Literature DB >> 24973595

How to balance cardiorenometabolic benefits and risks of statins.

Soo Lim1, Pyung Chun Oh2, Ichiro Sakuma3, Kwang Kon Koh4.   

Abstract

Statins, 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, are important for preventing adverse cardiovascular events not only in patients with a high risk of vascular disease but also in those with a low risk, by reducing the levels of low-density lipoprotein cholesterol. Statin is associated with deteriorating glucose homeostasis and an increased risk of diabetes mellitus. Moreover, these off-target effects are dose-dependent; it has also been suggested that renal insult can be caused dose-dependently by statin treatment, in contrast to previous studies showing a renoprotective effect. The 2013 American College of Cardiology/American Heart Association guidelines recommend the use of high-intensity statin therapy, and extend its use to more people at risk of vascular diseases. However, a European committee has expressed concerns about the potential side effects of using statins in a large fraction of the population for extended periods. This is true of Asian people, for whom the disease burden from cardiovascular disorders is not as great as among Western ethnic groups. There are still many unanswered questions on how to balance the cardiovascular benefits with the potential renometabolic risks of statins. Therefore, genetic or pharmacogenetic approaches are needed to define who is more vulnerable to developing diabetes mellitus or acute kidney injury. In particular, more information is required regarding the metabolism of statins, and their off-target or unknown actions and overall impact. These different renometabolic effects of statins should help in formulating optimal therapeutic strategies for patients for reducing overall morbidity and mortality and not just those associated with cardiovascular diseases.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Benefits and risks; Cardiovascular disease; Diabetes; Renal injury; Statins

Mesh:

Substances:

Year:  2014        PMID: 24973595     DOI: 10.1016/j.atherosclerosis.2014.06.001

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  6 in total

1.  Crystal structures of human NSDHL and development of its novel inhibitor with the potential to suppress EGFR activity.

Authors:  Dong-Gyun Kim; Sujin Cho; Kyu-Yeon Lee; Seung-Ho Cheon; Hye-Jin Yoon; Joo-Youn Lee; Dongyoon Kim; Kwang-Soo Shin; Choong-Hyun Koh; Ji Sung Koo; Yuri Choi; Hyung Ho Lee; Yu-Kyoung Oh; Yoo-Seong Jeong; Suk-Jae Chung; Moonkyu Baek; Kwan-Young Jung; Hyo Jin Lim; Hyoun Sook Kim; Sung Jean Park; Jeong-Yeon Lee; Sang Jae Lee; Bong-Jin Lee
Journal:  Cell Mol Life Sci       Date:  2020-03-05       Impact factor: 9.261

2.  A randomized, double-blind, placebo-controlled study of the effect of ezetimibe on glucose metabolism in subjects with type 2 diabetes mellitus and hypercholesterolemia.

Authors:  Itori Saito; Kyoichi Azuma; Taro Kakikawa; Nobuyuki Oshima; Mary E Hanson; Andrew M Tershakovec
Journal:  Lipids Health Dis       Date:  2015-05-01       Impact factor: 3.876

3.  Effect of Berberine on promoting the excretion of cholesterol in high-fat diet-induced hyperlipidemic hamsters.

Authors:  Xiao-Yang Li; Zhen-Xiong Zhao; Min Huang; Ru Feng; Chi-Yu He; Chao Ma; Shi-Heng Luo; Jie Fu; Bao-Ying Wen; Long Ren; Jia-Wen Shou; Fang Guo; Yangchao Chen; Xin Gao; Yan Wang; Jian-Dong Jiang
Journal:  J Transl Med       Date:  2015-08-27       Impact factor: 5.531

4.  Moderate-intensity statin therapy seems ineffective in primary cardiovascular prevention in patients with type 2 diabetes complicated by nephropathy. A multicenter prospective 8 years follow up study.

Authors:  Ferdinando Carlo Sasso; Nadia Lascar; Antonella Ascione; Ornella Carbonara; Luca De Nicola; Roberto Minutolo; Teresa Salvatore; Maria Rosaria Rizzo; Plinio Cirillo; Giuseppe Paolisso; Raffaele Marfella
Journal:  Cardiovasc Diabetol       Date:  2016-10-13       Impact factor: 9.951

5.  FR171456 is a specific inhibitor of mammalian NSDHL and yeast Erg26p.

Authors:  Stephen B Helliwell; Shantanu Karkare; Marc Bergdoll; Alain Rahier; Juliet R Leighton-Davis; Celine Fioretto; Thomas Aust; Ireos Filipuzzi; Mathias Frederiksen; John Gounarides; Dominic Hoepfner; Andreas Hofmann; Pierre-Eloi Imbert; Rolf Jeker; Richard Knochenmuss; Philipp Krastel; Anais Margerit; Klaus Memmert; Charlotte V Miault; N Rao Movva; Alban Muller; Hans-Ulrich Naegeli; Lukas Oberer; Vivian Prindle; Ralph Riedl; Sven Schuierer; Jessica A Sexton; Jianshi Tao; Trixie Wagner; Hong Yin; Juan Zhang; Silvio Roggo; Stefan Reinker; Christian N Parker
Journal:  Nat Commun       Date:  2015-10-12       Impact factor: 14.919

Review 6.  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

  6 in total

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