Effects of statins in patients with coronary artery spasm: A nationwide population-based study.

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Cts-Clinical and Translational Science Pub Date : 2024-11-01 DOI:10.1111/cts.70087
Yu-Ching Lee, Ming-Jui Hung, Tien-Hsing Chen, Chun-Tai Mao, Chi-Tai Yeh, Nicholas G Kounis, Ian Y Chen, Patrick Hu, Ming-Yow Hung
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Abstract

Controversies regarding the benefits of statin treatment on clinical outcomes in coronary artery spasm (CAS) without obstructive coronary artery disease (CAD) persist due to limited data. In this retrospective nationwide population-based cohort study from the Taiwan National Health Insurance Research Database during the period 2000-2012, the matched cohorts consisted of 12,000 patients with CAS. After propensity score matching with 1:1 ratio, 2216 patients were eligible for outcome analysis in either statin or nonstatin group, with the mean follow-up duration of 4.8 and 4.6 years, respectively. Statin users versus nonusers had a significantly reduced risk of major adverse cardiovascular events (MACEs) (6.7% vs. 9.5%, hazard ratio [HR] 0.68; 95% confidence interval [CI] 0.55-0.84) and all-cause mortality (6.0% vs. 7.6%; HR 0.77; 95% CI 0.61-0.96). While the results of MACEs were mainly contributed by cardiovascular death (1.9% vs. 3.2%; HR 0.56; 95% CI 0.38-0.83) and ischemic stroke (3.8% vs. 5.4%; subdistribution HR 0.69; 95% CI 0.52-0.91), they were primarily driven by reductions in ischemic but not hemorrhagic stroke. The benefit of statins was significantly pronounced in patients with hypertension and diabetes. Nevertheless, the effect on MACEs was consistent irrespective of age, sex, dyslipidemia, and mental disorder. Statins significantly reduced the risk of MACEs and all-cause mortality in CAS patients. The benefit of statin therapy in reducing MACEs appeared to be linear, with greater risk reduction with higher doses and longer duration without upper threshold, reflecting the dose-dependent relationship of statins with MACEs in CAS patients.

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他汀类药物对冠状动脉痉挛患者的影响:一项基于全国人口的研究。
由于数据有限,他汀类药物治疗对无阻塞性冠状动脉疾病(CAD)的冠状动脉痉挛(CAS)患者的临床预后的益处一直存在争议。在这项基于台湾国民健康保险研究数据库的回顾性全国人群队列研究(2000-2012 年)中,匹配队列包括 12,000 名 CAS 患者。按 1:1 的比例进行倾向得分匹配后,他汀或非他汀组中有 2216 名患者符合结果分析条件,平均随访时间分别为 4.8 年和 4.6 年。他汀类药物使用者与非使用者发生主要不良心血管事件(MACEs)(6.7% 对 9.5%,危险比 [HR] 0.68;95% 置信区间 [CI] 0.55-0.84)和全因死亡率(6.0% 对 7.6%;HR 0.77;95% CI 0.61-0.96)的风险明显降低。虽然MACEs的结果主要由心血管死亡(1.9% vs. 3.2%;HR 0.56;95% CI 0.38-0.83)和缺血性卒中(3.8% vs. 5.4%;亚分布HR 0.69;95% CI 0.52-0.91)造成,但其主要驱动因素是缺血性卒中的减少,而非出血性卒中的减少。他汀类药物对高血压和糖尿病患者的益处更为明显。然而,无论年龄、性别、血脂异常和精神障碍如何,他汀类药物对 MACEs 的影响是一致的。他汀类药物能明显降低 CAS 患者的 MACE 和全因死亡风险。他汀类药物治疗在降低MACEs方面的益处似乎是线性的,剂量越大、持续时间越长,降低的风险越大,但没有阈值上限,这反映了他汀类药物与CAS患者MACEs之间的剂量依赖关系。
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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