Key result
Liraglutide added to metformin significantly reduced carotid intima-media thickness from 1.13 mm to 0.92 mm and decreased atherogenic small dense LDL-3 subfractions over 4 months in patients with type 2 diabetes.
Why the study?
Liraglutide has non-glycemic effects contributing to cardiovascular benefit, but the exact underlying mechanisms remain unclear.
Does liraglutide reduce carotid intima-media thickness and atherogenic small dense LDL in patients with type 2 diabetes?
Observational (n=62)
Single-blind (outcome assessors)
No
Does liraglutide reduce carotid intima-media thickness and atherogenic small dense LDL in patients with type 2 diabetes?
Absolute Event Rate: 0.92% vs 1.13%
p-value: p=<0.0001
Liraglutide reduces carotid intima-media thickness in patients with type 2 diabetes, an anti-atherogenic effect that is independently predicted by reductions in small dense LDL-3 subfractions.
Links cIMT reduction on liraglutide to sdLDL-3 changes in T2DM; hypothesis-generating and requires prospective confirmation.
INTRODUCTION: Liraglutide has several non-glycemic effects, including those on plasma lipids and lipoproteins, contributing to its cardiovascular benefit; however, the exact underlying mechanisms remain unclear. We investigated a novel anti-atherogenic effect of liraglutide in a real-world prospective study on patients with type 2 diabetes (T2DM). METHODS: Sixty-two patients with T2DM (31 men, 31 women; mean age ± standard deviation 61 ± 9 years) naïve to incretin-based therapies were treated with liraglutide (1.2 mg/day) as add-on therapy to metformin (1500-3000 mg/day) for 4 months. Laboratory analyses included the assessment of lipoprotein subclass profile by gel electrophoresis (Lipoprint; Quantimetrix Corp., Redondo Beach, CA, USA). Carotid intima-media thickness (cIMT) was assessed by Doppler ultrasonography. Statistical analyses included the paired t test, Spearman correlation and multiple regression analysis. RESULTS: The addition of liraglutide to metformin monotherapy resulted in significant reductions in fasting glycemia, hemoglobin A1c, body mass index, waist circumference, total cholesterol, triglycerides and low-density lipoprotein (LDL)-cholesterol, as well as in cIMT. There was an increase in the large LDL-1 subfraction, with a concomitant reduction in atherogenic small dense LDL-3 and LDL-4 subfractions. Correlation analysis revealed a significant association between changes in cIMT and changes in small dense LDL-3 subfraction (r = 0.501; p < 0.0001). Multivariate analysis, including all of the measured anthropometric and laboratory parameters, revealed that only changes in the small dense LDL-3 subfraction were independent predictors of changes in cIMT (p < 0.0001). CONCLUSION: Our findings are the first to show that the vascular benefit of liraglutide in patients with T2DM is associated with reductions in atherogenic small dense LDL. This effect is independent of glycemic control and body weight reduction and may represent one of the key mechanisms by which liraglutide is able to reduce cardiovascular events. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01715428.
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Nikolić et al. (2020) conducted an observational in Type 2 Diabetes (n=62). Liraglutide vs. Baseline (no control group) was evaluated on Carotid intima-media thickness (cIMT) (p=<0.0001). Liraglutide added to metformin significantly reduced carotid intima-media thickness from 1.13 mm to 0.92 mm and decreased atherogenic small dense LDL-3 subfractions over 4 months in patients with type 2 diabetes.
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