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Can glucose-lowering medications improve outcomes in non-diabetic heart failure patients? A Bayesian network
Trevor Yeong1, Aaron Shengting Mai1, Oliver Z H Lim1
1Yong Loo Lin School of Medicine, National University of Singapore, 10 Medical Dr, 117597, Singapore.
Insights
Sodium-glucose transporter 2 inhibitors (SGLT2i) show superior efficacy in improving heart failure outcomes for non-diabetic patients compared to other glucose-lowering drugs. SGLT2i significantly enhances left ventricular ejection fraction and reduces NT-proBNP levels.
Area of Science:
- Cardiology
- Pharmacology
- Metabolic Diseases
Background:
- Glucose-lowering medications are known for cardioprotective effects in diabetic patients with heart failure (HF).
- Emerging evidence suggests these benefits extend to non-diabetic HF patients.
- This study evaluates various glucose-lowering drugs in this population.
Purpose of the Study:
- To conduct a Bayesian network meta-analysis on glucose-lowering medications in non-diabetic HF patients.
- To compare the efficacy of different drug classes on key HF outcomes.
Main Methods:
- Searched Medline and Embase for relevant randomized controlled trials (RCTs) up to August 2021.
- Included 7 RCTs with 2897 patients, assessing NT-proBNP, LVEF, and PVO2.
- Performed Bayesian network meta-analysis and assessed risk-of-bias using ROB2.
Main Results:
- Sodium-glucose transporter 2 inhibitors (SGLT2i) significantly reduced NT-proBNP compared to GLP-1 RAs, metformin, and placebo.
- SGLT2i demonstrated superior improvement in LVEF for HF with reduced ejection fraction patients versus GLP-1 RAs and placebo.
- SGLT2i and GLP-1 RAs improved PVO2 compared to placebo, with comparable safety profiles across drugs.
Conclusions:
- SGLT2i are superior to GLP-1 RAs and metformin in improving LVEF, PVO2, and NT-proBNP in non-diabetic HF patients.
- These findings highlight SGLT2i as a promising therapeutic option for non-diabetic HF.
- Further large-scale prospective studies are warranted to confirm these results.
Aims:
The cardioprotective effects of glucose-lowering medications in diabetic patients with heart failure (HF) are well known. Several large randomized controlled trials (RCTs) have recently suggested that the cardioprotective effects of glucose-lowering medications extend to HF patients regardless of diabetic status. The aim of this study was to conduct a Bayesian network meta-analysis to evaluate the impact of various glucose-lowering medications on the outcomes of non-diabetic HF patients.
Methods And Results:
Medline and Embase were searched for RCTs investigating the use of glucose-lowering medications in non-diabetic HF patients in August 2021. Studies were included in accordance with the inclusion and exclusion criteria, and data were extracted with a pre-defined datasheet. Primary outcomes include serum N-terminal prohormone of brain natriuretic peptide (NT-proBNP) levels, left ventricular ejection fraction (LVEF), and maximal oxygen consumption (PVO2 ). A Bayesian network meta-analysis was performed to compare the effectiveness of different classes of glucose-lowering medications in improving HF outcomes. Risk-of-bias was assessed using Cochrane Risk-of-Bias tool 2.0 for randomized trials (ROB2). Seven RCTs involving 2897 patients were included. Sodium-glucose transporter 2 inhibitor (SGLT2i) was the most favourable in lowering NT-proBNP, with the significant reduction in NT-proBNP when compared with glucagon-like peptide-1 receptor agonists (GLP1-RA) [mean differences (MD): -229.59 pg/mL, 95%-credible intervals (95%-CrI): -238.31 to -220.91], metformin (MD: -237.15 pg/mL, 95%-CrI: -256.19 to -218.14), and placebo (MD: -228.00 pg/mL, 95%-CrI: -233.99 to -221.99). SGLT2i was more effective in improving LVEF for HF with reduced ejection fraction patients relative to GLP1-RA (MD: 8.09%, 95%-CrI: 6.30 to 9.88) and placebo (MD: 6.10%, 95%-CrI: 4.37 to 7.84). SGLT2i and GLP1-RA were more favourable to placebo in improving PVO2 , with significant increase of PVO2 at a MD of 1.60 mL/kg/min (95%-CrI: 0.63 to 2.57) and 0.86 mL/kg/min (95%-CrI: 0.66 to 1.06), respectively. All three drugs had comparable safety profiles when compared with placebo.
Conclusions:
This Bayesian network meta-analysis demonstrated that SGLT2i, when compared with GLP1-RA and metformin, was superior in improving LVEF in HF with reduced ejection fraction patients, as well as improving PVO2 and NT-proBNP in non-diabetic HF patients. Further large-scale prospective studies are needed to confirm these preliminary findings.
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