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Genetic determinants of cerebral vasospasm, delayed cerebral ischemia, and outcome after aneurysmal subarachnoid hemorrhage

机译:脑血管痉挛,延迟性脑缺血和动脉瘤性蛛网膜下腔出血后结局的遗传决定因素

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摘要

Despite extensive effort to elucidate the cellular and molecular bases for delayed cerebral injury after aneurysmal subarachnoid hemorrhage (aSAH), the pathophysiology of these events remains poorly understood. Recently, much work has focused on evaluating the genetic underpinnings of various diseases in an effort to delineate the contribution of specific molecular pathways as well as to uncover novel mechanisms. The majority of subarachnoid hemorrhage genetic research has focused on gene expression and linkage studies of these markers as they relate to the development of intracranial aneurysms and their subsequent rupture. Far less work has centered on the genetic determinants of cerebral vasospasm, the predisposition to delayed cerebral injury, and the determinants of ensuing functional outcome after aSAH. The suspected genes are diverse and encompass multiple functional systems including fibrinolysis, inflammation, vascular reactivity, and neuronal repair. To this end, we present a systematic review of 21 studies suggesting a genetic basis for clinical outcome after aSAH, with a special emphasis on the pathogenesis of cerebral vasospasm and delayed cerebral ischemia. In addition, we highlight potential pitfalls in the interpretation of genetic association studies, and call for uniformity of design of larger multicenter studies in the future.
机译:尽管为阐明动脉瘤性蛛网膜下腔出血(aSAH)后延迟性脑损伤的细胞和分子基础做出了巨大努力,但对这些事件的病理生理学仍知之甚少。最近,许多工作集中于评估各种疾病的遗传基础,以描绘特定分子途径的作用以及发现新机制。蛛网膜下腔出血的大多数遗传研究都集中在这些标志物的基因表达和连锁研究上,因为它们与颅内动脉瘤的发展及其随后的破裂有关。很少有工作集中在脑血管痉挛的遗传决定因素,迟发性脑损伤的易感性以及aSAH后导致功能预后的决定因素上。可疑的基因是多种多样的,涵盖了多种功能系统,包括纤维蛋白溶解,炎症,血管反应性和神经元修复。为此,我们提出了对21项研究的系统评价,这些研究提出了aSAH后临床结局的遗传基础,并特别强调了脑血管痉挛和延迟性脑缺血的发病机制。此外,我们强调了遗传关联研究的解释中的潜在陷阱,并呼吁将来大型多中心研究的设计统一。

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