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Dipeptidyl peptidase-4 inhibitors and cardiovascular risks in patients with pre-existing heart failure
Shuo-Ming Ou1,2, Hung-Ta Chen2,3, Shu-Chen Kuo2,4,5
1Division of Nephrology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Insights
Dipeptidyl peptidase-4 (DPP-4) inhibitors reduced mortality and cardiovascular events in type 2 diabetes patients with heart failure. DPP-4 inhibitor use did not increase heart failure hospitalization risk in this population.
Area of Science:
- Cardiology
- Endocrinology
- Pharmacology
Background:
- Recent trials questioned heart failure (HF) risk with dipeptidyl peptidase-4 (DPP-4) inhibitors.
- Limited data exist on cardiovascular risks of DPP-4 inhibitors in patients with pre-existing HF.
Purpose of the Study:
- To evaluate the cardiovascular safety and efficacy of DPP-4 inhibitors in patients with type 2 diabetes mellitus (T2DM) and pre-existing HF.
- To assess the association between DPP-4 inhibitor use and outcomes including all-cause mortality, myocardial infarction (MI), ischemic stroke, and HF hospitalization.
Main Methods:
- A nationwide cohort study using Taiwan's National Health Insurance Research Database (2009-2013).
- Identified 196,986 T2DM patients with prior HF history.
- Compared 30,204 DPP-4 inhibitor users with 166,782 propensity score-matched non-users, analyzing mortality, MI, ischemic stroke, and HF hospitalization.
Main Results:
- DPP-4 inhibitor users showed significantly lower risks of all-cause mortality (HR 0.67) and the composite of MI and ischemic stroke (HR 0.81).
- Specific reductions were observed for MI (HR 0.80) and ischemic stroke (HR 0.83) in DPP-4 inhibitor users.
- Crucially, no significant difference in HF hospitalization risk was found between DPP-4 inhibitor users and non-users.
Conclusions:
- DPP-4 inhibitor use is associated with reduced mortality and major adverse cardiovascular events in T2DM patients with pre-existing HF.
- DPP-4 inhibitors are safe regarding HF hospitalization risk in this high-risk T2DM population.
- Findings support the use of DPP-4 inhibitors for glycemic control without increasing HF risk in T2DM patients with HF history.
Background:
Although recent clinical trials raised concerns about the risk for heart failure (HF) in dipeptidyl peptidase-4 (DPP-4) inhibitor use, data on the cardiovascular risks in the patients with pre-existing HF are still lacking.
Methods:
We used Taiwan's National Health Insurance Research Database to identify 196 986 patients diagnosed with type 2 diabetes mellitus (T2DM) who had previous history of HF between 2009 and 2013. This population included 30 204 DPP-4 inhibitor users and 166 782 propensity score-matched DPP-4 inhibitor non-users. The outcomes of interest were all-cause mortality, combination of myocardial infarction (MI) and ischaemic stroke, and hospitalisation for HF.
Results:
The incidence in DPP-4 users compared with non-users was 67.02 vs 102.85 per 1000 person-years for all-cause mortality, 37.89 vs 47.54 per 1000 person-years for the combination of MI and ischaemic stroke, 12.70 vs 16.18 per 1000 person-years for MI and 26.37 vs 32.46 per 1000 person-years for ischaemic stroke. The risk of all-cause mortality was lower in DPP-4 inhibitor users (HR 0.67, 95% CI 0.64 to 0.70), combination of MI and stroke (HR 0.81, 95% CI 0.76 to 0.87), MI (HR 0.80, 95% CI 0.71 to 0.89) and ischaemic stroke (HR 0.83, 95% CI 0.76 to 0.89) than in non-users. Notably, the risk of hospitalisation for HF did not differ significantly between groups. The results were similar after accounting for death as a competing risk.
Conclusions:
In this nationwide T2DM cohort, the risks of mortality and the combination of MI and ischaemic stroke were lower for patients receiving DPP-4 inhibitors than for those who did not receive such treatment. DPP-4 inhibitor use was not associated with a higher risk of hospitalisation for HF even in patients with pre-existing HF.
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