Biswas Santanu, Ghoshal Pradip K, Halder Bhubaneswar, Ganguly Kajal, DasBiswas Arup, Mandal Nripendranath
Division of Molecular Medicine, Bose Institute, P-1/12 CIT Scheme VIIM, Kolkata 700054, India.
Department of Cardiology, N.R.S. Medical College & Hospital, 138 A.J.C. Bose Road, Kolkata 700014, India.
Indian Heart J. 2013 Dec;65(6):658-65. doi: 10.1016/j.ihj.2013.10.003. Epub 2013 Oct 30.
The present study was designed to investigate whether the three-apolipoprotein (AI, B, E) gene polymorphisms were related to alter their plasma protein levels and hence associated to coronary artery disease (CAD).
We determined distribution of MspI apo AI, EcoRI apo B, HhaI apo E gene polymorphisms, plasma apolipoproteins and lipids levels among 150 patients having CAD admitted to the Department of Cardiology, N.R.S. Medical College & Hospital, Kolkata, India during June 2010-June 2012 and 150 age sex matched healthy controls.
We found that ApoAI concentration of studied population was significantly different in each genotypes of -75 G/A apo AI (p < 0.0001) gene polymorphism. A significant association was found in multivariate analysis for the genotypes with apo E4 allele [odds ratio (OR): 3.639; 95% confidence interval (CI): 1.019-12.995, p = 0.040] with four conventional risk factors (i.e. smoking, low-density lipoprotein, ApoAI and ApoB) with CAD. In contrast E2 allele has reverse effect, but the genotypes with apo E2 allele was no longer significant in the multivariate model (OR: 1.788; 95% CI: 0.400-8.001, p = 0.447) where as being significant in univariate analysis (OR: 0.219; 95% CI: 0.087-0.552, p = 0.001).
Our findings suggest that the polymorphisms apo AI MspI and apo B EcoRI do not seem to affect CAD. But the genotype with E4 allele of apo E gene independent of other risk factors is associated with this disease.
本研究旨在调查三种载脂蛋白(AI、B、E)基因多态性是否与血浆蛋白水平改变相关,进而与冠状动脉疾病(CAD)相关。
我们测定了2010年6月至2012年6月期间入住印度加尔各答N.R.S.医学院附属医院心脏病科的150例CAD患者以及150例年龄和性别匹配的健康对照者中MspI载脂蛋白AI、EcoRI载脂蛋白B、HhaI载脂蛋白E基因多态性的分布、血浆载脂蛋白和血脂水平。
我们发现,在-75 G/A载脂蛋白AI(p < 0.0001)基因多态性的每种基因型中,研究人群的载脂蛋白AI浓度存在显著差异。在多变量分析中,发现载脂蛋白E4等位基因的基因型与CAD的四个传统危险因素(即吸烟、低密度脂蛋白、载脂蛋白AI和载脂蛋白B)存在显著关联[比值比(OR):3.639;95%置信区间(CI):1.019 - 12.995,p = 0.040]。相比之下,E2等位基因具有相反的作用,但在多变量模型中,载脂蛋白E2等位基因的基因型不再显著(OR:1.788;95% CI:0.400 - 8.001,p = 0.447),而在单变量分析中显著(OR:0.219;95% CI:0.087 - 0.552,p = 0.001)。
我们的研究结果表明,载脂蛋白AI MspI和载脂蛋白B EcoRI基因多态性似乎不影响CAD。但载脂蛋白E基因E4等位基因的基因型独立于其他危险因素与该疾病相关。