Department of Psychiatry and Psychotherapy, Universitätsklinikum Erlangen, Erlangen, Germany.
J Alzheimers Dis. 2010;19(4):1199-203. doi: 10.3233/JAD-2010-1313.
Neurochemical Dementia Diagnostics (NDD), i.e., analysis of the cerebrospinal fluid (CSF) concentrations of amyloid-beta peptides and tau/phospho-tau proteins plays important role in the diagnosis of neurodegeneration and dementias. Several studies show alterations of these biomarkers in Alzheimer's disease (AD), however, only a few reports address alterations of other CSF biomarkers (albumin and immunoglobulins' quotients, cell count, lactate concentration, etc.) in the pathophysiology and diagnostic procedures of dementias. Therefore, we analyzed these biomarkers in patients diagnosed for dementia syndromes and carefully characterized with the state-of-the-art NDD analysis: Abeta1-42, Abetax-42, Abetax-42/x-40 ratio, tau, and ptau181. We found intrathecal IgG synthesis in 5 out of 112 patients showing alterations of the NDD biomarkers, and in four out of these five subjects, we could not find any satisfying reason for the intrathecal humoral response. In 25.9% of the patients with altered NDD biomarkers, we found an increased albumin quotient indicating a dysfunction of the blood-CSF barrier; however a similar figure of 25.2% was found in the group of patients without alterations in the NDD. Our findings suggest that at least some patients with increased CSF concentrations of tau/ptau proteins and decreased concentrations of Abeta{42} peptides show simultaneously CSF alterations found otherwise in neuroinflammatory processes. This, in turn, suggests that extended diagnosis should be performed in patients with "isolated" alterations of NDD biomarkers or intrathecal immunoglobulin synthesis.
神经化学性痴呆诊断(NDD),即分析脑脊液(CSF)中淀粉样β肽和 tau/磷酸化 tau 蛋白的浓度,在神经退行性疾病和痴呆的诊断中发挥着重要作用。几项研究表明这些生物标志物在阿尔茨海默病(AD)中发生了改变,然而,只有少数报告涉及其他 CSF 生物标志物(白蛋白和免疫球蛋白比值、细胞计数、乳酸浓度等)在痴呆的病理生理学和诊断程序中的改变。因此,我们分析了这些在被诊断为痴呆综合征的患者中的生物标志物,并仔细进行了最先进的 NDD 分析:Abeta1-42、Abetax-42、Abetax-42/x-40 比值、tau 和 ptau181。我们发现,在 112 名患者中有 5 名出现了 NDD 生物标志物改变,其中有 5 名患者出现了这种改变,并且在其中 4 名患者中,我们无法找到任何合理的理由来解释这种鞘内体液反应。在改变了 NDD 生物标志物的患者中,有 25.9%的患者发现白蛋白比值增加,表明血脑屏障功能障碍;然而,在没有改变 NDD 的患者中,也有 25.2%的患者出现了这种情况。我们的发现表明,至少有一些 CSF 中 tau/ptau 蛋白浓度增加和 Abeta{42} 肽浓度降低的患者同时存在 CSF 改变,这些改变通常与神经炎症过程有关。这反过来表明,在“孤立性”改变 NDD 生物标志物或鞘内免疫球蛋白合成的患者中,应进行扩展诊断。