Use of Low-Dose Colchicine Safe for Prevention of Coronary artery Disease, new Study Reveals

Findings:

• One of the key findings highlighted in the review is the overwhelmingly positive safety profile of low-dose colchicine.
• According to the data collated, the most commonly reported side effect is mild diarrhea, typically occurring during the initiation phase of treatment and subsiding within a week for the vast majority of patients.
• Crucially, the review found no significant adverse effects of low-dose colchicine on renal, liver, or cognitive function.
• Furthermore, the medication does not appear to impact bleeding, wound healing, fertility, or pregnancy outcomes.
• No evidence was found to suggest an increased risk of cancer, serious infection, or cause-specific mortality associated with its use.
• Of particular interest is the investigation into potential interactions between low-dose colchicine and statin therapy, a commonly prescribed treatment for cardiovascular disease.
• Contrary to concerns, the data indicate that patients concurrently taking statins do not face heightened risks of myelosuppression, myotoxicity, or serious drug interactions when prescribed low-dose colchicine.

The implications of these findings are profound for clinical practice. Physicians, pharmacists, and patients can now approach the use of low-dose colchicine with greater confidence, especially in the context of reducing cardiovascular risk among individuals with atherosclerosis. Importantly, the review suggests that when appropriately prescribed to patients without significant renal or hepatic impairment, the risks associated with continuous use of low-dose colchicine are minimal. This study marks a significant milestone in our understanding of low-dose colchicine, paving the way for its wider adoption in clinical practice as a safe and effective therapy for cardiovascular disease.

Further research: Nidorf, Stefan Mark et al. “Low-dose colchicine for atherosclerosis: long-term safety.” European heart journal, ehae208. 10 Apr. 2024, doi:10.1093/eurheartj/ehae208.