Lipoprotein(a) and the effect of alirocumab on coronary and non-coronary revascularization following acute coronary syndrome

التفاصيل البيبلوغرافية
العنوان: Lipoprotein(a) and the effect of alirocumab on coronary and non-coronary revascularization following acute coronary syndrome
المؤلفون: P Steg, M Szarek, M Valgimigli, S Islam, A M Zeiher, D L Bhatt, V A Bittner, R Diaz, S G Goodman, R A Harrington, J W Jukema, R Pordy, M Scemama, H D White, G G Schwartz
المصدر: European Heart Journal. 43
بيانات النشر: Oxford University Press (OUP), 2022.
سنة النشر: 2022
مصطلحات موضوعية: Cardiology and Cardiovascular Medicine
الوصف: Background Many patients require arterial revascularization after an index ACS. Lipoprotein(a) is thought to play a pathogenic role in atherothrombosis. In the ODYSSEY OUTCOMES trial, the PCSK9 inhibitor alirocumab reduced major adverse cardiovascular events after ACS, with greater reduction among those with higher lipoprotein(a). Objectives We determined whether the risk of first coronary or any (coronary, peripheral artery or carotid) revascularization after ACS was modified by the level of lipoprotein(a) and treatment with alirocumab or placebo. Methods The ODYSSEY OUTCOMES trial (NCT01663402) compared alirocumab with placebo in 18,924 patients with ACS and elevated atherogenic lipoproteins despite optimized statin treatment. Treatment effects were summarized by competing-risks proportional hazard models. Results A total of 1559 (8.2%) patients had coronary, 204 (1.1%) peripheral artery, and 40 (0.2%) carotid revascularization after randomization. Alirocumab reduced first coronary revascularization (9.6% vs. 11.3% at 4 years; hazard ratio [HR] 0.88, 95% confidence interval [CI] 0.80–0.97; p=0.01) and any first revascularization (10.8% vs. 13.0%; HR 0.85, 95% CI 0.78–0.94; p=0.001). Baseline lipoprotein(a) quartile was directly associated with risk of coronary or any revascularization in the placebo arm (ptrend Conclusions Alirocumab reduced revascularization after ACS. The risk of revascularization and reduction in that risk with alirocumab were greatest in patients with elevated lipoprotein(a) at baseline. Funding Acknowledgement Type of funding sources: Private company. Main funding source(s): SanofiRegeneron Pharmaceuticals
تدمد: 1522-9645
0195-668X
0166-3402
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0456672f162cdcab57c1da7d3fcee816
https://doi.org/10.1093/eurheartj/ehac544.1386
حقوق: CLOSED
رقم الأكسشن: edsair.doi...........0456672f162cdcab57c1da7d3fcee816
قاعدة البيانات: OpenAIRE
الوصف
تدمد:15229645
0195668X
01663402