Clinical study: endothelial function
Improved endothelial function with metformin in type 2 diabetes mellitus

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Abstract

OBJECTIVES

This study was designed to assess the effect of metformin on impaired endothelial function in type 2 diabetes mellitus.

BACKGROUND

Abnormalities in vascular endothelial function are well recognized among patients with type 2 (insulin-resistant) diabetes mellitus. Insulin resistance itself may be central to the pathogenesis of endothelial dysfunction. The effects of metformin, an antidiabetic agent that improves insulin sensitivity, on endothelial function have not been reported.

METHODS

Subjects with diet-treated type 2 diabetes but without the confounding collection of cardiovascular risk factors seen in the metabolic syndrome were treated with metformin 500 mg twice daily (n = 29) or placebo (n = 15) for 12 weeks. Before and after treatment, blood flow responses to intraarterial administration of endothelium-dependent (acetylcholine), endothelium-independent (sodium nitroprusside) and nitrate-independent (verapamil) vasodilators were measured using forearm plethysmography. Whole-body insulin resistance was assessed on both occasions using the homeostasis model (HOMA-IR).

RESULTS

Subjects who received metformin demonstrated statistically significant improvement in acetylcholine-stimulated flows compared with those treated with placebo (p = 0.0027 by 2-way analysis of variance), whereas no significant effect was seen on nitroprusside-stimulated (p = 0.27) or verapamil-stimulated (p = 0.40) flows. There was a significant improvement in insulin resistance with metformin (32.5% reduction in HOMA-IR, p = 0.01), and by stepwise multivariate analysis insulin resistance was the sole predictor of endothelium-dependent blood flow following treatment (r = −0.659, p = 0.0012).

CONCLUSIONS

Metformin treatment improved both insulin resistance and endothelial function, with a strong statistical link between these variables. This supports the concept of the central role of insulin resistance in the pathogenesis of endothelial dysfunction in type 2 diabetes mellitus. This has important implications for the investigation and treatment of vascular disease in patients with type 2 diabetes mellitus.

Abbreviations

Ach
acetylcholine
ANCOVA
analysis of covariance
ANOVA
analysis of variance
BMI
body mass index
CV
coefficient of variation
DM
diabetes mellitus
FBF
forearm blood flow
FFA
free fatty acid
HOMA-IR
homeostasis model assessment of insulin resistance
IR
insulin resistance
LDL
low density lipoprotein
SNP
sodium nitroprusside
VER
verapamil

Cited by (0)

This study was supported by the Alberta Heart and Stroke Foundation, Edmonton, Alberta, Canada. We gratefully acknowledge the financial support of the Dr. Howard MacEwan Diabetes Center Research Fund. At the time of this study, Dr. Mather was supported by a Clinical Research Fellowship from the Alberta Heritage Fund for Medical Research (AHFMR). Dr. Verma was also supported by the AHFMR. Dr. Anderson is an AHFMR Scholar.