Department of Clinical Neuroscience and Therapeutics, Hiroshima University Graduate School of Biomedical and Health Sciences.
Center for Clinical Research, Kobe University Hospital.
J Atheroscler Thromb. 2018 Mar 1;25(3):262-268. doi: 10.5551/jat.40196. Epub 2017 Sep 16.
The J-STARS study examined whether pravastatin (10 mg/day) reduces recurrence of stroke in non-cardioembolic ischemic stroke patients who were enrolled within 1 month to 3 years after initial stroke events (ClinicalTrials.gov, NCT00221104). The main results showed that the frequency of atherothrombotic stroke was low in pravastatin-treated patients, although no effect of pravastatin was found for the other stroke subtypes. We evaluated differences of early (within 6 months) or late (after 6 months) pravastatin treatment benefits on the incidence of stroke or transient ischemic attack (TIA), as well as atherothrombotic stroke and the other subtypes.
Subjects in the J-STARS study were classified into two cohorts, depending on whether they enrolled early (1 to 6 months) or late (6 months to 3 years) following initial stroke events.
A total of 1578 patients (491 female, 66.2±8.5 years) were randomly assigned to either the pravastatin group (n=793; n=426 in the early cohort, n=367 in the late cohort) or the control group (n=785; n=417 in the early cohort, n=368 in the late cohort). During the follow-up of 4.9± 1.4 years, the rate of atherothrombotic stroke was lower in the pravastatin group compared to controls in the early cohort (0.24 vs. 0.88%/year, p=0.01) but not in the late cohort (0.17 vs. 0.39%/year, p=0.29). However, this difference of pravastatin effect on atherothrombotic stroke was not significantly interacted by the early or late cohort (p=0.59). The incidence rates of other stroke subtype were not different in between pravastatin and control groups despite the timing of entry.
Pravastatin is likely to reduce atherothrombotic stroke in patients enrolled within 6 months after stroke onset. However, the clinical efficacy for prevention of recurrent stroke was not conclusive with earlier statin treatment.
J-STARS 研究旨在探讨普伐他汀(10mg/天)是否能降低非心源性缺血性卒中患者在首次卒中发作后 1 个月至 3 年内复发卒中的风险(ClinicalTrials.gov,NCT00221104)。主要结果表明,普伐他汀治疗组的动脉粥样硬化血栓性卒中的发生率较低,尽管普伐他汀对其他卒中亚型没有影响。我们评估了早期(6 个月内)或晚期(6 个月后)普伐他汀治疗对卒中或短暂性脑缺血发作(TIA)、动脉粥样硬化血栓性卒中和其他亚型的影响。
J-STARS 研究的受试者分为两组,根据他们在首次卒中事件后是早期(1 至 6 个月)还是晚期(6 个月至 3 年)入组。
共有 1578 名患者(491 名女性,66.2±8.5 岁)被随机分配至普伐他汀组(n=793;早期队列 426 例,晚期队列 367 例)或对照组(n=785;早期队列 417 例,晚期队列 368 例)。在 4.9±1.4 年的随访中,与对照组相比,早期队列中普伐他汀组的动脉粥样硬化血栓性卒中发生率较低(0.24 比 0.88%/年,p=0.01),但晚期队列中无差异(0.17 比 0.39%/年,p=0.29)。然而,普伐他汀对动脉粥样硬化血栓性卒中的影响的这种差异与早期或晚期队列无关(p=0.59)。尽管入组时间不同,但普伐他汀组和对照组其他卒中亚型的发生率无差异。
在卒中发作后 6 个月内入组的患者中,普伐他汀可能降低动脉粥样硬化血栓性卒中的发生。然而,早期应用他汀类药物预防复发性卒中的疗效尚不确定。