• 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

瑞舒伐他汀与阿托伐他汀治疗对已确诊心血管疾病且高密度脂蛋白胆固醇水平低的男性对氧磷酶-1活性的影响。

Effect of rosuvastatin versus atorvastatin treatment on paraoxonase-1 activity in men with established cardiovascular disease and a low HDL-cholesterol.

作者信息

Bergheanu S C, Van Tol A, Dallinga-Thie G M, Liem A, Dunselman P H J, Van der Bom J G, Jukema J W

机构信息

Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Curr Med Res Opin. 2007 Sep;23(9):2235-40. doi: 10.1185/030079907X226104.

DOI:10.1185/030079907X226104
PMID:17692153
Abstract

OBJECTIVE

Paraoxonase-1 (PON-1) is a high-density lipoprotein (HDL) associated enzyme involved in the protective mechanisms of HDL. Our aim was to compare the effect of treatment with rosuvastatin and atorvastatin on serum PON-1 activity.

METHODS

We performed a prespecified prospective study in 68 patients, part of a larger, multicentre randomized study--RADAR (Rosuvastatin and Atorvastatin in different Dosages And Reverse cholesterol transport). Patients aged 40-80 years, all men, with established cardiovascular disease and high-density lipoprotein cholesterol (HDL-C) < 1.0 mmol/L (< 40 mg/dL) entered a 6-week dietary run-in period before receiving treatment with rosuvastatin 10 mg or atorvastatin 20 mg daily for 6-weeks. Doses were increased after 6 weeks to rosuvastatin 20 mg or atorvastatin 40 mg and after 12 weeks to rosuvastatin 40 mg or atorvastatin 80 mg daily. Serum PON-1 activity and lipid profile were determined at baseline, 6 and 18 weeks.

RESULTS

After 18 weeks, the rosuvastatin arm showed a significant increase of PON-1 activity (6.39 U/L, p = 0.02) whereas this was not observed in the atorvastatin arm (1.84 U/L, p = 0.77). The difference between groups did not reach significance (p = 0.11). Both rosuvastatin and atorvastatin resulted in significant (p = 0.0001) and similar increases in HDL-C after 6 weeks [0.06 mmol/L (2.32 mg/dL) vs. 0.05 mmol/L (1.93 mg/dL)] and after 18 weeks [0.10 mmol/L (3.87 mg/dL) vs. 0.10 mmol/L (3.87 mg/dL)].

CONCLUSIONS

Rosuvastatin treatment resulted in a significant increment of serum PON-1 activity with increasing dose while this was not observed with atorvastatin.

摘要

目的

对氧磷酶-1(PON-1)是一种与高密度脂蛋白(HDL)相关的酶,参与HDL的保护机制。我们的目的是比较瑞舒伐他汀和阿托伐他汀治疗对血清PON-1活性的影响。

方法

我们在68例患者中进行了一项预先设定的前瞻性研究,这些患者是一项更大的多中心随机研究——RADAR(不同剂量瑞舒伐他汀和阿托伐他汀与逆向胆固醇转运)的一部分。年龄在40-80岁的男性患者,患有确诊的心血管疾病且高密度脂蛋白胆固醇(HDL-C)<1.0 mmol/L(<40 mg/dL),在接受每日10 mg瑞舒伐他汀或20 mg阿托伐他汀治疗6周之前,先进入为期6周的饮食导入期。6周后剂量增加至瑞舒伐他汀20 mg或阿托伐他汀40 mg,12周后剂量增加至瑞舒伐他汀40 mg或阿托伐他汀80 mg每日。在基线、6周和18周时测定血清PON-1活性和血脂谱。

结果

18周后,瑞舒伐他汀组的PON-1活性显著增加(6.39 U/L,p = 0.02),而阿托伐他汀组未观察到这种情况(1.84 U/L,p = 0.77)。两组之间的差异未达到显著水平(p = 0.11)。瑞舒伐他汀和阿托伐他汀在6周后[0.06 mmol/L(2.32 mg/dL)对0.05 mmol/L(1.93 mg/dL)]和18周后[0.10 mmol/L(3.87 mg/dL)对0.10 mmol/L(3.87 mg/dL)]均导致HDL-C显著(p = 0.0001)且相似的升高。

结论

瑞舒伐他汀治疗随着剂量增加导致血清PON-1活性显著增加,而阿托伐他汀未观察到这种情况。

相似文献

1
Effect of rosuvastatin versus atorvastatin treatment on paraoxonase-1 activity in men with established cardiovascular disease and a low HDL-cholesterol.瑞舒伐他汀与阿托伐他汀治疗对已确诊心血管疾病且高密度脂蛋白胆固醇水平低的男性对氧磷酶-1活性的影响。
Curr Med Res Opin. 2007 Sep;23(9):2235-40. doi: 10.1185/030079907X226104.
2
LDL-C/HDL-C ratio in subjects with cardiovascular disease and a low HDL-C: results of the RADAR (Rosuvastatin and Atorvastatin in different Dosages And Reverse cholesterol transport) study.心血管疾病且高密度脂蛋白胆固醇(HDL-C)水平低的受试者的低密度脂蛋白胆固醇(LDL-C)/HDL-C 比值:RADAR(瑞舒伐他汀和阿托伐他汀不同剂量与胆固醇逆向转运)研究结果
Curr Med Res Opin. 2005 Nov;21(11):1865-74. doi: 10.1185/030079905X74952.
3
Twelve-week, multicenter, randomized, open-label comparison of the effects of rosuvastatin 10 mg/d and atorvastatin 10 mg/d in high-risk adults: a DISCOVERY study.瑞舒伐他汀10毫克/天与阿托伐他汀10毫克/天对高危成年人影响的12周多中心随机开放标签比较:一项探索性研究
Clin Ther. 2004 Nov;26(11):1821-33. doi: 10.1016/j.clinthera.2004.11.015.
4
Efficacy and safety of rosuvastatin and atorvastatin in patients with hypercholesterolemia and a high risk of coronary heart disease: a randomized, controlled trial.瑞舒伐他汀与阿托伐他汀治疗高胆固醇血症合并冠心病高危患者的疗效及安全性:一项随机对照试验
Am Heart J. 2004 Jul;148(1):e4. doi: 10.1016/j.ahj.2004.01.020.
5
The DISCOVERY PENTA study: a DIrect Statin COmparison of LDL-C Value--an Evaluation of Rosuvastatin therapY compared with atorvastatin.探索五联研究:一项直接比较他汀类药物降低低密度脂蛋白胆固醇(LDL-C)值的研究——瑞舒伐他汀与阿托伐他汀治疗效果的评估
Curr Med Res Opin. 2005 Aug;21(8):1307-15. doi: 10.1185/030079905X56529.
6
Effects of rosuvastatin versus atorvastatin, simvastatin, and pravastatin on non-high-density lipoprotein cholesterol, apolipoproteins, and lipid ratios in patients with hypercholesterolemia: additional results from the STELLAR trial.瑞舒伐他汀与阿托伐他汀、辛伐他汀及普伐他汀对高胆固醇血症患者非高密度脂蛋白胆固醇、载脂蛋白及脂质比值的影响:STELLAR试验的额外结果
Clin Ther. 2004 Sep;26(9):1388-99. doi: 10.1016/j.clinthera.2004.09.006.
7
A comparative study with rosuvastatin in subjects with metabolic syndrome: results of the COMETS study.一项在代谢综合征患者中与瑞舒伐他汀的对比研究:COMETS研究结果
Eur Heart J. 2005 Dec;26(24):2664-72. doi: 10.1093/eurheartj/ehi482. Epub 2005 Sep 5.
8
Effects of rosuvastatin on lipids, lipoproteins and apolipoproteins in the dyslipidaemia of diabetes.瑞舒伐他汀对糖尿病血脂异常患者脂质、脂蛋白及载脂蛋白的影响。
Diabet Med. 2007 May;24(5):541-9. doi: 10.1111/j.1464-5491.2007.02095.x. Epub 2007 Mar 15.
9
Comparison of the efficacy of rosuvastatin versus atorvastatin, simvastatin, and pravastatin in achieving lipid goals: results from the STELLAR trial.瑞舒伐他汀与阿托伐他汀、辛伐他汀及普伐他汀在实现血脂目标方面的疗效比较:STELLAR试验结果
Curr Med Res Opin. 2003;19(8):689-98. doi: 10.1185/030079903125002405.
10
Achieving LDL cholesterol, non-HDL cholesterol, and apolipoprotein B target levels in high-risk patients: Measuring Effective Reductions in Cholesterol Using Rosuvastatin therapY (MERCURY) II.使高危患者的低密度脂蛋白胆固醇、非高密度脂蛋白胆固醇和载脂蛋白B达到目标水平:使用瑞舒伐他汀治疗评估胆固醇的有效降低(MERCURY)II
Am Heart J. 2006 May;151(5):975.e1-9. doi: 10.1016/j.ahj.2005.12.013.

引用本文的文献

1
Comparative efficacy and safety among high-intensity statins. Systematic Review and Meta-Analysis.高强度他汀类药物的疗效和安全性比较。系统评价和荟萃分析。
J Comp Eff Res. 2023 Mar;12(3):e220163. doi: 10.57264/cer-2022-0163. Epub 2023 Feb 27.
2
HDL and Oxidation.高密度脂蛋白与氧化
Adv Exp Med Biol. 2022;1377:63-77. doi: 10.1007/978-981-19-1592-5_5.
3
Antioxidative activity of high-density lipoprotein (HDL): Mechanistic insights into potential clinical benefit.高密度脂蛋白(HDL)的抗氧化活性:对潜在临床益处的机制性见解。
BBA Clin. 2017 Aug 19;8:66-77. doi: 10.1016/j.bbacli.2017.07.002. eCollection 2017 Dec.
4
Paraoxonase-1 and Simvastatin Treatment in Patients with Stable Coronary Artery Disease.对稳定型冠状动脉疾病患者进行对氧磷酶-1和辛伐他汀治疗。
Int J Vasc Med. 2016;2016:6312478. doi: 10.1155/2016/6312478. Epub 2016 Apr 11.
5
Lipid-lowering efficacy of atorvastatin.阿托伐他汀的降脂疗效。
Cochrane Database Syst Rev. 2015 Mar 12;2015(3):CD008226. doi: 10.1002/14651858.CD008226.pub3.
6
Lipid-lowering efficacy of rosuvastatin.瑞舒伐他汀的降脂疗效。
Cochrane Database Syst Rev. 2014 Nov 21;2014(11):CD010254. doi: 10.1002/14651858.CD010254.pub2.
7
Association between serum free fatty acid levels and possible related factors in patients with type 2 diabetes mellitus and acute myocardial infarction.2型糖尿病合并急性心肌梗死患者血清游离脂肪酸水平与可能相关因素的关联
BMC Cardiovasc Disord. 2014 Nov 14;14:159. doi: 10.1186/1471-2261-14-159.
8
PPARs in Regulation of Paraoxonases: Control of Oxidative Stress and Inflammation Pathways.过氧化物酶体增殖物激活受体在对氧磷酶调控中的作用:氧化应激和炎症通路的控制。
PPAR Res. 2012;2012:616371. doi: 10.1155/2012/616371. Epub 2012 Jan 24.