Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis
Abstract Aims We sought to conduct a meta‐analysis regarding the safety and efficacy of sodium‐glucose co‐transporter 2 (SGLT2) inhibitors in patients with heart failure (HF). Methods and results MEDLINE, Scopus, Cochrane CENTRAL, and ClinicalTrials.gov were searched from their inception to November...
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doaj-ce6a29d7cf9d48ecb3a195f8066e8b972021-02-24T06:51:28ZengWileyESC Heart Failure2055-58222020-12-01763298330910.1002/ehf2.13169Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysisJaved Butler0Muhammad Shariq Usman1Muhammad Shahzeb Khan2Stephen J. Greene3Tim Friede4Muthiah Vaduganathan5Gerasimos Filippatos6Andrew J. Stewart Coats7Stefan D. Anker8Department of Medicine University of Mississippi Medical Center 2500 N. State Street Jackson MS 39216 USADepartment of Medicine Dow University of Health Sciences Karachi PakistanDepartment of Medicine University of Mississippi Medical Center 2500 N. State Street Jackson MS 39216 USADivision of Cardiology Duke University Medical Center Durham NC USADepartment of Medical Statistics University Medical Center Goettingen Goettingen GermanyHeart and Vascular Center Brigham and Women's Hospital Boston MA USANational and Kapodistrian University of Athens School of Medicine Athens University Hospital Attikon Athens GreeceDepartment of Cardiology IRCCS San Raffaele Pisana Rome ItalyDepartment of Cardiology (CVK) and Berlin Institute of Health Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research (DZHK), partner site Berlin Charité Universitätsmedizin Berlin Augustenburger Platz 1 D‐13353 Berlin GermanyAbstract Aims We sought to conduct a meta‐analysis regarding the safety and efficacy of sodium‐glucose co‐transporter 2 (SGLT2) inhibitors in patients with heart failure (HF). Methods and results MEDLINE, Scopus, Cochrane CENTRAL, and ClinicalTrials.gov were searched from their inception to November 2020 for placebo‐controlled randomized controlled trials of SGLT2 inhibitors. Randomized controlled trials were selected if they reported at least one of the prespecified outcomes in patients with HF. Hazard ratios (HRs) or risk ratios and their corresponding 95% confidence intervals were pooled using a random‐effects model. A total of seven trials including 16 820 HF patients (N = 8884 in the SGLT2 inhibitor arms; N = 7936 in the placebo arms) were included. In the overall HF cohort, SGLT2 inhibitors compared with placebo significantly reduced the risk of the composite endpoint of first HF hospitalization or cardiovascular death [HR: 0.77 (0.72–0.83); P < 0.001; I2 = 0%], time to first HF hospitalization [HR: 0.71 (0.64–0.78); P < 0.001; I2 = 0], cardiovascular mortality [HR: 0.87 (0.79–0.96); P = 0.005; I2 = 0%], and all‐cause mortality [HR: 0.89 (0.82–0.96); P = 0.004; I2 = 0%]. Results remained consistent across HF‐specific trials and according to diabetes mellitus status. A trend towards benefit was observed in patients with HF with preserved ejection fraction for the composite of HF hospitalization and cardiovascular death [HR: 0.80 (0.63–1.00); P = 0.05; I2 = 29%]. No increased risk of hypovolaemia, hyperkalaemia, and hypotension was seen with SGLT2 inhibitors compared with placebo. Conclusions SGLT2 inhibitors significantly improve cardiovascular outcomes including cardiovascular and all‐cause mortality in patients with HF without an increased risk of serious adverse events. A trend towards benefit was observed in patients with HF with preserved ejection fraction.https://doi.org/10.1002/ehf2.13169 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Javed Butler Muhammad Shariq Usman Muhammad Shahzeb Khan Stephen J. Greene Tim Friede Muthiah Vaduganathan Gerasimos Filippatos Andrew J. Stewart Coats Stefan D. Anker |
spellingShingle |
Javed Butler Muhammad Shariq Usman Muhammad Shahzeb Khan Stephen J. Greene Tim Friede Muthiah Vaduganathan Gerasimos Filippatos Andrew J. Stewart Coats Stefan D. Anker Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis ESC Heart Failure |
author_facet |
Javed Butler Muhammad Shariq Usman Muhammad Shahzeb Khan Stephen J. Greene Tim Friede Muthiah Vaduganathan Gerasimos Filippatos Andrew J. Stewart Coats Stefan D. Anker |
author_sort |
Javed Butler |
title |
Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis |
title_short |
Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis |
title_full |
Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis |
title_fullStr |
Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis |
title_full_unstemmed |
Efficacy and safety of SGLT2 inhibitors in heart failure: systematic review and meta‐analysis |
title_sort |
efficacy and safety of sglt2 inhibitors in heart failure: systematic review and meta‐analysis |
publisher |
Wiley |
series |
ESC Heart Failure |
issn |
2055-5822 |
publishDate |
2020-12-01 |
description |
Abstract Aims We sought to conduct a meta‐analysis regarding the safety and efficacy of sodium‐glucose co‐transporter 2 (SGLT2) inhibitors in patients with heart failure (HF). Methods and results MEDLINE, Scopus, Cochrane CENTRAL, and ClinicalTrials.gov were searched from their inception to November 2020 for placebo‐controlled randomized controlled trials of SGLT2 inhibitors. Randomized controlled trials were selected if they reported at least one of the prespecified outcomes in patients with HF. Hazard ratios (HRs) or risk ratios and their corresponding 95% confidence intervals were pooled using a random‐effects model. A total of seven trials including 16 820 HF patients (N = 8884 in the SGLT2 inhibitor arms; N = 7936 in the placebo arms) were included. In the overall HF cohort, SGLT2 inhibitors compared with placebo significantly reduced the risk of the composite endpoint of first HF hospitalization or cardiovascular death [HR: 0.77 (0.72–0.83); P < 0.001; I2 = 0%], time to first HF hospitalization [HR: 0.71 (0.64–0.78); P < 0.001; I2 = 0], cardiovascular mortality [HR: 0.87 (0.79–0.96); P = 0.005; I2 = 0%], and all‐cause mortality [HR: 0.89 (0.82–0.96); P = 0.004; I2 = 0%]. Results remained consistent across HF‐specific trials and according to diabetes mellitus status. A trend towards benefit was observed in patients with HF with preserved ejection fraction for the composite of HF hospitalization and cardiovascular death [HR: 0.80 (0.63–1.00); P = 0.05; I2 = 29%]. No increased risk of hypovolaemia, hyperkalaemia, and hypotension was seen with SGLT2 inhibitors compared with placebo. Conclusions SGLT2 inhibitors significantly improve cardiovascular outcomes including cardiovascular and all‐cause mortality in patients with HF without an increased risk of serious adverse events. A trend towards benefit was observed in patients with HF with preserved ejection fraction. |
url |
https://doi.org/10.1002/ehf2.13169 |
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