Lipid profile evaluation and severe hypercholesterolaemia screening in the middle-aged population according to

Sandra Kutkiene1, Zaneta Petrulioniene1, Aleksandras Laucevicius1

  • 1Vilnius University, Faculty of Medicine, Clinic of Cardiac and Vascular Diseases, Santariskiu str. 2, LT-08661, Vilnius, Lithuania; Vilnius University, Faculty of Medicine, M. K. Ciurlionio str. 21, 03101, Vilnius, Lithuania; Vilnius University Hospital Santaros Klinikos, Santariskiu str. 2, 08661, Vilnius, Lithuania.

Atherosclerosis
|October 2, 2018
PubMed

Insights

Severe hypercholesterolaemia (SH) affects 3.2% of middle-aged Lithuanians without cardiovascular disease. Screening identified a slight decrease in SH prevalence from 2009-2016, indicating a need for further evaluation of familial hypercholesterolaemia.

Area of Science:

  • Cardiology
  • Public Health
  • Genetics

Background:

  • Cardiovascular disease (CVD) is a leading cause of premature death in Lithuania.
  • Abnormal lipid levels are prevalent in middle-aged Lithuanian adults.
  • Population-based screening for severe hypercholesterolaemia (SH) is crucial.

Purpose of the Study:

  • To evaluate the lipid profile of middle-aged Lithuanians.
  • To conduct population-based screening for severe hypercholesterolaemia (SH).
  • To assess trends in SH prevalence over time.

Main Methods:

  • Analysis of lipidograms from 92,373 adults (aged 40-64) in the Lithuanian High Cardiovascular Risk (LitHiR) program (2009-2016).
  • Inclusion criteria: no overt CVD.
  • Screening for SH (LDL-C ≥6 mmol/l).

Main Results:

  • Mean LDL cholesterol (LDL-C) was 3.87 mmol/l; 89.7% had dyslipidaemia.
  • SH (LDL-C ≥6 mmol/l) was detected in 3.2% of participants.
  • SH prevalence showed a slight decrease from 2.91% to 2.82% (2009-2016).

Conclusions:

  • Severe hypercholesterolaemia (SH) affects 3.2% of middle-aged Lithuanians without overt CVD.
  • A slight decrease in SH prevalence was observed between 2009 and 2016.
  • Further clinical and genetic evaluation is needed to identify familial hypercholesterolaemia in individuals with SH.
Abstract

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