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Published on: April 4, 2018
Gene polymorphism of 3'APO-VNTR in Egyptians with coronary artery disease
1Mansoura University, Faculty of Science, Chemistry Department, Division of Biochemistry, Mansoura, Egypt.
Insights
The 3'APOB-VNTR gene may be a risk factor for coronary artery diseases (CAD). This genetic marker could aid in the early diagnosis of CAD, a leading global cause of death.
Area of Science:
- Genetics
- Cardiology
- Molecular Biology
Background:
- Coronary artery diseases (CAD) represent a significant global health burden and a leading cause of mortality worldwide.
- Dyslipidemia is a known risk factor that elevates the likelihood of developing CAD.
- Investigating genetic factors like the 3'APOB-VNTR gene is crucial for understanding CAD etiology.
Purpose of the Study:
- To investigate the potential impact of the 3'APOB-VNTR gene polymorphism on the incidence of coronary artery diseases (CAD).
- To explore the association between specific 3'APOB-VNTR genotypes and the presence of CAD.
Main Methods:
- The study enrolled 80 patients diagnosed with CAD and 93 healthy control volunteers.
- Lipid parameters were measured in all participants.
- Polymerase Chain Reaction (PCR) was employed to analyze the 3'APOB-VNTR gene polymorphism.
Main Results:
- Specific genotypes (31/31, 31/37, 37/37, 31/44) were prevalent in both CAD patients and controls.
- The 24/31 genotype was observed in 13.7% of CAD patients but was absent in the control group.
- An increased frequency of certain genotypes (e.g., 17/31, 21/34) was noted in the control group compared to the CAD patient group.
Conclusions:
- The 3'APOB-VNTR gene is suggested as a potential risk factor for coronary artery diseases (CAD).
- Analysis of this gene polymorphism may contribute to the early diagnosis of CAD.
Background:
Coronary artery diseases (CAD) are big health problem in both developed and developing countries. It is considered one of the main causes of death in the world. Dyslipidemia increases the risk of CAD incidences. It is aimed in this worktop study the impact of 3'APOBVNTRgene on CAD incidences.
Methods:
Eighty CAD patients and ninety-three healthy volunteers are enrolled in this study. Lipid parameters were estimated in both groups and PCR technique has been performed to analyze 3'APOB-VNTR gene polymorphism.
Results:
The genotypes 31/31, 31/37, 37/37 and 31/44 are more predominant in both groups. The frequency of 24/31 in CAD patients is (0.137) while it is completely absent in the control group. Our results show that there is an increase in the frequency of various genotypes (e.g., 17/31 and 21/34 genotypes) in the control group compared to theca patients group.
Conclusions:
3'APOB-VNTR gene could probably be considered a risk factor for CAD incidences and may help to early diagnose them.
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