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Possible gene-gender interaction between the SLCO1B1 polymorphism and statin treatment efficacy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F12%3A00058445" target="_blank" >RIV/00023001:_____/12:00058445 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.nel.edu/home.htm" target="_blank" >http://www.nel.edu/home.htm</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Possible gene-gender interaction between the SLCO1B1 polymorphism and statin treatment efficacy

  • Original language description

    OBJECTIVES: A significant inter-individual variability in statin treatment efficacy is likely to have a strong genetic background. A candidate gene with the potential to influence statin treatment efficacy is SLCO1B1. This gene codes for the solute carrier organic anion transporter, which has been shown to regulate the hepatic uptake of statins and some other drugs. MATERIALS AND METHODS: The SLCO1B1 rs4149056 (T>C) polymorphism was successfully analysed in a group of 253 patients with dyslipidemia (treated with simvastin or atorvastatin, 10 or 20 mg per day) and 470 healthy normolipidemic controls. The polymorphism was analysed using nested PCR-RFLP. Lipid levels (total, LDL and HDL cholesterol; triglycerides) were analysed before and after 10-13 weeks of treatment. RESULTS: After treatment, as expected, there was a significant decrease both in the total cholesterol (7.60+-1.36 -> 5.37+-1.12 mmol/L, p<0.001) and LDL cholesterol (5.04+-1.34 -> 3.17+-0.99 mmol/L, p<0.001) levels. The di

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FA - Cardiovascular diseases including cardio-surgery

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NT11307" target="_blank" >NT11307: Analysis of the genetic predisposition to the statin-induced side effects</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Neuroendocrinology letters

  • ISSN

    0172-780X

  • e-ISSN

  • Volume of the periodical

    33

  • Issue of the periodical within the volume

    suppl. 2

  • Country of publishing house

    SE - SWEDEN

  • Number of pages

    4

  • Pages from-to

    22-25

  • UT code for WoS article

  • EID of the result in the Scopus database