Department of Neurology, Boston University Medical Center and Boston University School of Medicine, Boston, MA, USA.
J Alzheimers Dis. 2022;87(2):803-805. doi: 10.3233/JAD-220133.
An accurate diagnosis of sporadic cerebral amyloid angiopathy (CAA) is critical for patient management and research (including clinical trials) for this common small vessel pathology of the brain. While the "big bang" of the CAA field has been the device and wide adoption of the clinico-radiological Boston criteria which allowed for CAA diagnosis during life, these criteria are not without major shortcoming. As it is now becoming evident that CAA is probably not a single disease, but rather represents divergent pathophysiological phenotypes and clinical trajectories, new biomarker-driven diagnostic approaches should be sought. One such complimentary approach for CAA diagnosis is the use of cerebrospinal fluid biomarkers (CSF), which could provide dynamic measures of the underlying disease process and is discussed in this commentary given exciting new advances. A hint on how the practicing clinician could apply the current CSF data for CAA diagnosis is also provided.
准确诊断散发型脑淀粉样血管病(CAA)对于患者管理和该种常见的脑小血管疾病的研究(包括临床试验)至关重要。虽然“大爆炸”是指 CAA 领域中设备和临床-影像学波士顿标准的广泛应用,这些标准允许在有生之年进行 CAA 诊断,但它们并非没有主要缺陷。随着人们越来越意识到 CAA 可能不是一种单一的疾病,而是代表不同的病理生理表型和临床轨迹,因此应该寻求新的基于生物标志物的诊断方法。CAA 诊断的一种补充方法是使用脑脊液生物标志物(CSF),它可以提供潜在疾病过程的动态测量,鉴于这一领域的令人兴奋的新进展,在本评论中进行了讨论。还提供了关于临床医生如何应用当前 CSF 数据进行 CAA 诊断的提示。