Key result
PCSK9 inhibitor initiation linked to ~43% lower 1-year risk of new-onset HF versus statins.
Why the study?
It was unclear whether PCSK9 inhibitors lower the risk of incident heart failure beyond statins in patients with dyslipidaemia and coronary artery disease.
Does PCSK9 inhibitor therapy reduce new-onset heart failure in adults with dyslipidaemia and coronary artery disease compared to statin therapy?
Cohort (n=41,396)
Yes
Does PCSK9 inhibitor therapy reduce new-onset heart failure in adults with dyslipidaemia and coronary artery disease compared to statin therapy?
Effect estimate: HR 0.566 (95% CI 0.506-0.634)
Absolute Event Rate: 2.25% vs 4.08%
p-value: p=<0.0001
In adults with dyslipidaemia and CAD, initiation of a PCSK9 inhibitor is associated with a significantly lower 1-year risk of incident heart failure, MACE, and mortality compared to statins.
Background/Introduction Whether proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) lower the risk of incident heart failure (HF) beyond statins in patients with dyslipidaemia and coronary artery disease (CAD) is unclear. Purpose To compare 1-year risk of new-onset HF between PCSK9i and statin therapy among adults with dyslipidaemia and CAD. Methods We performed a retrospective cohort study on a large federated electronic health record network. Adults (≥18 years) with dyslipidaemia and CAD who newly initiated a PCSK9i (alirocumab, evolocumab or inclisiran) or a statin (ATC C10AA) between 2015–2025 were eligible. One-to-one propensity score matching (caliper 0.1 SD) balanced demographics, comorbidities, laboratory values and concomitant medications. Follow-up began the day after index prescription and continued to 365 days. Primary outcome: new-onset HF. Secondary outcomes: three-point major adverse cardiovascular events (MACE; myocardial infarction, stroke, cardiovascular death) and all-cause mortality. Cox models estimated hazard ratios (HRs) with 95% CIs. Results After matching, 20,698 patients remained in each group. Over 1 year, PCSK9i users had fewer primary events than statin users (466 vs 844), yielding HR 0.566 (95% CI 0.506–0.634; p<0.0001). Three-point MACE was also lower (483 vs 840; HR 0.594, 95% CI 0.532–0.665; p<0.0001). All-cause mortality was markedly reduced (166 vs 532; HR 0.325, 95% CI 0.273–0.387; p<0.0001). Results were robust in sensitivity analyses; a negative control outcome showed no association. Conclusions In adults with dyslipidaemia and CAD, initiation of a PCSK9i was associated with a significantly lower 1-year risk of new-onset HF, alongside reductions in three-point MACE and all-cause mortality versus statins. These real-world findings support a potential secondary-prevention role of PCSK9i for HF risk reduction and warrant prospective confirmation.For image description, please refer to the figure legend and surrounding text.
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Lin et al. (2026) conducted a cohort in dyslipidaemia and coronary artery disease (n=41,396). PCSK9 inhibitors (alirocumab, evolocumab or inclisiran) vs. statin was evaluated on new-onset heart failure (HR 0.566, 95% CI 0.506-0.634, p=<0.0001). Initiation of a PCSK9 inhibitor was associated with a significantly lower 1-year risk of new-onset heart failure compared to statins (HR 0.566; 95% CI 0.506–0.634; p<0.0001).
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