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脑白质疏松症的遗传关联表明了白质病变病因中的病理生理机制。

Genetic associations of leukoaraiosis indicate pathophysiological mechanisms in white matter lesions etiology.

作者信息

Lin Qing, Huang Wen-Qing, Tzeng Chi-Meng

出版信息

Rev Neurosci. 2015;26(3):343-58. doi: 10.1515/revneuro-2014-0082.

Abstract

Leukoaraiosis (LA), also called white matter lesions (WMLs) and white matter hyperintensities (WMHs), is a frequent neuroimaging finding commonly seen on magnetic resonance imaging brain scans of elderly people with prevalence ranging from 50% to 100%. Although it remains asymptomatic, LA is not considered to be benign, and it is showed to be related to a host of poor clinical outcomes and increases the risk of disability, dementia, depression, stroke, and the overall morbidity and mortality. Pathologically, LA is characterized by loss of myelin and axons, patchy demyelination, and denudation of ependyma in regions of WMH. Age and hypertension are the most importantly established risk factors for LA. However, the precise pathogenic mechanisms remain unclear. Together with the previous findings, our recent genetic results strongly supported that LA is associated with immune response and neuroinflammation. Therefore, we confidently hypothesized that LA was not only a common neuroimaging phenomenon in the elderly but also an emerging neuroinflammatory disorder in the central nervous system. This article focusing on neuroimaging classification, genetics basis, and putative molecular mechanism introduced the basic knowledge and current status of LA and put forward some of our research ideas and results from our molecular genetics research, which may pave the way for deciphering the putative pathogenic mechanism, risk factor, epigenetic index, and its application in diagnostic agents or drug target for prevention and treatment. Thus, it could provide clinicians and researchers with a specific and modern overview of LA to enable the understanding of recent progress and future directions in this illness.

摘要

脑白质疏松症(LA),也称为白质病变(WMLs)和白质高信号(WMHs),是一种常见的神经影像学表现,常见于老年人的脑部磁共振成像扫描中,患病率在50%至100%之间。尽管LA通常无症状,但它并非被认为是良性的,并且已显示与一系列不良临床结局相关,会增加残疾、痴呆、抑郁、中风以及总体发病率和死亡率的风险。在病理上,LA的特征是髓鞘和轴突丢失、斑片状脱髓鞘以及白质高信号区域的室管膜剥脱。年龄和高血压是LA最重要的确立的危险因素。然而,确切的致病机制仍不清楚。结合先前的研究结果,我们最近的遗传学结果有力地支持了LA与免疫反应和神经炎症有关。因此,我们有信心地假设,LA不仅是老年人中常见的神经影像学现象,也是中枢神经系统中一种新出现的神经炎症性疾病。本文聚焦于神经影像学分类、遗传学基础和假定的分子机制,介绍了LA的基础知识和现状,并提出了我们分子遗传学研究的一些思路和结果,这可能为破译假定的致病机制、危险因素、表观遗传指标及其在预防和治疗的诊断试剂或药物靶点中的应用铺平道路。因此,它可以为临床医生和研究人员提供关于LA的具体而现代的概述,以便理解这种疾病的最新进展和未来方向。

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