Molaeimanesh Zahra, Kashipazha Davood, Shalilahmadi Davood, Shamsaei Gholamreza, Mohammadi Shooka
Department of Neurology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Rev Recent Clin Trials. 2025;20(1):59-67. doi: 10.2174/0115748871325292240904060109.
It has been proposed that colchicine may have the potential to prevent cardiovascular and cerebrovascular dysfunctions.
This study evaluated the impact of colchicine on preventing recurrent stroke in patients with both ischemic stroke (IS) and atrial fibrillation (AF).
A randomized, double-blinded, placebo-controlled trial was conducted at Golestan Hospital (Ahvaz, Iran) over one year, involving IS patients with AF. Demographic and clinical data were collected from the participants, who were then assigned to either the intervention or placebo groups. The experimental group was administered colchicine at a dosage of 0.05 mg twice daily for one year, while the control group received a placebo at a comparable dosage over the same timeframe.
In one year, 108 patients completed the study. There were 55 patients in the intervention group and 53 patients in the placebo group. During the second trimester of the trial, three patients in the colchicine group and 10 patients in the placebo group experienced recurrent strokes. Gastrointestinal issues were the most commonly reported complications (33 cases) among the two groups, followed by myalgia (8 patients). There were significant differences in the frequency of recurrent stroke and serum levels of C-reactive protein (CRP) between the colchicine and placebo groups (p < 0.05) after intervention.
In this study, colchicine was effective in reducing recurrent stroke and CRP levels in IS patients with AF compared to the control group. Further randomized controlled trials with larger sample sizes and extended durations are recommended to validate the results of this trial.
有人提出秋水仙碱可能具有预防心血管和脑血管功能障碍的潜力。
本研究评估了秋水仙碱对预防缺血性卒中(IS)合并心房颤动(AF)患者复发性卒中的影响。
在伊朗阿瓦士的戈勒斯坦医院进行了一项为期一年的随机、双盲、安慰剂对照试验,纳入IS合并AF的患者。收集参与者的人口统计学和临床数据,然后将其分为干预组或安慰剂组。实验组每日两次服用0.05毫克秋水仙碱,持续一年,而对照组在相同时间内接受相同剂量的安慰剂。
一年内,108名患者完成了研究。干预组有55名患者,安慰剂组有53名患者。在试验的第二个三个月期间,秋水仙碱组有3名患者,安慰剂组有10名患者发生复发性卒中。胃肠道问题是两组中最常报告的并发症(33例),其次是肌痛(8例患者)。干预后,秋水仙碱组和安慰剂组在复发性卒中频率和血清C反应蛋白(CRP)水平方面存在显著差异(p<0.05)。
在本研究中,与对照组相比,秋水仙碱在降低IS合并AF患者的复发性卒中和CRP水平方面有效。建议进行进一步的大样本量和更长持续时间的随机对照试验,以验证本试验的结果。