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The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy : 2014 Update

Ramsey, L. B. (author)
Johnson, S. G. (author)
Caudle, K. E. (author)
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Haidar, C. E. (author)
Voora, D. (author)
Wilke, R. A. (author)
Maxwell, W. D. (author)
McLeod, L. (author)
Krauss, R. M. (author)
Roden, D. M. (author)
Feng, Q. (author)
Cooper-DeHoff, R. M. (author)
Gong, L. (author)
Klein, T. E. (author)
Wadelius, Mia (author)
Uppsala universitet,Klinisk farmakogenomik och osteoporos,Science for Life Laboratory, SciLifeLab
Niemi, M. (author)
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 (creator_code:org_t)
2014-06-11
2014
English.
In: Clinical Pharmacology and Therapeutics. - : Springer Science and Business Media LLC. - 0009-9236 .- 1532-6535. ; 96:4, s. 423-428
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Simvastatin is among the most commonly used prescription medications for cholesterol reduction. A single coding single-nucleotide polymorphism, rs4149056T>C, in SLCO1B1 increases systemic exposure to simvastatin and the risk of muscle toxicity. We summarize evidence from the literature supporting this association and provide therapeutic recommendations for simvastatin based on SLCO1B1 genotype. This article is an update to the 2012 Clinical Pharmacogenetics Implementation Consortium guideline for SLCO1B1 and simvastatin-induced myopathy.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

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