Systematic review of sodium‐glucose cotransporter 2 inhibitors: a hopeful prospect in tackling heart failure‐related events

Author:

Aziri Buena1ORCID,Begic Edin12,Jankovic Slobodan3,Mladenovic Zorica4,Stanetic Bojan5,Kovacevic‐Preradovic Tamara5,Iglica Amer6,Mujakovic Aida2

Affiliation:

1. Sarajevo Medical School Sarajevo School of Science and Technology Sarajevo Bosnia and Herzegovina

2. General Hospital “Prim. Dr. Abdulah Nakas” Sarajevo Bosnia and Herzegovina

3. Faculty of Medical Sciences University of Kragujevac Kragujevac Serbia

4. Military Medical Academy University of Defense Belgrade Serbia

5. Faculty of Medicine University of Banja Luka, University Clinical Centre of the Republic of Srpska Banja Luka Republic of Srpska Bosnia and Herzegovina

6. Clinic for Heart, Blood Vessel and Rheumatic Diseases Clinical Center University of Sarajevo Sarajevo Bosnia and Herzegovina

Abstract

AbstractIn modern cardiology, sodium‐glucose cotransporter 2 (SGLT2) inhibitors are critical components of heart failure (HF) treatment algorithms and exert their effects primarily by preventing glucose reabsorption and facilitating its urinary excretion. The objective was to systematically review randomized controlled trials (RCTs) assessing the effects of SGLT2 inhibitors, particularly canagliflozin, empagliflozin, dapagliflozin, ertugliflozin, sotagliflozin (dual SGLT inhibitor), and their use in HF. Systematic searches of PubMed/Medline, The Cochrane Central Register of Controlled Trials (CENTRAL), and ClinicalTrials.gov databases were performed. There were no restrictions imposed on the date and status of publication; however, there were restrictions on language for the searched studies. A total of 1139 records were identified in the bibliographic searches from both databases and the register of choice for this systematic review. Following duplicate removal, screening for titles and abstracts, and thorough assessment of full‐text articles, 12 RCTs met the inclusion criteria. Altogether, 83 878 patients were included in this review. Among the included studies, two RCTs, with six respective reports, investigated canagliflozin, four RCTs with 13 derived reports investigated dapagliflozin, three RCTs with 12 separate reports studied the effects of empagliflozin, one RCT and its three respective reports assessed ertugliflozin's effects, and two RCTs with one added report investigated the dual inhibitor sotagliflozin. Pooled meta‐analytic effects of SGLT2 inhibitors were as follows: on atrial fibrillation odds ratio (OR) = 0.83, 95% confidence interval (CI): 0.68–1.01, prediction interval (PI): 0.57–1.19; on HF hospitalization OR = 0.69, 95% CI: 0.60–0.78, PI: 0.60–0.78; on cardiovascular death OR = 0.82, 95% CI: 0.58–1.15, PI: 0.42–1.60; and on major adverse cardiovascular events OR = 0.90, 95% CI: 0.77–1.06, PI: 0.71–1.15. SGLT2 inhibitors significantly improve the quality of life in HF patients. Their beneficial effects on HF, especially in left ventricular dysfunction, have made their use possible irrespective of diabetes mellitus or atrial fibrillation status.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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