Myocardial Infarction
Conditions
Keywords
myocardial infarction, colchicine, anti-inflammatory
Brief summary
The aim of this study is to determine the immuno-modulatory mechanistic effects of colchicine in patients with myocardial infarction (MI). Investigators hypothesize that colchicine exerts its anti-inflammatory properties by switching the metabolism of neutrophils, thereby reducing the expression of adhesion molecules responsible for their recruitment in MI.
Detailed description
This is a pilot study to explore the mechanistic effects of colchicine in patients with MI. The study will be conducted sequentially in 3 parts: 1. Blood will be collected from up to 10 healthy volunteers for protocol development. (Group 1). 2. Blood will be collected from 20 MI patients within 24 hours of presentation at New York University (NYU) Langone Medical Center and Bellevue Hospital Center (BHC). Neutrophil adhesion to human aortic endothelial cells, quantitative expression of adhesion molecules on the surface of neutrophils, quantitative levels of adhesion molecules on neutrophils and endothelial cells, and neutrophil metabolism, using a Seahorse Analyzer will be evaluated pre- and post-addition of in vitro colchicine. (Group 2) 3. The standard low-dose loading regimen of colchicine (1.2 mg followed by 0.6 mg one hour later) will be administered to 20 patients with MI at BHC. Blood will be collected prior to drug administration, 2 to 3 hours after completion of the colchicine load, and 23 to 24 hours after the completion of the colchicine load. Neutrophil adhesion to human aortic endothelial cells, quantitative expression of adhesion molecules on the surface of neutrophils, quantitative levels of adhesion molecules on neutrophils and endothelial cells, and neutrophil metabolism will be evaluated pre- and post-addition of in vitro colchicine (exact markers will be determined based on the results of in viro studies above). (Group 3)
Interventions
DRUGColchicine 0.6 mg tablets
1.2 mg PO followed by 0.6 mg PO 1 hour later
Sponsors
NYU Langone Health
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* 18 years of age for the healthy volunteer subset. * 18 years of age and within 24 hours of an MI for the MI subset.
Exclusion criteria
Subjects in all 3 groups will be excluded if they meet one of the following criteria * history of myelodysplasia; * Use of anti-inflammatory medications, with the exception of aspirin, within 5 half-lives; * medications known to interact with colchicine; * known creatinine clearance \<30 cc/minute (severe kidney disease); * pregnant; or * Unable to consent. MI subjects who will have oral colchicine administered will have the following additional
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of neutrophils adherent to TNFα-stimulated endothelial cells | 1 Day | Metabolism of neutrophils will be measured using the Seahorse assay. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Levels of adhesion molecules on neutrophils and endothelial cells quantified using PCR | 1 Day | Metabolism of neutrophils will be measured using the Seahorse assay. |
| Expression of adhesion molecules on the surface of neutrophils assessed via flow cytometry | 1 Day | Measurements of L-selectin, CD11b, and active CD11b will be made via an Accuri C6 flow cytometer using standard antibodies on an aliquot of whole blood. |
| Measures of neutrophil metabolism (e.g. O2 consumption) | 1 Day | Metabolism of neutrophils will be measured using the Seahorse assay. |
Outcome results
None listed