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Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia

Pitavastatin was first developed in Japan and is expanding the regions in which it is clinically available. A considerable number of clinical studies have been conducted and published to date on the usefulness of pitavastatin for patients with primary hypercholesterolemia or combined dyslipidemia. P...

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Detalles Bibliográficos
Autor principal: Sasaki, Jun
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988623/
https://www.ncbi.nlm.nih.gov/pubmed/21127702
http://dx.doi.org/10.2147/VHRM.S7802
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author Sasaki, Jun
author_facet Sasaki, Jun
author_sort Sasaki, Jun
collection PubMed
description Pitavastatin was first developed in Japan and is expanding the regions in which it is clinically available. A considerable number of clinical studies have been conducted and published to date on the usefulness of pitavastatin for patients with primary hypercholesterolemia or combined dyslipidemia. Pitavastatin demonstrates potent low-density lipoprotein cholesterol reduction at low doses of 1–4 mg/day. It also affects the regression of coronary plaques, as observed in intravascular ultrasound-guided percutaneous coronary intervention studies. Moreover, the persistent, long-term high-density lipoprotein cholesterol elevation observed in the populations treated with pitavastatin is worthy of further attention. The reported improvements in lipid profiles are consistent among the studies conducted in Japan, Korea, Thailand, and Europe. In light of accumulating clinical experience worldwide, pitavastatin is now expected to establish its position for preventing and treating cardiovascular disease.
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spelling pubmed-29886232010-12-02 Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia Sasaki, Jun Vasc Health Risk Manag Review Pitavastatin was first developed in Japan and is expanding the regions in which it is clinically available. A considerable number of clinical studies have been conducted and published to date on the usefulness of pitavastatin for patients with primary hypercholesterolemia or combined dyslipidemia. Pitavastatin demonstrates potent low-density lipoprotein cholesterol reduction at low doses of 1–4 mg/day. It also affects the regression of coronary plaques, as observed in intravascular ultrasound-guided percutaneous coronary intervention studies. Moreover, the persistent, long-term high-density lipoprotein cholesterol elevation observed in the populations treated with pitavastatin is worthy of further attention. The reported improvements in lipid profiles are consistent among the studies conducted in Japan, Korea, Thailand, and Europe. In light of accumulating clinical experience worldwide, pitavastatin is now expected to establish its position for preventing and treating cardiovascular disease. Dove Medical Press 2010 2010-11-02 /pmc/articles/PMC2988623/ /pubmed/21127702 http://dx.doi.org/10.2147/VHRM.S7802 Text en © 2010 Sasaki, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Sasaki, Jun
Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title_full Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title_fullStr Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title_full_unstemmed Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title_short Pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
title_sort pitavastatin approved for treatment of primary hypercholesterolemia and combined dyslipidemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988623/
https://www.ncbi.nlm.nih.gov/pubmed/21127702
http://dx.doi.org/10.2147/VHRM.S7802
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