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The Clinical Pharmacogenomics Implementation Consortium : CPIC Guideline for SLCO1B1 and Simvastatin-Induced Myopathy

Wilke, R. A. (author)
Ramsey, L. B. (author)
Johnson, S. G. (author)
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Maxwell, W. D. (author)
McLeod, H. L. (author)
Voora, D. (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
Niemi, M. (author)
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 (creator_code:org_t)
2012-05-23
2012
English.
In: Clinical Pharmacology and Therapeutics. - : Springer Science and Business Media LLC. - 0009-9236 .- 1532-6535. ; 92:1, s. 112-117
  • Journal article (peer-reviewed)
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  • Cholesterol reduction from statin therapy has been one of the greatest public health successes in modern medicine. Simvastatin is among the most commonly used prescription medications. A non-synonymous coding single-nucleotide polymorphism (SNP), rs4149056, in SLCO1B1 markedly increases systemic exposure to simvastatin and the risk of muscle toxicity. This guideline explores the relationship between rs4149056 (c.521T>C, p.V174A) and clinical outcome for all statins. The strength of the evidence is high for myopathy with simvastatin. We limit our recommendations accordingly.

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