诊断阿尔茨海默病的脑脊液生物标志物

Imran Sarker, M. R. K. Khan, A. Haque, Md Rafiqul Islam
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摘要

阿尔茨海默病是老年人痴呆症的最常见原因。阿尔茨海默病的主要病理特征是神经元的丧失,细胞外老年斑的发生以及细胞内神经原纤维缠结(NFT)。大脑中的生化变化反映在脑脊液(CSF)中,人们已经进行了大量的研究工作,以开发AD中心致病过程的生物标志物,并将其用作诊断工具。生物标志物是疾病管理的重要组成部分,因为它们对于诊断、监测疾病进展、发现疾病的早期发病、监测治疗干预的效果以及避免疾病的错误诊断至关重要。不幸的是,目前可用的生物标志物都不能单独完成疾病诊断。三种脑脊液生物标志物,a - 42、总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)被发现具有最高的诊断潜力。孟加拉国神经科学杂志2015;Vol. 31 (1): 34-41
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cerebrospinal Fluid Biomarkers for Diagnosis of Alzheimer’s Disease
Alzheimer’s disease is the most common cause of dementia among elderly people. The major pathological hallmarks of AD are the loss of neurons, occurrence of extracellular senile plaques as well as intracellular neurofibrillary tangles (NFT). Biochemical changes in the brain are reflected in the cerebrospinal fluid (CSF), and intense research efforts have been made to develop biomarkers for the central pathogenic processes in AD that can be used as diagnostic tools. Biomarkers are essential part of disease management as they are essential for diagnosis, monitoring the disease progression, detecting early onset of the disease, monitoring the effect of therapeutic intervention, and also avoiding false diagnosis of the disease. Unfortunately, none of the biomarkers presently available are able to accomplish the disease diagnosis single-handedly. Three CSF biomarkers, Aâ42, Total-tau (t-tau), and phosphorylated-tau (p-tau), have been found to have the highest diagnostic potential. Bangladesh Journal of Neuroscience 2015; Vol. 31 (1): 34-41
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