Literature DB >> 24263182

The SLCO1B1 c.521T>C polymorphism is associated with dose decrease or switching during statin therapy in the Rotterdam Study.

Catherine E de Keyser1, Bas J M Peters, Matthijs L Becker, Loes E Visser, André G Uitterlinden, Olaf H Klungel, Céline Verstuyft, Albert Hofman, Anke-Hilse Maitland-van der Zee, Bruno H Stricker.   

Abstract

OBJECTIVE: The SLCO1B1 c.521T>C polymorphism is associated with statin plasma levels and simvastatin-induced adverse drug reactions. We studied whether the c.521T>C polymorphism is associated with dose decreases or switches to other cholesterol-lowering drugs during simvastatin and atorvastatin therapy, because these events are indicators of adverse drug reactions.
MATERIALS AND METHODS: We identified 1939 incident simvastatin and atorvastatin users in the Rotterdam Study, a population-based cohort study. Associations were studied using Cox proportional hazards analysis. Meta-analysis was performed with data from the Utrecht Cardiovascular Pharmacogenetics study.
RESULTS: Simvastatin users with the c.521 CC genotype had a significantly higher risk of a dose decrease or switch than users with the TT genotype [hazard ratio (HR) 1.74, 95% confidence interval (CI) 1.05-2.88]. Female sex, age below 70 years, and low starting dose were risk factors. In atorvastatin users with starting dose of more than 20 mg, the risk of a dose decrease or switch was higher in users carrying a C allele than in users with the TT genotype (HR 3.26, 95% CI 1.47-7.25). In the meta-analysis the association in simvastatin users remained, with a significantly higher risk of a dose decrease or switch in simvastatin users with two minor alleles (HR 1.69, 95% CI 1.05-2.73). For atorvastatin users no significant association was found.
CONCLUSION: In simvastatin users in the Rotterdam Study, we demonstrated an association between the c.521T>C polymorphism and dose decrease or switching, as indicators of adverse drug reactions, and provided risk factors for this association. For atorvastatin, an association was found in users with a starting dose of more than 20 mg.

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Year:  2014        PMID: 24263182     DOI: 10.1097/FPC.0000000000000018

Source DB:  PubMed          Journal:  Pharmacogenet Genomics        ISSN: 1744-6872            Impact factor:   2.089


  21 in total

1.  The Rotterdam Study: 2016 objectives and design update.

Authors:  Albert Hofman; Guy G O Brusselle; Sarwa Darwish Murad; Cornelia M van Duijn; Oscar H Franco; André Goedegebure; M Arfan Ikram; Caroline C W Klaver; Tamar E C Nijsten; Robin P Peeters; Bruno H Ch Stricker; Henning W Tiemeier; André G Uitterlinden; Meike W Vernooij
Journal:  Eur J Epidemiol       Date:  2015-09-19       Impact factor: 8.082

2.  Effects of SLCO1B1 and GATM gene variants on rosuvastatin-induced myopathy are unrelated to high plasma exposure of rosuvastatin and its metabolites.

Authors:  Xue Bai; Bin Zhang; Ping Wang; Guan-Lei Wang; Jia-Li Li; Ding-Sheng Wen; Xing-Zhen Long; Hong-Shuo Sun; Yi-Bin Liu; Min Huang; Shi-Long Zhong
Journal:  Acta Pharmacol Sin       Date:  2018-06-27       Impact factor: 6.150

3.  SLCO1B1 521T > C polymorphism associated with rosuvastatin-induced myotoxicity in Chinese coronary artery disease patients: a nested case-control study.

Authors:  Ju-E Liu; Xiao-Ying Liu; Sheng Chen; Yan Zhang; Li-Yun Cai; Min Yang; Wei-Hua Lai; Bin Ren; Shi-Long Zhong
Journal:  Eur J Clin Pharmacol       Date:  2017-08-15       Impact factor: 2.953

4.  Performance of exome sequencing for pharmacogenomics.

Authors:  Eric R Londin; Peter Clark; Marialuisa Sponziello; Larry J Kricka; Paolo Fortina; Jason Y Park
Journal:  Per Med       Date:  2014       Impact factor: 2.512

5.  The Integrating Pharmacogenetics in Clinical Care (I-PICC) Study: Protocol for a point-of-care randomized controlled trial of statin pharmacogenetics in primary care.

Authors:  Jason L Vassy; Charles A Brunette; Nilla Majahalme; Sanjay Advani; Lauren MacMullen; Cynthia Hau; Andrew J Zimolzak; Stephen J Miller
Journal:  Contemp Clin Trials       Date:  2018-10-24       Impact factor: 2.226

Review 6.  Pharmacogenetics to guide cardiovascular drug therapy.

Authors:  Julio D Duarte; Larisa H Cavallari
Journal:  Nat Rev Cardiol       Date:  2021-05-05       Impact factor: 32.419

7.  Association of SLCO1B1 c.521T>C (rs4149056) with discontinuation of atorvastatin due to statin-associated muscle symptoms.

Authors:  Derek W Linskey; Joseph D English; Daniel A Perry; Heather M Ochs-Balcom; Changxing Ma; Paul J Isackson; Georgirene D Vladutiu; Jasmine A Luzum
Journal:  Pharmacogenet Genomics       Date:  2020-12       Impact factor: 2.000

8.  SLCO1B1 polymorphism is not associated with risk of statin-induced myalgia/myopathy in a Czech population.

Authors:  Jaroslav A Hubáček; Dana Dlouhá; Vera Adámková; Lukáš Zlatohlavek; Ondřej Viklický; Petra Hrubá; Richard Češka; Michal Vrablík
Journal:  Med Sci Monit       Date:  2015-05-20

9.  The frequency of SLCO1B1*5 polymorphism genotypes among Russian and Sakha (Yakutia) patients with hypercholesterolemia.

Authors:  Dmitrij Alekseevitch Sychev; Grigorij Nikolaevich Shuev; Jana Valer'evna Chertovskih; Nadezhda Romanovna Maksimova; Andrej Vladimirovich Grachev; Ol'ga Aleksandrovna Syrkova
Journal:  Pharmgenomics Pers Med       Date:  2016-05-25

10.  SLCO1B1 c.388A>G Polymorphism Is Associated with HDL-C Levels in Response to Atorvastatin in Chilean Individuals.

Authors:  Yalena Prado; Nicolás Saavedra; Tomás Zambrano; Jenny Lagos; Alexy Rosales; Luis A Salazar
Journal:  Int J Mol Sci       Date:  2015-08-31       Impact factor: 5.923

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