接受 PCSK9 单克隆抗体治疗的已确诊心血管疾病患者体内的循环内皮祖细胞

IF 4.3 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of preventive cardiology Pub Date : 2024-11-16 DOI:10.1016/j.ajpc.2024.100896
Chen Gurevitz , Osnat Itzhaki Ben Zadok , Dorit Leshem-Lev , Lital Hodeda , Aviad Rotholz , Ran Kornowski , Alon Eisen
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引用次数: 0

摘要

背景循环内皮祖细胞(cEPCs)在血管修复中的作用及其与心血管保护的关系已得到公认。我们研究了高胆固醇血症和心血管疾病成人患者中的丙蛋白转换酶亚基克星 9 型单克隆抗体(PCSK9 mAb)对 cEPCs 的影响,旨在确定其多级效应。使用流式细胞术通过 CD34/CD133 和血管内皮生长因子受体 (VEGFR)-2 的表达评估 cEPCs,并通过集落形成单位 (CFU) 的形成和线粒体四氮唑 (MTT) 试验评估 cEPCs 的功能,以显示 cEPCs 的活力。结果51名患者(中位年龄67(IQR 63,74)岁;63%为男性,中位低密度脂蛋白胆固醇(LDL-C)125(102,165)毫克/分升)开始接受PCSK9 mAb治疗(evolocumab n = 22,alirocumab n = 29),以进行二级预防。使用 PCSK9 mAb 治疗 3 个月后,CD34(+)VEGFR-2(+) 和 CD133(+)VEGFR-2(+) 水平有所提高(分别为 0.50 % [IQR 0.30,1.04] 至 1.36 % [0.89, 1.73],p < 0.001;0.57 % [0.25,0.88] 至 1.18 % [0.74, 1.66],p < 0.001)。从功能上看,EPCs-CFUs明显增加(0.5 [0.0,1.0] 到 2.0 [1.5,2.5],p <0.001),MTT也随之增加(0.11 [0.09,0.15] 到 0.17 [0.12,0.21],p <0.001)。结论在接受 PCSK9 mAb 治疗的高胆固醇血症心血管疾病患者中,cEPCs 水平和功能较基线水平均有所提高。这些发现在 evolocumab 和 alirocumab 中都持续存在,可能暗示了一种新的多效应类作用。
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Circulating Endothelial Progenitor Cells in Patients with Established Cardiovascular Disease Treated with PCSK9 Monoclonal Antibodies

Background

The role of circulating endothelial progenitor cells (cEPCs) in vascular repair and their association to cardiovascular protection is well established.

Objectives

We examined the effect of proprotein convertase subtilisin kexin type 9 monoclonal antibodies (PCSK9 mAb) on cEPCs in adults with hypercholesterolemia and cardiovascular disease, aiming to establish a pleotropic class effect.

Methods

Non-interventional prospective study in patients with cardiovascular disease treated with either evolocumab or alirocumab. Patients were sampled for cEPCs at baseline, 1- and 3-months following initiation of PCSK9 mAb. cEPCs were assessed using flow cytometry by expression of CD34/CD133 and vascular endothelial growth factor receptor (VEGFR)-2, and functionally by formation of colony forming units (CFUs) and by Mitochondrial Tetrazolium (MTT) assay, indicative of cEPCs viability.

Results

51 patients (median age 67 (IQR 63,74) years;63 % male, median low-density lipoprotein-cholesterol (LDL-C) 125 (102,165) mg/dL) were initiated on PCSK9 mAb therapy (evolocumab n = 22, alirocumab n = 29) for secondary prevention. Following 3-month treatment with PCSK9 mAb, there was an increase in CD34(+)VEGFR-2(+) and CD133(+)VEGFR-2(+) levels (0.50 % [IQR 0.30,1.04] to 1.36 % [0.89, 1.73], p < 0.001 and 0.57 % [0.25,0.88] to 1.18 % [0.74,1.66], p < 0.001, respectively). Functionally, increase in EPCs-CFUs was evident (0.5 [0.0,1.0] to 2.0 [1.5,2.5], p < 0.001) with concomitant increase in MTT (0.11 [0.09,0.15] to 0.17 [0.12,0.21], p < 0.001). Stratifying by PCSK9 mAb, both agents were associated with an increase in cEPCs level and function.

Conclusions

In hypercholesterolemic patients with cardiovascular disease treated with PCSK9 mAb, there is an increase in cEPCs levels and function from baseline levels. These findings, which persist in both evolocumab and alirocumab, might suggest a novel pleiotropic class effect.
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
CiteScore
6.60
自引率
0.00%
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0
审稿时长
76 days
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