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Early Administration of Proprotein Convertase Subtilisin/Kexin Type 9 (Pcsk9) Inhibitors in Patients With Acute Coronary Syndrome: A Systematic Review and Meta-Analysis Publisher Pubmed



Hosseini K1, 2 ; Soleimani H1, 2, 3 ; Maleki S1, 4 ; Nasrollahizadeh A1, 2 ; Tayebi S5 ; Nelson J6 ; Heffron SP7
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Authors Affiliations
  1. 1. Cardiac Primary Prevention Research Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, 1419733141, Iran
  2. 2. Cardiovascular Diseases Research Institute, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, 1419733141, Iran
  3. 3. Non-Communicable Diseases Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, 1411713139, Iran
  4. 4. School of Medicine, Guilan University of Medical Sciences (GUMS), Guilan Province, Rasht, Iran
  5. 5. Centre for Clinical Research Sormland, Uppsala University, Uppsala, SE, Sweden
  6. 6. California Cardiovascular Institute, Fresno, CA, United States
  7. 7. Center for the Prevention of Cardiovascular Disease, Leon H. Charney Division of Cardiology, NYU Langone Health, New York University Grossman School of Medicine, New York, NY, United States

Source: BMC Cardiovascular Disorders Published:2024


Abstract

Background: High-intensity statin therapy is currently recommended initial guideline therapy in ACS treatment. However, only a minority of patients are achieving LDL-C attainment goal at 6 months. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are on recommended guideline therapy post-ACS if LDL-C goal attainment is not achieved after high-intensity statin (4–6 weeks) and after the addition of ezetimibe if guideline goal attainment is not achieved after an additional 4–6 weeks. Thus, it has been recommended that PCSK9 inhibitors be considered earlier post-ACS. However, the efficacy of early PCSK9 inhibitors initiation in ACS patients remains uncertain. Methods: This systematic review and meta-analysis was conducted following PRISMA guidelines. Randomized controlled trials (RCTs) and observational studies involving ACS patients who received PCSK9 inhibitors within 48 h of hospitalization were included. Common and random effects models were used to evaluate the pooled effect of early PCSK9 inhibitor administration. Nine RCTs and three cohort studies were included. Results: Early PCSK9 inhibitor administration reduced the incidence of MI, ACS hospitalization, and revascularization at 6–18 months post-ACS. Although there was a drift towards reduced stroke, all-cause mortality, and cardiovascular death, no statistically significant reduction was observed. Additionally, PCSK9 inhibitors significantly enhanced lipid control at 4–12 weeks after index hospitalization. Conclusion: Early PCSK9 inhibitors initiation in ACS patients reduces MACE and improves lipid profiles. While the results propose promising benefits in terms of stroke and mortality, further research with longer follow-up is required for more decisive evidence. © The Author(s) 2024.
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