Bailout inclisiran-based triple lipid-lowering therapy reduces plaque lipid content in stable coronary artery disease patients

医学 以兹提米比 冠状动脉疾病 内科学 他汀类 心脏病学 经皮冠状动脉介入治疗 胃肠病学 心肌梗塞
作者
Kārlis Trušinskis,Maris Lapsovs,Baiba Kokina,Mairita Karantajere,Evija Knoka,Laima Caunite,Sanda Jēgere,Inga Narbute,Dace Sondore,Ana Sofia Grave,Indulis Kumsārs,Andrejs Ērglis
出处
期刊:European Heart Journal [Oxford University Press]
卷期号:44 (Supplement_2) 被引量:2
标识
DOI:10.1093/eurheartj/ehad655.1313
摘要

Abstract Background Low-density lipoprotein cholesterol (LDL-C) has a causal role in atherosclerotic cardiovascular disease. Genetic studies and variability in individual response to lipid-lowering therapies suggest combining hypolipidaemic medications with different mechanisms of action. Purpose The aim of this study was to evaluate the effect of triple inclisiran-based hypolipidaemic therapy in patients not reaching LDL-C target on maximum statin/ezetimibe treatment. Methods This prospective study enrolled 37 stable coronary artery disease patients admitted for elective percutaneous coronary intervention after 4-6 weeks on maximum tolerated statin and/or ezetimibe therapy during run-in period. Afterwards, patients with LDL-C level >1.8 mmol/l at the time of inclusion were assigned to receive add-on inclisiran (triple therapy group). In all participants near-infrared spectroscopy (NIRS) was performed at baseline and after 15 months for atherosclerotic plaque evaluation in the segment of interest, defined as 20-50% lesion in the proximal or middle third of a coronary artery. Statistical analysis was carried out with SPSS Statistics software. Results Average LDL-C level among screened patients was 2.81 (±1.17) mmol/l. In 19 patients LDL-C level remained >1.8 mmol/l on maximally tolerated statin and/or ezetimibe treatment, and after 15 months of triple therapy mean LDL-C reached 1.81 (±1.02) mmol/l with a significant LDL-C percentage change of 35.59% (95%CI -47.31 to -9.18, P=0.006) in this group. 17 patients continued statin/ezetimibe as mono or dual treatment and at 15-month follow-up mean LDL-C level comprised 1.67 (±0.61) mmol/l among these participants. According to NIRS data, maximum lipid-core burden index within 4 mm (maxLCBI4 mm) was significantly reduced by 28.85 (95%CI -189.39 to 17.64, P=0.041) in triple therapy group and by 114.72 in mono or dual therapy group (-194.76 to 23.01, P=0.004), with no statistically significant difference established between both groups (P=0.494). Conclusions Triple therapy demonstrated significant atherosclerotic plaque lipid content reduction along with LDL-C level lowering in patients with insufficient effectiveness of statin/ezetimibe treatment.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Glovexx完成签到,获得积分20
刚刚
Lucas的应助被Twinkle采纳,获得10
刚刚
顺其自然发布了新的文献求助10
1秒前
俏皮道之完成签到,获得积分10
2秒前
LOnlyT发布了新的文献求助10
3秒前
蓝天的应助被higvhsd采纳,获得10
3秒前
3秒前
4秒前
yyyyy发布了新的文献求助10
4秒前
4秒前
蒸馒头争气完成签到,获得积分10
4秒前
6秒前
科研通AI6.2的应助被飞利浦采纳,获得10
7秒前
风堇发布了新的文献求助10
7秒前
科研通AI6.2的应助被快乐星球采纳,获得10
7秒前
8秒前
yulin完成签到,获得积分10
9秒前
Pursuit发布了新的文献求助10
9秒前
DACHIYIJING完成签到,获得积分10
10秒前
11秒前
11秒前
aaaaa完成签到,获得积分10
11秒前
yuu发布了新的文献求助10
11秒前
11秒前
王欣发布了新的文献求助10
11秒前
老的火龙果的应助被PENG采纳,获得10
12秒前
xx完成签到,获得积分10
12秒前
顺其自然完成签到,获得积分10
12秒前
知性的凝云完成签到,获得积分10
13秒前
FashionBoy的应助被wuyongxiang采纳,获得10
13秒前
Millllllo完成签到,获得积分10
14秒前
14秒前
14秒前
15秒前
leungzzz完成签到 ,获得积分10
15秒前
jj发布了新的文献求助10
16秒前
LY发布了新的文献求助10
16秒前
16秒前
Orange的应助被跳跃早晨采纳,获得30
16秒前
CynthiaLi完成签到,获得积分10
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Issues in Task-Based Language Teaching 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7783710
求助须知:如何正确求助?哪些是违规求助? 9322987
关于积分的说明 20392570
捐赠科研通 7372332
什么是DOI,文献DOI怎么找? 3320737
关于科研通互助平台的介绍 2468747
邀请新用户注册赠送积分活动 2336971