Chintamaneni Meena, Bhaskar Manju
Department of Clinical Pharmacy, Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, Vile Parle, Mumbai 400056, India.
ISRN Pharmacol. 2012;2012:984786. doi: 10.5402/2012/984786. Epub 2012 Jun 28.
Alzheimer's disease is the most common form of dementia affecting millions of individuals worldwide. It is currently diagnosed only via clinical assessments and confirmed by postmortem brain pathology. The development of validated biomarkers for Alzheimer's disease is essential to improve diagnosis and accelerate the development of new therapies. Biochemical and neuroimaging markers could facilitate diagnosis, predict AD progression from a pre-AD state of mild cognitive impairment (MCI), and be used to monitor efficacies of disease-modifying therapies. Cerebrospinal fluid (CSF) levels of Aβ40, Aβ42, total tau, and phosphorylated tau have diagnostic values in AD. Measurements of the above CSF markers in combination are useful in predicting the risk of progression from MCI to AD. New potential biomarkers are emerging, and CSF or plasma marker profiles may eventually become part of the clinician's toolkit for accurate AD diagnosis and management. These biomarkers along with clinical assessment, neuropsychological testing, and neuroimaging could achieve a much higher diagnostic accuracy for AD and related disorders in the future.
阿尔茨海默病是痴呆最常见的形式,影响着全球数百万人。目前仅通过临床评估进行诊断,并通过死后脑病理学确诊。开发经过验证的阿尔茨海默病生物标志物对于改善诊断和加速新疗法的开发至关重要。生化和神经影像标志物有助于诊断,预测从轻度认知障碍(MCI)的阿尔茨海默病前期状态发展为阿尔茨海默病,并用于监测疾病修饰疗法的疗效。脑脊液(CSF)中Aβ40、Aβ42、总tau蛋白和磷酸化tau蛋白水平在阿尔茨海默病中具有诊断价值。联合测量上述脑脊液标志物有助于预测从MCI发展为阿尔茨海默病的风险。新的潜在生物标志物正在出现,脑脊液或血浆标志物谱最终可能会成为临床医生准确诊断和管理阿尔茨海默病的工具之一。这些生物标志物与临床评估、神经心理学测试和神经影像检查相结合,未来可能会大大提高阿尔茨海默病及相关疾病的诊断准确性。