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连续磁共振成像显示,PCSK9 抑制剂阿利西尤单抗可快速降低斑块脂质含量。

Serial magnetic resonance imaging detects a rapid reduction in plaque lipid content under PCSK9 inhibition with alirocumab.

机构信息

University of Washington, 850 Republican St, Seattle, WA, 98109, USA.

Westside Medical Associates of Los Angeles, Beverly Hills, CA, USA.

出版信息

Int J Cardiovasc Imaging. 2021 Apr;37(4):1415-1422. doi: 10.1007/s10554-020-02115-w. Epub 2021 Jan 3.

Abstract

PCSK9 inhibitors lower low-density lipoprotein cholesterol (LDL-C) and reduce cardiovascular events. The clinical benefits presumably result from favorable effects on atherosclerotic plaques. Lipid-core and plaque inflammation have been recognized as main determinants of risk for plaque rupture and cardiovascular events. Both can be noninvasively assessed with carotid MRI. We studied if PCSK9 inhibition with alirocumab induces regression in lipid-core or plaque inflammation within 6 months as measured by MRI. Patients with non-calcified carotid plaque(s) and baseline LDL-C ≥ 70 mg/dl, who were statin-intolerant or taking a low-dose statin (≤ 10 mg per day of atorvastatin or an equivalent), received subcutaneous alirocumab 150 mg every 2 weeks. Carotid MRI was performed at baseline and 6 months after treatment, including pre- and post-contrast images for measuring percent lipid-core volume (%LC) and dynamic contrast-enhanced images for measuring microvessel leakiness (K), a marker of inflammation. Twenty-eight patients completed the study (69 ± 9 years; 64% male). Alirocumab led to significant changes in LDL-C (p < 0.001) and high-density lipoprotein cholesterol (HDL-C) (p = 0.003). At 6 months, there was a significant reduction in %LC (mean: - 2.1% [- 3.5, - 0.7], p = 0.005; a 17% reduction from baseline of 9.9%) without significant changes in lumen/wall area or in the inflammatory index K. Carotid plaque lipid content was reduced by 17% after 6 months of PCSK9 inhibition with alirocumab. This was seen before observable changes in lumen or wall areas, which supports pursing plaque lipid content as a more sensitive marker of therapeutic response compared to lumen or wall areas in future technical developments and serial studies.

摘要

PCSK9 抑制剂可降低低密度脂蛋白胆固醇(LDL-C)并减少心血管事件。临床获益可能源自对动脉粥样硬化斑块的有利影响。脂质核心和斑块炎症已被认为是斑块破裂和心血管事件风险的主要决定因素。两者均可通过颈动脉 MRI 进行非侵入性评估。我们研究了在 6 个月内用阿利西尤单抗进行 PCSK9 抑制是否会导致脂质核心或斑块炎症的消退,该消退可通过 MRI 测量。患有非钙化性颈动脉斑块(s)和基线 LDL-C≥70mg/dl 的患者,他汀类药物不耐受或服用低剂量他汀类药物(每天阿托伐他汀或等效药物≤10mg),接受皮下注射阿利西尤单抗 150mg,每两周一次。在治疗前和治疗后 6 个月进行颈动脉 MRI,包括对比前和对比后的图像,用于测量脂质核心体积百分比(%LC)和动态对比增强图像,用于测量微血管渗漏率(K),炎症标志物。28 名患者完成了研究(69±9 岁;64%为男性)。阿利西尤单抗可显著改变 LDL-C(p<0.001)和高密度脂蛋白胆固醇(HDL-C)(p=0.003)。在 6 个月时,%LC 显著降低(平均:-2.1%[-3.5,-0.7],p=0.005;与基线相比降低 9.9%的 17%),管腔/壁面积或炎症指数 K 无明显变化。阿利西尤单抗抑制 PCSK9 6 个月后,颈动脉斑块脂质含量减少 17%。这是在管腔或壁面积出现可观察变化之前观察到的,这支持与管腔或壁面积相比,将斑块脂质含量作为治疗反应的更敏感标志物,这在未来的技术发展和系列研究中是值得追求的。

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