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The APOE locus and the pharmacogenetics of lipid response.

机译:APOE基因座和脂质反应的药物遗传学。

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摘要

Genetic variation at the APOE locus has been associated with plasma lipoprotein concentrations in the fasting (low-density, and high-density lipoproteins and triglycerides), and in the postprandial (triglyceride-rich lipoproteins) states. Resulting from these associations, the APOE locus has been found to be a significant genetic determinant of cardiovascular disease in the general population. Beyond the traditional association studies, APOE genetic variation has been shown to play a significant role, which explains some of the individual variations in therapies aimed at normalizing plasma lipid concentrations. Thus, the APOE E4 allele has been shown in some studies to be associated with increased response to dietary intervention. Conversely, APOE E2 carriers appear to be more responsive to statin therapy. The mechanisms behind these observations, however, have not been elucidated. Moreover, several other gene:environment and gene:therapy interactions have recently been demonstrated, thus further increasing the interest in this remarkable apolipoprotein.
机译:在禁食状态(低密度,高密度脂蛋白和甘油三酸酯)和餐后(富含甘油三酸酯的脂蛋白)状态下,APOE位点的遗传变异与血浆脂蛋白浓度相关。由于这些关联,已发现APOE基因座是普通人群中心血管疾病的重要遗传决定因素。除了传统的关联研究,APOE基因变异已显示出重要作用,这解释了旨在使血浆脂质浓度正常化的疗法中的一些个体变异。因此,一些研究显示,APOE E4等位基因与饮食干预反应增强有关。相反,APOE E2携带者似乎对他汀类药物治疗反应更强。但是,尚未阐明这些观察结果的机制。此外,最近还证明了其他几种基因:环境和基因:疗法的相互作用,从而进一步增加了对这种显着载脂蛋白的兴趣。

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