Simvastatin is one of the most commonly used statins for cholesterol reduction in the world. The inadequate drug dose can lead to adverse side-effects and cause muscle-related health problems, myopathy, in some patients. The adverse drug reactions appear to be dose-dependent, especially when statins are administered at higher doses and together with certain other medications [2-4].
Is one of the most commonly used statins for cholesterol reduction.
May cause muscle-related adverse effects in some patients.
Its dosage influences these adverse drug reactions.
The pharmacogenetics study defines the drug optimal dose therapy or recommends for alternative statin therapy. SLCO1B1 genetic variants are associated with increased risk of composite adverse events in patients with hypercholesterolemia when treated with statins (atorvastatin, pravastatin or simvastatin).
Benefits of genetic testing
The pharmacogenetic test includes the study of 3 genetic variants in SLCO1B1 gene associated with myopathy risk. In patients taking statins could improve treatment adherence and efficacy.
By evaluating SLCO1B1 genetic variants it is possible to:
> evaluate the patient response to simvastatin
> prescribe an adequate dose
> avoid the adverse side-effects of non-optimal simvastatin dosage
The genetic test includes the evaluation of 3 genetic variants in SLCO1B1 gene. The selected variants were approved by the FDA and also by the International Warfarin Pharmacogenomics Consortium to guide therapy.
SLCO1B1 – Solute Carrier Organic Anion Transporter Family, member 1B1
International Medical Guidelines
Genetic testing is recommended by several renowned international organizations, such as the Food and Drug Administration (FDA) and the Clinical Pharmacogenetics Implementation Consortium (CPIC)
In order to reduce the risk of muscle injury, the FDA recommends against 80 daily simvastatin dosage in new patients and also in those already taking lower doses of the drug. According to the FDA, the risk of myopathy is higher during the first year of treatment and approximately 60% of the cases are associated with SLCO1B1 genetic variants. These are strongly associated with an increased risk of statin-induced myopathy. Genotyping these variants may help to achieve the benefits of statin therapy more safely and effectively.
“The Clinical Pharmacogenetics Implementation Consortium (CPIC) that develops peer-reviewed gene-drug guidelines based on new developments in the field, has established several recommendations on simvastatin dosage based on SLCO1B1 genotype.”
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