Buckley Leo F, Chebrolu Bhavya, Al Zaria Mohsen, Blankstein Ron, Libby Peter, Weber Brittany N
Department of Pharmacy, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Department of Pharmacy, Brigham and Women's Hospital, Boston, Massachusetts, USA; Bouvé College of Health Sciences, Northeastern University, Boston, Massachusetts, USA.
JACC Adv. 2025 Mar;4(3):101622. doi: 10.1016/j.jacadv.2025.101622. Epub 2025 Feb 15.
In the COLCOT (Colchicine Cardiovascular Outcomes Trial) and LoDoCo2 (Low-Dose Colchicine 2) coronary artery disease trials, low-dose colchicine decreased the risk of major adverse cardiovascular events (MACEs) by 23% to 31% beyond statin therapy with a strong safety profile. The number of MACE potentially preventable by widespread colchicine use in the United States remains uncertain.
The objective of this study was to estimate the current and potential impact of colchicine on cardiovascular outcomes.
We first calculated the number of new colchicine users with coronary artery disease before and after COLCOT and LoDoCo2 publication at an integrated health care system in southeastern New England from 2018 to 2023. Second, we estimated the number of potentially avoidable MACEs with widespread colchicine use using incidence rates and the relative risk reduction from the LoDoCo2 trial and the nationally representative National Health And Nutrition Examination Survey study.
From January 2018 to December 2019 (before COLCOT and LoDoCo2 publication), the number of new colchicine users varied between 126 and 151 every 6 months. From January 2020 to June 2023, the number of new colchicine users increased from 141 to 181 every 6 months (<1% of adults with coronary artery disease at Mass General Brigham). Among the estimated 9.2 million adults with stable coronary artery disease on a statin in the United States, adding colchicine to standard medical management is estimated to prevent 226,000 MACE over a 3-year period.
Adding colchicine to standard cardiovascular management may prevent 226,000 MACE in the United States over a 3-year period.
在COLCOT(秋水仙碱心血管结局试验)和LoDoCo2(低剂量秋水仙碱2)冠状动脉疾病试验中,低剂量秋水仙碱在他汀类药物治疗基础上,将主要不良心血管事件(MACE)风险降低了23%至31%,且安全性良好。在美国,通过广泛使用秋水仙碱可能预防的MACE数量仍不确定。
本研究的目的是评估秋水仙碱对心血管结局的当前和潜在影响。
我们首先计算了2018年至2023年在新英格兰东南部一个综合医疗系统中,COLCOT和LoDoCo2发表前后新使用秋水仙碱的冠心病患者数量。其次,我们使用发病率以及LoDoCo2试验和具有全国代表性的美国国家健康与营养检查调查研究中的相对风险降低率,估算了广泛使用秋水仙碱可能避免的MACE数量。
2018年1月至2019年12月(COLCOT和LoDoCo2发表之前),每6个月新使用秋水仙碱的患者数量在126至151人之间。2020年1月至2023年6月,每6个月新使用秋水仙碱的患者数量从141人增加到181人(在麻省总医院布莱根分院的冠心病成年患者中占比不到1%)。在美国,估计有920万服用他汀类药物的稳定型冠心病成年患者,在标准药物治疗中添加秋水仙碱,预计在3年内可预防22.6万例MACE。
在美国,在标准心血管治疗中添加秋水仙碱,可能在3年内预防22.6万例MACE。