Evolocumab Safe and Efficacious for Lowering LDL-C

HealthDay News – For patients with or without dysglycemia or metabolic syndrome (MetS), evolocumab is safe and efficacious for reducing low-density lipoprotein cholesterol (LDL-C) at 52 weeks, according to research published online September 13 in Diabetes, Obesity and Metabolism.

Dirk J. Blom, MB, ChB, from the University of Cape Town in South Africa, and colleagues examined the lipid and glycemic effects of 52 weeks of evolocumab treatment in a post-hoc analysis of data from the DESCARTES randomized trial involving 905 patients from 88 study centers. Nine hundred one patients received at least one dose of study drug. Patients were categorized by baseline glycemic status: type 2 diabetes (120 patients), impaired fasting glucose (IFG; 293 patients), MetS (289 patients [194 also had IFG]), or none (393 patients).

The researchers found that evolocumab reduced LDL-C by >50% in all subgroups at week 52, with favorable effects on other lipids. There was no significant between-group difference in any subgroup for fasting plasma glucose, hemoglobin A1C, insulin, C-peptide, or homeostasis model assessment. The overall incidence of new-onset diabetes was not significantly different for placebo and evolocumab (6.6% and 5.6%, respectively); the incidences were 1.9% and 2.7%, respectively, in those with baseline normoglycemia. The incidence of adverse events was similar between the groups.

“Evolocumab showed encouraging safety and efficacy at 52 weeks in patients with or without dysglycemia or MetS,” the authors wrote. “Changes in glycemic parameters did not differ between evolocumab- and placebo-treated patients within the glycemic subgroups examined.”

Disclosures: Several authors disclosed financial ties to pharmaceutical companies, including Amgen, which manufactures evolocumab.

Reference

Blom DJ, Koren MJ, Roth E, et al. Evaluation of the efficacy, safety, and glycemic effects of evolocumab (AMG 145) in hypercholesterolemia patietns stratified by glycemic status and metabolic syndrome. Diabetes Obes Metab. 2016. doi:10.1111/dom.12788.