Studying the efficacy of low-dose colchicine on clinical outcomes of patients with STEMI: a randomized controlled trial.

Mojtaba Yousefzadeh, Ali Khosrobeigi, Ayoub Salehi
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Abstract

Background: Numerous studies have underscored the essential role of inflammation across all stages of atherosclerosis. While various anti-inflammatory interventions have been implemented to mitigate inflammation-induced injuries, outcomes have been conflicting. Given the essential role of inflammation in these patients and limited data regarding the efficacy of low-dose Colchicine as an anti-inflammatory drug, we aimed to study the efficacy of low-dose Colchicine on clinical outcomes of patients with STEMI in Iran.

Results: Participants presented with STEMI and qualified revascularization at Shahid Beheshti Hospital in Qom during 2022 and 2023 were included into the study. This study included 172 STEMI patients (114 males and 58 females) within the mean age of 58.93 ± 7.79. Results indicate that colchicine (2 mg for loading dose and 0.5 mg daily for 30 days) and placebo group were not significant differences in identical profiles regarding age and gender. Analyses revealed no significant differences in clinical outcome after the 40-day follow-up period.

Conclusions: This study revealed that the addition of colchicine did not yield a significant benefit in enhancing the outcomes of patients with STEMI.

Clinical trial registration: This study was prospectively registered on Iranian registry of clinical trials, with registration number (IRCT20231001059578N1).

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研究小剂量秋水仙碱对 STEMI 患者临床疗效的影响:随机对照试验。
背景:大量研究强调了炎症在动脉粥样硬化各个阶段的重要作用。虽然已经采取了各种抗炎干预措施来减轻炎症引起的损伤,但结果却相互矛盾。鉴于炎症在这些患者中的重要作用,以及有关小剂量秋水仙碱作为抗炎药物疗效的数据有限,我们旨在研究小剂量秋水仙碱对伊朗 STEMI 患者临床疗效的影响:研究对象包括 2022 年和 2023 年期间在库姆 Shahid Beheshti 医院就诊的 STEMI 患者,他们均符合血管重建的条件。本研究共纳入 172 名 STEMI 患者(男性 114 人,女性 58 人),平均年龄为 58.93 ± 7.79 岁。结果显示,秋水仙碱组(负荷剂量为 2 毫克,每天 0.5 毫克,持续 30 天)和安慰剂组在年龄和性别方面没有显著差异。分析表明,在 40 天的随访期后,临床结果无明显差异:本研究显示,加用秋水仙碱并不能显著改善 STEMI 患者的预后:本研究在伊朗临床试验登记处进行了前瞻性登记,登记号为(IRCT20231001059578N1)。
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