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1
An Unnecessary Pain: Using Pharmacogenetics for Statin-related Skeletal Muscle Toxicity.一种不必要的痛苦:利用药物基因组学应对他汀类药物相关的骨骼肌毒性
Cureus. 2018 Apr 30;10(4):e2557. doi: 10.7759/cureus.2557.
2
Assessment of pharmacogenomic SLCO1B1 assay for prediction of neuromuscular pain in type 2 diabetes mellitus and cardiovascular patients: preliminary results.评估 SLCO1B1 基因多态性检测对 2 型糖尿病和心血管病患者神经肌肉疼痛的预测作用:初步研究结果。
Eur Rev Med Pharmacol Sci. 2020 Jan;24(1):469-477. doi: 10.26355/eurrev_202001_19948.
3
Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.SLCO1B1 基因 rs4149056 变异对辛伐他汀和阿托伐他汀相关肌病的影响差异。
Pharmacogenomics J. 2012 Jun;12(3):233-7. doi: 10.1038/tpj.2010.92. Epub 2011 Jan 18.
4
Pharmacogenomics and adverse drug reactions: the case of statins.药物基因组学与药物不良反应:以他汀类药物为例。
Expert Opin Pharmacother. 2011 Jul;12(10):1499-509. doi: 10.1517/14656566.2011.563734. Epub 2011 Mar 29.
5
Association between SLCO1B1 T521C polymorphism and risk of statin-induced myopathy: a meta-analysis.SLCO1B1基因T521C多态性与他汀类药物所致肌病风险的关联:一项荟萃分析
Pharmacogenomics J. 2018 Dec;18(6):721-729. doi: 10.1038/s41397-018-0054-0. Epub 2018 Sep 24.
6
SLCO1B1 polymorphism is not associated with risk of statin-induced myalgia/myopathy in a Czech population.在捷克人群中,SLCO1B1基因多态性与他汀类药物诱发的肌痛/肌病风险无关。
Med Sci Monit. 2015 May 20;21:1454-9. doi: 10.12659/MSM.893007.
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Pharmacogenomics of statins: understanding susceptibility to adverse effects.他汀类药物的药物基因组学:了解不良反应易感性
Pharmgenomics Pers Med. 2016 Oct 3;9:97-106. doi: 10.2147/PGPM.S86013. eCollection 2016.
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Impact of SLCO1B1 (OATP1B1) and ABCG2 (BCRP) genetic polymorphisms and inhibition on LDL-C lowering and myopathy of statins.溶质载体有机阴离子转运体1B1(OATP1B1)和ATP结合盒转运体G2(ABCG2)基因多态性及抑制作用对他汀类药物降低低密度脂蛋白胆固醇(LDL-C)水平及引发肌病的影响
Xenobiotica. 2011 Aug;41(8):639-51. doi: 10.3109/00498254.2011.562566. Epub 2011 Mar 22.
9
Statin-associated muscle symptoms and SLCO1B1 rs4149056 genotype in patients with familial hypercholesterolemia.家族性高胆固醇血症患者的他汀类药物相关肌肉症状与SLCO1B1 rs4149056基因型
Am Heart J. 2016 Sep;179:1-9. doi: 10.1016/j.ahj.2016.05.015. Epub 2016 Jun 9.
10
Polymorphism of the hepatic influx transporter organic anion transporting polypeptide 1B1 is associated with increased cholesterol synthesis rate.肝脏摄取转运体有机阴离子转运多肽1B1的多态性与胆固醇合成速率增加有关。
Pharmacogenet Genomics. 2008 Oct;18(10):921-6. doi: 10.1097/FPC.0b013e32830c1b5f.

本文引用的文献

1
Proposal for a Pharmacogenetic Decision Algorithm.药物遗传学决策算法提案。
Cureus. 2017 May 30;9(5):e1289. doi: 10.7759/cureus.1289.
2
Statin Therapy: Review of Safety and Potential Side Effects.他汀类药物治疗:安全性及潜在副作用综述
Acta Cardiol Sin. 2016 Nov;32(6):631-639. doi: 10.6515/acs20160611a.
3
Association Between SLCO1B1 Gene T521C Polymorphism and Statin-Related Myopathy Risk: A Meta-Analysis of Case-Control Studies.SLCO1B1基因T521C多态性与他汀类药物相关肌病风险的关联:病例对照研究的荟萃分析
Medicine (Baltimore). 2015 Sep;94(37):e1268. doi: 10.1097/MD.0000000000001268.
4
The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.临床药物基因组学实施联盟关于SLCO1B1与辛伐他汀所致肌病的指南:2014年更新版
Clin Pharmacol Ther. 2014 Oct;96(4):423-8. doi: 10.1038/clpt.2014.125. Epub 2014 Jun 11.
5
An assessment by the Statin Muscle Safety Task Force: 2014 update.他汀类药物肌肉安全性工作组评估:2014 年更新。
J Clin Lipidol. 2014 May-Jun;8(3 Suppl):S58-71. doi: 10.1016/j.jacl.2014.03.004.

一种不必要的痛苦:利用药物基因组学应对他汀类药物相关的骨骼肌毒性

An Unnecessary Pain: Using Pharmacogenetics for Statin-related Skeletal Muscle Toxicity.

作者信息

Alzghari Saeed K

机构信息

Gulfstream Genomics, Gulfstream Diagnostics, Dallas, USA.

出版信息

Cureus. 2018 Apr 30;10(4):e2557. doi: 10.7759/cureus.2557.

DOI:10.7759/cureus.2557
PMID:29974012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6029739/
Abstract

Statins are an important class of medications in reducing the risk of cardiovascular events as well as overall mortality. However, a well-known adverse effect of statins is skeletal muscle toxicity, which may lead to abrupt discontinuation of the statin. In turn, patients may miss out on the benefits of statin therapy. An important factor to consider is a patient's solute carrier organic anion transporter 1B1 (SLCO1B1) gene T521C polymorphism status. Herein, an overview of the pharmacogenetics of SLCO1B1 is provided as well as recommendations for use in practice.

摘要

他汀类药物是降低心血管事件风险以及总体死亡率的一类重要药物。然而,他汀类药物一个众所周知的不良反应是骨骼肌毒性,这可能导致他汀类药物突然停用。相应地,患者可能无法获得他汀类药物治疗的益处。一个需要考虑的重要因素是患者的溶质载体有机阴离子转运体1B1(SLCO1B1)基因T521C多态性状态。本文提供了SLCO1B1药物遗传学的概述以及在实践中的使用建议。