• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用阿尔茨海默病神经影像队列数据在认知测试分数之间进行交叉转换的方法。

Methods to crosswalk between cognitive test scores using data from the Alzheimer's Disease Neuroimaging Cohort.

作者信息

Ackley Sarah F, Wang Jingxuan, Chen Ruijia, Hill-Jarrett Tanisha G, Rojas-Saunero L Paloma, Stokes Andrew, Shah Sachin J, Glymour M Maria

机构信息

Department of Epidemiology, Brown University, Providence, Rhode Island, USA.

Department of Epidemiology & Biostatistics, UCSF, San Francisco, California, USA.

出版信息

Alzheimers Dement. 2025 Feb;21(2):e14597. doi: 10.1002/alz.14597.

DOI:10.1002/alz.14597
PMID:40000573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11859661/
Abstract

INTRODUCTION

Studies use multiple different instruments to measure dementia-related outcomes, making head-to-head comparisons of interventions difficult.

METHODS

To address this gap, we developed two methods to crosswalk estimated treatment effects on cognitive outcomes that are flexible, broadly applicable, and do not rely on strong distributional assumptions.

RESULTS

We present two methods to crosswalk effect estimates using one measure to estimates using another measure, illustrated with global cognitive measures from the Alzheimer's Disease Neuroimaging Initiative (ADNI). Specifically, we develop crosswalks for the following measures and associated change scores over time: the clinical dementia rating scale sum of box (CDR-SB), Montreal Cognitive Assessment (MoCA), and Mini-Mental State Examination (MMSE) scores. Finally, a setting in which crosswalking is not appropriate is illustrated with plasma phosphorylated tau (p-tau) concentration and global cognitive measures.

DISCUSSION

Given the inconsistent collection and reporting of dementia and cognitive outcomes across studies, these crosswalking methods offer a valuable approach to harmonizing and comparing results reported on different scales.

HIGHLIGHTS

Developed methods to crosswalk from one cognitive outcome to another in studies of dementia interventions. Methods illustrated using combinations of global cognitive tests: the CDR-SB, MoCA, and MMSE. Illustrates scenarios where crosswalking may not be appropriate for certain combinations of measures. Crosswalking methods support comparison of interventions with accurate error propagation. Facilitates inclusion of more studies in meta-analyses by increasing data comparability.

摘要

引言

多项研究使用多种不同工具来测量与痴呆症相关的结果,这使得对干预措施进行直接比较变得困难。

方法

为填补这一空白,我们开发了两种方法来对认知结果的估计治疗效果进行相互转换,这两种方法灵活、广泛适用且不依赖于强分布假设。

结果

我们提出了两种将一种测量方法的效应估计值转换为另一种测量方法的效应估计值的方法,并以阿尔茨海默病神经影像倡议(ADNI)的整体认知测量为例进行说明。具体而言,我们针对以下测量方法及随时间的相关变化分数开发了相互转换方法:临床痴呆评定量表总和(CDR-SB)、蒙特利尔认知评估量表(MoCA)和简易精神状态检查表(MMSE)分数。最后,以血浆磷酸化tau蛋白(p-tau)浓度和整体认知测量为例,说明了相互转换不适用的情况。

讨论

鉴于不同研究中痴呆症和认知结果的收集与报告不一致,这些相互转换方法为协调和比较不同量表上报告的结果提供了一种有价值的方法。

要点

在痴呆症干预研究中开发了从一种认知结果转换为另一种认知结果的方法。使用整体认知测试组合(CDR-SB、MoCA和MMSE)对方法进行了说明。说明了某些测量组合相互转换可能不适用的情况。相互转换方法支持对干预措施进行比较,并能准确传播误差。通过提高数据可比性,有助于在荟萃分析中纳入更多研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e3/11859661/3f1541906f7e/ALZ-21-e14597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e3/11859661/4af67b20dde7/ALZ-21-e14597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e3/11859661/3f1541906f7e/ALZ-21-e14597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e3/11859661/4af67b20dde7/ALZ-21-e14597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57e3/11859661/3f1541906f7e/ALZ-21-e14597-g001.jpg

相似文献

1
Methods to crosswalk between cognitive test scores using data from the Alzheimer's Disease Neuroimaging Cohort.利用阿尔茨海默病神经影像队列数据在认知测试分数之间进行交叉转换的方法。
Alzheimers Dement. 2025 Feb;21(2):e14597. doi: 10.1002/alz.14597.
2
Bridging the gap: A conversion framework for CDR-SB and MoCA scores in Alzheimer's disease and related dementia.弥合差距:阿尔茨海默病及相关痴呆症中CDR-SB与MoCA评分的转换框架
J Prev Alzheimers Dis. 2025 Sep;12(8):100226. doi: 10.1016/j.tjpad.2025.100226. Epub 2025 Jun 7.
3
Extension and external validation of mapping between the Mini-Mental State Examination and the Clinical Dementia Rating scale in patients with Alzheimer's disease.阿尔茨海默病患者简易精神状态检查表与临床痴呆评定量表之间映射关系的扩展及外部验证
Alzheimers Dement. 2025 Jun;21(6):e70163. doi: 10.1002/alz.70163.
4
Mini-Mental State Examination (MMSE) for the detection of Alzheimer's disease and other dementias in people with mild cognitive impairment (MCI).用于检测轻度认知障碍(MCI)患者中阿尔茨海默病及其他痴呆症的简易精神状态检查表(MMSE)。
Cochrane Database Syst Rev. 2015 Mar 5;2015(3):CD010783. doi: 10.1002/14651858.CD010783.pub2.
5
¹⁸F-FDG PET for the early diagnosis of Alzheimer's disease dementia and other dementias in people with mild cognitive impairment (MCI).¹⁸F - 氟代脱氧葡萄糖正电子发射断层显像(¹⁸F - FDG PET)用于轻度认知障碍(MCI)患者中阿尔茨海默病性痴呆及其他痴呆的早期诊断。
Cochrane Database Syst Rev. 2015 Jan 28;1(1):CD010632. doi: 10.1002/14651858.CD010632.pub2.
6
CSF tau and the CSF tau/ABeta ratio for the diagnosis of Alzheimer's disease dementia and other dementias in people with mild cognitive impairment (MCI).脑脊液tau蛋白及脑脊液tau蛋白与β淀粉样蛋白比值在轻度认知障碍(MCI)患者中用于诊断阿尔茨海默病性痴呆及其他痴呆。
Cochrane Database Syst Rev. 2017 Mar 22;3(3):CD010803. doi: 10.1002/14651858.CD010803.pub2.
7
Plasma and cerebrospinal fluid amyloid beta for the diagnosis of Alzheimer's disease dementia and other dementias in people with mild cognitive impairment (MCI).血浆和脑脊液β淀粉样蛋白用于诊断轻度认知障碍(MCI)患者的阿尔茨海默病性痴呆及其他痴呆。
Cochrane Database Syst Rev. 2014 Jun 10;2014(6):CD008782. doi: 10.1002/14651858.CD008782.pub4.
8
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.
9
Multi-domain interventions for the prevention of dementia and cognitive decline.多领域干预措施预防痴呆和认知能力下降。
Cochrane Database Syst Rev. 2021 Nov 8;11(11):CD013572. doi: 10.1002/14651858.CD013572.pub2.
10
Selegiline for Alzheimer's disease.司来吉兰用于治疗阿尔茨海默病。
Cochrane Database Syst Rev. 2003(1):CD000442. doi: 10.1002/14651858.CD000442.

本文引用的文献

1
Considerations for Use of Blood-Based Biomarkers in Epidemiologic Dementia Research.考虑在流行病学痴呆研究中使用基于血液的生物标志物。
Am J Epidemiol. 2024 Feb 5;193(3):527-535. doi: 10.1093/aje/kwad197.
2
Causal inference in medical records and complementary systems pharmacology for metformin drug repurposing towards dementia.基于病历的因果推断和补充系统药理学在二甲双胍药物重用到痴呆症的研究
Nat Commun. 2022 Dec 10;13(1):7652. doi: 10.1038/s41467-022-35157-w.
3
Lecanemab in Early Alzheimer's Disease.早期阿尔茨海默病中的lecanemab
N Engl J Med. 2023 Jan 5;388(1):9-21. doi: 10.1056/NEJMoa2212948. Epub 2022 Nov 29.
4
Harmonizing Depression Measures Across Studies: a Tutorial for Data Harmonization.协调研究间的抑郁测量:数据协调教程。
Prev Sci. 2023 Nov;24(8):1569-1580. doi: 10.1007/s11121-022-01381-5. Epub 2022 Jul 7.
5
Two Randomized Phase 3 Studies of Aducanumab in Early Alzheimer's Disease.两项早期阿尔茨海默病中阿杜卡努单抗的随机 3 期研究。
J Prev Alzheimers Dis. 2022;9(2):197-210. doi: 10.14283/jpad.2022.30.
6
Clinical Outcome Measure Crosswalks in Alzheimer's Disease: A Systematic Review.阿尔茨海默病临床结局测量转换标准:系统评价。
J Alzheimers Dis. 2021;83(2):591-608. doi: 10.3233/JAD-210060.
7
A comparison of test-retest reliability of four cognitive screening tools in people with dementia.痴呆患者四种认知筛查工具重测信度的比较。
Disabil Rehabil. 2022 Jul;44(15):4090-4095. doi: 10.1080/09638288.2021.1891466. Epub 2021 Mar 9.
8
Time course of phosphorylated-tau181 in blood across the Alzheimer's disease spectrum.阿尔茨海默病谱中血液磷酸化 tau181 的时间进程。
Brain. 2021 Feb 12;144(1):325-339. doi: 10.1093/brain/awaa399.
9
Data Harmonization: Establishing Measurement Invariance across Different Assessments of the Same Construct across Adolescence.数据协调:在青少年时期对同一结构的不同评估中建立测量不变性。
J Clin Child Adolesc Psychol. 2019 Jul-Aug;48(4):555-567. doi: 10.1080/15374416.2019.1622124. Epub 2019 Jun 11.
10
Data Harmonization in Aging Research: Not so Fast.衰老研究中的数据协调:没那么快。
Exp Aging Res. 2015;41(5):475-95. doi: 10.1080/0361073X.2015.1085748.