Abstract
Rosuvastatin (ZD4522) and pitavastatin (NK-104) are novel HMG-CoA reductase inhibitors with a peculiar pharmacological profile. In particular, they show a high potency in decreasing LDL-C and their catabolism is not mediated by the cytochrome P-450 3A4, thus reducing the potential for drug-drug interaction and improving the management of blood cholesterol. As the magnitude of LDL-C reduction is directly associated with the decrease in the incidence of myocardial infarction and mortality for CAD, statins with increased LDL-C lowering potency may ensure the achievement of target LDL-C levels and offer a more aggressive cholesterol control, further improving CAD morbidity and mortality.
MeSH terms
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Animals
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Cholesterol, LDL / blood
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Clinical Trials as Topic
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Coronary Disease / blood
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Coronary Disease / etiology
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Coronary Disease / prevention & control
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Fluorobenzenes / pharmacokinetics
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Fluorobenzenes / pharmacology
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Fluorobenzenes / therapeutic use
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Humans
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Hydroxymethylglutaryl-CoA Reductase Inhibitors / pharmacology*
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Hypercholesterolemia / complications
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Hypercholesterolemia / drug therapy
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Naphthalenes / pharmacokinetics
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Naphthalenes / pharmacology
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Naphthalenes / therapeutic use
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Pyrimidines*
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Quinolines / pharmacokinetics
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Quinolines / pharmacology
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Quinolines / therapeutic use
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Rosuvastatin Calcium
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Sulfonamides*
Substances
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Cholesterol, LDL
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Fluorobenzenes
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Hydroxymethylglutaryl-CoA Reductase Inhibitors
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LFA703
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Naphthalenes
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Pyrimidines
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Quinolines
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Sulfonamides
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Rosuvastatin Calcium
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pitavastatin