CSF total and phosphorylated tau protein, regional glucose metabolism and dementia severity in Alzheimer’s disease

楔前 医学 痴呆 内科学 阿尔茨海默病 τ蛋白 额上回 海马旁回 内分泌学 正电子发射断层摄影术 认知障碍 心脏病学 颞叶 病理 核医学 疾病 认知 精神科 癫痫
作者
Cathleen Haense,Katharina Büerger,Elke Kalbe,Alexander Drzezga,Stefan Teipel,Paweł Markiewicz,Karl Herholz,W.-D. Heiß,Harald Hampel
出处
期刊:European Journal of Neurology [Wiley]
卷期号:15 (11): 1155-1162 被引量:54
标识
DOI:10.1111/j.1468-1331.2008.02274.x
摘要

We investigated associations between severity of cognitive impairment, cerebrospinal fluid (CSF) concentrations of total-tau (t-tau) protein and tau phosphorylated at threonin 181 (p-tau(181)) and regional glucose metabolism measured with 18F-fluorodeoxyglucose-positron emission tomography (18F-FDG-PET) in patients with probable Alzheimer's disease (AD).In 38 patients (mean age 66.5 +/- 8.0 years) with AD, Mini-Mental State Examination (MMSE) scores were evaluated and CSF levels of t-tau and p-tau(181) measured. All patients underwent an 18F-FDG-PET scan. Image analysis including correlation analysis and principal component analysis (PCA) were performed using SPM5 and VINCI.Dementia severity (MMSE 21.2 +/- 4.9) correlated well with metabolic impairment especially in left hemisphere association areas that are typically affected in patients with AD (e.g. inferior parietal lobule, r = 0.512; medial temporal gyrus, r = 0.478; inferior temporal gyrus, r = 0.488; precuneus, r = 0.468; PCA: r = 0.639, F = 7.751; all P < 0.001). There were no associations between t-tau and p-tau(181) with dementia severity and only weak correlations between t-tau and cerebral glucose metabolism (superior parietal gyrus, r = -0.325, P < 0.05; precentral gyrus r = -0.418, P < 0.01; amygdala r = -0.362, P < 0.05). No correlations were found between p-tau(181) and regional hypometabolism in FDG-PET.MMSE and CSF t-tau represent different aspects of disease severity. Whilst MMSE is closely related to impaired cerebral glucose metabolism, CSF t-tau is less closely related and appears to be less well suited for assessment of disease progression.
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