open access

Vol 30, No 2 (2023)
Review Article
Submitted: 2021-08-07
Accepted: 2021-08-27
Published online: 2021-10-08
Get Citation

Colchicine — From rheumatology to the new kid on the block: Coronary syndromes and COVID-19

Stanisław Surma1, Marcin Basiak1, Monika Romańczyk1, Krzysztof J. Filipiak2, Bogusław Okopień1
·
Pubmed: 34642922
·
Cardiol J 2023;30(2):297-311.
Affiliations
  1. Department of Internal Medicine and Clinical Pharmacology, Medical University of Silesia, Katowice, Poland
  2. Department of Clinical Sciences, Maria Sklodowska-Curie Medical Academy, Warsaw, Poland

open access

Vol 30, No 2 (2023)
Review articles — Clinical cardiology
Submitted: 2021-08-07
Accepted: 2021-08-27
Published online: 2021-10-08

Abstract

Colchicine is an effective anti-inflammatory agent used to treat gout, coronary artery disease, viral
pericarditis, and familial Mediterranean fever. It has been found to act by preventing the polymerization
of the protein called tubulin, thus inhibiting inflammasome activation, proinflammatory chemokines,
and cellular adhesion molecules. Accumulating evidence suggests that some patients with coronavirus
disease 2019 (COVID-19) suffer from “cytokine storm” syndrome. The ideal anti-inflammatory in this
setting would be one that is readily available, cheap, orally administered, with a good safety profile, well-
tolerated, and that prevents or modulates inflammasome activation. The researchers selected colchicine
for their study. This paper is a review of the literature describing the effects of colchicine, which is a drug
that is being increasingly used, especially when standard therapy fails. Colchicine was shown to reduce
inflammatory lung injury and respiratory failure by interfering with leukocyte activation and recruitment.
In this publication, we try to systematically review the current data on new therapeutic options for
colchicine. The article focuses on new data from clinical trials in COVID-19, rheumatic, cardiovascular,
and other treatment such as familial Mediterranean fever, chronic urticaria, and PFAPA syndrome
(periodic fever, aphthous, stomatitis, pharyngitis, and cervical adenitis). We also summarize new reports
on the side effects, drug interactions, and safety of colchicine.

Abstract

Colchicine is an effective anti-inflammatory agent used to treat gout, coronary artery disease, viral
pericarditis, and familial Mediterranean fever. It has been found to act by preventing the polymerization
of the protein called tubulin, thus inhibiting inflammasome activation, proinflammatory chemokines,
and cellular adhesion molecules. Accumulating evidence suggests that some patients with coronavirus
disease 2019 (COVID-19) suffer from “cytokine storm” syndrome. The ideal anti-inflammatory in this
setting would be one that is readily available, cheap, orally administered, with a good safety profile, well-
tolerated, and that prevents or modulates inflammasome activation. The researchers selected colchicine
for their study. This paper is a review of the literature describing the effects of colchicine, which is a drug
that is being increasingly used, especially when standard therapy fails. Colchicine was shown to reduce
inflammatory lung injury and respiratory failure by interfering with leukocyte activation and recruitment.
In this publication, we try to systematically review the current data on new therapeutic options for
colchicine. The article focuses on new data from clinical trials in COVID-19, rheumatic, cardiovascular,
and other treatment such as familial Mediterranean fever, chronic urticaria, and PFAPA syndrome
(periodic fever, aphthous, stomatitis, pharyngitis, and cervical adenitis). We also summarize new reports
on the side effects, drug interactions, and safety of colchicine.

Get Citation

Keywords

colchicine, rheumatic diseases, cardiovascular diseases, COVID-19

About this article
Title

Colchicine — From rheumatology to the new kid on the block: Coronary syndromes and COVID-19

Journal

Cardiology Journal

Issue

Vol 30, No 2 (2023)

Article type

Review Article

Pages

297-311

Published online

2021-10-08

Page views

4794

Article views/downloads

1550

DOI

10.5603/CJ.a2021.0123

Pubmed

34642922

Bibliographic record

Cardiol J 2023;30(2):297-311.

Keywords

colchicine
rheumatic diseases
cardiovascular diseases
COVID-19

Authors

Stanisław Surma
Marcin Basiak
Monika Romańczyk
Krzysztof J. Filipiak
Bogusław Okopień

References (67)
  1. Montealegre-Gómez G, Garcia-Botero A, Cantini J, et al. Potential effect of colchicine in the prevention of acute respiratory distress syndrome (ARDS) in patients with Covid-19 infection. Int J Surg Surgical Tech. 2020; 4: 000146.
  2. Dzieciatkowski T, Filipiak KJ. SARS-CoV-2 coronavirus - update 2021 on diagnostic tools, vaccinations, and drugs. PZWL Publishing House, Warsaw 2021.
  3. Montealegre-Gómez G, Garavito E, Gómez-López A, et al. Colchicine: A potential therapeutic tool against COVID-19. Experience of 5 patients. Reumatol Clin. 2021; 17(7): 371–375.
  4. Golpour M, Mousavi T, Alimohammadi M, et al. The effectiveness of Colchicine as an anti-inflammatory drug in the treatment of coronavirus disease 2019: Meta-analysis. Int J Immunopathol Pharmacol. 2021; 35: 20587384211031763.
  5. Mizel SB, Wilson L. Nucleoside transport in mammalian cells. Inhibition by colchicine. Biochemistry. 1972; 11(14): 2573–2578.
  6. Viktorov AV, Yurkiv VA. Albendazole and colchicine modulate LPS-induced secretion of inflammatory mediators by liver macrophages. Bull Exp Biol Med. 2011; 151(6): 683–685.
  7. Takenouchi T, Iwamaru Y, Sugama S, et al. Lysophospholipids and ATP mutually suppress maturation and release of IL-1 beta in mouse microglial cells using a Rho-dependent pathway. J Immunol. 2008; 180(12): 7827–7839.
  8. Leung YY, Yao Hui LLi, Kraus VB. Colchicine: Update on mechanisms of action and therapeutic uses. Semin Arthritis Rheum. 2015; 45(3): 341–350.
  9. Terkeltaub RA, Furst DE, Bennett K, et al. High versus low dosing of oral colchicine for early acute gout flare: Twenty-four-hour outcome of the first multicenter, randomized, double-blind, placebo-controlled, parallel-group, dose-comparison colchicine study. Arthritis Rheum. 2010; 62(4): 1060–1068.
  10. Roddy E, Clarkson K, Blagojevic-Bucknall M, et al. Open-label randomised pragmatic trial (CONTACT) comparing naproxen and low-dose colchicine for the treatment of gout flares in primary care. Ann Rheum Dis. 2020; 79(2): 276–284.
  11. Aran S, Malekzadeh S, Seifirad S. A double-blind randomized controlled trial appraising the symptom-modifying effects of colchicine on osteoarthritis of the knee. Clin Exp Rheumatol. 2011; 29(3): 513–518.
  12. Erden M, Ediz L, Hız Ö, et al. Effect of Colchicine on Total Antioxidant Capacity, Antioxidant Enzymes and Oxidative Stress Markers in Patients with Knee Osteoarthritis. Int J Clin Med. 2012; 3(5): 377–382.
  13. Leung YY, Haaland B, Huebner JL, et al. Colchicine lack of effectiveness in symptom and inflammation modification in knee osteoarthritis (COLKOA): a randomized controlled trial. Osteoarthritis Cartilage. 2018; 26(5): 631–640.
  14. Restrepo-Escobar M, Carmona-Franceschi M, Gómez JD. Colchicine treatment in adult patients with knee osteoarthritis: Systematic review of the literature. Rev Colomb Reumatol (English Edition). 2017; 24(2): 102–111.
  15. Davatchi F, Abdollahi BS, Banihashemi AT, et al. Colchicine versus placebo in Behçet’s disease: randomized, double-blind, controlled crossover trial. Mod Rheumatol. 2014; 19(5): 542–549.
  16. Sun A, Wang YP, Chia JS, et al. Treatment with levamisole and colchicine can result in a significant reduction of IL-6, IL-8 or TNF-alpha level in patients with mucocutaneous type of Behcet's disease. J Oral Pathol Med. 2009; 38(5): 401–405.
  17. Papageorgiou N, Briasoulis A, Lazaros G, et al. Colchicine for prevention and treatment of cardiac diseases: A meta-analysis. Cardiovasc Ther. 2017; 35(1): 10–18.
  18. Imazio M, Brucato A, Forno D, et al. Efficacy and safety of colchicine for pericarditis prevention. Systematic review and meta-analysis. Heart. 2012; 98(14): 1078–1082.
  19. Lennerz C, Barman M, Tantawy M, et al. Colchicine for primary prevention of atrial fibrillation after open-heart surgery: Systematic review and meta-analysis. Int J Cardiol. 2017; 249: 127–137.
  20. Salih M, Smer A, Charnigo R, et al. Colchicine for prevention of post-cardiac procedure atrial fibrillation: Meta-analysis of randomized controlled trials. Int J Cardiol. 2017; 243: 258–262.
  21. Shojaeifard M, Pakbaz M, Beheshti R, et al. The effect of colchicine on the echocardiographic constrictive physiology after coronary artery bypass graft surgery. Echocardiography. 2020; 37(3): 399–403.
  22. Adler Y, Charron P, Imazio M, et al. 2015 ESC Guidelines for the diagnosis and management of pericardial diseases: The Task Force for the Diagnosis and Management of Pericardial Diseases of the European Society of Cardiology (ESC)Endorsed by: The European Association for Cardio-Thoracic Surgery (EACTS). Eur Heart J. 2015; 36(42): 2921–2964.
  23. Morel N, Bonjour M, Le Guern V, et al. Colchicine: a simple and effective treatment for pericarditis in systemic lupus erythematosus? A report of 10 cases. Lupus. 2015; 24(14): 1479–1485.
  24. Fiolet ATL, Silvis MJM, Opstal TSJ, et al. Short-term effect of low-dose colchicine on inflammatory biomarkers, lipids, blood count and renal function in chronic coronary artery disease and elevated high-sensitivity C-reactive protein. PLoS One. 2020; 15(8): e0237665.
  25. Martínez GJ, Robertson S, Barraclough J, et al. Colchicine acutely suppresses local cardiac production of inflammatory cytokines in patients with an acute coronary syndrome. J Am Heart Assoc. 2015; 4(8): e002128.
  26. Vaidya K, Arnott C, Martínez GJ, et al. Colchicine therapy and plaque stabilization in patients with acute coronary syndrome: a CT coronary angiography study. JACC Cardiovasc Imaging. 2018; 11(2 Pt 2): 305–316.
  27. Tucker B, Kurup R, Barraclough J, et al. Colchicine as a novel therapy for suppressing chemokine production in patients with an acute coronary syndrome: a pilot study. Clin Ther. 2019; 41(10): 2172–2181.
  28. Samuel M, Tardif JC, Bouabdallaoui N, et al. Colchicine for secondary prevention of cardiovascular disease: a systematic review and meta-analysis of randomized controlled trials. Can J Cardiol. 2021; 37(5): 776–785.
  29. Tardif JC, Kouz S, Waters DD, et al. Efficacy and safety of low-dose colchicine after myocardial infarction. N Engl J Med. 2019; 381(26): 2497–2505.
  30. Bouabdallaoui N, Tardif JC, Waters DD, et al. Time-to-treatment initiation of colchicine and cardiovascular outcomes after myocardial infarction in the Colchicine Cardiovascular Outcomes Trial (COLCOT). Eur Heart J. 2020; 41(42): 4092–4099.
  31. Nidorf SM, Fiolet ATL, Mosterd A, et al. Colchicine in patients with chronic coronary disease. N Engl J Med. 2020; 383(19): 1838–1847.
  32. Bytyçi I, Bajraktari G, Penson PE, et al. Efficacy and safety of colchicine in patients with coronary artery disease: A systematic review and meta-analysis of randomized controlled trials. Br J Clin Pharmacol. 2021 [Epub ahead of print].
  33. Roubille F, Tardif JC. Colchicine for secondary cardiovascular prevention in coronary disease. Circulation. 2020; 142(20): 1901–1904.
  34. Masson W, Lobo M, Molinero G, et al. Role of colchicine in stroke prevention: an updated meta-analysis. J Stroke Cerebrovasc Dis. 2020; 29(5): 104756.
  35. Cheng G, Chang FJ, Wang Yi, et al. Factors influencing stent restenosis after percutaneous coronary intervention in patients with coronary heart disease: a clinical trial based on 1-year follow-up. Med Sci Monit. 2019; 25: 240–247.
  36. Liu L, Liu B, Ren J, et al. Comparison of drug-eluting balloon versus drug-eluting stent for treatment of coronary artery disease: a meta-analysis of randomized controlled trials. BMC Cardiovasc Disord. 2018; 18(1): 46.
  37. Demirtas K. Inflammation and In-Stent Restenosis. Angiology. 2018; 69(1): 89.
  38. Deftereos S, Giannopoulos G, Raisakis K, et al. Colchicine treatment for the prevention of bare-metal stent restenosis in diabetic patients. J Am Coll Cardiol. 2013; 61(16): 1679–1685.
  39. Tien YY, Huang HK, Shih MC, et al. Drug repurposing? Cardiovascular effect of colchicine on patients with coronary artery disease: A systematic review and meta-analysis. J Cardiol. 2021; 77(6): 576–582.
  40. Ratajczak MZ, Kucia M. SARS-CoV-2 infection and overactivation of Nlrp3 inflammasome as a trigger of cytokine "storm" and risk factor for damage of hematopoietic stem cells. Leukemia. 2020; 34(7): 1726–1729.
  41. Cocco G, Chu DCC, Pandolfi S. Colchicine in clinical medicine. A guide for internists. Eur J Intern Med. 2010; 21(6): 503–508.
  42. Dupuis J, Sirois MG, Rhéaume E, et al. Colchicine reduces lung injury in experimental acute respiratory distress syndrome. PLoS One. 2020; 15(12): e0242318.
  43. Fiorucci E, Lucantoni G, Paone G, et al. Colchicine, cyclophosphamide and prednisone in the treatment of mild-moderate idiopathic pulmonary fibrosis: comparison of three currently available therapeutic regimens. Eur Rev Med Pharmacol Sci. 2008; 12(2): 105–111.
  44. Scarsi M, Piantoni S, Colombo E, et al. Association between treatment with colchicine and improved survival in a single-centre cohort of adult hospitalised patients with COVID-19 pneumonia and acute respiratory distress syndrome. Ann Rheum Dis. 2020; 79(10): 1286–1289.
  45. Deftereos SG, Giannopoulos G, Vrachatis DA, et al. Effect of colchicine vs standard care on cardiac and inflammatory biomarkers and clinical outcomes in patients hospitalized with coronavirus disease 2019: the GRECCO-19 randomized clinical trial. JAMA Netw Open. 2020; 3(6): e2013136.
  46. Salehzadeh F, Pourfarzi F, Ataei S. The impact of colchicine on the COVID-19 patients; a clinical trial study. Research Square. 2020.
  47. Tardif J, Bouabdallaoui N, L’Allier PL, et al. Efficacy of colchicine in non-hospitalized patients with COVID-19. MedRxiv. 2021: medRxiv.
  48. Mareev VYu, Orlova YaA, Plisyk AG, et al. Proactive anti-inflammatory therapy with colchicine in the treatment of advanced stages of new coronavirus infection. The first results of the COLORIT study. Kardiologiia. 2021; 61(2): 15–27.
  49. Haslak F, Yildiz M, Adrovic A, et al. Management of childhood-onset autoinflammatory diseases during the COVID-19 pandemic. Rheumatol Int. 2020; 40(9): 1423–1431.
  50. Hariyanto TI, Halim DA, Jodhinata C, et al. Colchicine treatment can improve outcomes of coronavirus disease 2019 (COVID-19): A systematic review and meta-analysis. Clin Exp Pharmacol Physiol. 2021; 48(6): 823–830.
  51. Nawangsih E, Kusmala Y, Rakhmat I, et al. Colchicine and mortality in patients with coronavirus disease 2019 (COVID-19) pneumonia: A systematic review, meta-analysis, and meta-regression. Int Immunopharmacol. 2021; 96: 107723.
  52. Salah HM, Mehta JL. Meta-analysis of the effect of colchicine on mortality and mechanical ventilation in COVID-19. Am J Cardiol. 2021; 145: 170–172.
  53. Chiu L, Lo CH, Shen M, et al. Colchicine use in patients with COVID-19: a systematic review and meta-analysis. medRxiv. 2021.
  54. Vrachatis DA, Giannopoulos GV, Giotaki SG, et al. Impact of colchicine on mortality in patients with COVID-19: A meta-analysis. Hellenic J Cardiol. 2021 [Epub ahead of print].
  55. Elshafei MN, El-Bardissy A, Khalil A, et al. Colchicine use might be associated with lower mortality in COVID-19 patients: A meta-analysis. Eur J Clin Invest. 2021; 51(9): e13645.
  56. Dinarello CA, Wolff SM, Goldfinger SE, et al. Colchicine therapy for familial mediterranean fever. A double-blind trial. N Engl J Med. 1974; 291(18): 934–937.
  57. Lidar M, Scherrmann J, Shinar Y, et al. Colchicine nonresponsiveness in familial mediterranean fever: clinical, genetic, pharmacokinetic, and socioeconomic characterization. Semin Arthritis Rheum. 2004; 33(4): 273–282.
  58. Lidar M, Kedem R, Langevitz P, et al. Intravenous colchicine for treatment of patients with familial Mediterranean fever unresponsive to oral colchicine. J Rheumatol. 2003; 30(12): 2620–2623.
  59. Rozenbaum M, Boulman N, Feld J, et al. Intravenous colchicine treatment for six months: adjunctive therapy in familial Mediterranean fever (FMF) unresponsive to oral colchicine. Clin Exp Rheumatol. 2009; 27(2 Suppl 53): S105.
  60. Grossman C, Farberov I, Feld O, et al. Efficacy and safety of long-term treatment with intravenous colchicine for familial Mediterranean fever (FMF) refractory to oral colchicine. Rheumatol Int. 2019; 39(3): 517–523.
  61. Criado RFJ, Criado PR, Martins JE, et al. Urticaria unresponsive to antihistaminic treatment: an open study of therapeutic options based on histopathologic features. J Dermatolog Treat. 2008; 19(2): 92–96.
  62. Quintana-Ortega C, Seoane-Reula E, Fernández L, et al. Colchicine treatment in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome: A multicenter study in Spain. Eur J Rheumatol. 2020 [Epub ahead of print].
  63. Stewart S, Yang KC, Atkins K, et al. Adverse events during oral colchicine use: a systematic review and meta-analysis of randomised controlled trials. Arthritis Res Ther. 2020; 22(1): 28.
  64. Indraratna PL, Virk S, Gurram D, et al. Use of colchicine in pregnancy: a systematic review and meta-analysis. Rheumatology (Oxford). 2018; 57(2): 382–387.
  65. Davis MW, Wason S, Digiacinto JL. Colchicine-antimicrobial drug interactions: what pharmacists need to know in treating gout. Consult Pharm. 2013; 28(3): 176–183.
  66. Colchicine: serious interactions. Prescrire Int. 2008; 17(96): 151–153.
  67. Imai S, Momo K, Kashiwagi H, et al. Prescription of colchicine with other dangerous concomitant medications: a nation-wide survey using the japanese claims database. Biol Pharm Bull. 2020; 43(10): 1519–1525.

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