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Colchicine in Patients With Chronic Coronary Disease in Relation to Prior Acute Coronary Syndrome
Tjerk S J Opstal1, Aernoud T L Fiolet2, Amber van Broekhoven3
1Department of Cardiology, Radboud University Medical Center, Nijmegen, the Netherlands; Department of Cardiology, Northwest Clinics, Alkmaar, the Netherlands.
Insights
Colchicine consistently reduces cardiovascular events in patients with chronic coronary disease, regardless of their history or the timing of previous acute coronary syndrome (ACS). This finding supports its use in secondary cardiovascular prevention.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Colchicine demonstrates efficacy in reducing cardiovascular events post-myocardial infarction and in chronic coronary disease.
- The impact of treatment timing relative to acute coronary syndrome (ACS) on colchicine's benefits is not well-established.
Purpose of the Study:
- To investigate major adverse cardiovascular events in relation to the history and timing of prior ACS.
- To determine if colchicine's benefits are consistent across different prior ACS statuses.
Main Methods:
- The LoDoCo2 trial randomized patients with chronic coronary disease to colchicine or placebo.
- Analysis compared cardiovascular event rates based on prior ACS history: none, recent (6-24 months), remote (2-7 years), or very remote (>7 years).
- Interaction between ACS status and colchicine treatment effect was assessed.
Main Results:
- In 5,522 patients, colchicine consistently reduced the primary endpoint (cardiovascular death, myocardial infarction, stroke, revascularization) across all prior ACS groups.
- Hazard ratios for colchicine vs. placebo ranged from 0.55 to 0.81, with no significant interaction (P=0.59).
- Specific results showed reduced events in no prior ACS (HR 0.81), recent ACS (HR 0.75), remote ACS (HR 0.55), and very remote ACS (HR 0.70).
Conclusions:
- Colchicine provides consistent cardiovascular benefits irrespective of the history and timing of prior acute coronary syndrome.
- These findings support the use of colchicine for secondary prevention in patients with chronic coronary disease, regardless of their ACS timeline.
Background:
Colchicine reduces risk of cardiovascular events in patients post-myocardial infarction and in patients with chronic coronary disease. It remains unclear whether this effect is related to the time of onset of treatment following an acute coronary syndrome (ACS).
Objectives:
This study investigates risk for major adverse cardiovascular events in relation to history and timing of prior ACS, to determine whether the benefits of colchicine are consistent independent of prior ACS status.
Methods:
The LoDoCo2 (Low-Dose Colchicine 2) trial randomly allocated patients with chronic coronary disease to colchicine 0.5 mg once daily or placebo. The rate of the composite of cardiovascular death, spontaneous myocardial infarction, ischemic stroke, or ischemia-driven coronary revascularization was compared between patients with no prior, recent (6-24 months), remote (2-7 years), or very remote (>7 years) ACS; interaction between ACS status and colchicine treatment effect was assessed.
Results:
In 5,522 randomized patients, risk of the primary endpoint was independent of prior ACS status. Colchicine consistently reduced the primary endpoint in patients with no prior ACS (incidence: 2.8 vs 3.4 events per 100 person-years; hazard ratio [HR]: 0.81; 95% confidence interval [CI]: 0.52-1.27), recent ACS (incidence: 2.4 vs 3.3 events per 100 person-years; HR: 0.75; 95% CI: 0.51-1.10), remote ACS (incidence: 1.8 vs 3.2 events per 100 person-years, HR: 0.55; 95% CI: 0.37-0.82), and very remote ACS (incidence: 3.0 vs 4.3 events per 100 person-years, HR: 0.70; 95% CI: 0.51-0.96) (P for interaction = 0.59).
Conclusions:
The benefits of colchicine are consistent irrespective of history and timing of prior ACS. (The LoDoCo2 Trial: Low Dose Colchicine for secondary prevention of cardiovascular disease [LoDoCo2] ACTRN12614000093684).
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