Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2839668 | Clínica e Investigación en Arteriosclerosis | 2012 | 10 Pages |
Abstract
Pitavastatin belongs to the statin group that fulfils the above-mentioned requirements. Pitavastatin is a synthetic statin, moderately lipophilic with a good oral absorption and low risk of drug-food interaction and a high biodisponibility. It produces an important change in the overall lipid profile with a significant reduction in LDLc levels. Pitavastatin, at equivalent doses to other strong statins, gets decreases in LDLc up to 45%, about 90% of patients treated with pitavastatin reach the EAS treatment target, it increases HDLc up to 14% (even to 24,6% in patients with a very high level of HDLc), decreases TG by 17% and positively changes the rest of other lipid parameters, in the long term. Pitavastatin is not metabolized in significant by CYP450 3A4, therefore it has a low drug-drug interaction profile, especially in the polymedicated patients (elderly, diabetic, nephropathic, hypertensive, heart disease and patients with a high risk cardiovascular). Also, pitavastatin has statins class pleiotropic effects and specific ones effects about carbohydrate metabolism, glomerular filtration, adiponectin⦠beyond lipid lowering, which can be added to the reduction of residual risk. Pitavastatin is well tolerated, not toxicity and safety data are supported by a significant number of patients currently treated.
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Authors
Ángel DÃaz RodrÃguez, Adalberto Serrano Cumplido, David Fierro González, Luis Alberto RodrÃguez Arroyo, Francisco-Javier GarcÃa-Norro Herreros, SerafÃn de Abajo Olea, Isidro López RodrÃguez, Josefa MarÃa Panisello Royo,