Pollex Rebecca L, Hegele Robert
Blackburn Cardiovascular Genetics Laboratory, Robarts Research Institute, 100 Perth Drive, London, Ontario, Canada.
Curr Atheroscler Rep. 2006 May;8(3):206-15. doi: 10.1007/s11883-006-0075-z.
Atherosclerosis is a complex disease with various intermediate phenotypes that are themselves complex and influenced by many factors. Through the use of carotid ultrasound techniques, the intermediate stages of vascular disease can be imaged and studied for association with potential genetic determinants. In this article we review the most recent available data (reports published since 2004) on the genetic determinants of atherosclerosis, as measured by one-, two-, and three-dimensional ultrasonography of the carotid arteries. In general, associations are disparate and modest. For intima-media thickness, promising associations have been found for both TNFRSF1A R92Q and PPARG P12A, but associations also differed in the same individuals depending on the specific ultrasound trait studied (eg, linear intima-media thickness versus total plaque volume in carotid arteries). Some of the challenging issues for future studies include accounting for gene-environment interactions, sex-specific associations, and the distinctiveness of different carotid ultrasound measures.
动脉粥样硬化是一种复杂的疾病,具有多种中间表型,这些表型本身也很复杂且受多种因素影响。通过使用颈动脉超声技术,可以对血管疾病的中间阶段进行成像,并研究其与潜在遗传决定因素的关联。在本文中,我们回顾了自2004年以来发表的关于动脉粥样硬化遗传决定因素的最新可用数据,这些数据通过颈动脉的一维、二维和三维超声测量得出。总体而言,关联是分散且适度的。对于内膜中层厚度,已发现TNFRSF1A R92Q和PPARG P12A都有有前景的关联,但在同一个体中,关联也因所研究的特定超声特征(例如,颈动脉的线性内膜中层厚度与总斑块体积)而有所不同。未来研究面临的一些具有挑战性的问题包括考虑基因-环境相互作用、性别特异性关联以及不同颈动脉超声测量的独特性。