Literature DB >> 8875970

Review of the major intervention trials of lowering coronary artery disease risk through cholesterol reduction.

R M Stark1.   

Abstract

Results of primary and secondary prevention trials have shown that lowering total cholesterol and low-density lipoprotein (LDL) cholesterol leads to a reduction in both fatal and nonfatal ischemic events. The reduced coronary artery disease (CAD) risk associated with cholesterol lowering appears to be unrelated to the intervention used, whether it be a low-fat/low-cholesterol diet, partial ileal bypass surgery, or pharmacologic intervention with an agent such as a bile resin, a fibrate, or niacin. Data emerging on the 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors have shown that this newest class of cholesterol-lowering agents also reduces the risk for CAD. The studies provide increasing evidence that high LDL cholesterol levels not only contribute to atherosclerotic plaque formation but also interfere with normal endothelial control of arterial vasomotor tone. Because the small amount of plaque regression observed on angiographic studies is not sufficient to explain the magnitude of CAD risk reduction associated with lowered levels of LDL cholesterol, these studies suggest that vasomotor control and plaque stabilization may have a greater impact on clinical events than the stenosis caused by atherosclerotic plaques.

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Year:  1996        PMID: 8875970     DOI: 10.1016/s0002-9149(96)00657-1

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


  3 in total

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Authors:  H D Langtry; A Markham
Journal:  Drugs       Date:  1999-04       Impact factor: 9.546

2.  CP-MLR/PLS directed QSAR study on apical sodium-codependent bile acid transporter inhibition activity of benzothiepines.

Authors:  Brij Kishore Sharma; Prithvi Singh; Pradeep Pilania; Kirti Sarbhai; Yenamandra S Prabhakar
Journal:  Mol Divers       Date:  2010-01-13       Impact factor: 2.943

3.  A novel class of apical sodium--dependent bile salt transporter inhibitors: 1-(2,4-bifluorophenyl)-7-dialkylamino-1,8-naphthyridine-3-carboxamides.

Authors:  Hongtao Liu; Guoxun Pang; Jinfeng Ren; Yue Zhao; Juxian Wang
Journal:  Acta Pharm Sin B       Date:  2016-12-23       Impact factor: 11.413

  3 in total

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