Inflammation as potential target for therapy to target residual risk post ACS
This lecture was part of a CME accredited symposium: How to address residual risk post ACS: LDL-c, dyslipidemia, and inflammation held at ESC 2016 in Rome
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Residual inflammatory risk versus residual cholesterol risk 00:23
Lowering hsCRP to reduce CV events 02:21
Targeting inflammatory pathways for the treatment of CVD 04:27
From CRP to IL-6 to IL-1: moving upstream to identify novel targets for atheroprotection 05:37
CIRT trial: low-dose methotrexate for reducing CV events 06:45
CANTOS-trial (canakinumab): background and design 08:18
Other ongoing areas of inflammation biology 11:14
Educational information
The educational objectives of this symposum were to:
- Discuss the potential of current and future strategies targeting inflammation in reducing residual risk in post ACS patients
- Outline current ongoing clinical development programs aimed at testing the inflammation hypothesis of cardiovascular disease
- Understand the unmet need for additional LDL-C-lowering therapies beyond current optimal statin-based therapy as a strategy for addressing lipid-related CV risk in patients post ACS
- Describe the potential impact of PCSK9-based therapies in development in patients who require additional LDL-C reduction
- To review the clinical significance of additional lipid lowering pathways, such as ezetimibe, in the management of patients with ACS
- Understand the implications of new guidelines for lipid management
Faculty
Paul M Ridker, MD, MPH: Eugene Braunwald Professor of Medicine, Harvard Medical School, Director, Center for Cardiovascular Disease Prevention, Brigham and Women’s Hospital, Boston, Massachusetts
Disclosures
This EBAC accredited symposium was funded by an unrestricted educational grants received from Novartis, MSD, Amgen
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The information and data provided in this program were updated and correct at the time of the program development, but may be subject to change.
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