Literature DB >> 11018193

Pravastatin reduces restenosis two years after percutaneous transluminal coronary angioplasty (REGRESS trial).

H J Mulder1, E T Bal, J W Jukema, A H Zwinderman, M J Schalij, A J van Boven, A V Bruschke.   

Abstract

The Regression Growth Evaluation Statin Study (REGRESS) is a placebo-controlled multicenter study designed to assess the effect of 2-year treatment with pravastatin on the progression and regression of angiographically documented coronary artery disease. One of the secondary end points was the occurrence of 2-year restenosis in the percutaneous transluminal coronary angioplasty (PTCA) block. We randomly assigned eligible patients to receive pravastatin 40 mg once daily or placebo. The end point was the percent diameter stenosis of the target lesion at 24 months, as assessed by (semi)quantitative coronary angiography. Two hundred twenty-one patients underwent scheduled PTCA, which was considered successful in 201 patients. One hundred seventy-eight patients underwent angiographic restudy (89%). The patients in the pravastatin group (n = 109) and placebo group (n = 112) were similar at baseline. Percent diameter stenosis before angioplasty was 78 +/- 14% (mean +/- SD) in the pravastatin group and 80 +/- 14% in the placebo group (p = 0.46). At follow-up, the percent diameter stenosis was 32 +/- 23% in the pravastatin group and 45 +/- 29% in the placebo group (p < 0.001). Clinical restenosis was significantly lower in the pravastatin group (7%) compared with the placebo group (29%) (p < 0.001). Risk reduction for all events was 58%. We conclude that treatment with pravastatin reduces 2-year clinical and angiographic restenosis.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11018193     DOI: 10.1016/s0002-9149(00)01073-0

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  8 in total

Review 1.  Atherosclerosis: Making a U Turn.

Authors:  Ira J Goldberg; Gaurav Sharma; Edward A Fisher
Journal:  Annu Rev Med       Date:  2020-01-27       Impact factor: 13.739

2.  Liposomal simvastatin attenuates neointimal hyperplasia in rats.

Authors:  Eyal Afergan; Meital Ben David; Hila Epstein; Nickolay Koroukhov; Dalia Gilhar; Keren Rohekar; Haim D Danenberg; Gershon Golomb
Journal:  AAPS J       Date:  2010-02-09       Impact factor: 4.009

Review 3.  Therapeutic potential of oral antiproliferative agents in the prevention of coronary restenosis.

Authors:  Pramod Kuchulakanti; Ron Waksman
Journal:  Drugs       Date:  2004       Impact factor: 9.546

4.  Pravastatin and endothelium dependent vasomotion after coronary angioplasty: the PREFACE trial.

Authors:  H J Mulder; M J Schalij; B Kauer; R F Visser; P R van Dijkman; J W Jukema; A H Zwinderman; A V Bruschke
Journal:  Heart       Date:  2001-11       Impact factor: 5.994

5.  Beneficial effects of statins after percutaneous coronary intervention.

Authors:  Zhi-Jiang Zhang; Oscar C Marroquin; Joel L Weissfeld; Roslyn A Stone; Suresh R Mulukutla; David O Williams; Faith Selzer; Kevin E Kip
Journal:  Eur J Cardiovasc Prev Rehabil       Date:  2009-08

6.  Temporal gene expression analysis of human coronary artery endothelial cells treated with Simvastatin.

Authors:  Li Qin Zhang; Shwu-Fan Ma; Dmitry Grigoryev; Tera L Lavoie; Hui Qing Xiao; Robert Setterquist; Hailong Li; Jeffrey Jacobson; Joe G N Garcia; Shui Qing Ye
Journal:  Gene Expr       Date:  2008

Review 7.  Monocyte-mediated drug delivery systems for the treatment of cardiovascular diseases.

Authors:  Gil Aizik; Etty Grad; Gershon Golomb
Journal:  Drug Deliv Transl Res       Date:  2018-08       Impact factor: 4.617

8.  Medical angioplasty - hope and expectations: an optimistic overview.

Authors:  Mohammed F Abdul-Mohsen
Journal:  J Family Community Med       Date:  2011-09
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.