Low-Dose Colchicine for Atherosclerosis: Key Points
- Authors:
- Nidorf SM, Ben-Chetrit E, Ridker PM.
- Citation:
- Low-Dose Colchicine for Atherosclerosis: Long-Term Safety. Eur Heart J 2024;Apr 10:[Epub ahead of print].
The following are key points to remember from a state-of-the-art review on the long-term safety of low-dose colchicine for atherosclerosis:
- Colchicine 0.5 mg daily is FDA-approved for secondary prevention in patients with coronary artery disease (CAD).
- These recommendations are rooted in the findings of the LoDoCo2 and COLCOT trials that showed a 31% drop in cardiovascular events in patients with clinically stable atherosclerosis. A similar drop of 23% was seen in patients with recent myocardial infarction.
- The experience of most clinicians with colchicine is for gout and pericarditis. The higher doses used for these conditions are often fraught with side effects.
- Many clinicians may be hesitant to use the lower dose of colchicine recommended for CAD out of concern of the potential for significant side effects.
- This review looked at a 20-year experience of continuous use colchicine for a variety of indications.
- The main finding was that the 0.5 mg daily dose of colchicine in appropriate patients has side effects like placebo. This includes myelosuppression, myotoxicity, and cancer.
- There is minimal evidence that colchicine increases the risk of serious or fatal infection.
- Patients on low-dose colchicine often report mild diarrhea after the medication is started, but it typically resolves quickly.
- Colchicine at a low dose has no negative effect on bleeding, wound healing, fertility, or pregnancy.
- This lack of significant adverse effects includes patients who are on statins.
- Even low-dose colchicine should NOT be used in patients with estimated glomerular filtration rate <45 mL/min/173 m2, cytopenia, advanced liver dysfunction, creatine kinase or alanine transaminase >3 x the upper limits of normal.
- Colchicine should be held in patients taking clarithromycin, ketoconazole, fluconazole, cyclosporine, ritonavir, or other strong CYP3A4 inhibitors or P-glycoprotein inhibitors.
- Long-term use of low-dose colchicine in patients with normal renal and hepatic function is otherwise very safe.
- The clear safety of low-dose colchicine in appropriate patients suggests that it is a medication that should be used far more widely for secondary prevention of CAD in patients with normal renal and hepatic function.
Clinical Topics: Prevention
Keywords: Atherosclerosis, Colchicine, Secondary Prevention
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