Key result
DPP-4 inhibitors increase HF hospitalization ~27% in moderate renal dysfunction without increasing primary CV events.
Why the study?
Recent studies suggested that the increased risk of heart failure by DPP-4 inhibitors may be related to patients' baseline renal function, necessitating investigation of cardiovascular safety in T2D patients with renal impairment.
Do DPP-4 inhibitors increase the risk of cardiovascular events or heart failure in type 2 diabetes patients with renal impairment?
Meta-Analysis (n=11,789)
Do DPP-4 inhibitors increase the risk of cardiovascular events or heart failure in type 2 diabetes patients with renal impairment?
While DPP-4 inhibitors do not increase overall cardiovascular events in T2D patients with renal impairment, they significantly increase the risk of heart failure hospitalization specifically in those with moderate renal dysfunction.
Advise caution with DPP-4 inhibitors in moderate renal dysfunction; extends HF risk signal to renally impaired patients.
Background: Recent studies suggested that the increased risk of heart failure by DPP-4 inhibitors may have an interconnection with patients' baseline eGFR. We decided to investigate the effect of DPP-4 inhibitors and the degree of renal function on cardiovascular (CV) safety in type 2 diabetes (T2D) patients. Materials and Methods: Systemic search of literature that examined the DPP-4 inhibitors and reported cardiovascular outcomes in diabetes patients with renal impairment were performed. Studies were examined for inclusion criteria: Randomized controlled trials with reduced renal function taking DPP-4 inhibitors alone or in combination with other anti-diabetes agents reporting evaluable CV events for at least 24 weeks. Result: Analysis of four CV outcome studies (11,789 patients with eGFR ≤60 ml/min/1.73m2) did not find any increase in primary composite endpoints with DPP-4 inhibitors in patients stratified by baseline renal function. Rate of hospitalization due to heart failure (hHF) is found to be non-inferior to placebo group in patients with renal insufficiency (RR 1.07; 95% CI, 0.96-1.20 P = 0.26). In moderate renal dysfunction, there is a significant increase in heart failure risk compared to placebo. (RR 1.27; 95% CI, 1.033 -1.5 8; P = 0.024). Conclusion: Treatment with DPP-4 inhibitors did not affect the risk of cardiovascular events regardless of baseline renal function, however, an increase in the risk of hHF in moderate renal function in T2D patients with high CV risk merits careful consideration. Further research would be necessitated to reach definitive conclusion to understand the effect of declining renal function on CV safety of DPP-4 inhibitors.
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Khalse et al. (2020) conducted a meta-analysis in Type 2 diabetes with renal impairment (n=11,789). DPP-4 inhibitors vs. Placebo was evaluated on Hospitalization due to heart failure (hHF) in patients with renal insufficiency (RR 1.07, 95% CI 0.96-1.20, p=0.26). DPP-4 inhibitors did not increase primary cardiovascular endpoints but increased heart failure hospitalization in patients with moderate renal dysfunction (RR 1.27; 95% CI 1.033-1.58; P=0.024).
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