Key result
Dipeptidyl peptidase-4 (DPP-4) inhibitors were associated with a 13% increased risk of heart failure compared to placebo or no therapy (RR 1.13; 95% CI 1.01-1.26).
Why the study?
Do DPP-4 inhibitors increase the risk of heart failure compared to placebo or no therapy?
Meta-Analysis (n=79,867)
Yes
Do DPP-4 inhibitors increase the risk of heart failure compared to placebo or no therapy?
Relative Risk: 1.13 (95% CI 1.01–1.26)
Meta-analysis of RCTs suggests a potential 13% increased risk of heart failure with DPP-4 inhibitors, though significant heterogeneity exists between individual agents.
May warrant caution prescribing DPP-4 inhibitors to patients at heart failure risk; confirms signals from prior trials.
Background: Given recent discrepant results from randomized controlled trials (RCTs), we examined the totality of RCT evidence assessing the association between dipeptidyl peptidase-4 (DPP-4) inhibitors and heart failure. Methods: MEDLINE, Embase and ClinicalTrials.gov were searched without language restrictions to August 2016 for RCTs comparing DPP-4 inhibitors to placebo or no therapy for a period of 24 weeks or more. We included all heart failure outcomes when listed either as a serious adverse event or adverse event. Pooled analyses used random-effects. Results: We identified 100 RCTs (n = 79 867) - 3 large cardiovascular-safety RCTs (SAVOR-TIMI 53[saxagliptin]/n = 16 492, EXAMINE[alogliptin]/n = 5380, and TECOS[sitagliptin]/n = 14 735), and 97 smaller RCTs with a primary outcome that was usually change in glycated hemoglobin. Virtually all RCTs were high-quality, multicentre, placebo-controlled trials. A total of 96% (1192/1244) of heart failure events were prespecified, blindly adjudicated and required hospital admission. Pooled results suggested a 13% increase in heart failure (relative risk [RR] 1.13, 95% confidence interval [CI] 1.01-1.26, I2 = 0%; 32 RCTs, n = 54 640, 1244 events). When including only the 3 large RCTs, the increase was similar, but not significant (RR 1.14, 95% CI 0.97-1.32; 3 RCTs, n = 36 543, 1169 adjudicated events; number needed to harm 246) owing to heterogeneity (I2 = 42%), which lead to wider CIs, because SAVOR-TIMI 53 showed increased heart failure (RR 1.26, 95% CI 1.06-1.49) and TECOS showed no effect (RR 1.00, 95% CI 0.83-1.19). Interpretation: Despite pooled data from 79 867 patients, whether DPP-4 inhibitors increase heart failure overall or exhibit within-class differences remains unresolved. Our results highlight the importance of ongoing trials that are comparing DPP-4 inhibitors to placebo, although no large cardiovascular-safety RCTs are comparing different DPP-4 inhibitors to each other; consequently, these will address the overall but not class-difference question.
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Verma et al. (2017) reported a meta-analysis. Dipeptidyl peptidase-4 (DPP-4) inhibitors vs. placebo or no therapy was evaluated on heart failure (RR 1.13, 95% CI 1.01-1.26). Dipeptidyl peptidase-4 (DPP-4) inhibitors were associated with a 13% increased risk of heart failure compared to placebo or no therapy (RR 1.13; 95% CI 1.01-1.26).
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