Continuum (Minneap Minn). 2022 Jun 1;28(3):822-833. doi: 10.1212/CON.0000000000001083.
This article discusses how fluid biomarkers can augment the routine dementia evaluation and improve diagnostic accuracy. The tests that are currently available and the indications for their use are described. Further, tests that are under development and likely to be used in the future are identified.
Technical improvements in assay sensitivity and precision have led to the rapid development of blood-based biomarkers for Alzheimer disease (AD) over the past several years. Studies have found that the ratio of amyloid-β (Aβ) peptides (Aβ42/Aβ40) and concentrations of phosphorylated tau isoforms in plasma can identify individuals with AD brain pathology. Blood-based tests may enable much broader use of AD biomarkers in the evaluation of patients with cognitive impairment.
Even after a detailed history, examination, routine laboratory testing, and brain imaging, the cause of dementia sometimes remains unclear. CSF and blood-based biomarkers can evaluate for a range of neurologic disorders that are associated with dementia, including AD. Integrating data from fluid biomarker tests and the routine dementia evaluation may improve the accuracy of dementia diagnosis.
本文讨论了液体生物标志物如何增强常规痴呆评估并提高诊断准确性。描述了目前可用的测试及其使用指征。此外,还确定了正在开发的、未来可能使用的测试。
过去几年,检测灵敏度和精度的技术改进促使针对阿尔茨海默病(AD)的血液生物标志物迅速发展。研究发现,血浆中淀粉样蛋白-β(Aβ)肽(Aβ42/Aβ40)的比值和磷酸化tau 同工型的浓度可以识别具有 AD 脑病理的个体。基于血液的测试可能使 AD 生物标志物在评估认知障碍患者方面得到更广泛的应用。
即使进行了详细的病史、检查、常规实验室检查和脑部成像,痴呆的原因有时仍不清楚。CSF 和基于血液的生物标志物可评估与痴呆相关的一系列神经疾病,包括 AD。整合来自液体生物标志物测试和常规痴呆评估的数据可能会提高痴呆诊断的准确性。