Polymorphisms rs2167444 and rs508384 in the SCD1 Gene Are Linked with High ApoB-48 Levels and Adverse Profile of

B Staňková1, J Macášek1, M Zeman1

  • 14th Department of Medicine, First Faculty of Medicine, Charles University and General University Hospital, Prague, Czech Republic.

Folia Biologica
|January 7, 2020
PubMed

Insights

Elevated apolipoprotein B-48 (apoB-48) is linked to cardiovascular disease risk. Lower frequencies of specific Stearoyl-CoA desaturase-1 (SCD1) gene variants are associated with higher apoB-48 levels, suggesting a genetic role.

Area of Science:

  • Cardiovascular Disease Research
  • Metabolic Syndrome Studies
  • Lipid Metabolism and Genetics

Background:

  • Elevated plasma apolipoprotein B-48 (apoB-48) is a recognized risk factor for cardiovascular disease.
  • Stearoyl-CoA desaturase-1 (SCD1), a key lipogenic enzyme, influences fuel metabolism.
  • Understanding factors associated with apoB-48 is crucial for managing cardiometabolic risk.

Purpose of the Study:

  • To investigate associations between clinical, biochemical, and genetic factors and apoB-48 levels in individuals at increased cardiometabolic risk.
  • To identify specific SCD1 gene polymorphisms related to apoB-48 concentrations.
  • To characterize the metabolic profile of individuals with high apoB-48 levels.

Main Methods:

  • Study included 220 subjects with at least one metabolic syndrome component.
  • Collected clinical, anthropometric, and laboratory data, including apoB-48 levels.
  • Genotyped specific SCD1 polymorphisms (rs2167444, rs508384).

Main Results:

  • High apoB-48 levels correlated with increased systolic blood pressure, higher prevalence of metabolic syndrome, and more small-dense LDL particles.
  • Individuals with high apoB-48 exhibited elevated triglycerides, non-HDL-cholesterol, lower HDL-cholesterol, and increased insulin resistance (HOMA-IR).
  • Lower frequencies of SCD1 minor genotypes (rs2167444, rs508384) were observed in subjects with elevated apoB-48.

Conclusions:

  • Elevated apoB-48 is associated with an adverse lipid profile, hypertension, insulin resistance, and oxidative stress.
  • Genetic factors, specifically lower proportions of minor SCD1 genotypes, may play a role in the pathogenesis of high apoB-48 levels.
  • These findings highlight the interplay between genetics and metabolic dysfunction in cardiovascular risk.

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