Baird A E
Stroke Neuroscience Unit, NINDS (National Institute of Neurological Disorders and Stroke)/NIH (National Institutes of Health), 10 Center Drive, MSC 1294, Room 3N258, Bethesda, MD 20892-1294, USA.
Biochem Soc Trans. 2006 Dec;34(Pt 6):1313-7. doi: 10.1042/BST0341313.
Findings from gene expression profiling studies are leading to new diagnostic and therapeutic strategies that can be applied in medical practice, especially in the field of oncology. Promising results of gene expression profiling of the peripheral blood in patients with ischaemic stroke have been obtained in recent pilot studies, demonstrating a partially reproducible gene signature of acute cerebral ischaemia. However, questions remain. Given that blood is at least in part a surrogate tissue for ischaemic stroke, the specificity of these signatures needs to be evaluated. Furthermore, it needs to be determined whether standardization of this methodology is required and whether clinical signatures can be identified that are improvements over the tools currently used in clinical practice. Clinically useful signatures would include those of haemorrhagic as well as ischaemic stroke, reclassification of stroke type and prognosis, and vascular disease risk. If these conditions are met, then it should be possible to develop cost-effective and rapid assays.
基因表达谱研究的结果正催生新的诊断和治疗策略,这些策略可应用于医学实践,尤其是肿瘤学领域。近期的初步研究已在缺血性中风患者的外周血基因表达谱分析中取得了有前景的结果,证明了急性脑缺血存在部分可重复的基因特征。然而,问题依然存在。鉴于血液至少在一定程度上是缺血性中风的替代组织,这些特征的特异性需要评估。此外,还需确定是否需要对该方法进行标准化,以及能否识别出比目前临床实践中使用的工具更优的临床特征。临床上有用的特征将包括出血性和缺血性中风的特征、中风类型和预后的重新分类以及血管疾病风险。如果满足这些条件,那么开发具有成本效益且快速的检测方法应该是可行的。