Mechanisms
Neither a liraglutide RCT nor a 1,611-person cohort finds any link between liver fat content and circulating CETP, despite CETP's hepatic Kupffer-cell origin (Sci Rep 2019)
Original title: Hepatic triglyceride content does not affect circulating CETP: lessons from a liraglutide intervention trial and a population-based cohort
Cholesteryl ester transfer protein (CETP) is mainly expressed by Kupffer cells in the liver, and reducing hepatic triglyceride content (HTGC) with pioglitazone or caloric restriction has been shown to lower circulating CETP. Since GLP-1 analogues also reduce HTGC, the authors tested whether liraglutide decreases CETP, and separately examined the HTGC-CETP association in a population cohort. In a placebo-controlled trial, 50 patients with type 2 diabetes received liraglutide or placebo added to standard care; HTGC and CETP were also measured in 1,611 participants of the Netherlands Epidemiology of Obesity (NEO) study. HTGC decreased in both the liraglutide (-6.3%) and placebo (-4.0%) groups with no between-group difference, and CETP was not decreased by either liraglutide or placebo. No association was found between HTGC and CETP at baseline, after treatment, or in the cohort, indicating circulating CETP is not determined by hepatic triglyceride content.
Original abstract
Cholesteryl ester transfer protein (CETP) is mainly expressed by Kupffer cells in the liver. A reduction of hepatic triglyceride content (HTGC) by pioglitazone or caloric restriction is accompanied by a decrease in circulating CETP. Since GLP-1 analogues also reduce HTGC, we assessed whether liraglutide decreases CETP. Furthermore, we investigated the association between HTGC and CETP in a population-based cohort. In a placebo-controlled trial, 50 patients with type 2 diabetes were randomly assigned to treatment with liraglutide or placebo added to standard care. In this trial and in 1,611 participants of the Netherlands Epidemiology of Obesity (NEO) study, we measured HTGC and circulating CETP by proton magnetic resonance spectroscopy and ELISA, respectively. The HTGC was decreased in the liraglutide group (-6.3%; 95%CI of difference [-9.5, -3.0]) but also in the placebo group (-4.0%; 95%CI[-6.0, -2.0]), without between-group differences. CETP was not decreased by liraglutide (-0.05 µg/mL; 95%CI[-0.13, 0.04]) or placebo (-0.04 µg/mL; 95%CI[-0.12, 0.04]). No association was present between HTGC and CETP at baseline (β: 0.002 µg/mL per %TG, 95%CI[-0.005, 0.009]) and between the changes after treatment with liraglutide (β: 0.003 µg/mL per %TG, 95%CI[-0.010, 0.017]) or placebo (β: 0.006 µg/mL per %TG, 95%CI[-0.012,0.024]). Also, in the cohort n o association between HTGC and CETP was present (β: -0.001 µg/mL per SD TG, 95%CI[-0.005, 0.003]). A reduction of HTGC after treatment with liraglutide or placebo does not decrease circulating CETP. Also, no association between HTGC and CETP was present in a large cohort. These findings indicate that circulating CETP is not determined by HTGC.Clinical Trial Registration: Clinicaltrials.gov (NCT01761318).
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.