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Randomized Trial of Anti-inflammatory Medications and Coronary Endothelial Dysfunction in Patients With Stable
Allison G Hays1, Michael Schär2, Gabriele Bonanno2
1Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Insights
Anti-inflammatory drugs, including methotrexate and colchicine, did not improve coronary endothelial function in patients with stable coronary artery disease (CAD). This study found no significant benefits for vascular health markers in CAD patients treated with these therapies.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Medical Imaging
Background:
- Inflammation is a key factor in coronary artery disease (CAD) pathogenesis.
- Impaired coronary endothelial function (CEF) drives atherosclerosis in CAD patients.
- The efficacy of anti-inflammatory therapies on CEF in stable CAD is not well understood.
Purpose of the Study:
- To investigate if anti-inflammatory approaches improve CEF in stable CAD patients.
- To test the hypothesis that methotrexate (MTX), low dose colchicine (LDC), or their combination (MTX+LDC) enhance CEF.
- To assess the impact of these therapies on coronary atherosclerosis markers.
Main Methods:
- A single-center, randomized, placebo-controlled, double-blinded trial involving 94 stable CAD patients.
- Assessed CEF using non-invasive MRI measures, focusing on coronary cross-sectional area changes during isometric handgrip exercise (IHE).
- Collected data on coronary/systemic endothelial function and inflammatory markers at baseline, 8, and 24 weeks.
Main Results:
- Anti-inflammatory drugs (MTX, LDC, MTX+LDC) were well-tolerated.
- No significant differences in CEF parameters were observed among the four groups (MTX, LDC, MTX+LDC, placebo) at 8 or 24 weeks.
- Serum inflammatory markers and systemic endothelial function measures also showed no significant group differences.
Conclusions:
- This is the first study to evaluate MTX, LDC, or combination therapy for CEF in stable CAD.
- These anti-inflammatory approaches, while tolerated, did not improve coronary endothelial function in the studied population.
- The findings suggest these therapies may not be beneficial for improving vascular health markers in stable CAD patients.
Abstract:
Aims: Inflammation plays a critical role in the pathogenesis of coronary artery disease (CAD), however the impact of anti-inflammatory therapies to reduce those processes which promote atherosclerosis in CAD patients is unknown. We aimed to test the hypothesis that anti-inflammatory approaches improve impaired coronary endothelial function (CEF), a driver of coronary atherosclerosis, in stable CAD patients. Methods and Results: We performed a single-center, randomized, placebo-controlled, double-blinded trial to assess whether low dose methotrexate (MTX), low dose colchicine (LDC), and/or their combination (MTX+LDC), improves CEF using non-invasive MRI measures in patients with stable CAD (N = 94). The primary endpoint was the MRI-detected change in coronary cross-sectional area from rest to isometric handgrip exercise (IHE), a predominantly nitric oxide-dependent endothelial dependent stressor. Coronary and systemic endothelial endpoints, and serum inflammatory markers, were collected at baseline, 8 and 24 weeks. Anti-inflammatory study drugs were well-tolerated. There were no significant differences in any of the CEF parameters among the four groups (MTX, LDC, MTX+LDC, placebo) at 8 or 24 weeks. Serum markers of inflammation and systemic endothelial function measures were also not significantly different among the groups. Conclusion: This is the first study to examine the effects of the anti-inflammatory approaches using MTX, LDC, and/or the combination in stable CAD patients on CEF, a marker of vascular health and the primary endpoint of the study. Although these anti-inflammatory approaches were relatively well-tolerated, they did not improve coronary endothelial function in patients with stable CAD. Clinical Trial Registration: www.clinicaltrials.gov, identifier: NCT02366091.
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