Wiltfang Jens
Klinik für Psychiatrie und Psychotherapie, Universitätsmedizin Göttingen.
Ther Umsch. 2015 Apr;72(4):271-8. doi: 10.1024/0040-5930/a000675.
Cerebrospinal fluid-based neurochemical dementia diagnostics (CSF-NDD) is meanwhile validated on S3 evidence level and international dementia guidelines like those of the German neuropsychiatric associations (DGPPN, DGN; http://www.DGPPN.de) recommend CSF-NDD for the improved early and differential diagnostics of multigenetic (sporadic) Alzheimer's Dementia (AD). CSF-NDD does also offer a predictive diagnosis of incipient AD for high-risk patients when they are still within the prodromal stage of mild cognitive impairment (MCI). But since currently no (secondary) preventive therapy of AD is available, the use of CSF-NDD for the predictive molecular diagnosis of AD is not recommended by the latter guidelines. However, molecular diagnostics of preclinical AD by CSF-NDD and/or [18F]Amyloid-PET has meanwhile gained high clinical relevance for therapeutic clinical research, as this novel clinical model allows to systematically screen for promising (secondary) preventive therapy options. Moreover, future blood based neurochemical diagnostics of preclinical or early AD by means of multiplex assays seems to be promising. However, so far blood assays were not consistently validated by independent research groups and in contrast to CSF-NDD a blood-based diagnosis of AD is not yet available.
基于脑脊液的神经化学性痴呆诊断(CSF-NDD)同时已在S3证据水平上得到验证,德国神经精神协会(DGPPN、DGN;http://www.DGPPN.de)等国际痴呆指南推荐使用CSF-NDD来改善多基因(散发性)阿尔茨海默病(AD)的早期诊断和鉴别诊断。当高危患者仍处于轻度认知障碍(MCI)前驱期时,CSF-NDD也能对早期AD进行预测性诊断。但由于目前尚无AD的(二级)预防性治疗方法,后述指南不建议使用CSF-NDD进行AD的预测性分子诊断。然而,通过CSF-NDD和/或[18F]淀粉样蛋白PET对临床前AD进行分子诊断,目前已在治疗性临床研究中具有高度临床相关性,因为这种新的临床模型能够系统地筛选出有前景的(二级)预防性治疗方案。此外,未来通过多重检测对临床前或早期AD进行基于血液的神经化学诊断似乎很有前景。然而,到目前为止,血液检测尚未得到独立研究小组的一致验证,与CSF-NDD不同,基于血液的AD诊断目前仍不可用。