TIMI Study Group, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Cardiology Division, Department of Medicine, Geneva University Hospitals, Geneva, Switzerland.
J Am Coll Cardiol. 2020 May 12;75(18):2283-2293. doi: 10.1016/j.jacc.2020.03.039.
The EBBINGHAUS (Evaluating PCSK9 Binding Antibody Influence on Cognitive Health in High Cardiovascular Risk Subjects) trial demonstrated that evolocumab added to a background statin did not affect cognitive performance in a subset of 1,204 patients enrolled in FOURIER (Further Cardiovascular Outcomes Research With PCSK9 inhibitors in Subjects With Elevated Risk).
The authors describe patient-reported cognition in the entire FOURIER trial using a self-survey.
FOURIER was a randomized, double-blind, placebo-controlled trial involving patients with atherosclerotic cardiovascular disease and low-density lipoprotein cholesterol (LDL-C) levels ≥70 mg/dl or non-high-density cholesterol ≥100 mg/dl despite statin therapy. At the final visit, patients completed a 23-item survey on memory and executive domains from the Everyday Cognition (ECog) scale. Patients compared their levels of everyday function at the end of the trial with their levels at the beginning and scored as 1 (no change or improvement), 2 (occasionally worse), 3 (consistently little worse), or 4 (consistently much worse). ECog scores were compared by the 2 randomized treatment arms and by achieved LDL-C at 4 weeks.
A total of 22,655 patients completed ECog after a median duration of 2.2 years. The proportions of patients reporting cognitive decline (ECog score ≥2) at the end of the study were similar for placebo versus evolocumab, both for total score 3.6% versus 3.7% (p = 0.62) and for subdomains (memory, 5.8% vs. 6.0%; total executive, 3.6% vs. 3.7%). The proportion of patients reporting a decline in total cognitive score was similar among the 2,338 patients who achieved very low LDL-C levels (<20 mg/dl) compared to the 3,613 patients with LDL-C ≥100 mg/dl (3.8% vs. 4.5%, p = 0.57).
The addition of evolocumab to maximally tolerated statin therapy had no impact on patient-reported cognition after an average of 2.2 years of treatment, even among patients who achieved LDL-C <20 mg/dl.
EBBINGHAUS(评价 PCSK9 结合抗体对高心血管风险人群认知健康的影响)试验表明,在 FOURIER 试验(依洛尤单抗在高胆固醇血症患者中的心血管结局研究)中入组的 1204 例患者亚组中,依洛尤单抗联合背景他汀类药物治疗并未影响认知功能。
作者使用自我调查描述了整个 FOURIER 试验中的患者报告认知。
FOURIER 是一项随机、双盲、安慰剂对照试验,纳入了动脉粥样硬化性心血管疾病患者和低密度脂蛋白胆固醇(LDL-C)水平≥70mg/dl 或非高密度胆固醇≥100mg/dl 且他汀类药物治疗后仍未达标的患者。在最后一次就诊时,患者完成了一项来自日常认知(ECog)量表的 23 项关于记忆和执行域的调查。患者将试验结束时的日常功能水平与试验开始时的水平进行比较,并评分 1(无变化或改善)、2(偶尔更差)、3(持续稍差)或 4(持续明显更差)。比较了两种随机治疗组和治疗 4 周时达到的 LDL-C 的 ECog 评分。
共有 22655 例患者在中位 2.2 年的时间后完成了 ECog 调查。安慰剂与依洛尤单抗组在研究结束时报告认知下降(ECog 评分≥2)的患者比例相似,总评分分别为 3.6%和 3.7%(p=0.62),亚域(记忆:5.8%比 6.0%;总执行:3.6%比 3.7%)。与 LDL-C≥100mg/dl 的 3613 例患者相比,在 LDL-C 水平非常低(<20mg/dl)的 2338 例患者中,报告总认知评分下降的患者比例相似(3.8%比 4.5%,p=0.57)。
在平均 2.2 年的治疗后,依洛尤单抗联合最大耐受剂量他汀类药物治疗对患者报告的认知功能没有影响,即使在 LDL-C<20mg/dl 的患者中也是如此。