Leblanc Gabrielle G, Meschia James F, Stuss Donald T, Hachinski Vladimir
The Neurogenetics Group, National Institute of Neurological Disorders and Stroke, Bethesda, MD 20892, USA.
Stroke. 2006 Jan;37(1):248-55. doi: 10.1161/01.STR.0000195177.61184.49. Epub 2005 Dec 8.
This review considers the current state of knowledge of genetic factors underlying vascular cognitive impairment (VCI).
We argue here that genes conferring susceptibility to VCI must be of 2 nonmutually exclusive classes: (1) genes that confer susceptibility to cerebrovascular disease, and (2) genes that determine brain tissue responses to cerebrovascular disease (ie, render parenchymal tissue more or less susceptible to injury or able to repair itself after injury). Although some progress has been made in identifying genes of the first class, little has been done to explore genes of the second class. Evidence for the existence of such genes is presented. We discuss the advantages and disadvantages of different forms of cerebrovascular disease for studying these genes, and different study designs that might be used.
The most critical challenge for genetic studies of VCI is to identify quantifiable phenotypes that can be reliably and effectively determined in large samples of subjects.
本综述探讨了血管性认知障碍(VCI)潜在遗传因素的当前知识状态。
我们在此认为,赋予VCI易感性的基因必须属于两个并非相互排斥的类别:(1)赋予脑血管疾病易感性的基因,以及(2)决定脑组织对脑血管疾病反应的基因(即使实质组织或多或少易受损伤或在损伤后能够自我修复)。虽然在识别第一类基因方面已取得一些进展,但在探索第二类基因方面几乎没有开展工作。本文提供了此类基因存在的证据。我们讨论了不同形式的脑血管疾病在研究这些基因方面的优缺点,以及可能采用的不同研究设计。
VCI基因研究最关键的挑战是识别可在大量受试者样本中可靠且有效地确定的可量化表型。