Journal
DIABETIC MEDICINE
Volume 29, Issue 9, Pages 1115-1118Publisher
WILEY
DOI: 10.1111/j.1464-5491.2012.03589.x
Keywords
asymmetric dimethylarginin; atherosclerosis; endothelium; glucagon-like peptide 1; vascular
Categories
Funding
- Novo Nordisk
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Diabet. Med. 29, 11151118 (2012) Abstract Aims The aim of this study was to investigate the vascular effects of liraglutide in patients well controlled on metformin monotherapy. Methods Forty-four patients with Type 2 diabetes were included in the study. Main inclusion criteria were: pretreatment with metformin on a stable dosage, HbA1c < 53 mmol/mol (7.0%), age 3065 years. Patients were randomized to receive additional liraglutide or to remain on metformin monotherapy. After 6 weeks (1.2 mg) and after 12 weeks (1.8 mg), venous blood was taken for the measurement of several laboratory markers characterizing vascular and endothelial function. In addition, retinal microvascular endothelial function and arterial stiffness were measured. Results HbA1c levels declined from 45 +/- 4 mmol/mol (6.3 +/- 0.4%; mean +/- sd) to 40 +/- 3 mmol/mol (5.8 +/- 0.3%) during liraglutide treatment. Asymmetric dimethylarginin was reduced by liraglutide treatment from 0.39 +/- 0.08 to 0.35 +/- 0.06 mu mol/l, E-selectin from 43.6 +/- 15.4 to 40.8 +/- 15.1 ng/ml, plasminogen activator inhibitor 1 from 861.6 +/- 584.3 to 666.1 +/- 499.4 ng/ml and intact proinsulin from 9.0 +/- 7.2 to 7.0 +/- 4.8 pmol/l at 12 weeks of treatment. The microvascular response to flicker light increased from 7.0 +/- 15.1 to 15.4 +/- 11.5% after 6 weeks and to 11.1 +/- 9.9% after 12 weeks. No change could be observed for high-sensitivity C-reactive protein, monocyte chemotactic protein 1, vascular cell adhesion molecule or arterial stiffness parameters. Conclusions In patients with Type 2 diabetes, well controlled with metformin monotherapy, addition of liraglutide improves several cardiovascular risk markers beyond glycaemic control.
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