Effect of colchicine on progression of known coronary atherosclerosis in patients with stable coronary artery disease: EKSTROM randomized placebo controlled trial

Inflammation plays a crucial role in atherosclerosis and coronary artery disease progression. Colchicine, an inexpensive anti-inflammatory medication, has shown promising results in reducing cardiovascular events in patients with stable coronary artery disease (CAD). However, its effect on coronary plaque progression remains unclear. We investigated whether colchicine, as an adjunct to standard of care therapy, affects coronary plaque components in patients with stable CAD.

We performed a prospective, randomized, double-blinded, placebo-controlled trial in 84 patients with stable CAD to receive either colchicine (0.5 mg/day) or placebo for 12 months. All enrolled patients had proven coronary artery disease as evidenced by coronary angiography, CT coronary angiography, or a Coronary Artery Calcium Score >400. The primary outcome was the rate of change in low attenuation plaque (LAP) volume, as measured by serial coronary computed tomography angiography (CCTA), utilizing volumetric plaque quantification software at 12 months between colchicine and placebo groups. The secondary endpoint was total plaque percent atheroma volume (PAV%). The sample size was set assuming a treatment difference of at least 8 mm³ change in LAP volume in favour of colchicine compared to placebo. The mean age of the 72 participants who completed the study was 64.6 ± 7.3 years, with 63 (88%) subjects being male. Baseline demographics, risk factors, medications, vitals, and inflammatory markers were not significantly different between the colchicine and placebo groups. One exception was that the colchicine group had significantly higher use of hypertension medications (75% vs. 44%) at the study start. There was no significant difference in the change in total LAP between the colchicine group with median (IQR) 0.1 (−02, 0.2) vs. 0.0 (−0.2, 0.3) in placebo, un-adjusted P = 0.342. Multivariable models, including known CV risk factors and baseline LAP, also showed no significant difference between the changes in LAP between treatment and placebo groups. A treatment effect was observed in the total PAV%. Follow-up total PAV at 12-month scan was significantly lower at median (IQR) 0.3 (−0.1, 1.3) in the colchicine group vs. 1.4 (0.4, 2.6) in placebo, P = 0.008 (unadjusted). In multivariate models, colchicine treatment was associated with lower PAV at 1 year, P = 0.015. Trends toward regression in non-calcified and fibro-fatty plaque were observed. Inflammatory markers were reduced with colchicine, but did not achieve statistical significance.

In the EKSTROM trial, low-dose colchicine did not significantly reduce low attenuation plaque volume in patients with stable coronary artery disease over 12 months, but did achieve a significant reduction in total plaque burden (percent atheroma volume) and dense calcified plaque compared to placebo. Colchicine was well tolerated, with no major safety concerns. In this stable well-treated CAD population, LAP was rare and not significantly reduced; however, it slowed overall plaque progression, supporting further investigation of its role in secondary prevention of coronary artery disease.

NCT06342609.