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本文引用的文献

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Development of a protocol to assess within-subject, regional white matter hyperintensity changes in aging and dementia.制定方案以评估衰老和痴呆个体内、区域性脑白质高信号变化。
J Neurosci Methods. 2021 Aug 1;360:109270. doi: 10.1016/j.jneumeth.2021.109270. Epub 2021 Jun 24.
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Value-Generating Exploratory Trials in Neurodegenerative Dementias.神经退行性痴呆的产生价值探索性试验。
Neurology. 2021 May 18;96(20):944-954. doi: 10.1212/WNL.0000000000011774. Epub 2021 Mar 5.
3
MarkVCID cerebral small vessel consortium: I. Enrollment, clinical, fluid protocols.马克 VCID 脑小血管联盟:一、入组、临床、液体方案。
Alzheimers Dement. 2021 Apr;17(4):704-715. doi: 10.1002/alz.12215. Epub 2021 Jan 21.
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MarkVCID cerebral small vessel consortium: II. Neuroimaging protocols.马克 VCID 脑小血管联盟:二、神经影像学协议。
Alzheimers Dement. 2021 Apr;17(4):716-725. doi: 10.1002/alz.12216. Epub 2021 Jan 21.
5
The Effects of Longitudinal White Matter Hyperintensity Change on Cognitive Decline and Cortical Thinning over Three Years.纵向白质高信号变化对三年认知衰退和皮质变薄的影响。
J Clin Med. 2020 Aug 17;9(8):2663. doi: 10.3390/jcm9082663.
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Normative performance of older individuals on the Hopkins Verbal Learning Test-Revised (HVLT-R) according to ethno-racial group, gender, age and education level.不同种族群体、性别、年龄和教育水平的老年人在霍普金斯词语学习测试修订版(HVLT-R)上的规范表现。
Clin Neuropsychol. 2021 Aug;35(6):1174-1190. doi: 10.1080/13854046.2020.1730444. Epub 2020 Feb 26.
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Post-acquisition processing confounds in brain volumetric quantification of white matter hyperintensities.脑白质高信号体积定量的后处理处理混杂因素。
J Neurosci Methods. 2019 Nov 1;327:108391. doi: 10.1016/j.jneumeth.2019.108391. Epub 2019 Aug 10.
8
White Matter Hyperintensity Regression: Comparison of Brain Atrophy and Cognitive Profiles with Progression and Stable Groups.白质高信号减退:脑萎缩与认知特征在进展组和稳定组中的比较
Brain Sci. 2019 Jul 19;9(7):170. doi: 10.3390/brainsci9070170.
9
Cognitive consequences of regression of cerebral small vessel disease.脑小血管病消退的认知后果。
Eur Stroke J. 2019 Mar;4(1):85-89. doi: 10.1177/2396987318820790. Epub 2018 Dec 21.
10
Cross-sectional and longitudinal associations between total and regional white matter hyperintensity volume and cognitive and motor function in Parkinson's disease.横断面和纵向研究帕金森病患者全脑和局部脑白质高信号体积与认知和运动功能的相关性。
Neuroimage Clin. 2019;23:101870. doi: 10.1016/j.nicl.2019.101870. Epub 2019 May 23.

MarkVCID 脑白质高信号增长和消退协议的多中心、跨中心、观察者间和重测信度以及构念效度。

Multi-Site Cross-Site Inter-Rater and Test-Retest Reliability and Construct Validity of the MarkVCID White Matter Hyperintensity Growth and Regression Protocol.

机构信息

Department of Neurology, University of Kentucky, College of Medicine, Lexington, KY, USA.

Sanders-Brown Center on Aging, University of Kentucky, College of Medicine, Lexington, KY, USA.

出版信息

J Alzheimers Dis. 2023;96(2):683-693. doi: 10.3233/JAD-230629.

DOI:10.3233/JAD-230629
PMID:37840499
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11009792/
Abstract

BACKGROUND

White matter hyperintensities (WMH) that occur in the setting of vascular cognitive impairment and dementia (VCID) may be dynamic increasing or decreasing volumes or stable over time. Quantifying such changes may prove useful as a biomarker for clinical trials designed to address vascular cognitive-impairment and dementia and Alzheimer's Disease.

OBJECTIVE

Conducting multi-site cross-site inter-rater and test-retest reliability of the MarkVCID white matter hyperintensity growth and regression protocol.

METHODS

The NINDS-supported MarkVCID Consortium evaluated a neuroimaging biomarker developed to track WMH change. Test-retest and cross-site inter-rater reliability of the protocol were assessed. Cognitive test scores were analyzed in relation to WMH changes to explore its construct validity.

RESULTS

ICC values for test-retest reliability of WMH growth and regression were 0.969 and 0.937 respectively, while for cross-site inter-rater ICC values for WMH growth and regression were 0.995 and 0.990 respectively. Word list long-delay free-recall was negatively associated with WMH growth (p < 0.028) but was not associated with WMH regression.

CONCLUSIONS

The present data demonstrate robust ICC validity of a WMH growth/regression protocol over a one-year period as measured by cross-site inter-rater and test-retest reliability. These data suggest that this approach may serve an important role in clinical trials of disease-modifying agents for VCID that may preferentially affect WMH growth, stability, or regression.

摘要

背景

血管性认知障碍和痴呆(VCID)患者的脑白质高信号(WMH)可能会出现动态增加或减少体积,或者随时间稳定。量化这些变化可能有助于作为临床试验的生物标志物,旨在解决血管性认知障碍和痴呆以及阿尔茨海默病。

目的

对 MarkVCID 脑白质高信号增长和消退方案进行多中心交叉站点间和测试-重测的可靠性评估。

方法

NINDS 支持的 MarkVCID 联合会评估了一种神经影像学生物标志物,用于跟踪 WMH 变化。评估了该方案的测试-重测和跨站点间的可靠性。分析认知测试分数与 WMH 变化的关系,以探索其结构有效性。

结果

WMH 增长和消退的测试-重测可靠性的 ICC 值分别为 0.969 和 0.937,而 WMH 增长和消退的跨站点间的 ICC 值分别为 0.995 和 0.990。词汇表长延迟自由回忆与 WMH 增长呈负相关(p < 0.028),但与 WMH 消退无关。

结论

本数据显示,通过跨站点间和测试-重测可靠性,在一年时间内,WMH 增长/消退方案的 ICC 有效性很强。这些数据表明,这种方法可能在血管性认知障碍疾病修饰药物的临床试验中发挥重要作用,这些药物可能优先影响 WMH 增长、稳定性或消退。