• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

瑞舒伐他汀和二十碳五烯酸对新动脉粥样硬化的影响:LINK-IT 试验。

Effect of rosuvastatin and eicosapentaenoic acid on neoatherosclerosis: the LINK-IT Trial.

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.

出版信息

EuroIntervention. 2019 Dec 20;15(12):e1099-e1106. doi: 10.4244/EIJ-D-18-01073.

DOI:10.4244/EIJ-D-18-01073
PMID:31334703
Abstract

AIMS

We aimed to assess the effect of 10 mg/day of rosuvastatin plus eicosapentaenoic acid (EPA) versus 2.5 mg/day of rosuvastatin on the extent of neoatherosclerosis using optical coherence tomography (OCT).

METHODS AND RESULTS

We randomly assigned 50 patients with non-obstructive neoatherosclerotic plaques detected on OCT to receive either rosuvastatin 10 mg/day and EPA 1,800 mg/day (intensive therapy group) or rosuvastatin 2.5 mg (standard therapy group). Follow-up OCT was performed one year later to evaluate serial changes in neoatherosclerosis. The serum low-density lipoprotein cholesterol (LDL-C) level decreased significantly from baseline to 12-month follow-up in the intensive therapy group (89 mg/dL to 70 mg/dL; p<0.001), while no change occurred in the standard therapy group. Lipid index change and percent changes in macrophage grade were significantly lower in the intensive therapy group than in the standard therapy group (-53.6 vs 310.1, p=0.001; -37.0% vs 35.3%, p<0.001; respectively). Percent changes in lipid index and macrophage grade were positively correlated with the changes in serum LDL-C and C-reactive protein levels, and negatively correlated with the change in serum EPA/arachidonic acid and 18-hydroxyeicosapentaenoic acid (EPA bioactive metabolite) level.

CONCLUSIONS

Compared with rosuvastatin 2.5 mg/day, rosuvastatin 10 mg/day and EPA 1,800 mg/day significantly stabilised non-obstructive neoatherosclerotic plaques.

CLINICAL TRIAL REGISTRATION

UMIN ID: UMIN000012576. https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014711.

摘要

目的

我们旨在使用光学相干断层扫描(OCT)评估每天 10 毫克瑞舒伐他汀加二十碳五烯酸(EPA)与每天 2.5 毫克瑞舒伐他汀对新动脉粥样硬化程度的影响。

方法和结果

我们随机分配 50 名经 OCT 检测到非阻塞性新动脉粥样硬化斑块的患者,分别接受瑞舒伐他汀 10 毫克/天和 EPA 1800 毫克/天(强化治疗组)或瑞舒伐他汀 2.5 毫克(标准治疗组)治疗。一年后进行随访 OCT,以评估新动脉粥样硬化的连续变化。强化治疗组的血清低密度脂蛋白胆固醇(LDL-C)水平从基线到 12 个月随访时显著降低(89 毫克/分升降至 70 毫克/分升;p<0.001),而标准治疗组无变化。强化治疗组的脂质指数变化和巨噬细胞分级的百分比变化明显低于标准治疗组(-53.6 对 310.1,p=0.001;-37.0%对 35.3%,p<0.001;分别)。脂质指数和巨噬细胞分级的百分比变化与血清 LDL-C 和 C 反应蛋白水平的变化呈正相关,与血清 EPA/花生四烯酸和 18-羟基二十碳五烯酸(EPA 生物活性代谢物)水平的变化呈负相关。

结论

与每天 2.5 毫克瑞舒伐他汀相比,每天 10 毫克瑞舒伐他汀和 1800 毫克 EPA 显著稳定了非阻塞性新动脉粥样硬化斑块。

临床试验注册

UMIN ID:UMIN000012576。https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014711。

相似文献

1
Effect of rosuvastatin and eicosapentaenoic acid on neoatherosclerosis: the LINK-IT Trial.瑞舒伐他汀和二十碳五烯酸对新动脉粥样硬化的影响:LINK-IT 试验。
EuroIntervention. 2019 Dec 20;15(12):e1099-e1106. doi: 10.4244/EIJ-D-18-01073.
2
Concomitant Use of Rosuvastatin and Eicosapentaenoic Acid Significantly Prevents Native Coronary Atherosclerotic Progression in Patients With In-Stent Neoatherosclerosis.瑞舒伐他汀与二十碳五烯酸联合应用可显著预防支架内新动脉粥样硬化患者的原位冠状动脉粥样硬化进展。
Circ J. 2020 Sep 25;84(10):1826-1836. doi: 10.1253/circj.CJ-20-0199. Epub 2020 Aug 5.
3
Effects of Fatty Acid Therapy in Addition to Strong Statin on Coronary Plaques in Acute Coronary Syndrome: An Optical Coherence Tomography Study.在强化他汀治疗基础上加用脂肪酸治疗对急性冠脉综合征患者冠脉斑块的影响:一项光学相干断层成像研究。
J Am Heart Assoc. 2020 Aug 18;9(16):e015593. doi: 10.1161/JAHA.119.015593. Epub 2020 Aug 1.
4
Stabilizing effect of combined eicosapentaenoic acid and statin therapy on coronary thin-cap fibroatheroma.联合二十碳五烯酸和他汀类药物治疗对冠状动脉薄帽纤维粥样瘤的稳定作用。
Atherosclerosis. 2014 May;234(1):114-9. doi: 10.1016/j.atherosclerosis.2014.02.025. Epub 2014 Mar 5.
5
Effects of 6-month eicosapentaenoic acid treatment on postprandial hyperglycemia, hyperlipidemia, insulin secretion ability, and concomitant endothelial dysfunction among newly-diagnosed impaired glucose metabolism patients with coronary artery disease. An open label, single blinded, prospective randomized controlled trial.6个月二十碳五烯酸治疗对新诊断的合并冠状动脉疾病的糖代谢受损患者餐后高血糖、高脂血症、胰岛素分泌能力及伴随的内皮功能障碍的影响。一项开放标签、单盲、前瞻性随机对照试验。
Cardiovasc Diabetol. 2016 Aug 26;15(1):121. doi: 10.1186/s12933-016-0437-y.
6
One-year efficacy and safety of rosuvastatin + fenofibric acid combination therapy in patients with mixed dyslipidemia: evaluation of dose response.瑞舒伐他汀联合非诺贝特治疗混合性血脂异常患者的一年疗效和安全性:剂量反应评估。
Am J Cardiovasc Drugs. 2012 Apr 1;12(2):117-25. doi: 10.2165/11597940-000000000-00000.
7
Comparison of the Effect of Rosuvastatin 2.5 mg vs 20 mg on Coronary Plaque Determined by Angioscopy and Intravascular Ultrasound in Japanese With Stable Angina Pectoris (from the Aggressive Lipid-Lowering Treatment Approach Using Intensive Rosuvastatin for Vulnerable Coronary Artery Plaque [ALTAIR] Randomized Trial).瑞舒伐他汀2.5毫克与20毫克对日本稳定型心绞痛患者经血管内镜和血管内超声测定的冠状动脉斑块影响的比较(来自使用强化瑞舒伐他汀治疗易损冠状动脉斑块的积极降脂治疗方法[ALTAIR]随机试验)
Am J Cardiol. 2016 Apr 15;117(8):1206-12. doi: 10.1016/j.amjcard.2016.01.013. Epub 2016 Jan 28.
8
Efficacy and safety of adding alirocumab to rosuvastatin versus adding ezetimibe or doubling the rosuvastatin dose in high cardiovascular-risk patients: The ODYSSEY OPTIONS II randomized trial.在心血管高危患者中,与添加依折麦布或将瑞舒伐他汀剂量加倍相比,添加阿利西尤单抗至瑞舒伐他汀的疗效和安全性:ODYSSEY OPTIONS II随机试验
Atherosclerosis. 2016 Jan;244:138-46. doi: 10.1016/j.atherosclerosis.2015.11.010. Epub 2015 Nov 14.
9
The impact of the time of drug administration on the effectiveness of combined treatment of hypercholesterolemia with Rosuvastatin and Ezetimibe (RosEze): study protocol for a randomized controlled trial.药物给药时间对瑞舒伐他汀和依折麦布联合治疗高胆固醇血症(RosEze)有效性的影响:一项随机对照试验的研究方案
Trials. 2017 Jul 11;18(1):316. doi: 10.1186/s13063-017-2047-8.
10
A Phase III, Multicenter, Randomized, Double-blind, Active Comparator Clinical Trial to Compare the Efficacy and Safety of Combination Therapy With Ezetimibe and Rosuvastatin Versus Rosuvastatin Monotherapy in Patients With Hypercholesterolemia: I-ROSETTE (Ildong Rosuvastatin & Ezetimibe for Hypercholesterolemia) Randomized Controlled Trial.一项 III 期、多中心、随机、双盲、阳性对照临床试验,旨在比较依折麦布和瑞舒伐他汀联合治疗与瑞舒伐他汀单药治疗在高胆固醇血症患者中的疗效和安全性:I-ROSETTE(Ildong 瑞舒伐他汀和依折麦布治疗高胆固醇血症)随机对照试验。
Clin Ther. 2018 Feb;40(2):226-241.e4. doi: 10.1016/j.clinthera.2017.12.018.

引用本文的文献

1
Role of Lipid-Lowering and Anti-Inflammatory Therapies on Plaque Stabilization.降脂和抗炎疗法对斑块稳定的作用。
J Clin Med. 2024 May 25;13(11):3096. doi: 10.3390/jcm13113096.
2
Efficacy and Safety of TiNO-Coated Stents versus Drug-Eluting Stents in Acute Coronary Syndrome: Systematic Literature Review and Meta-Analysis.急性冠状动脉综合征中钛氮涂层支架与药物洗脱支架的疗效和安全性:系统文献综述与荟萃分析
Biomedicines. 2022 Dec 7;10(12):3159. doi: 10.3390/biomedicines10123159.
3
Dirty Jobs: Macrophages at the Heart of Cardiovascular Disease.
脏活:巨噬细胞是心血管疾病的核心因素
Biomedicines. 2022 Jul 2;10(7):1579. doi: 10.3390/biomedicines10071579.
4
Mid-Term Clinical Outcomes Following Drug-Coated Balloons in Coronary Artery Disease.药物涂层球囊治疗冠状动脉疾病的中期临床结果
J Clin Med. 2022 Mar 27;11(7):1859. doi: 10.3390/jcm11071859.
5
In Stent Neo-Atherosclerosis: Pathophysiology, Clinical Implications, Prevention, and Therapeutic Approaches.支架内新生动脉粥样硬化:病理生理学、临床意义、预防及治疗方法
Life (Basel). 2022 Mar 8;12(3):393. doi: 10.3390/life12030393.
6
Lipid-lowering therapy and percutaneous coronary interventions.降脂治疗与经皮冠状动脉介入治疗。
EuroIntervention. 2021 Apr 20;16(17):1389-1403. doi: 10.4244/EIJ-D-20-00999.
7
Rosuvastatin exerts anti-atherosclerotic effects by improving macrophage-related foam cell formation and polarization conversion via mediating autophagic activities.瑞舒伐他汀通过调节自噬活性改善巨噬细胞相关泡沫细胞形成和极化转化,发挥抗动脉粥样硬化作用。
J Transl Med. 2021 Feb 10;19(1):62. doi: 10.1186/s12967-021-02727-3.
8
Drug-eluting stent thrombosis: current and future perspectives.药物洗脱支架血栓形成:当前和未来的观点。
Cardiovasc Interv Ther. 2021 Apr;36(2):158-168. doi: 10.1007/s12928-021-00754-x. Epub 2021 Jan 13.