TY - JOUR
T1 - Colchicine in Cardiovascular Disease
T2 - In-Depth Review
AU - Deftereos, Spyridon G.
AU - Beerkens, Frans J.
AU - Shah, Binita
AU - Giannopoulos, George
AU - Vrachatis, Dimitrios A.
AU - Giotaki, Sotiria G.
AU - Siasos, Gerasimos
AU - Nicolas, Johny
AU - Arnott, Clare
AU - Patel, Sanjay
AU - Parsons, Mark
AU - Tardif, Jean Claude
AU - Kovacic, Jason C.
AU - Dangas, George D.
N1 - Funding Information:
C.A. holds a National Health and Medical Research Council/Medical Research Future Fund Priority Investigator Grant and an New South Wales Health Early-Mid Career Research Grant (both of which are not for colchicine studies). S.P. holds the following Australian National Health and Medical Research Council/Medical Research Future Fund colchicine grants: COLCARDIO-ACS GA65779, CASPER GA82107, and IMPACT-ICO GA85492. These studies are supported by Aspen Pharmacare Australia, who are providing drug and placebo. S.P. also holds a New South Wales Cardiovascular Health Fellowship to support colchicine research. M.P. receives funding from the National Health and Medical Research Council Program Grant in Stroke (ID 1113352). J.C.K. received funding from the National Institutes of Health (R01HL130423, R01HL135093, R01HL148167-01A1) and a New South Wales health grant (RG194194).
Funding Information:
B. Shah reports funding from the Veterans Affairs Office of Research and Development (iK2CX001074) and the National Heart, Lung, and Blood Institute of the National Institutes of Health (R01HL146206) for studies of colchicine in coronary artery disease; is on the advisory board for Philips Volcano; and serves as a consultant for Terumo Medical. Dr Tardif has received research grants from Amarin, AstraZeneca, Ceapro, DalCor Pharmaceuticals, Esperion, Ionis, Novartis, Pfizer, RegenXBio, and Sanofi; has received honoraria from AstraZeneca, DalCor Pharmaceuticals, HLS Pharmaceuticals, and Pendopharm; has received minor equity interest from DalCor Pharmaceuticals; and is an author of patents on pharmacogenomics-guided cholesteryl ester transfer protein inhibition, use of colchicine after MI, and use of colchicine in coronavirus infection (Dr Tardiff has waived his rights in patents on colchicine and does not stand to gain financially). The other authors report no conflicts.
Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/1/4
Y1 - 2022/1/4
N2 - Inflammation plays a prominent role in the development of atherosclerosis and other cardiovascular diseases, and anti-inflammatory agents may improve cardiovascular outcomes. For years, colchicine has been used as a safe and well-tolerated agent in diseases such as gout and familial Mediterranean fever. The widely available therapeutic has several anti-inflammatory effects, however, that have proven effective in a broad spectrum of cardiovascular diseases as well. It is considered standard-of-care therapy for pericarditis, and several clinical trials have evaluated its role in postoperative and postablation atrial fibrillation, postpericardiotomy syndrome, coronary artery disease, percutaneous coronary interventions, and cerebrovascular disease. We aim to summarize colchicine's pharmacodynamics and the mechanism behind its anti-inflammatory effect, outline thus far accumulated evidence on treatment with colchicine in cardiovascular disease, and present ongoing randomized clinical trials. We also emphasize real-world clinical implications that should be considered on the basis of the merits and limitations of completed trials. Altogether, colchicine's simplicity, low cost, and effectiveness may provide an important addition to other standard cardiovascular therapies. Ongoing studies will address complementary questions pertaining to the use of low-dose colchicine for the treatment of cardiovascular disease.
AB - Inflammation plays a prominent role in the development of atherosclerosis and other cardiovascular diseases, and anti-inflammatory agents may improve cardiovascular outcomes. For years, colchicine has been used as a safe and well-tolerated agent in diseases such as gout and familial Mediterranean fever. The widely available therapeutic has several anti-inflammatory effects, however, that have proven effective in a broad spectrum of cardiovascular diseases as well. It is considered standard-of-care therapy for pericarditis, and several clinical trials have evaluated its role in postoperative and postablation atrial fibrillation, postpericardiotomy syndrome, coronary artery disease, percutaneous coronary interventions, and cerebrovascular disease. We aim to summarize colchicine's pharmacodynamics and the mechanism behind its anti-inflammatory effect, outline thus far accumulated evidence on treatment with colchicine in cardiovascular disease, and present ongoing randomized clinical trials. We also emphasize real-world clinical implications that should be considered on the basis of the merits and limitations of completed trials. Altogether, colchicine's simplicity, low cost, and effectiveness may provide an important addition to other standard cardiovascular therapies. Ongoing studies will address complementary questions pertaining to the use of low-dose colchicine for the treatment of cardiovascular disease.
KW - atrial fibrillation
KW - cerebrovascular
KW - colchicine
KW - coronary artery disease
KW - disorders
KW - inflammation
KW - percutaneous coronary intervention
KW - pericarditis
KW - postpericardiotomy syndrome
UR - http://www.scopus.com/inward/record.url?scp=85125005995&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.121.056171
DO - 10.1161/CIRCULATIONAHA.121.056171
M3 - Review article
C2 - 34965168
AN - SCOPUS:85125005995
SN - 0009-7322
VL - 145
SP - 61
EP - 78
JO - Circulation
JF - Circulation
IS - 1
ER -