Key result
Dapagliflozin therapy for 12 weeks did not improve flow-mediated dilation compared to placebo in patients with T2DM and ischemic heart disease.
Why the study?
The study was conducted to evaluate the effect of the SGLT2 inhibitor dapagliflozin on endothelial function in patients with high-risk type 2 diabetes mellitus.
Does dapagliflozin improve endothelial function in patients with high-risk T2DM and ischemic heart disease on metformin and insulin?
RCT (n=81)
Double-blind
randomized
Does dapagliflozin improve endothelial function in patients with high-risk T2DM and ischemic heart disease on metformin and insulin?
In patients with T2DM and ischemic heart disease, 12 weeks of dapagliflozin improved glycemic control and some surrogate markers of endothelial function (ICAM-1) but did not significantly improve flow-mediated dilation compared to placebo.
Answers are grounded in this paper and cite their sources.
Dapagliflozin may stabilize endothelial function via surrogate markers in high-risk T2DM; leaves open clinical relevance pending larger trials.
Objectives To evaluate the effect of the sodium-glucose cotransporter 2 inhibitor (SGLT2-I) dapagliflozin on endothelial function in patients with high-risk type 2 diabetes mellitus (T2DM). Methods This was a prospective, double-blind, randomized, placebo-controlled, clinical trial of patients with T2DM with underlying ischemic heart disease who were receiving metformin and insulin therapy (n = 81). After 12-weeks of additional therapy with either dapagliflozin (n = 40) or placebo (n = 41), systemic endothelial function was evaluated by change in flow-mediated dilation (ΔFMD), change in nitroglycerin-mediated dilation (ΔNMD) and surrogate markers including intercellular adhesion molecule 1 (ICAM-1), endothelial nitric oxide synthase (eNOS), high-sensitivity C-reactive protein (hs-CRP), and lipoprotein(a) (Lp[a]). Glycemic and lipid profiles were also measured. Results The dapagliflozin group demonstrated significant reductions of hemoglobin A1c (HbA1c) and fasting blood glucose (FBG) compared to the placebo group (ΔHbA1c –0.83 ± 1.47% vs –0.16 ± 1.25%, P = 0.042 and ΔFBG vs –0.73 ± 4.55 mmol/L vs –1.90 ± 4.40 mmol/L, P = 0.015, respectively). The placebo group showed worsening of ΔFMD while the dapagliflozin group maintained similar measurements pre- and posttherapy (P = not significant). There was a reduction in ICAM-1 levels in the dapagliflozin group (–83.9 ± 205.9 ng/mL, P < 0.02), which remained unchanged in the placebo group (–11.0 ± 169.1 ng/mL, P = 0.699). Univariate correlation analysis revealed a significant negative correlation between HbA1c and ΔFMD within the active group. Conclusion A 12-week therapy with dapagliflozin, in addition to insulin and metformin therapies, in high-risk patients resulted in significant reductions in HbA1c, FBG, and surrogate markers of the endothelial function. Although the dapagliflozin group demonstrated a significant association between reduction in HbA1c and improvement in FMD, there was no significant difference in FMD between the 2 groups.
No takes yet. Share an insight, caveat, or question.
Zainordin et al. (2019) conducted an RCT in type 2 diabetes mellitus with established ischemic heart disease (n=81). dapagliflozin vs. placebo was evaluated on change in flow-mediated dilation (ΔFMD) (p=not significant). Dapagliflozin therapy for 12 weeks did not improve flow-mediated dilation compared to placebo in patients with T2DM and ischemic heart disease.
Synapse has enriched 10 related papers. Consider them for comparative context: