Risk of Hemorrhagic Stroke among Patients Treated with High-Intensity Statins versus Pitavastatin-Ezetimibe: A Population Based Study.

IF 1.7 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Tohoku Journal of Experimental Medicine Pub Date : 2024-06-28 Epub Date: 2024-02-22 DOI:10.1620/tjem.2024.J019
Po-Sheng Chen, Jia-Ling Lin, Hui-Wen Lin, Sheng-Hsiang Lin, Yi-Heng Li
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Abstract

High-intensity statin (HIS) is recommended for high-risk patients in current guidelines. However, the risk of hemorrhagic stroke (HS) with HIS is a concern for Asians. Pitavastatin carries pharmacological differences compared with other statins. We compared the risk of HS in patients treated with pitavastatin-ezetimibe vs. HIS. We conducted a population-based, propensity score-matched cohort study using data from the Taiwan National Health Insurance Research Database. From January 2013 to December 2018, adults (≥ 18 years) who received pitavastatin 2-4 mg/day plus ezetimibe 10 mg/day (combination group, N = 3,767) and those who received atorvastatin 40 mg/day or rosuvastatin 20 mg/day (HIS group, N = 37,670) were enrolled. The primary endpoint was HS. We also assessed the difference of a composite safety endpoint of hepatitis or myopathy requiring hospitalization and new-onset diabetes mellitus. Multivariable Cox proportional hazards model was used to evaluate the relationship between study endpoints and different treatment. After a mean follow-up of 3.05 ± 1.66 years, less HS occurred in combination group (0.74%) than in HIS group (1.35%) [adjusted hazard ratio (aHR) 0.65, 95% confidence interval (CI) 0.44-0.95]. In subgroup analysis, the lower risk of HS in combination group was consistent among all pre-specified subgroups. There was no significant difference of the composite safety endpoint between the 2 groups (aHR 0.91, 95% CI 0.81-1.02). In conclusion, pitavastatin-ezetimibe combination treatment had less HS compared with high-intensity atorvastatin and rosuvastatin. Pitavastatin-ezetimibe may be a favorable choice for Asians who need strict lipid control but with concern of HS.

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高强度他汀类药物与匹伐他汀-依折麦布治疗患者的出血性中风风险:一项基于人群的研究。
现行指南推荐高危患者服用高强度他汀类药物(HIS)。然而,亚洲人担心服用高强度他汀类药物会有出血性中风(HS)的风险。与其他他汀类药物相比,匹伐他汀具有药理差异。我们比较了接受匹伐他汀-依折麦布与 HIS 治疗的患者发生 HS 的风险。我们利用台湾国民健康保险研究数据库的数据开展了一项基于人群的倾向得分匹配队列研究。从2013年1月至2018年12月,我们招募了接受匹伐他汀2-4毫克/天加依折麦布10毫克/天治疗的成人(≥18岁)(联合组,N = 3,767)和接受阿托伐他汀40毫克/天或罗苏伐他汀20毫克/天治疗的成人(HIS组,N = 37,670)。主要终点为 HS。我们还评估了需要住院治疗的肝炎或肌病以及新发糖尿病的复合安全终点的差异。我们采用了多变量考克斯比例危险模型来评估研究终点与不同治疗方法之间的关系。平均随访 3.05 ± 1.66 年后,联合治疗组的 HS 发生率(0.74%)低于 HIS 组(1.35%)[调整后危险比(aHR)为 0.65,95% 置信区间(CI)为 0.44-0.95]。在亚组分析中,在所有预先指定的亚组中,联合组发生 HS 的风险较低,这一点是一致的。两组间的复合安全性终点无明显差异(aHR 0.91,95% CI 0.81-1.02)。总之,与高强度阿托伐他汀和罗苏伐他汀相比,匹伐他汀-依折麦布联合疗法的HS较低。对于需要严格控制血脂但又担心HS的亚洲人来说,匹伐他汀-依泽替米贝可能是一个不错的选择。
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CiteScore
3.60
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4.50%
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