at baseline and follow-up. Higher body mass index (BMI; odds ratio [OR] 1.06 per kg/m&lt;sup>2&lt;/sup> , 1.03-1.09) and diabetes (OR 2.01 [1.65-2.46]) were independently associated with advanced fibrosis at baseline, whereas statin use was protective (OR 0.46 [0.35-0.60]; P &lt; 0.0001 for all). The imp</pubmed_abstract><journal>Hepatology communications</journal><pubmed_title>Dysmetabolism, Diabetes and Clinical Outcomes in Patients Cured of Chronic Hepatitis C: A Real-Life Cohort Study.</pubmed_title><pmcid>PMC8948549</pmcid><funding_grant_id>Gilead Fellowship 2018 Italy</funding_grant_id><funding_grant_id>PR‐0391</funding_grant_id><funding_grant_id>RC100017A</funding_grant_id><funding_grant_id>777377</funding_grant_id><funding_grant_id>CV PREVITAL</funding_grant_id><funding_grant_id>RF‐2016‐02364358</funding_grant_id><funding_grant_id>Gilead_IN‐IT‐989‐5790</funding_grant_id><funding_grant_id>101016726</funding_grant_id><pubmed_authors>Terreni N</pubmed_authors><pubmed_authors>Pelusi S</pubmed_authors><pubmed_authors>D'Ambrosio R</pubmed_authors><pubmed_authors>D'Arminio Monforte A</pubmed_authors><pubmed_authors>Zuccaro V</pubmed_authors><pubmed_authors>Colombo MC</pubmed_authors><pubmed_authors>Valenti L</pubmed_authors><pubmed_authors>Fagiuoli S</pubmed_authors><pubmed_authors>Degasperi E</pubmed_authors><pubmed_authors>Pan A</pubmed_authors><pubmed_authors>Lorini G</pubmed_authors><pubmed_authors>Buscarini E</pubmed_authors><pubmed_authors>Rumi MG</pubmed_authors><pubmed_authors>Aghemo A</pubmed_authors><pubmed_authors>Prati D</pubmed_authors><pubmed_authors>Quirino T</pubmed_authors><pubmed_authors>Bonfanti P</pubmed_authors><pubmed_authors>Lampertico P</pubmed_authors><pubmed_authors>Pasulo L</pubmed_authors><pubmed_authors>Memoli M</pubmed_authors><pubmed_authors>Spinetti A</pubmed_authors><pubmed_authors>Bianco C</pubmed_authors><pubmed_authors>Carriero C</pubmed_authors><pubmed_authors>Mendeni M</pubmed_authors><pubmed_authors>Gritti S</pubmed_authors><pubmed_authors>Re T</pubmed_authors><pubmed_authors>Iegri C</pubmed_authors><pubmed_authors>Autolitano A</pubmed_authors><pubmed_authors>Puoti M</pubmed_authors><pubmed_authors>Soria A</pubmed_authors><pubmed_authors>Cologni G</pubmed_authors><pubmed_authors>Del Poggio P</pubmed_authors><pubmed_authors>Spinelli O</pubmed_authors><pubmed_authors>Giorgini A</pubmed_authors><pubmed_authors>Aimo G</pubmed_authors><pubmed_authors>NAVIGATORE-Lombardia Network</pubmed_authors><pubmed_authors>Pigozzi MG</pubmed_authors><pubmed_authors>Vigano M</pubmed_authors><pubmed_authors>Colombo M</pubmed_authors><pubmed_authors>Carderi I</pubmed_authors><pubmed_authors>Menzaghi B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dysmetabolism, Diabetes and Clinical Outcomes in Patients Cured of Chronic Hepatitis C: A Real-Life Cohort Study.</name><description>The aim of this study was to examine the impact of features of dysmetabolism on liver disease severity, evolution, and clinical outcomes in a real-life cohort of patients treated with direct acting antivirals for chronic hepatitis C virus (HCV) infection. To this end, we considered 7,007 patients treated between 2014 and 2018, 65.3% with advanced fibrosis, of whom 97.7% achieved viral eradication (NAVIGATORE-Lombardia registry). In a subset (n = 748), liver stiffness measurement (LSM) was available at baseline and follow-up. Higher body mass index (BMI; odds ratio [OR] 1.06 per kg/m&lt;sup>2&lt;/sup> , 1.03-1.09) and diabetes (OR 2.01 [1.65-2.46]) were independently associated with advanced fibrosis at baseline, whereas statin use was protective (OR 0.46 [0.35-0.60]; P &lt; 0.0001 for all). The imp</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-05T14:43:30.627Z</modification><creation>2025-04-05T14:43:30.627Z</creation></dates><accession>S-EPMC8948549</accession><cross_references><pubmed>34811949</pubmed><doi>10.1002/hep4.1851</doi></cross_references></HashMap>