Suppr超能文献

阿利西尤单抗与依洛尤单抗在高胆固醇血症患者中降脂效果比较的真实世界数据。

Real-World Data on Comparison of Lipid-Lowering Effects between Alirocumab and Evolocumab in Patients with Hypercholesterolemia.

作者信息

Lin Dai-Yi, Tsai Chia-Ling, Chang Ya-Hui, Liang Chih-Hung, Chuang Jen-Yu, Chen Yi-Han, Yeh Hung-I, Lin Chao-Feng

机构信息

Department of Cardiology.

Department of Pharmacy.

出版信息

Acta Cardiol Sin. 2022 Nov;38(6):778-783. doi: 10.6515/ACS.202211_38(6).20220705A.

Abstract

BACKGROUND

Even though the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, alirocumab and evolocumab, have been approved to reduce plasma low-density lipoprotein cholesterol (LDL-C) and the risk of atherosclerotic cardiovascular disease in high-risk patients, real-world data showing comparisons of the lipid-lowering effects between alirocumab and evolocumab are scarce because of the low prescription rates of PCSK9 inhibitors in clinical practice.

METHODS

Between Feb 2018 and Sep 2021, 22 patients who received alirocumab and 22 patients who received evolocumab at a tertiary medical center were enrolled. The patients' baseline characteristics, prescribed medications, plasma LDL-C levels, and percentages of reduction in LDL-C were compared between alirocumab users and evolocumab users.

RESULTS

The alirocumab users more frequently received ezetimibe treatment (72.7% vs. 40.9%, p = 0.03) and had higher baseline LDL-C (165.6 ± 63.2 mg/dL vs. 130.8 ± 56.3 mg/dL, p = 0.04) compared with the evolocumab users. At 6 months of follow-up, the plasma LDL-C levels in the alirocumab users were similar to those in the evolocumab users (79.3 ± 64.0 mg/dL vs. 63.5 ± 44.1 mg/dL, p = 0.48). Additionally, the percentages of LDL-C reduction following treatment were similar between the alirocumab users and evolocumab users (-47.0% ± 45.0% vs. -49.8 ± 24.9%, p = 0.66).

CONCLUSIONS

The LDL-C lowering effects of alirocumab are similar to those of evolocumab in clinical practice.

摘要

背景

尽管前蛋白转化酶枯草溶菌素/克新9型(PCSK9)抑制剂阿利西尤单抗和依洛尤单抗已被批准用于降低高危患者的血浆低密度脂蛋白胆固醇(LDL-C)及动脉粥样硬化性心血管疾病风险,但由于临床实践中PCSK9抑制剂的处方率较低,显示阿利西尤单抗和依洛尤单抗降脂效果比较的真实世界数据较少。

方法

2018年2月至2021年9月,纳入在一家三级医疗中心接受阿利西尤单抗治疗的22例患者和接受依洛尤单抗治疗的22例患者。比较阿利西尤单抗使用者和依洛尤单抗使用者的基线特征、处方药物、血浆LDL-C水平以及LDL-C降低百分比。

结果

与依洛尤单抗使用者相比,阿利西尤单抗使用者更频繁接受依折麦布治疗(72.7%对40.9%,p = 0.03),且基线LDL-C更高(165.6±63.2mg/dL对130.8±56.3mg/dL,p = 0.04)。随访6个月时,阿利西尤单抗使用者的血浆LDL-C水平与依洛尤单抗使用者相似(79.3±64.0mg/dL对63.5±44.1mg/dL,p = 0.48)。此外,阿利西尤单抗使用者和依洛尤单抗使用者治疗后LDL-C降低百分比相似(-47.0%±45.0%对-49.8±24.9%,p = 0.66)。

结论

在临床实践中,阿利西尤单抗降低LDL-C的效果与依洛尤单抗相似。

相似文献

3
PCSK-9 Inhibitors in a Real-World Setting and a Comparison Between Alirocumab and Evolocumab in Heterozygous FH Patients.
J Endocr Soc. 2020 Nov 18;5(1):bvaa180. doi: 10.1210/jendso/bvaa180. eCollection 2021 Jan 1.
4
10
Proprotein convertase subtilisin/kexin type 9 inhibitors for reduction of cardiovascular events.
Am J Health Syst Pharm. 2018 Jun 1;75(11):747-754. doi: 10.2146/ajhp170707.

本文引用的文献

2
5
PCSK-9 Inhibitors in a Real-World Setting and a Comparison Between Alirocumab and Evolocumab in Heterozygous FH Patients.
J Endocr Soc. 2020 Nov 18;5(1):bvaa180. doi: 10.1210/jendso/bvaa180. eCollection 2021 Jan 1.
7
PCSK9 Inhibitor Use in the Real World: Data From the National Patient-Centered Research Network.
J Am Heart Assoc. 2019 May 7;8(9):e011246. doi: 10.1161/JAHA.118.011246.
10
Alirocumab and Cardiovascular Outcomes after Acute Coronary Syndrome.
N Engl J Med. 2018 Nov 29;379(22):2097-2107. doi: 10.1056/NEJMoa1801174. Epub 2018 Nov 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验