Circulating PCSK9 levels are not associated with the severity of hepatic steatosis and NASH in a high-risk population
Affiliation auteurs | !!!! Error affiliation !!!! |
Titre | Circulating PCSK9 levels are not associated with the severity of hepatic steatosis and NASH in a high-risk population |
Type de publication | Journal Article |
Year of Publication | 2018 |
Auteurs | Wargny M, Ducluzeau P-H, Petit J-M, Le May C, Smati S, Arnaud L, Pichelin M, Bouillet B, Lannes A, Blanchet O, Lefebvre P, Francque S, Van Gaal L, Staels B, Verges B, Boursier J, Cariou B |
Journal | ATHEROSCLEROSIS |
Volume | 278 |
Pagination | 82-90 |
Date Published | NOV |
Type of Article | Article |
ISSN | 0021-9150 |
Mots-clés | LDL-cholesterol, Liver biopsy, Liver fibrosis, Liver steatosis, mri, PCSK9 |
Résumé | {Background and aims: Some studies suggested that proprotein convertase subtilisin kexin type 9 (PCSK9) is linked to liver steatosis severity and non-alcoholic steatohepatitis (NASH). We aimed to assess whether circulating PCSK9 levels are associated with either liver fat content (LFC) or histological markers of NASH in high-risk patients. Methods: We present results from three cross-sectional studies from two French Hospitals: Dijon and Numevox (departments of Endocrinology) and Angers (department of Hepatology). Only patients without lipid-lowering therapy were included. All 132 patients had type 2 diabetes in Dijon, compared to 55/224 in Numevox (25%) and 39/122 in Angers (32%). LFC was assessed on MRI (Dijon and Numevox), and NASH lesion on liver biopsy (Angers). Additionally, we included mRNA results from 138 overweight patients of a Belgian Hospital (Antwerp). Results: While circulating levels of PCSK9 were positively correlated with total cholesterol, LDL-C, triglycerides and non-HDL-C in all 3 cohorts, no significant association was found between PCSK9 and transaminases. Furthermore, no association was found between plasma PCSK9 levels and LFC in both Numevox (beta(adjusted) = 0.71 +/- 1.33 |
DOI | 10.1016/j.atherosclerosis.2018.09.008 |