Systematic review of colchicine neuromyopathy: Risk factors, duration and resolution

被引:5
作者
McEwan, Tim [1 ]
Bhambra, Jaspreet [1 ]
Liew, David F. [2 ,3 ,4 ]
Robinson, Philip C. [1 ,5 ,6 ]
机构
[1] Univ Queensland, Sch Clin Med, Fac Med, Herston, Qld 4029, Australia
[2] Dept Rheumatol, Austin Hlth, Heidelberg, Vic 3084, Australia
[3] Austin Hlth, Dept Clin Pharmacol & Therapeut, Heidelberg, Vic 3084, Australia
[4] Univ Melbourne, Dept Med, Parkville, Vic 3052, Australia
[5] Metro North Hosp & Hlth Serv, Royal Brisbane & Womens Hosp, Herston, Qld 4029, Australia
[6] Univ Queensland, Royal Brisbane & Womens Hosp, Sch Clin Med, Dept Rheumatol, Bowen Bridge Rd, Herston, Qld 4006, Australia
关键词
Colchicine; Myopathy; Neuropathy; Creatine kinase; Nerve; Muscle; Liver dysfunction; Renal dysfunction; Drug interactions; GOUT; OVERDOSE;
D O I
10.1016/j.semarthrit.2022.152150
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To identify reports of colchicine-induced neuropathy and myopathy and ascertain risk factors asso-ciated with this toxicity at commonly used doses.Methods: A systematic review of case reports was conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA methodology). PubMed and EMBASE were searched through October 2021 for case reports of neuropathy and/or myopathy associated with the use of colchicine at thera-peutic doses.Results: A total of 143 cases of neuromyopathy from 99 articles were identified as having a "definite" or "probable" association with colchicine usage, as assessed by the Naranjo algorithm. Most of these cases presented with features of both neuropathy and myopathy (n=72, 51%) but symptoms of myopathy were predominant. The mean total daily dose was 1.25 +/- 0.60 mg and 48% had been taking colchicine for more than 12 months before presenting with neuromyopathy. A total of 117 (82%) of all reports had either a significant co-morbidity or possible colchicine drug-drug interaction, while 57 (40%) had both risk factors. A total of 26 cases (18%) had no significant risk factor but only 15 of these reports contained complete descriptions of the patient's co-morbidities and co-medications. Cessation of colchicine generally led to complete resolution of symptoms in 70% of cases within a median of 21 days. There were 3 deaths reported which were due to multi-organ failure despite cessation of colchicine and medical management. Colchicine was restarted at reduced doses in 15 cases and 73% had no symptom recurrence.Conclusion: Neuromyopathy is an uncommon but reported adverse effect of colchicine. Cases generally present with proximal myopathy symptoms. Cases of colchicine neuromyopathy are largely reported in patients on commonly used doses. Renal and hepatic dysfunction and medications that inhibit cytochrome P450 3A4 isozyme (CYP3A4) and P-glycoprotein (P-gp) appear to be the most significant risk factors. Fortunately, cessation of colchicine generally leads to complete resolution of symptoms. Recommencement of colchicine at reduced doses appeared to be usually safe.
引用
收藏
页数:8
相关论文
共 50 条
[31]   Colchicine for Patients With Coronary Artery Disease: A Systematic Review and Meta-analysis [J].
Shrestha, Dhan B. ;
Budhathoki, Pravash ;
Sedhai, YubRaj ;
Khadka, Manoj ;
Pokharel, Subashchandra ;
Yadav, Stuti ;
Patel, Toralben ;
Elgendy, Islam ;
Mir, Wasey Ali Yadullahi ;
Patel, Nimesh K. .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2022, 79 (04) :420-430
[32]   The Role of Colchicine in Pericarditis - A Systematic Review and Meta-analysis of Randomised Trials [J].
Raval, Jwalant ;
Nagaraja, Vinayak ;
Eslick, Guy D. ;
Denniss, A. Robert .
HEART LUNG AND CIRCULATION, 2015, 24 (07) :660-666
[33]   The relationship between common risk factors and the pathology of pressure ulcer development: a systematic review [J].
Blackburn, Joanna ;
Ousey, Karen ;
Taylor, Lauren ;
Moore, Barry ;
Patton, Declan ;
Moore, Zena ;
Avsar, Pinar .
JOURNAL OF WOUND CARE, 2020, 29 (03) :S4-S12
[34]   Predictive risk factors for hospitalization and response to colchicine in patients with COVID-19 [J].
Tardif, Jean-Claude ;
Cossette, Marieve ;
Guertin, Marie-Claude ;
Bouabdallaoui, Nadia ;
Dube, Marie-Pierre ;
Boivin, Guy .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2022, 116 :387-390
[35]   Colchicine-related life-threatening toxicity: Risk factors and management [J].
Hantson, Philippe .
TOXICOLOGY LETTERS, 2016, 258 :S35-S35
[36]   A systematic review of the drug-drug interaction between statins and colchicine: Patient characteristics, etiologies, and clinical management strategies [J].
Schwier, Nicholas C. ;
Cornelio, Cyrille K. ;
Boylan, Paul M. .
PHARMACOTHERAPY, 2022, 42 (04) :320-333
[37]   Evaluating the Utility of Colchicine in Acute Coronary Syndrome: A Systematic Review and Meta-Analysis [J].
Bao, Yu-Lin ;
Gu, Ling-Feng ;
Du, Chong ;
Wang, Ya-Xin ;
Wang, Lian-Sheng .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2022, 80 (05) :639-647
[38]   Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials [J].
Verma, Subodh ;
Eikelboom, John W. ;
Nidorf, Stefan M. ;
Al-Omran, Mohammed ;
Gupta, Nandini ;
Teoh, Hwee ;
Friedrich, Jan O. .
BMC CARDIOVASCULAR DISORDERS, 2015, 15
[39]   Colchicine in cardiac disease: a systematic review and meta-analysis of randomized controlled trials [J].
Subodh Verma ;
John W. Eikelboom ;
Stefan M. Nidorf ;
Mohammed Al-Omran ;
Nandini Gupta ;
Hwee Teoh ;
Jan O. Friedrich .
BMC Cardiovascular Disorders, 15
[40]   Risk factors for the development of a parastomal hernia in patients with enterostomy: a systematic review and meta-analysis [J].
Niu, Niu ;
Du, Shizheng ;
Yang, Dongliang ;
Zhang, Liuliu ;
Wu, Bainv ;
Zhi, Xiaoxu ;
Li, Jun ;
Xu, Dejing ;
Zhang, Yinan ;
Meng, Aifeng .
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE, 2022, 37 (03) :507-519