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Published on: May 28, 2019
Effects of routine early treatment with PCSK9 inhibitors in patients undergoing primary percutaneous coronary
Shamir R Mehta1,2,3, Guillaume Pare1,2,3,4, Eva M Lonn1,2,3
1Population Health Research Institute, Hamilton, ON, Canada.
Insights
Early PCSK9 inhibitor therapy with alirocumab significantly reduced LDL cholesterol by 22% in STEMI patients. This strategy, added to high-intensity statins, offers a promising approach for acute myocardial infarction management.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Early high-intensity statin therapy is standard for ST-segment elevation myocardial infarction (STEMI).
- The role of adding proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors early for LDL cholesterol reduction in STEMI is under investigation.
Purpose of the Study:
- To evaluate the effect of early alirocumab initiation, alongside high-intensity statins, on LDL cholesterol levels in patients with acute STEMI.
Main Methods:
- A randomized, double-blind trial involving 68 STEMI patients undergoing primary percutaneous coronary intervention (PCI).
- Patients received either subcutaneous alirocumab 150 mg or a matching sham control, with the first dose before PCI, followed by doses at 2 and 4 weeks.
- The primary outcome was the percentage reduction in LDL cholesterol up to 6 weeks.
Main Results:
- Alirocumab reduced LDL cholesterol by 72.9% compared to 48.1% in the sham group (mean difference -22.3%, p<0.001) at a median of 45 days.
- 92.1% of patients in the alirocumab group achieved the guideline target LDL ≤1.4 mmol/L versus 56.7% in the sham group (p<0.001).
- LDL cholesterol declined slightly more rapidly within the first 24 hours in the alirocumab group.
Conclusions:
- Routine early initiation of PCSK9 inhibitors (alirocumab) significantly reduces LDL cholesterol in STEMI patients on high-intensity statins.
- This simplified approach warrants further investigation in larger trials to confirm its impact on cardiovascular outcomes.
Background:
In patients with ST-segment elevation myocardial infarction (STEMI), early initiation of high-intensity statin therapy, regardless of low-density lipoprotein (LDL) cholesterol levels, is the standard of practice worldwide. Aims: We sought to determine the effect of a similar early initiation strategy, using a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor added to the high-intensity statin, on LDL cholesterol in acute STEMI.
Methods:
In a randomised, double-blind trial we assigned 68 patients with STEMI undergoing primary percutaneous coronary intervention (PCI) to early treatment with alirocumab 150 mg subcutaneously or to a matching sham control. The first injection was given before primary PCI regardless of the baseline LDL level, then at 2 and 4 weeks. The primary outcome was the percent reduction in direct LDL cholesterol up to 6 weeks, analysed using a linear mixed model. Results: High-intensity statin use was 97% and 100% in the alirocumab and sham-control groups, respectively. At a median of 45 days, the primary outcome of LDL cholesterol decreased by 72.9% with alirocumab (2.97 mmol/L to 0.75 mmol/L) versus 48.1% with the sham control (2.87 mmol/L to 1.30 mmol/L), for a mean between-group difference of -22.3% (p<0.001). More patients achieved the European Society of Cardiology/European Atherosclerosis Society dyslipidaemia guideline target of LDL ≤1.4 mmol/L in the alirocumab group (92.1% vs 56.7%; p<0.001). Within the first 24 hours, LDL declined slightly more rapidly in the alirocumab group than in the sham-control group (-0.01 mmol/L/hour; p=0.03) with similar between-group mean values. Conclusions: In this randomised trial of routine early initiation of PCSK9 inhibitors in patients undergoing primary PCI for STEMI, alirocumab reduced LDL cholesterol by 22% compared with sham control on a background of high-intensity statin therapy. A large trial is needed to determine if this simplified approach followed by long-term therapy improves cardiovascular outcomes in patients with acute STEMI. (ClinicalTrials.gov: NCT03718286).
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