PCSK9 inhibitors are monoclonal antibodies that have been shown to lower LDL cholesterol levels by up to 60% independent of other therapies. They are currently recommended for secondary prevention of cardiovascular events due to their high cost, though trials have demonstrated their ability to reduce cardiovascular events when added to other treatments. PCSK9 inhibitors work by inhibiting the PCSK9 protein in the liver that prevents the removal of LDL cholesterol from the bloodstream.
PCSK9 inhibitors are monoclonal antibodies that have been shown to lower LDL cholesterol levels by up to 60% independent of other therapies. They are currently recommended for secondary prevention of cardiovascular events due to their high cost, though trials have demonstrated their ability to reduce cardiovascular events when added to other treatments. PCSK9 inhibitors work by inhibiting the PCSK9 protein in the liver that prevents the removal of LDL cholesterol from the bloodstream.
PCSK9 inhibitors are monoclonal antibodies that have been shown to lower LDL cholesterol levels by up to 60% independent of other therapies. They are currently recommended for secondary prevention of cardiovascular events due to their high cost, though trials have demonstrated their ability to reduce cardiovascular events when added to other treatments. PCSK9 inhibitors work by inhibiting the PCSK9 protein in the liver that prevents the removal of LDL cholesterol from the bloodstream.
PCSK-9 inhibitors are relatively new monoclonal antibody
agents and have demonstrated improvement in LDL-C by up to 60%, and this effect is thought to be independent of additional therapy already initiated. Their use is currently recommended in secondary prevention, as they can be difficult to access and their high cost prohibitive for most patients/health systems. The JUPITER trial was one of the first to demonstrate an inflammatory component to atherosclerosis, and the FOURIER and ODYSSEY trials have since demonstrated a reduction in cardiovascular events with the addition of PCSK- 9 inhibitors.
Cardiovascular Risk in Clopidogrel-Treated Patients According To Cytochrome P450 2C19 2 Loss-of-Function Allele or Proton Pump Inhibitor Coadministration