Key result
Dapagliflozin improves cardiorespiratory fitness, increasing VO2peak by ~11% vs control at three months.
Why the study?
The study evaluated the effect of dapagliflozin on cardiorespiratory fitness in patients with coronary heart disease and type 2 diabetes mellitus following PCI.
Does dapagliflozin improve cardiorespiratory fitness in patients with coronary heart disease and type 2 diabetes mellitus following PCI?
RCT (n=180)
Randomly divided
No
Does dapagliflozin improve cardiorespiratory fitness in patients with coronary heart disease and type 2 diabetes mellitus following PCI?
In patients with CHD and T2DM following PCI, the addition of dapagliflozin to standard therapy significantly improves short-term cardiorespiratory fitness and endothelial function while reducing adverse cardiovascular events.
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Supports dapagliflozin addition to standard care post-PCI; extends SGLT2i evidence to cardiorespiratory fitness gains in CHD-T2DM.
To evaluate the effect of dapagliflozin on cardiorespiratory fitness (CRF) in patients with coronary heart disease (CHD) and type 2 diabetes mellitus (T2DM) following percutaneous coronary intervention (PCI). A total of 180 patients with CHD and T2DM who underwent PCI at Yuebei People’s Hospital between April 2021 and April 2023 were enrolled and randomly divided into the dapagliflozin group and the non-dapagliflozin group. CRF, brachial artery flow-mediated dilation (FMD), as well as the incidence of cardiovascular events and adverse reactions were compared between the two groups. After 3 months of intervention, compared with the non-dapagliflozin group, the dapagliflozin group exhibited significantly higher peak oxygen uptake (VO2peak) (Adjusted mean difference [AMD] in VO2peak for the dapagliflozin group: 21.87 ml/kg/min, 95% confidence interval [CI]: 21.05–22.69; AMD in VO2peak for the non-dapagliflozin group: 19.65 ml/kg/min, 95% CI: 18.2–20.48; P < 0.001), and a similar beneficial effect was observed for FMD (AMD in FMD for the dapagliflozin group: 5.63%, 95% CI: 5.12–6.14; AMD in FMD for the non-dapagliflozin group: 3.22%, 95% CI: 2.7–3.74; P < 0.001). No statistically significant between-group differences were detected in the remaining indicators (all P > 0.05). Over a 3-month observational period, dapagliflozin improved CRF, vascular endothelial function, and reduced the incidence of adverse cardiovascular events in patients with CHD and T2DM following PCI. This trial was registered with the Chinese Clinical Trial Registry (ChiCTR), registration number ChiCTR2100047856, on June 27, 2021 (retrospective registration). The study protocol adheres to the CONSORT guidelines.
Yang et al. (2026) conducted an RCT in Coronary heart disease and type 2 diabetes mellitus following PCI (n=180). Dapagliflozin vs. Conventional therapy without dapagliflozin was evaluated on VO2peak (ml/kg/min) (p=<0.001). Dapagliflozin significantly improved cardiorespiratory fitness, increasing adjusted mean VO2peak to 21.87 ml/kg/min compared to 19.65 ml/kg/min in the control group over 3 months.
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