Literature DB >> 1493355

HMG-CoA reductase inhibitor use in the aged. A review of clinical experience.

C J Lintott1, R S Scott.   

Abstract

While the benefit of cholesterol-lowering in the elderly has yet to be proven in clinical trials, individuals at high risk of coronary events who otherwise enjoy a good quality of life, should not be denied cholesterol-lowering therapy on the basis of age alone. Moreover, hypolipidaemic drugs are already extensively used in the aged. The HMG-CoA reductase inhibitors lovastatin, simvastatin and pravastatin are potent well tolerated hypolipidaemic therapies in young subjects. Although there have been few studies on their use in elderly subjects, the available data suggest the efficacy and safety of HMG-CoA reductase inhibitors in similar to that established for younger age groups.

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Year:  1992        PMID: 1493355     DOI: 10.2165/00002512-199202060-00007

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  78 in total

1.  ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium.

Authors:  A Endo; M Kuroda; Y Tsujita
Journal:  J Antibiot (Tokyo)       Date:  1976-12       Impact factor: 2.649

Review 2.  Hypercholesterolaemia in aged patients. To treat or not to treat?

Authors:  M J Tikkanen; R S Tilvis
Journal:  Drugs Aging       Date:  1991 Nov-Dec       Impact factor: 3.923

3.  Safety and efficacy of combined gemfibrozil-lovastatin therapy for primary dyslipoproteinemias.

Authors:  C J Glueck; J Speirs; T Tracy
Journal:  J Lab Clin Med       Date:  1990-05

4.  Treatment of familial hypercholesterolaemia: a controlled trial of the effects of pravastatin or cholestyramine therapy on lipoprotein and apolipoprotein levels.

Authors:  O Wiklund; B Angelin; G Fager; M Eriksson; S O Olofsson; L Berglund; T Lindén; A Sjöberg; G Bondjers
Journal:  J Intern Med       Date:  1990-09       Impact factor: 8.989

5.  The efficacy and safety of pravastatin, compared to and in combination with bile acid binding resins, in familial hypercholesterolaemia.

Authors:  N Hoogerbrugge; M J Mol; J J Van Dormaal; C Rustemeijer; E Muls; A F Stalenhoef; J C Birkenhäger
Journal:  J Intern Med       Date:  1990-09       Impact factor: 8.989

6.  HMG-CoA reductase inhibitors for hypercholesterolemia.

Authors: 
Journal:  N Engl J Med       Date:  1988-11-03       Impact factor: 91.245

7.  Effects of simvastatin and cholestyramine in familial and nonfamilial hypercholesterolemia. Multicenter Group I.

Authors:  E Stein; R Kreisberg; V Miller; G Mantell; L Washington; D R Shapiro
Journal:  Arch Intern Med       Date:  1990-02

8.  Effect of lovastatin on hemorheology in type II hyperlipoproteinemia.

Authors:  R Koppensteiner; E Minar; H Ehringer
Journal:  Atherosclerosis       Date:  1990-07       Impact factor: 5.162

9.  Lovastatin. Warfarin interaction.

Authors:  S Ahmad
Journal:  Arch Intern Med       Date:  1990-11

10.  Effects of fluvastatin (XU 62-320), an HMG-CoA reductase inhibitor, on the distribution and composition of low density lipoprotein subspecies in humans.

Authors:  J N Yuan; M Y Tsai; J Hegland; D B Hunninghake
Journal:  Atherosclerosis       Date:  1991-04       Impact factor: 5.162

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  3 in total

Review 1.  How well tolerated are lipid-lowering drugs?

Authors:  B Tomlinson; P Chan; W Lan
Journal:  Drugs Aging       Date:  2001       Impact factor: 3.923

2.  Efficacy and safety of fluvastatin, a new HMG CoA reductase inhibitor, in elderly hypercholesterolaemic women.

Authors:  G Baggio; O De Candia; P L Forte; F Mello; A Andriolli; S Donazzan; G Valerio; M Milani; G Crepaldi
Journal:  Drugs       Date:  1994       Impact factor: 9.546

Review 3.  Treatment of non-insulin-dependent diabetes mellitus and its complications. A state of the art review.

Authors:  A Ilarde; M Tuck
Journal:  Drugs Aging       Date:  1994-06       Impact factor: 3.923

  3 in total

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