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脑动脉瘤的发生——最新进展

Genesis of cerebral aneurysms--an update.

作者信息

Krex D, Schackert H K, Schackert G

机构信息

Department of Neurosurgery, Universitätsklinikum Carl Gustav Carus, University of Technology Dresden, Germany.

出版信息

Acta Neurochir (Wien). 2001;143(5):429-48; discussion 448-9. doi: 10.1007/s007010170072.

Abstract

To elucidate the molecular pathogenesis of diseases has become a crucial step in the development of new treatment strategies. Although the pathogenesis of cerebral aneurysms has been studied intensively, it is poorly understood. Endogenous factors like elevated arterial blood pressure, the special anatomy of the Circle of Willis or the effect of haemodynamic factors, particularly originating at vessel bifurcation, are all known to be involved in the growth and rupture of an aneurysm. There is an ongoing discussion as to whether these factors also contribute to the very early steps of pathogenesis. Arteriosclerosis and secondary inflammatory reactions are thought to be elementary preconditions. Exogenous factors like cigarette smoking, heavy alcohol consumption or certain medications known to help generate arteriosclerosis and elevated blood pressure have also been found to be related to the occurrence of cerebral aneurysms. Furthermore, there has been a long-lasting debate on whether aneurysms might develop as a result of an inborn genetic defect. First-degree relatives of patients with cerebral aneurysms have a higher risk of having an aneurysm. In addition, the elevated prevalence of cerebral aneurysms in patients suffering from various inherited diseases points to a genetic background in the development of an aneurysm. Recent advances in molecular biology provide evidence that genetic variants of different candidate genes are associated with the occurrence of cerebral aneurysms. The aim of this review is to expose the current status of these various hypotheses and their contribution to the pathogenesis of cerebral aneurysms in order to provide a basis for future investigations in this field.

摘要

阐明疾病的分子发病机制已成为开发新治疗策略的关键步骤。尽管脑动脉瘤的发病机制已得到深入研究,但仍了解甚少。诸如动脉血压升高、 Willis 环的特殊解剖结构或血流动力学因素的影响(尤其是起源于血管分叉处的因素)等内源性因素,均已知与动脉瘤的生长和破裂有关。关于这些因素是否也在发病机制的早期阶段起作用,目前仍在讨论中。动脉硬化和继发性炎症反应被认为是基本前提条件。吸烟、大量饮酒或某些已知会导致动脉硬化和血压升高的药物等外源性因素,也被发现与脑动脉瘤的发生有关。此外,关于动脉瘤是否可能由先天性遗传缺陷引起,长期以来一直存在争论。脑动脉瘤患者的一级亲属患动脉瘤的风险更高。此外,患有各种遗传性疾病的患者中脑动脉瘤患病率升高,这表明动脉瘤的发生存在遗传背景。分子生物学的最新进展提供了证据,表明不同候选基因的遗传变异与脑动脉瘤的发生有关。本综述的目的是揭示这些各种假说的现状及其对脑动脉瘤发病机制的贡献,以便为该领域未来的研究提供基础。

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