Stomrud Erik, Hansson Oskar, Zetterberg Henrik, Blennow Kaj, Minthon Lennart, Londos Elisabet
Clinical Memory Research Unit, Department of Clinical Sciences, Malmö University Hospital, Lund University, Malmö, Sweden.
Arch Neurol. 2010 Feb;67(2):217-23. doi: 10.1001/archneurol.2009.316.
Abnormal cerebrospinal fluid (CSF) biomarker levels predict development of Alzheimer disease with good accuracy and are thought to precede cognitive deterioration.
To investigate whether changes in CSF biomarker levels over time in healthy older adults are associated with a concurrent decline in cognitive performance.
Retrospective analysis of longitudinal CSF biomarker levels and clinical data.
A combined academic dementia disorder research center and dementia clinic.
Thirty-seven cognitively healthy older volunteers (mean age, 73 years).
Longitudinal CSF total tau protein, hyperphosphorylated tau protein 181, and beta-amyloid(1-42) protein levels and cognitive assessments at baseline and at follow-up 4 years later.
Low levels of CSF beta-amyloid(1-42) protein at follow-up were associated with decreased delayed word recall score on the Alzheimer Disease Assessment Scale-cognitive subscale (r(s) = -0.437, P < .01) and with slower results on A Quick Test of Cognitive Speed (r(s) = -0.540, P < .001). Individuals with a decrease during the 4-year study of 15% or more in CSF beta-amyloid(1-42) protein level performed worse on the Alzheimer Disease Assessment Scale-cognitive subscale delayed word recall (z = -2.18, P < .05) and A Quick Test of Cognitive Speed (z = -2.35, P < .05) at follow-up. An increase over time of 20% or more in CSF hyperphosphorylated tau protein 181 level correlated with slower results on A Quick Test of Cognitive Speed at follow-up (z = -2.13, P < .05). Furthermore, the presence of the APOE-epsilon4 (OMIM 107741) allele was associated with a greater longitudinal decrease in CSF beta-amyloid(1-42) protein level (chi(2) = 10.47, P < .05) and with a higher CSF total tau protein level at follow-up (chi(2) = 8.83, P < .05). No correlation existed between baseline CSF biomarker levels and baseline or follow-up cognitive scores.
In this group of healthy older adults, changes in CSF biomarker levels previously associated with Alzheimer disease correlated with a decline in cognitive functions. Changes in CSF biomarker levels may identify early neurodegenerative processes of Alzheimer disease.
脑脊液(CSF)生物标志物水平异常可准确预测阿尔茨海默病的发生,且被认为先于认知功能恶化出现。
探讨健康老年人脑脊液生物标志物水平随时间的变化是否与同期认知功能下降相关。
对脑脊液生物标志物水平和临床数据进行纵向回顾性分析。
一个综合性学术痴呆症研究中心和痴呆症诊所。
37名认知健康的老年志愿者(平均年龄73岁)。
基线及4年后随访时脑脊液总tau蛋白、磷酸化tau蛋白181和β-淀粉样蛋白(1-42)水平,以及认知评估。
随访时脑脊液β-淀粉样蛋白(1-42)水平较低与阿尔茨海默病评估量表认知子量表上的延迟词语回忆得分降低相关(r(s)= -0.437,P <.01),且与认知速度快速测试结果较慢相关(r(s)= -0.540,P <.001)。在4年研究期间脑脊液β-淀粉样蛋白(1-42)水平下降15%或更多的个体,在随访时阿尔茨海默病评估量表认知子量表延迟词语回忆(z = -2.18,P <.05)和认知速度快速测试(z = -2.35,P <.05)中表现更差。随访时脑脊液磷酸化tau蛋白181水平随时间增加20%或更多与认知速度快速测试结果较慢相关(z = -2.13,P <.05)。此外,APOE-ε4(OMIM 107741)等位基因的存在与脑脊液β-淀粉样蛋白(1-42)水平更大的纵向下降相关(χ(2)= 10.47,P <.05),且与随访时更高的脑脊液总tau蛋白水平相关(χ(2)= 8.83,P <.05)。基线脑脊液生物标志物水平与基线或随访认知得分之间无相关性。
在这组健康老年人中,先前与阿尔茨海默病相关的脑脊液生物标志物水平变化与认知功能下降相关。脑脊液生物标志物水平的变化可能识别出阿尔茨海默病早期神经退行性变过程。