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一种用于预测阿尔茨海默病病理或疑似非阿尔茨海默病病理患者从轻度认知障碍进展为痴呆的综合视觉评定量表。

A Comprehensive Visual Rating Scale for Predicting Progression from Mild Cognitive Impairment to Dementia in Patients with Alzheimer's Pathology or Suspected Non-Alzheimer's Pathology.

作者信息

Park Sang Won, Kim Seongheon, Park Jeonghoon, Jang Jae Won, Kim SangYun

机构信息

Department of Neuroscience, Kangwon National University School of Medicine, Chuncheon, Korea.

Department of Neurology, Kangwon National University Hospital, Chuncheon, Korea.

出版信息

Dement Neurocogn Disord. 2020 Dec;19(4):129-139. doi: 10.12779/dnd.2020.19.4.129.

DOI:10.12779/dnd.2020.19.4.129
PMID:33377666
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7781734/
Abstract

BACKGROUND AND PURPOSE

To identify biomarkers for prediction of the progression to dementia in mild cognitive impairment (MCI) patients, evaluation of brain structure changes has been validated by a comprehensive visual grading scale (CVRS) through magnetic resonance imaging (MRI). In this study, we specifically elucidated for the cognitive change of MCI patients classified based on AT(N) pathological status classification during the follow-up period of 3 years through the CVRS.

METHODS

The 301 patients with initial MCI visited at least once for follow-up period. The data used in this study were obtained from the Alzheimer's disease (AD) Neuroimaging Initiative study. Brain atrophy was assessed by CVRS using MRI. AT(N) profiles were classified by cerebrospinal fluid abnormality. Based on the AT(N) assessment, all individuals in this study were divided into 3 groups (normal state biomarker, suspected non-Alzheimer's pathology [SNAP], or Alzheimer's continuum). The cox regression was used to analyze the hazard ratios of CVRS for progression to dementia.

RESULTS

Sixty-three progressed and 238 remained stable to dementia and the CVRS (mean±standard deviation) had significant difference between progressive MCI and stable MCI (p<0.001). Univariate and multivariate cox regression results (p<0.001) showed the independence of initial CVRS as a predictor for the progression to dementia. Moreover, comparing the classified AT(N) pathology group, SNAP and AD, effectiveness of CVRS as a predictor was verified only in Alzheimer's continuum.

CONCLUSIONS

The initial CVRS score as a predictor of dementia progression was independently validated at the stage of Alzheimer's progression among AT(N) pathologically differentiated MCI.

摘要

背景与目的

为了识别预测轻度认知障碍(MCI)患者发展为痴呆症的生物标志物,通过磁共振成像(MRI)的综合视觉分级量表(CVRS)对脑结构变化进行评估已得到验证。在本研究中,我们通过CVRS特别阐明了在3年随访期内基于AT(N)病理状态分类的MCI患者的认知变化。

方法

301例初始MCI患者在随访期至少就诊一次。本研究使用的数据来自阿尔茨海默病(AD)神经影像学倡议研究。使用MRI通过CVRS评估脑萎缩。通过脑脊液异常对AT(N)特征进行分类。基于AT(N)评估结果,本研究中的所有个体被分为3组(正常状态生物标志物、疑似非阿尔茨海默病病理[SNAP]或阿尔茨海默病连续体)。采用Cox回归分析CVRS进展为痴呆症的风险比。

结果

63例进展为痴呆症,238例保持稳定,进展性MCI和稳定性MCI之间的CVRS(均值±标准差)存在显著差异(p<0.001)。单因素和多因素Cox回归结果(p<0.001)表明初始CVRS作为进展为痴呆症预测指标的独立性。此外,比较分类后的AT(N)病理组、SNAP和AD,仅在阿尔茨海默病连续体中验证了CVRS作为预测指标的有效性。

结论

在AT(N)病理分化的MCI中,阿尔茨海默病进展阶段,初始CVRS评分作为痴呆症进展预测指标得到独立验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040c/7781734/1cb972a76c45/dnd-19-129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040c/7781734/7105731e1c5c/dnd-19-129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040c/7781734/1cb972a76c45/dnd-19-129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040c/7781734/7105731e1c5c/dnd-19-129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/040c/7781734/1cb972a76c45/dnd-19-129-g002.jpg

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本文引用的文献

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PLoS One. 2018 Aug 20;13(8):e0201852. doi: 10.1371/journal.pone.0201852. eCollection 2018.
2
The A/T/N biomarker scheme and patterns of brain atrophy assessed in mild cognitive impairment.轻度认知障碍中 A/T/N 生物标志物方案和脑萎缩模式评估。
Sci Rep. 2018 May 30;8(1):8431. doi: 10.1038/s41598-018-26151-8.
3
NIA-AA Research Framework: Toward a biological definition of Alzheimer's disease.
NIA-AA 研究框架:迈向阿尔茨海默病的生物学定义。
Alzheimers Dement. 2018 Apr;14(4):535-562. doi: 10.1016/j.jalz.2018.02.018.
4
The Alzheimer's disease metabolic brain pattern in mild cognitive impairment.轻度认知障碍中的阿尔茨海默病代谢脑模式。
J Cereb Blood Flow Metab. 2017 Dec;37(12):3643-3648. doi: 10.1177/0271678X17732508. Epub 2017 Sep 20.
5
Identification of clusters of rapid and slow decliners among subjects at risk for Alzheimer's disease.鉴定阿尔茨海默病高危人群中的快速和缓慢下降者聚类。
Sci Rep. 2017 Jul 28;7(1):6763. doi: 10.1038/s41598-017-06624-y.
6
Distinct subtypes of Alzheimer's disease based on patterns of brain atrophy: longitudinal trajectories and clinical applications.基于脑萎缩模式的阿尔茨海默病的不同亚型:纵向轨迹和临床应用。
Sci Rep. 2017 Apr 18;7:46263. doi: 10.1038/srep46263.
7
White matter hyperintensities are associated with disproportionate progressive hippocampal atrophy.白质高信号与不成比例的进行性海马萎缩相关。
Hippocampus. 2017 Mar;27(3):249-262. doi: 10.1002/hipo.22690. Epub 2017 Jan 9.
8
A/T/N: An unbiased descriptive classification scheme for Alzheimer disease biomarkers.A/T/N:阿尔茨海默病生物标志物的无偏描述性分类方案。
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9
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10
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