Literature DB >> 23251745

Pitavastatin: finding its place in therapy.

Leiv Ose.   

Abstract

Dyslipidaemia is a major risk factor for cardiovascular (CV) disease. Despite the widespread availability of effective lipid-lowering agents, an unacceptably large proportion of patients fail to attain their target low-density lipoprotein cholesterol (LDL-C) level in clinical practice. Reasons for this include undertreatment, poor adherence/persistence with therapy and failure to address non-LDL-C residual risk factors such as high levels of triglycerides, low high-density lipoprotein cholesterol (HDL-C) concentrations and raised apolipoprotein B: apolipoprotein A1 ratios. Pitavastatin is a novel, well-tolerated statin with a noninferior or superior lipid-lowering efficacy to comparable doses of atorvastatin, simvastatin, and prava-statin in a wide range of patients with hypercholesterolemia or combined dyslipidaemia. Compared with other statins, pitavastatin produces consistently greater increases in HDL-C levels that are sustained over the long term. In addition to pravastatin's potent effects on lipid profiles, a number of pleiotropic benefits have been identified that may contribute to a reduction in residual cardiovascular risk in people with dyslipidaemia and could partly account for pitavastatin's ability to regress coronary plaques in patients with acute coronary syndrome. Pitavastatin's unique metabolic profile results in a high efficacy at low (1-4 mg) doses and minimal drug interactions with cytochrome CYP3A4 substrates, making it an excellent choice for people requiring multiple medications. Although future trials are required to assess the impact of pitavastatin treatment on CV morbidity and mortality, studies to date suggest that pitavastatin will play an important role in the future management of dyslipidaemia and in the overall reduction of CV risk.

Entities:  

Keywords:  cardiovascular; dyslipidaemia; hypercholesterolemia; lipid; pitavastatin; statin

Year:  2011        PMID: 23251745      PMCID: PMC3513875          DOI: 10.1177/2040622310389227

Source DB:  PubMed          Journal:  Ther Adv Chronic Dis        ISSN: 2040-6223            Impact factor:   5.091


  91 in total

1.  Influence of statins on glucose tolerance in patients with type 2 diabetes mellitus: subanalysis of the collaborative study on hypercholesterolemia drug intervention and their benefits for atherosclerosis prevention (CHIBA study).

Authors:  Koutaro Yokote; Yasushi Saito
Journal:  J Atheroscler Thromb       Date:  2009-06-26       Impact factor: 4.928

2.  Identification of genetic variants associated with response to statin therapy.

Authors:  Jessica L Mega; David A Morrow; Alison Brown; Christopher P Cannon; Marc S Sabatine
Journal:  Arterioscler Thromb Vasc Biol       Date:  2009-08-10       Impact factor: 8.311

3.  Synthesis and biological evaluations of quinoline-based HMG-CoA reductase inhibitors.

Authors:  M Suzuki; H Iwasaki; Y Fujikawa; M Kitahara; M Sakashita; R Sakoda
Journal:  Bioorg Med Chem       Date:  2001-10       Impact factor: 3.641

4.  Relative induction of mRNA for HMG CoA reductase and LDL receptor by five different HMG-CoA reductase inhibitors in cultured human cells.

Authors:  S Morikawa; M Umetani; S Nakagawa; H Yamazaki; H Suganami; K Inoue; M Kitahara; T Hamakubo; T Kodama; Y Saito
Journal:  J Atheroscler Thromb       Date:  2000       Impact factor: 4.928

5.  Fibrate and statin synergistically increase the transcriptional activities of PPARalpha/RXRalpha and decrease the transactivation of NFkappaB.

Authors:  Ikuo Inoue; Fumiaki Itoh; Shigemi Aoyagi; Shigeki Tazawa; Hiroshi Kusama; Masuo Akahane; Toshiyuki Mastunaga; Kenji Hayashi; Takuya Awata; Tugikazu Komoda; Sigehiro Katayama
Journal:  Biochem Biophys Res Commun       Date:  2002-01-11       Impact factor: 3.575

6.  Atorvastatin lowers C-reactive protein and improves endothelium-dependent vasodilation in type 2 diabetes mellitus.

Authors:  K C B Tan; W S Chow; S C F Tam; V H G Ai; C H L Lam; K S L Lam
Journal:  J Clin Endocrinol Metab       Date:  2002-02       Impact factor: 5.958

7.  Effect of intensive statin therapy on regression of coronary atherosclerosis in patients with acute coronary syndrome: a multicenter randomized trial evaluated by volumetric intravascular ultrasound using pitavastatin versus atorvastatin (JAPAN-ACS [Japan assessment of pitavastatin and atorvastatin in acute coronary syndrome] study).

Authors:  Takafumi Hiro; Takeshi Kimura; Takeshi Morimoto; Katsumi Miyauchi; Yoshihisa Nakagawa; Masakazu Yamagishi; Yukio Ozaki; Kazuo Kimura; Satoshi Saito; Tetsu Yamaguchi; Hiroyuki Daida; Masunori Matsuzaki
Journal:  J Am Coll Cardiol       Date:  2009-07-21       Impact factor: 24.094

8.  EUROASPIRE III: a survey on the lifestyle, risk factors and use of cardioprotective drug therapies in coronary patients from 22 European countries.

Authors:  Kornelia Kotseva; David Wood; Guy De Backer; Dirk De Bacquer; Kalevi Pyörälä; Ulrich Keil
Journal:  Eur J Cardiovasc Prev Rehabil       Date:  2009-04

9.  Reduction in C-reactive protein and LDL cholesterol and cardiovascular event rates after initiation of rosuvastatin: a prospective study of the JUPITER trial.

Authors:  Paul M Ridker; Eleanor Danielson; Francisco Ah Fonseca; Jacques Genest; Antonio M Gotto; John Jp Kastelein; Wolfgang Koenig; Peter Libby; Alberto J Lorenzatti; Jean G Macfadyen; Børge G Nordestgaard; James Shepherd; James T Willerson; Robert J Glynn
Journal:  Lancet       Date:  2009-03-28       Impact factor: 79.321

10.  Lipid treatment assessment project 2: a multinational survey to evaluate the proportion of patients achieving low-density lipoprotein cholesterol goals.

Authors:  David D Waters; Carlos Brotons; Cheng-Wen Chiang; Jean Ferrières; JoAnne Foody; J Wouter Jukema; Raul D Santos; Juan Verdejo; Michael Messig; Ruth McPherson; Ki-Bae Seung; Lisa Tarasenko
Journal:  Circulation       Date:  2009-06-22       Impact factor: 29.690

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