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.
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.
Abstract:
Elevated plasma concentration of apolipoprotein B-48 (apoB-48) is an independent risk factor of cardiovascular disease. Stearoyl-CoA desaturase-1 (SCD1) is a rate-limiting lipogenic enzyme and a key regulator of fuel metabolism. The aim of this study was to analyse associations between clinical, biochemical, and genetic factors and different apoB-48 levels in subjects at increased cardiometabolic risk. We examined 220 subjects exhibiting at least one metabolic syndrome (MetS) component. In conjunction with basic clinical, anthropometric and laboratory measurements, we analysed various polymorphisms of stearoyl-CoA desaturase-1 (SCD1). Subjects were divided into two groups according to the median apoB-48 level: (1) high apoB-48 (≥ 7.9 mg/l, N = 112) and (2) low apoB-48 (< 7.9 mg/l, N = 108). Neither group differed significantly in anthropometric measures. High plasma apoB-48 levels were associated with increased systolic blood pressure (+3 %; P < 0.05), MetS prevalence (59.8 vs. 32.4 %; P < 0.001), small-dense LDL frequency (46.4 vs. 20.4 %; P < 0.001), triglycerides (+97 %; P < 0.001), non-HDLcholesterol (+27 %; P < 0.001), and lower concentrations of HDL-cholesterol (-11 %; P < 0.01). This group was further characterized by a higher HOMA-IR index (+54 %; P < 0.001) and increased concentrations of conjugated dienes (+11 %; P < 0.001) and oxidatively modified LDL (+ 38 %; P < 0.05). Lower frequencies of SCD1 minor genotypes (rs2167444, rs508384, P < 0.05) were observed in subjects with elevated plasma concentrations of apoB-48. Elevated plasma concentrations of apoB-48 are associated with an adverse lipid profile, higher systolic blood pressure, insulin resistance, and oxidative stress. Lower proportions of minor SCD1 genotypes (rs2167444, rs508384) implicate the role of genetic factors in the pathogenesis of elevated levels of apoB-48.
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