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Authors
Advisor(s)
Abstract(s)
Background/Aim: Statins are the standard treatment for dyslipidaemia disorders, but there is a
wide (10-70%) variation in patient response to statin treatment and several
documented serious adverse effects. Studies of variants in genes regulating
drug absorption, metabolism, pharmacodynamics and excretion mechanisms,
have been implicated as reasons for this variability.
The aim of this study is to determine the prevalence of pharmacogenetic
relevant genotypes in the Portuguese population and in a sample of high
cardiovascular risk patients: familial hypercholesterolemia subjects.
Description
Keywords
Pharmacogenomics Dyslipidemia Portugal e_COR Familial Hypercholesterolaemia Doenças Cardio e Cérebro-vasculares
Pedagogical Context
Citation
Publisher
Instituto Nacional de Saúde Doutor Ricardo Jorge, IP
