Related Experiment Video
Updated: Nov 15, 2025

In Silico Clinical Trials for Cardiovascular Disease
Published on: May 27, 2022
Systematic review and meta-analysis: SGLT2 inhibitors, blood pressure and cardiovascular outcomes
Jamie L Benham1, Jane E Booth2, Ronald J Sigal3
1Departments of Medicine and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Objective:
Clinical trials suggest that SGLT2 inhibitors reduce the risk of cardiovascular mortality in patients with type 2 diabetes, however the mechanism is unclear. Our objective was to test the hypothesis that blood pressure reduction is one potential mechanism underlying the observed improvements in cardiovascular outcomes with SGLT2 inhibitors.
Methods:
We searched MEDLINE, EMBASE and Cochrane Central Register of Controlled Trials (inception-June 2019) for randomized controlled trials that reported the effect of SGLT2 inhibitors compared with placebo on cardiovascular outcomes in adults with type 2 diabetes. Two reviewers independently extracted data and assessed study quality. Random effects meta-analyses, stratified meta-analyses and meta-regressions were conducted to evaluate the association between blood pressure reduction in SGLT2 inhibitor treated patients and cardiovascular outcomes.
Results:
Of 11,232 articles identified, 40 articles (n = 54,279 participants) were included. The relative risk of cardiovascular mortality was reduced by 18% with the use of SGLT2 inhibitors compared with placebo (RR 0.82; 95%CI 0.74, 0.91, I2 = 0.0%). Meta-regression analysis revealed no detectable difference in cardiovascular mortality (RR 0.93; 95%CI 0.88, 1.13, p = 0.483), 3-point major adverse cardiovascular events (p = 0.839) or congestive heart failure hospitalizations (p = 0.844) with change in mean systolic blood pressure.
Conclusions:
Cardiovascular events are reduced in participants with type 2 diabetes treated with SGLT2 inhibitors compared with placebo. There was no significant relationship between the risk of developing adverse cardiovascular events and blood pressure reduction with SGLT2 inhibitors. There is insufficient evidence to suggest that blood pressure reduction is a significant contributor to the cardiovascular benefits observed.
Insights
Sodium-glucose cotransporter 2 (SGLT2) inhibitors reduce cardiovascular mortality in type 2 diabetes. However, blood pressure reduction does not appear to be a significant mechanism for these cardiovascular benefits.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- SGLT2 inhibitors are associated with reduced cardiovascular mortality in type 2 diabetes.
- The precise mechanisms underlying these benefits remain unclear.
Purpose of the Study:
- To investigate whether blood pressure reduction is a contributing mechanism to the cardiovascular benefits of SGLT2 inhibitors.
- To test the hypothesis that decreased blood pressure mediates improved cardiovascular outcomes.
Main Methods:
- A systematic literature search of MEDLINE, EMBASE, and Cochrane Central Register of Controlled Trials was performed.
- Randomized controlled trials comparing SGLT2 inhibitors with placebo in adults with type 2 diabetes were included.
- Random effects meta-analyses and meta-regressions were used to assess the association between blood pressure changes and cardiovascular outcomes.
Main Results:
- Data from 40 trials involving 54,279 participants were analyzed.
- SGLT2 inhibitors significantly reduced the risk of cardiovascular mortality (RR 0.82; 95%CI 0.74, 0.91).
- Meta-regression showed no significant association between changes in systolic blood pressure and cardiovascular mortality, MACE, or heart failure hospitalizations.
Conclusions:
- While SGLT2 inhibitors reduce cardiovascular events in type 2 diabetes, blood pressure reduction is not a significant contributing factor.
- The observed cardiovascular benefits are likely mediated by mechanisms other than blood pressure lowering.
Related Concept Videos
Antihypertensive Drugs: Angiotensin II Receptor Blockers
Antihypertensive Drugs: Direct Renin Inhibitors
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Dipeptidyl Peptidase 4 Inhibitors
Oral Hypoglycemic Agents: Biguanides and Glitazones
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
