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Age-Associated White Matter Lesions: The MRC Cognitive Function and Ageing Study

机译:与年龄相关的白色物质病变:MRC认知功能和衰老研究

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摘要

Cerebral white matter lesions (WML) are common in the aging brain and are associated with dementia and depression. They are associated with vascular risk factors and small vessel disease, suggesting an ischemic origin, but recent pathology studies suggest a more complex pathogenesis. Studies using samples from the population-representative Medical Research Council Cognitive Function and Ageing Study neuropathology cohort used post-mortem magnetic resonance imaging to identify WML for further study. Expression of hypoxia-related molecules and other injury and protective cellular pathways in candidate immunohistochemical and gene expression microarray studies support a role for hypoxia/ischemia. However, these approaches also suggest that immune activation, blood-brain barrier dysfunction, altered cell metabolic pathways and glial cell injury contribute to pathogenesis. These abnormalities are not confined to WML, but are also found in apparently normal white matter in brains with lesions, suggesting a field effect of white matter abnormality within which lesions arise. WML are an active pathology with a complex pathogenesis that may potentially offer a number of primary and secondary intervention targets.
机译:脑白质病变(WML)在衰老的大脑中很常见,并与痴呆和抑郁症相关。它们与血管危险因素和小血管疾病相关,表明是缺血性起源,但最近的病理学研究提示其发病机理更为复杂。使用来自具有代表性的医学研究委员会认知功能和衰老研究神经病理学研究的样本进行的研究使用验尸磁共振成像来识别WML,以进行进一步研究。在候选免疫组织化学和基因表达微阵列研究中,缺氧相关分子的表达以及其他损伤和保护性细胞途径支持缺氧/缺血的作用。但是,这些方法也表明免疫激活,血脑屏障功能障碍,改变的细胞代谢途径和神经胶质细胞损伤是发病的原因。这些异常不仅限于WML,而且还存在于具有病变的大脑中看似正常的白质中,这表明在其中出现病变的白质异常的场效应。 WML是具有复杂发病机制的活跃病理,可能潜在地提供许多主要和次要干预目标。

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