Key result
ApoB XbaI polymorphism shows no association with obesity or lipid profiles in Egyptian adults.
Why the study?
No data were available on the relationship between apoB XbaI gene polymorphism and lipid levels in Egyptian populations.
Is the apoB XbaI gene polymorphism associated with altered lipid profiles or obesity in an Egyptian population?
Case-Control (n=356)
No
Is the apoB XbaI gene polymorphism associated with altered lipid profiles or obesity in an Egyptian population?
Odds Ratio: 0.727 (95% CI 0.538–1.276)
Absolute Event Rate: 32.3% vs 32.9%
p-value: p=0.250
The apoB XbaI gene polymorphism does not appear to be a significant genetic determinant of obesity or altered lipid profiles in the Egyptian population.
No association between ApoB XbaI polymorphism and lipids or obesity in Egyptians; leaves open population-specific genetic effects on dyslipidemia.
BACKGROUND: Several environmental and genetic factors are associated with high levels of lipids in obese patients. Apolipoprotein B (ApoB) is the major protein component of low-density lipoproteins (LDL), very-low density lipoproteins (VLDL) and chylomicrons and plays a central role in lipid metabolism. Several apoB restriction fragment length polymorphisms (XbaI, EcoRI, MspI) have been reported to be associated with variation in lipid levels and obesity. To date, no data are available on the relationship between XbaI polymorphism and lipid levels in Egyptian populations. Following clinical profiling, 178 obese (body mass index [BMI] >25 kg/m(2)) and 178 age-matched non-obese (BMI ≤ 25 kg/m(2)) subjects were included in this case-control study. All samples were analysed for total cholesterol, triglycerides and HDL-cholesterol. Genetic analysis of apoB XbaI (X) was performed using Polymerase Chain Reaction-Restriction Fragment Length polymorphism (PCR-RFLP). The aim of this study was to assess the association of apoB XbaI gene polymorphism (X) and lipid profiles in obese and non-obese Egyptian populations. RESULTS: Obese subjects demonstrated significantly higher values of waist-to-hip ratio, blood pressure, and total lipid. However, in our sample we did not find significant differences in apoB XbaI gene polymorphism (X) genotype or allele frequencies. Moreover, none of the studied lipid parameters showed any association with the gene polymorphism. CONCLUSION: This study reveals no significant association of apoB XbaI gene polymorphism (X) with obesity or lipid profiles in an Egyptian population.
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Bogari et al. (2015) conducted a case-control in Obesity and dyslipidemia (n=356). apolipoprotein B (apoB) XbaI gene polymorphism vs. Wild-type genotype / non-obese controls was evaluated on Association of apoB XbaI T allele with obesity (OR 0.727, 95% CI 0.538-1.276, p=0.250). The apoB XbaI gene polymorphism showed no significant association with obesity (OR 0.727 for the T allele) or lipid profiles in an Egyptian population.
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