Literature DB >> 12149041

Who should receive HMG CoA reductase inhibitors?

Koon K Teo1, Jeffrey R Burton.   

Abstract

During the last decade, the development of the HMG CoA reductase inhibitors, commonly referred to as 'statins', has contributed greatly to cholesterol lowering therapy and cardiovascular risk reduction. These agents are well tolerated and efficacious. Data on nearly 30,000 patients from five long-term randomised, placebo-controlled trials of statins have clearly demonstrated that a broad range of individuals can benefit from such therapy. These include men or women, younger or older individuals, those with elevated or normal cholesterol levels, with or without myocardial infarction or symptomatic coronary heart disease, with or without hypertension or diabetes mellitus, and those who are smokers or non-smokers. Benefits include reductions in the risks for myocardial infarction, and coronary, cardiovascular and all-cause mortality, stroke and the need for coronary revascularisation. Results of the recently completed Heart Protection Trial have clearly confirmed the results of the earlier trials and support the use of statin therapy in secondary prevention. The role of statins in acute coronary syndromes is being actively evaluated and appears promising. In primary prevention, the data are not as convincing and generalisations cannot be made as to whether, and in which subgroup, drug therapy to lower low density lipoprotein (LDL) cholesterol should be initiated. There are important cost implications to consider and the use of statin therapy has to be judged on an individual basis, particularly in those with high or very high LDL cholesterol levels and/or with multiple risk factors rendering them at high short- and long-term risk of coronary heart disease. There is evidence of a 'care gap' in translating trial data into practice, even in secondary prevention, and this needs closing in order to improve patient outcomes.

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Year:  2002        PMID: 12149041     DOI: 10.2165/00003495-200262120-00001

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  34 in total

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Authors:  P M Ridker
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2.  Undertreatment of hyperlipidemia in the secondary prevention of coronary artery disease.

Authors:  S R Majumdar; J H Gurwitz; S B Soumerai
Journal:  J Gen Intern Med       Date:  1999-12       Impact factor: 5.128

3.  The care gap: improving delivery of patient care.

Authors:  K K Teo; L K Taylor
Journal:  Evid Based Cardiovasc Med       Date:  2000-12

4.  Lipid-lowering therapy in low-risk patients.

Authors:  T A Pearson
Journal:  JAMA       Date:  1998-05-27       Impact factor: 56.272

5.  Statin trials and goals of cholesterol-lowering therapy.

Authors:  S M Grundy
Journal:  Circulation       Date:  1998-04-21       Impact factor: 29.690

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Authors:  S M Grundy
Journal:  JAMA       Date:  1990-12-19       Impact factor: 56.272

7.  The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators.

Authors:  F M Sacks; M A Pfeffer; L A Moye; J L Rouleau; J D Rutherford; T G Cole; L Brown; J W Warnica; J M Arnold; C C Wun; B R Davis; E Braunwald
Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

8.  Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: results of AFCAPS/TexCAPS. Air Force/Texas Coronary Atherosclerosis Prevention Study.

Authors:  J R Downs; M Clearfield; S Weis; E Whitney; D R Shapiro; P A Beere; A Langendorfer; E A Stein; W Kruyer; A M Gotto
Journal:  JAMA       Date:  1998-05-27       Impact factor: 56.272

9.  Hyperlipidemia and coronary disease. Correction of the increased thrombogenic potential with cholesterol reduction.

Authors:  L Lacoste; J Y Lam; J Hung; G Letchacovski; C B Solymoss; D Waters
Journal:  Circulation       Date:  1995-12-01       Impact factor: 29.690

10.  Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group.

Authors:  J Shepherd; S M Cobbe; I Ford; C G Isles; A R Lorimer; P W MacFarlane; J H McKillop; C J Packard
Journal:  N Engl J Med       Date:  1995-11-16       Impact factor: 91.245

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  7 in total

1.  A qualitative study of barriers to the use of statins and the implementation of coronary heart disease prevention in primary care.

Authors:  John Kedward; Lorraine Dakin
Journal:  Br J Gen Pract       Date:  2003-09       Impact factor: 5.386

2.  An atomic-resolution mechanism of 3-hydroxy-3-methylglutaryl-CoA synthase.

Authors:  Brian J Bahnson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-11-16       Impact factor: 11.205

3.  Antileishmanial effect of mevastatin is due to interference with sterol metabolism.

Authors:  Neeradi Dinesh; Neelagiri Soumya; Sushma Singh
Journal:  Parasitol Res       Date:  2015-07-18       Impact factor: 2.289

4.  3-hydroxy-3-methylglutaryl-CoA synthase intermediate complex observed in "real-time".

Authors:  Michael J Theisen; Ila Misra; Dana Saadat; Nino Campobasso; Henry M Miziorko; David H T Harrison
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-21       Impact factor: 11.205

5.  The impact of statins on health services utilization and mortality in older adults discharged from hospital with ischemic heart disease: a cohort study.

Authors:  Charmaine A Cooke; Susan A Kirkland; Ingrid S Sketris; Jafna Cox
Journal:  BMC Health Serv Res       Date:  2009-11-04       Impact factor: 2.655

6.  Pyridines and pyrimidines mediating activity against an efflux-negative strain of Candida albicans through putative inhibition of lanosterol demethylase.

Authors:  Ed T Buurman; April E Blodgett; Kenneth G Hull; Daniel Carcanague
Journal:  Antimicrob Agents Chemother       Date:  2004-01       Impact factor: 5.191

7.  Statins impair antitumor effects of rituximab by inducing conformational changes of CD20.

Authors:  Magdalena Winiarska; Jacek Bil; Ewa Wilczek; Grzegorz M Wilczynski; Malgorzata Lekka; Patrick J Engelberts; Wendy J M Mackus; Elzbieta Gorska; Lukasz Bojarski; Tomasz Stoklosa; Dominika Nowis; Zuzanna Kurzaj; Marcin Makowski; Eliza Glodkowska; Tadeusz Issat; Piotr Mrowka; Witold Lasek; Anna Dabrowska-Iwanicka; Grzegorz W Basak; Maria Wasik; Krzysztof Warzocha; Maciej Sinski; Zbigniew Gaciong; Marek Jakobisiak; Paul W H I Parren; Jakub Golab
Journal:  PLoS Med       Date:  2008-03-25       Impact factor: 11.069

  7 in total

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