• 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

[Effect of a long-term treatment with simvastatin, an inhibitor of HMG-CoA reductase, in dyslipidemic patients at high risk].

作者信息

Strano A, Novo S, Notarbartolo A, Davì G, Abrignani M G, Alaimo G, Averna M R, Barbagallo C M, Marino G

出版信息

Cardiologia. 1989 Dec;34(12):1027-33.

PMID:2634479
Abstract

The reduction of total and LDL cholesterol (TC and LDLc), apoprotein B (ApoB) and in some instances triglycerides (TG) and the increase of HDL cholesterol (HDLc) and apoprotein A (ApoA) seem to be associated to a reduced coronary risk. Aim of our work was to evaluate the effects of a chronic treatment with the HMG-CoA reductase inhibitor simvastatin (MK-733), in a group of 8 dyslipidemic patients, 5 women and 3 men, aged between 48 and 69 years (mean age 59 +/- 8 years) at high risk being already affected by clinical compliances of atherosclerosis and not previously controlled by diet and/or other antidyslipidemic drugs. At the beginning and at the end (6 months) of this open study it was performed a clinical, ECG and ophthalmological examination, as well as an evaluation of the routine laboratory parameters. The initial dosage of simvastatin was a tablet of 10 mg/day, increased after a month to 20 mg and then to 40 mg/die. The mean dosage was 26.25 mg at the 3rd month and 21.25 mg at the 6th. Long-term simvastatin treatment was well tolerated (lack of important side effects as well as of significant changes of other clinical and laboratory parameters) and effective, reducing significantly (p less than 0.01) TC (317.9 +/- 30.8 vs 238.5 +/- 37.9 mg/dl), LDLc (210.6 +/- 48 vs 147.9 +/- 52 mg/dl), ApoB (144.7 +/- 17.5 vs 104.5 +/- 18), and TG (272.9 +/- 184 vs 200.5 +/- 117.6 mg/dl) and increasing in contrast HDL and ApoA values.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
[Effect of a long-term treatment with simvastatin, an inhibitor of HMG-CoA reductase, in dyslipidemic patients at high risk].
Cardiologia. 1989 Dec;34(12):1027-33.
2
Low-dose effect of simvastatin (MK-733) on serum lipids, lipoproteins, and apolipoproteins in patients with hypercholesterolemia.辛伐他汀(MK-733)对高胆固醇血症患者血清脂质、脂蛋白和载脂蛋白的低剂量效应。
Clin Ther. 1989 Mar-Apr;11(2):247-57.
3
[Simvastatin (MK-733), a new HMG-CoA reductase inhibitor, in the treatment of hypercholesterolemia in elderly patients with atherosclerosis].辛伐他汀(MK-733),一种新型HMG-CoA还原酶抑制剂,用于治疗老年动脉粥样硬化患者的高胆固醇血症
Arq Bras Cardiol. 1990 Jun;54(6):407-14.
4
Comparison of combined statin-fibrate treatment to monotherapy in patients with mixed hyperlipidemia.混合性高脂血症患者联合使用他汀类药物与贝特类药物治疗与单一药物治疗的比较。
Kardiol Pol. 2004 Jun;60(6):567-77.
5
[Mid-term clinical study of the effectiveness of and tolerability to simvastatin ++ in dyslipidemic patients].[辛伐他汀++对血脂异常患者有效性和耐受性的中期临床研究]
Minerva Med. 1992 Dec;83(12):815-8.
6
Effects of simvastatin on lipoprotein (a) and lipoprotein composition in patients with nephrotic syndrome.辛伐他汀对肾病综合征患者脂蛋白(a)及脂蛋白组成的影响。
Clin Nephrol. 1994 Mar;41(3):138-43.
7
[Effect of long-term cardiac training on lipids concentration in patients with chronic heart ischemic disease treated with simvastatin].[长期心脏训练对接受辛伐他汀治疗的慢性心脏缺血性疾病患者血脂浓度的影响]
Pol Merkur Lekarski. 2007 Feb;22(128):101-6.
8
The additional effects of acipimox to simvastatin in the treatment of combined hyperlipidaemia.
J Intern Med. 1997 Feb;241(2):151-5.
9
[Effects of simvastatin on plasma levels of lipids, lipoproteins and apolipoproteins in primary hypercholesterolemia].
Minerva Cardioangiol. 1989 Dec;37(12):509-15.
10
Effects of bezafibrate and of 2 HMG-CoA reductase inhibitors on lipoprotein (a) level in hypercholesterolemic patients.
Int J Clin Pharmacol Ther. 1995 Jun;33(6):345-50.