Effect of liraglutide on ectopic fat in polycystic ovary syndrome: A randomized clinical trial. Issue 1 (11th August 2017)

• Record Type: Journal Article
• Authors: Frøssing, Signe; Nylander, Malin; Chabanova, Elizaveta; Frystyk, Jan; Holst, Jens J.; Kistorp, Caroline; Skouby, Sven O.; Faber, Jens
• Is Part Of: Diabetes, obesity & metabolism. Volume 20:Issue 1(2018)
• Page Start: 215
• Page End: 218
• Publication Date: 2017-08-11
• Subjects: body composition -- clinical trial -- fatty liver -- GLP‐1 analogue -- insulin resistance; Diabetes -- Periodicals; Obesity -- Periodicals; Metabolism -- Disorders -- Periodicals; Clinical pharmacology -- Periodicals; 616.462
• DOI: 10.1111/dom.13053
• Languages: English
• ISSNs: 1462-8902

Abstract

Abstract : Women with polycystic ovary syndrome (PCOS) were treated with the GLP‐1 receptor agonist liraglutide to investigate the effect on liver fat content, visceral adipose tissue (VAT) and the prevalence of nonalcoholic fatty liver disease (NAFLD). In a double‐blind, placebo‐controlled, randomized clinical trial 72 women with PCOS, with a BMI > 25 kg/m 2 and/or insulin resistance, were treated with liraglutide or received placebo 1.8 mg/d (2:1) for 26 weeks. Liver fat content was assessed by 1 HMR spectroscopy, VAT by MRI, body composition by DXA, and glucose metabolism by oral glucose tolerance test. Compared with placebo, liraglutide treatment reduced body weight by 5.2 kg (5.6%), liver fat content by 44%, VAT by 18%, and the prevalence of NAFLD by two‐thirds (all P < .01). Sex‐hormone‐binding‐globulin (SHBG) levels increased by 19% ( P = .03), and free testosterone decreased by 19% ( P = .054). HbA1c, fasting glucose and leptin were reduced (all: P < .05), whereas measures of insulin resistance, adiponectin and glucagon did not change. In conclusion, 26 weeks of liraglutide treatment in PCOS resulted in significant reductions in liver fat content, VAT and the prevalence of NAFLD.