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Total and phosphorylated tau protein as biological markers of Alzheimer's disease.总tau 蛋白和磷酸化 tau 蛋白作为阿尔茨海默病的生物学标志物。
Exp Gerontol. 2010 Jan;45(1):30-40. doi: 10.1016/j.exger.2009.10.010. Epub 2009 Oct 22.
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Baseline MRI predictors of conversion from MCI to probable AD in the ADNI cohort.阿尔茨海默病神经成像计划(ADNI)队列中从轻度认知障碍(MCI)转变为可能的阿尔茨海默病(AD)的基线磁共振成像(MRI)预测指标。
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MRI and CSF biomarkers in normal, MCI, and AD subjects: predicting future clinical change.正常、轻度认知障碍和阿尔茨海默病患者的MRI及脑脊液生物标志物:预测未来临床变化
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Multidimensional classification of hippocampal shape features discriminates Alzheimer's disease and mild cognitive impairment from normal aging.海马体形状特征的多维分类可区分阿尔茨海默病和轻度认知障碍与正常衰老。
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Longitudinal progression of Alzheimer's-like patterns of atrophy in normal older adults: the SPARE-AD index.正常老年人中阿尔茨海默病样萎缩模式的纵向进展:SPARE-AD指数
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Cerebrospinal fluid biomarker signature in Alzheimer's disease neuroimaging initiative subjects.阿尔茨海默病神经影像学计划受试者的脑脊液生物标志物特征
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Decreased cerebrospinal fluid Abeta(42) correlates with brain atrophy in cognitively normal elderly.脑脊液β淀粉样蛋白42(Abeta[42])水平降低与认知正常老年人的脑萎缩相关。
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基于 MRI、CSF 生物标志物和模式分类预测 MCI 向 AD 的转化。

Prediction of MCI to AD conversion, via MRI, CSF biomarkers, and pattern classification.

机构信息

Section of Biomedical Image Analysis, Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Neurobiol Aging. 2011 Dec;32(12):2322.e19-27. doi: 10.1016/j.neurobiolaging.2010.05.023. Epub 2010 Jul 1.

DOI:10.1016/j.neurobiolaging.2010.05.023
PMID:20594615
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2951483/
Abstract

Magnetic resonance imaging (MRI) patterns were examined together with cerebrospinal fluid (CSF) biomarkers in serial scans of Alzheimer's Disease Neuroimaging Initiative (ADNI) participants with mild cognitive impairment (MCI). The SPARE-AD score, summarizing brain atrophy patterns, was tested as a predictor of short-term conversion to Alzheimer's disease (AD). MCI individuals that converted to AD (MCI-C) had mostly positive baseline SPARE-AD (Spatial Pattern of Abnormalities for Recognition of Early AD) and atrophy in temporal lobe gray matter (GM) and white matter (WM), posterior cingulate/precuneous, and insula. MCI individuals that converted to AD had mostly AD-like baseline CSF biomarkers. MCI nonconverters (MCI-NC) had mixed baseline SPARE-AD and CSF values, suggesting that some MCI-NC subjects may later convert. Those MCI-NC with most negative baseline SPARE-AD scores (normal brain structure) had significantly higher baseline Mini Mental State Examination (MMSE) scores (28.67) than others, and relatively low annual rate of Mini Mental State Examination decrease (-0.25). MCI-NC with midlevel baseline SPARE-AD displayed faster annual rates of SPARE-AD increase (indicating progressing atrophy). SPARE-AD and CSF combination improved prediction over individual values. In summary, both SPARE-AD and CSF biomarkers showed high baseline sensitivity, however, many MCI-NC had abnormal baseline SPARE-AD and CSF biomarkers. Longer follow-up will elucidate the specificity of baseline measurements.

摘要

磁共振成像(MRI)模式与脑脊液(CSF)生物标志物一起在阿尔茨海默病神经影像学倡议(ADNI)轻度认知障碍(MCI)参与者的连续扫描中进行了检查。总结大脑萎缩模式的 SPARE-AD 评分被测试为短期转化为阿尔茨海默病(AD)的预测因子。转化为 AD 的 MCI 个体(MCI-C)基线 SPARE-AD(早期 AD 识别的异常模式)大多为阳性,且颞叶灰质(GM)和白质(WM)、后扣带/楔前叶和脑岛存在萎缩。转化为 AD 的 MCI 个体具有类似 AD 的基线 CSF 生物标志物。未转化为 AD 的 MCI 个体(MCI-NC)具有混合的基线 SPARE-AD 和 CSF 值,表明一些 MCI-NC 患者可能随后会转化。那些基线 SPARE-AD 评分最低(正常脑结构)的 MCI-NC 患者的基线 Mini Mental State Examination(MMSE)评分(28.67)明显更高,且 MMSE 评分每年下降的幅度相对较低(-0.25)。基线 SPARE-AD 处于中等水平的 MCI-NC 表现出 SPARE-AD 每年递增速度更快(表明进展性萎缩)。SPAER-AD 和 CSF 联合使用可提高个体值的预测能力。综上所述,SPARE-AD 和 CSF 生物标志物均具有较高的基线敏感性,但是许多 MCI-NC 具有异常的基线 SPARE-AD 和 CSF 生物标志物。更长时间的随访将阐明基线测量的特异性。