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依洛尤单抗治疗与主动脉瓣狭窄进展缓慢的相关性。

Association between evolocumab use and slow progression of aortic valve stenosis.

机构信息

Division of Cardiology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, 232-0024, Japan.

Advanced Critical Care and Emergency Center, Yokohama City University Medical Center, Yokohama, Japan.

出版信息

Heart Vessels. 2024 Aug;39(8):725-734. doi: 10.1007/s00380-024-02386-6. Epub 2024 Mar 19.

DOI:10.1007/s00380-024-02386-6
PMID:38499696
Abstract

No medications have been reported to inhibit the progression of aortic valve stenosis (AS). The present study aimed to investigate whether evolocumab use is related to the slow progression of AS evaluated by serial echocardiography. This was a retrospective observational study from 2017 to 2022 at Yokohama City University Medical Center. Patients aged ≥ 18 with moderate AS were included. Exclusion criteria were (1) mild AS; (2) severe AS defined by maximum aortic valve (AV) velocity ≥ 4.0 m/s; and/or (3) no data of annual follow-up echocardiography. The primary endpoint was the association between evolocumab use and annual changes in the maximum AV-velocity or peak AV-pressure gradient (PG). A total of 57 patients were enrolled: 9 patients treated with evolocumab (evolocumab group), and the other 48 patients assigned to a control group. During a median follow-up of 33 months, the cumulative incidence of AS events (a composite of all-cause death, AV intervention, or unplanned hospitalization for heart failure) was 11% in the evolocumab group and 58% in the control group (P = 0.012). Annual change of maximum AV-velocity or peak AV-PG from the baseline to the next year was 0.02 (- 0.18 to 0.22) m/s per year or 0.60 (- 4.20 to 6.44) mmHg per year in the evolocumab group, whereas it was 0.29 (0.04-0.59) m/s per year or 7.61 (1.46-16.48) mmHg per year in the control group (both P < 0.05). Evolocumab use was associated with slow progression of AS and a low incidence of AS events in patients with moderate AS.

摘要

尚未有药物被报道可抑制主动脉瓣狭窄(AS)的进展。本研究旨在探究依洛尤单抗的使用是否与经连续超声心动图评估的 AS 缓慢进展有关。这是一项 2017 年至 2022 年在横滨市立大学医学中心进行的回顾性观察性研究。纳入年龄≥18 岁且患有中度 AS 的患者。排除标准为:(1)轻度 AS;(2)最大主动脉瓣(AV)速度≥4.0m/s 定义的重度 AS;和/或(3)无年度随访超声心动图数据。主要终点为依洛尤单抗使用与最大 AV 速度或峰值 AV 压力梯度(PG)的年度变化之间的关系。共纳入 57 例患者:9 例接受依洛尤单抗治疗(依洛尤单抗组),其余 48 例患者纳入对照组。中位随访 33 个月期间,依洛尤单抗组的 AS 事件(全因死亡、AV 干预或因心力衰竭计划外住院的复合终点)累计发生率为 11%,而对照组为 58%(P=0.012)。从基线到次年,最大 AV 速度或峰值 AV-PG 的年变化在依洛尤单抗组为 0.02(-0.18 至 0.22)m/s/年,而在对照组为 0.29(0.04-0.59)m/s/年(均 P<0.05)。依洛尤单抗组的年变化为 0.60(-4.20 至 6.44)mmHg/年,对照组为 7.61(1.46-16.48)mmHg/年(均 P<0.05)。在患有中度 AS 的患者中,依洛尤单抗的使用与 AS 的缓慢进展和 AS 事件的低发生率相关。

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本文引用的文献

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Aortic Stenosis Progression: A Systematic Review and Meta-Analysis.主动脉瓣狭窄进展:系统评价和荟萃分析。
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Lipoprotein(a) and aortic valve stenosis: work in progress.脂蛋白(a)与主动脉瓣狭窄:研究进行中。
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Lipoprotein(a) is associated with the onset but not the progression of aortic valve calcification.脂蛋白(a)与主动脉瓣钙化的发生有关,但与进展无关。
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Effect of Alirocumab on Lipoprotein(a) and Cardiovascular Risk After Acute Coronary Syndrome.依洛尤单抗对急性冠状动脉综合征后脂蛋白(a)和心血管风险的影响。
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Circulation. 2019 Mar 19;139(12):1483-1492. doi: 10.1161/CIRCULATIONAHA.118.037184.
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