Literature DB >> 23924053

Differential metabolic actions of specific statins: clinical and therapeutic considerations.

Soo Lim1, Ichiro Sakuma, Michael J Quon, Kwang Kon Koh.   

Abstract

SIGNIFICANCE: Statins, the most widely prescribed drugs in clinical practice, mainly act by reducing the plasma level of low-density lipoprotein (LDL)-cholesterol. A shift in redox homeostasis to an imbalance between reactive oxygen species generation and endogenous antioxidant mechanisms results in oxidative stress that has been implicated in the pathogenesis of various diseases, including those of the cardiovascular system. Beyond their efficacy in lowering LDL cholesterol, statins modulate redox systems that are implicated in the development of atherosclerosis, cardiovascular morbidity, and mortality. RECENT ADVANCES: Differences in specific statins or their dosages result in differential metabolic actions arising from off-target or unknown mechanisms of action that can have important implications for overall patient morbidity and mortality. CRITICAL ISSUES: A recent meta-analysis and a combined analysis have suggested that high doses of statins increase the risk of developing type 2 diabetes mellitus, but reduce the risk of cardiovascular events. Thus, it is important to consider the cardiovascular and metabolic context and natural history of diseases when choosing a specific statin therapy for optimal individual patient health over the long term. FUTURE DIRECTIONS: More information is needed regarding the metabolism of statins, and the off-target or unknown actions of statins in affecting insulin resistance and metabolic homeostasis. The differential metabolic effects of specific statins should be considered in formulating optimal therapeutic strategies to reduce not just cardiovascular-related but also overall patient morbidity and mortality.

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Year:  2013        PMID: 23924053      PMCID: PMC4692132          DOI: 10.1089/ars.2013.5531

Source DB:  PubMed          Journal:  Antioxid Redox Signal        ISSN: 1523-0864            Impact factor:   8.401


  117 in total

1.  Inhibition of isoprenoid biosynthesis causes insulin resistance in 3T3-L1 adipocytes.

Authors:  L H Chamberlain
Journal:  FEBS Lett       Date:  2001-11-02       Impact factor: 4.124

2.  Modulation of human T cells signaling transduction by lovastatin.

Authors:  Shu-Meng Cheng; Jenn-Haung Lai; Shih-Ping Yang; Tien-Ping Tsao; Ling-Jun Ho; Jun-Ting Liou; Cheng-Chung Cheng
Journal:  Int J Cardiol       Date:  2008-11-28       Impact factor: 4.164

3.  Effect of atorvastatin and irbesartan, alone and in combination, on postprandial endothelial dysfunction, oxidative stress, and inflammation in type 2 diabetic patients.

Authors:  Antonio Ceriello; Roberta Assaloni; Roberto Da Ros; Amabile Maier; Ludovica Piconi; Lisa Quagliaro; Katherine Esposito; Dario Giugliano
Journal:  Circulation       Date:  2005-05-02       Impact factor: 29.690

Review 4.  How to control residual cardiovascular risk despite statin treatment: focusing on HDL-cholesterol.

Authors:  Soo Lim; Yae Min Park; Ichiro Sakuma; Kwang Kon Koh
Journal:  Int J Cardiol       Date:  2012-04-12       Impact factor: 4.164

5.  Inhibition of nitric oxide synthase uncoupling by sepiapterin improves left ventricular function in streptozotocin-induced diabetic mice.

Authors:  Hiromi Jo; Hajime Otani; Fusakazu Jo; Takayuki Shimazu; Toru Okazaki; Kei Yoshioka; Masanori Fujita; Atsushi Kosaki; Toshiji Iwasaka
Journal:  Clin Exp Pharmacol Physiol       Date:  2011-08       Impact factor: 2.557

6.  Deterioration of glucose homeostasis in type 2 diabetic patients one year after beginning of statins therapy.

Authors:  Alfonso Bellia; Stefano Rizza; Marco Felice Lombardo; Giulia Donadel; Rossella Fabiano; Katia Andreadi; Michael J Quon; Paolo Sbraccia; Massimo Federici; Manfredi Tesauro; Carmine Cardillo; Davide Lauro
Journal:  Atherosclerosis       Date:  2012-05-08       Impact factor: 5.162

Review 7.  Potentially important considerations in choosing specific statin treatments to reduce overall morbidity and mortality.

Authors:  Soo Lim; Ichiro Sakuma; Michael J Quon; Kwang Kon Koh
Journal:  Int J Cardiol       Date:  2012-11-16       Impact factor: 4.164

8.  NADPH oxidase contributes to vascular inflammation, insulin resistance, and remodeling in the transgenic (mRen2) rat.

Authors:  Yongzhong Wei; Adam T Whaley-Connell; Kemin Chen; Javad Habibi; Grace M-E Uptergrove; Suzanne E Clark; Craig S Stump; Carlos M Ferrario; James R Sowers
Journal:  Hypertension       Date:  2007-05-28       Impact factor: 10.190

9.  Isoprenoid metabolism is required for stimulation of the respiratory burst oxidase of HL-60 cells.

Authors:  G M Bokoch; V Prossnitz
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

10.  A 52-week, randomized, open-label, parallel-group comparison of the tolerability and effects of pitavastatin and atorvastatin on high-density lipoprotein cholesterol levels and glucose metabolism in Japanese patients with elevated levels of low-density lipoprotein cholesterol and glucose intolerance.

Authors:  Jun Sasaki; Yoshihiko Ikeda; Tadanobu Kuribayashi; Keizou Kajiwara; Sadatoshi Biro; Kyosuke Yamamoto; Masato Ageta; Syozou Kobori; Tetsunori Saikawa; Takatoshi Otonari; Suminori Kono
Journal:  Clin Ther       Date:  2008-06       Impact factor: 3.393

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  2 in total

1.  Statins: pleiotropic regulators of cardiovascular redox state.

Authors:  Charalambos Antoniades; Keith M Channon
Journal:  Antioxid Redox Signal       Date:  2014-03-10       Impact factor: 8.401

Review 2.  Combining Potent Statin Therapy with Other Drugs to Optimize Simultaneous Cardiovascular and Metabolic Benefits while Minimizing Adverse Events.

Authors:  Kwang Kon Koh; Ichiro Sakuma; Kazunori Shimada; Toshio Hayashi; Michael J Quon
Journal:  Korean Circ J       Date:  2017-07-26       Impact factor: 3.243

  2 in total

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