Related Experiment Video
Updated: Jul 17, 2026

A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
Published on: July 14, 2016
Polymorphism in apoprotein-CIII gene and coronary heart disease
S S Hussain1, J Buraiki, N Dzimiri
1Departments of Biological and Medical Research, Cardiovascular Diseases, and Biomedical Statistics and Scientific Computing, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Insights
The apoprotein-CIII variant allele is not linked to high cholesterol or triglycerides. However, this genetic marker significantly increases the risk of coronary heart disease (CHD) in Saudi subjects.
Area of Science:
- Genetics
- Cardiovascular Disease Epidemiology
- Molecular Biology
Background:
- Apolipoprotein-CIII (Apo-CIII) plays a role in lipid metabolism.
- Genetic variations in Apo-CIII may influence lipid levels and cardiovascular risk.
- Previous studies have suggested potential links between Apo-CIII and dyslipidemia or coronary heart disease (CHD).
Purpose of the Study:
- To investigate the association between an apoprotein-CIII variant allele and hypertriglyceridemia, hypercholesterolemia, and coronary heart disease (CHD).
Main Methods:
- Genotyping of a C to G substitution in the 3' untranslated region of apoprotein-CIII was performed.
- The study included 92 Saudi subjects (65 males, 27 females) who underwent coronary angiography.
- Restriction fragment length polymorphism analysis using Sac I was employed for genotyping.
Main Results:
- The Apo-CIII variant allele showed no significant association with hypertriglyceridemia or hypercholesterolemia.
- A significant association (P<0.01) was observed between the Apo-CIII variant allele and coronary heart disease (CHD).
- Individuals with the rare allele had a 3.4-fold increased risk of CHD, independent of other risk factors, even in those over 45.
Conclusions:
- The study did not establish a link between the apoprotein-CIII variant allele and dyslipidemia (hypertriglyceridemia or hypercholesterolemia).
- A significant association was found between the apoprotein-CIII variant allele and an increased risk of coronary heart disease (CHD) in the studied Saudi population.
Background:
The aim of this study was to look into the association, if any, of apoprotein-CIII variant allele with hypertriglyceridemia, hypercholesterolemia and coronary heart disease (CHD).
Patients And Methods:
The prevalence of a C to G substitution in the 3' untranslated region of apoprotein-CIII was studied in a sample of 92 angiographed Saudi subjects, consisting of 65 males and 27 females. The subjects were genotyped by amplification followed by digestion of the gene fragment containing the polymorphic site with Sac I restriction enzyme.
Results:
The variant allele of apoprotein-CIII was found to be associated neither with hypertriglyceridemia nor with hypercholesterolemia. However, a significant association of this allele (P<0.01) was found with coronary heart disease, independent of other risk factors such as smoking, diabetes and hypertension. An estimation of odds ratio using logistic regression with various risk factors in the model showed that the individuals with this rare allele were 3.4 times more at risk of developing coronary heart disease. This estimate of risk held even after analyzing a subset of individuals above 45 years of age.
Conclusion:
While the association between apoprotein-CIII variant allele and dyslipidemia could not be established in this study, the relationship between this marker and CHD was highlighted in the studied subjects.
More Related Videos
07:26High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
Published on: July 18, 2017
03:45Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Coronary Artery Disease II: Pathophysiology
Pharmacogenomics: Identification of New Drug Targets
Coronary Artery Disease III: Clinical Manifestations
Coronary Artery Disease I: Introduction