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Liraglutide in combination with metformin may improve the atherogenic lipid profile and decrease C-reactive protein level in statin treated obese patients with coronary artery disease and newly diagnosed type 2 diabetes: A randomized trial. | LitMetric

AI Article Synopsis

  • Atherosclerosis in obesity and T2DM is linked to low-grade inflammation and harmful lipid profiles, particularly small, dense lipoproteins, prompting the study of liraglutide with metformin as a treatment.
  • A randomized trial was conducted to assess the effects of liraglutide combined with metformin on lipid density and inflammation markers in patients with stable coronary artery disease and newly diagnosed T2DM.
  • Results showed that while liraglutide alone had no significant impact on lipid profiles, its combination with metformin reduced harmful LDL subfractions and C-reactive protein levels, indicating potential cardiovascular benefits in treated patients.

Article Abstract

Background And Aims: Atherosclerosis in obesity and type 2 diabetes (T2DM) is associated with low-grade inflammation (LGI) and dyslipidemia, where especially small, dense lipoprotein particles are atherogenic. The glucagon-like peptide-1 receptor agonist, liraglutide, reduces cardiovascular events by poorly understood mechanisms. We investigated the effect of liraglutide combined with metformin on LGI and lipoprotein density profiles in patients with stable coronary artery disease (CAD) and newly diagnosed T2DM.

Methods: We conducted a randomized, double-blind, placebo-controlled, cross-over trial over a 12 + 12-week period, with ≥2-week wash-out.

Intervention: liraglutide/metformin vs. placebo/metformin. Lipoproteins were separated by continuous density gradient ultracentrifugation, and LDL divided into five subfractions between 226 and 270 Å, considering particle size ≤255 Å as the atherogenic pattern. Plasma C-reactive protein and tumor necrosis factor-α were assessed by the enzyme-linked immunosorbent-assay.

Results: 28 out of 41 randomized patients completed all visits. Intention-to-treat analysis was performed but one patient had statin dosage and was excluded from the analysis. 95% of the patients were on statin therapy. Overall, liraglutide did not affect lipid subfractions or markers of LGI compared to placebo. The combination of liraglutide and metformin reduced the total LDL subfractions, primarily by reducing the most atherogenic subfraction LDL, and reduced CRP but not TNF-α. Explorative analyses suggested that the subfraction LDL during the wash-out period rebounded significantly at least in a per-protocol analysis of the sub-group of patients starting the liraglutide therapy.

Conclusions: In patients with CAD and newly diagnosed T2DM on stable statin therapy, liraglutide combined with metformin may improve the atherogenic LDL lipid profile and CRP.

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Source
http://dx.doi.org/10.1016/j.atherosclerosis.2019.07.007DOI Listing

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