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Advisor(s)
Abstract(s)
Objectives: This project aims to identify novel biomarkers to distinguish
polygenic and monogenic dyslipidaemia, by an integrative
approach, based on the detailed characterization of the lipid
profile ID of patients with severe dyslipidaemia. This is expected
to contribute to an early and accurate diagnosis, allowing the
implementation of a successful therapeutic plan that can be
applied still in childhood to effectively abolish/decrease the
patient’s cardiovascular risk.
Background: Dyslipidaemia is one of the major cardiovascular risk factors. It can be due to primary causes (i.e. monogenic, characterized by a single gene mutation, or dyslipidaemia of polygenic/environmental causes), or secondary to specific disorders such as obesity, diabetes mellitus or hypothyroidism. Monogenic patients present the most severe phenotype and so they need to be identified at an early age, allowing the implementation of pharmacologic treatment able to decrease cardiovascular risk. However, the majority of hyperlipidemic patients most likely have a polygenic disease that can be controlled just by the implementation of a healthy lifestyle. Thus, the distinction between monogenic and polygenic dyslipidaemia is important for a prompt diagnosis, cardiovascular risk assessment, counselling and treatment. In spit of this, none of the current standard biomarkers (i.e. total cholesterol, LDL-c, HDL-c, triglycerides), can effectively make that discrimination between patients.
Description
Marta Correia acknowledges financial support from FCT (PD/BD/114387/2016).
Keywords
Dyslipidaemia Portuguese Familial Hypercholesterolemia Doenças Cardio e Cérebro-vasculares
