• 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

相似文献

1
Heterogeneous cortical atrophy patterns in MCI not captured by conventional diagnostic criteria.轻度认知障碍中异质性皮质萎缩模式未被传统诊断标准所捕捉。
Neurology. 2016 Nov 15;87(20):2108-2116. doi: 10.1212/WNL.0000000000003326. Epub 2016 Oct 19.
2
Patterns of longitudinal cortical atrophy over 3 years in empirically derived MCI subtypes.在经验衍生的 MCI 亚型中,3 年内纵向皮质萎缩的模式。
Neurology. 2020 Jun 16;94(24):e2532-e2544. doi: 10.1212/WNL.0000000000009462. Epub 2020 May 11.
3
Cortical Amyloid Burden Differences Across Empirically-Derived Mild Cognitive Impairment Subtypes and Interaction with APOE ɛ4 Genotype.基于经验得出的轻度认知障碍亚型的皮质淀粉样蛋白负荷差异以及与APOE ε4基因型的相互作用
J Alzheimers Dis. 2016 Mar 29;52(3):849-61. doi: 10.3233/JAD-150900.
4
Susceptibility of the conventional criteria for mild cognitive impairment to false-positive diagnostic errors.轻度认知障碍传统诊断标准出现假阳性诊断错误的易感性。
Alzheimers Dement. 2015 Apr;11(4):415-24. doi: 10.1016/j.jalz.2014.03.005. Epub 2014 May 22.
5
Neuropsychological criteria for mild cognitive impairment improves diagnostic precision, biomarker associations, and progression rates.轻度认知障碍的神经心理学标准提高了诊断准确性、生物标志物关联性和进展率。
J Alzheimers Dis. 2014;42(1):275-89. doi: 10.3233/JAD-140276.
6
Cortical atrophy patterns of incident MCI subtypes in the Mayo Clinic Study of Aging. Mayo 诊所老龄化研究中首发 MCI 亚型的皮质萎缩模式。
Alzheimers Dement. 2020 Jul;16(7):1013-1022. doi: 10.1002/alz.12108. Epub 2020 May 17.
7
Statistically Derived Subtypes and Associations with Cerebrospinal Fluid and Genetic Biomarkers in Mild Cognitive Impairment: A Latent Profile Analysis.轻度认知障碍中基于统计得出的亚型及其与脑脊液和基因生物标志物的关联:一项潜在类别分析
J Int Neuropsychol Soc. 2017 Aug;23(7):564-576. doi: 10.1017/S135561771700039X. Epub 2017 Jun 5.
8
Examining differences in neuropsychiatric symptom factor trajectories in empirically derived mild cognitive impairment subtypes.考察基于实证得出的轻度认知障碍亚型中神经精神症状因子轨迹的差异。
Int J Geriatr Psychiatry. 2018 Dec;33(12):1627-1634. doi: 10.1002/gps.4963. Epub 2018 Oct 1.
9
Alzheimer Disease Signature Neurodegeneration and APOE Genotype in Mild Cognitive Impairment With Suspected Non-Alzheimer Disease Pathophysiology.疑似非阿尔茨海默病病理生理的轻度认知障碍中的阿尔茨海默病特征性神经退行性变与APOE基因型
JAMA Neurol. 2017 Jun 1;74(6):650-659. doi: 10.1001/jamaneurol.2016.5349.
10
Increasing Inaccuracy of Self-Reported Subjective Cognitive Complaints Over 24 Months in Empirically Derived Subtypes of Mild Cognitive Impairment.主观认知主诉的自我报告在经验衍生的轻度认知障碍亚型中 24 个月的准确性逐渐降低。
J Int Neuropsychol Soc. 2018 Sep;24(8):842-853. doi: 10.1017/S1355617718000486.

引用本文的文献

1
Learning a Foreign Language in Older Adults Shapes the Functional Connectivity of Distinct Cerebellar Sub-Regions With Cortical Areas Rich in CB Receptor Expression.老年人学习外语会塑造不同小脑亚区域与富含CB受体表达的皮质区域之间的功能连接。
Brain Behav. 2025 May;15(5):e70565. doi: 10.1002/brb3.70565.
2
Revealing heterogeneity in mild cognitive impairment based on individualized structural covariance network.基于个体化结构协方差网络揭示轻度认知障碍的异质性。
Alzheimers Res Ther. 2025 May 15;17(1):106. doi: 10.1186/s13195-025-01752-4.
3
Adversarial Learning for MRI Reconstruction and Classification of Cognitively Impaired Individuals.用于认知障碍个体MRI重建与分类的对抗学习
IEEE Access. 2024;12:83169-83182. doi: 10.1109/access.2024.3408840. Epub 2024 Jun 3.
4
Definition and analysis of gray matter atrophy subtypes in mild cognitive impairment based on data-driven methods.基于数据驱动方法的轻度认知障碍中灰质萎缩亚型的定义与分析
Front Aging Neurosci. 2024 Jun 4;16:1328301. doi: 10.3389/fnagi.2024.1328301. eCollection 2024.
5
Cognition and Amyloid-β in Older Veterans: Characterization and Longitudinal Outcomes of Data-Derived Phenotypes.老年退伍军人的认知与β-淀粉样蛋白:数据衍生表型的特征及纵向结果
J Alzheimers Dis. 2024;99(1):417-427. doi: 10.3233/JAD-240077.
6
News event memory in amnestic and non-amnestic MCI, heritable risk for dementia, and subjective memory complaints.遗忘型和非遗忘型 MCI 中的新闻事件记忆、痴呆的遗传风险和主观记忆主诉。
Neuropsychologia. 2024 Jul 4;199:108887. doi: 10.1016/j.neuropsychologia.2024.108887. Epub 2024 Apr 15.
7
Data-driven classification of cognitively normal and mild cognitive impairment subtypes predicts progression in the NACC dataset.基于数据驱动的认知正常和轻度认知障碍亚型分类可预测 NACC 数据集的进展。
Alzheimers Dement. 2024 May;20(5):3442-3454. doi: 10.1002/alz.13793. Epub 2024 Apr 4.
8
Exploring Shared Biomarkers of Myocardial Infarction and Alzheimer's Disease via Single-Cell/Nucleus Sequencing and Bioinformatics Analysis.通过单细胞/核测序和生物信息学分析探索心肌梗死和阿尔茨海默病的共享生物标志物。
J Alzheimers Dis. 2023;96(2):705-723. doi: 10.3233/JAD-230559.
9
Cognitive phenotypes in late-onset epilepsy: results from the atherosclerosis risk in communities study.迟发性癫痫的认知表型:社区动脉粥样硬化风险研究结果
Front Neurol. 2023 Aug 24;14:1230368. doi: 10.3389/fneur.2023.1230368. eCollection 2023.
10
Heterogeneity in subjective cognitive decline in the Sino Longitudinal Study on Cognitive Decline(SILCODE): Empirically derived subtypes, structural and functional verification.主观认知衰退在认知衰退纵向研究(SILCODE)中的异质性:经验得出的亚型,结构和功能验证。
CNS Neurosci Ther. 2023 Dec;29(12):4032-4042. doi: 10.1111/cns.14327. Epub 2023 Jul 20.

本文引用的文献

1
Cortical Amyloid Burden Differences Across Empirically-Derived Mild Cognitive Impairment Subtypes and Interaction with APOE ɛ4 Genotype.基于经验得出的轻度认知障碍亚型的皮质淀粉样蛋白负荷差异以及与APOE ε4基因型的相互作用
J Alzheimers Dis. 2016 Mar 29;52(3):849-61. doi: 10.3233/JAD-150900.
2
The Sub-Classification of Amnestic Mild Cognitive Impairment Using MRI-Based Cortical Thickness Measures.基于 MRI 脑皮质厚度测量的遗忘型轻度认知障碍的亚分类。
Front Neurol. 2014 May 21;5:76. doi: 10.3389/fneur.2014.00076. eCollection 2014.
3
Susceptibility of the conventional criteria for mild cognitive impairment to false-positive diagnostic errors.轻度认知障碍传统诊断标准出现假阳性诊断错误的易感性。
Alzheimers Dement. 2015 Apr;11(4):415-24. doi: 10.1016/j.jalz.2014.03.005. Epub 2014 May 22.
4
Neuropsychological criteria for mild cognitive impairment improves diagnostic precision, biomarker associations, and progression rates.轻度认知障碍的神经心理学标准提高了诊断准确性、生物标志物关联性和进展率。
J Alzheimers Dis. 2014;42(1):275-89. doi: 10.3233/JAD-140276.
5
Biological heterogeneity in ADNI amnestic mild cognitive impairment.ADNI遗忘型轻度认知障碍中的生物学异质性。
Alzheimers Dement. 2014 Sep;10(5):511-521.e1. doi: 10.1016/j.jalz.2013.09.003. Epub 2014 Jan 10.
6
Are empirically-derived subtypes of mild cognitive impairment consistent with conventional subtypes?经验衍生的轻度认知障碍亚型与传统亚型是否一致?
J Int Neuropsychol Soc. 2013 Jul;19(6):635-45. doi: 10.1017/S1355617713000313. Epub 2013 Apr 3.
7
Gray matter atrophy patterns of mild cognitive impairment subtypes.轻度认知障碍亚型的灰质萎缩模式。
J Neurol Sci. 2012 Apr 15;315(1-2):26-32. doi: 10.1016/j.jns.2011.12.011. Epub 2012 Jan 26.
8
Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study.神经病理学定义的具有不同临床特征的阿尔茨海默病亚型:一项回顾性研究。
Lancet Neurol. 2011 Sep;10(9):785-96. doi: 10.1016/S1474-4422(11)70156-9. Epub 2011 Jul 27.
9
Global clinical dementia rating of 0.5 in MCI masks variability related to level of function.全球临床痴呆评定量表 0.5 分在 MCI 中掩盖了与功能水平相关的变异性。
Neurology. 2011 Feb 15;76(7):652-9. doi: 10.1212/WNL.0b013e31820ce6a5.
10
Dysexecutive versus amnesic phenotypes of very mild Alzheimer's disease are associated with distinct clinical, genetic and cortical thinning characteristics.非常轻度阿尔茨海默病的执行功能障碍与遗忘症表型与不同的临床、遗传和皮质变薄特征相关。
J Neurol Neurosurg Psychiatry. 2011 Jan;82(1):45-51. doi: 10.1136/jnnp.2009.199505. Epub 2010 Jun 20.

轻度认知障碍中异质性皮质萎缩模式未被传统诊断标准所捕捉。

Heterogeneous cortical atrophy patterns in MCI not captured by conventional diagnostic criteria.

作者信息

Edmonds Emily C, Eppig Joel, Bondi Mark W, Leyden Kelly M, Goodwin Bailey, Delano-Wood Lisa, McDonald Carrie R

机构信息

From the Department of Psychiatry (E.C.E., M.W.B., K.M.L., B.G., L.D.-W., C.R.M.), School of Medicine, University of California San Diego, La Jolla; Joint Doctoral Program in Clinical Psychology (J.E.), San Diego State University/University of California San Diego; and Veterans Affairs San Diego Healthcare System (M.W.B., L.D.-W.), CA.

出版信息

Neurology. 2016 Nov 15;87(20):2108-2116. doi: 10.1212/WNL.0000000000003326. Epub 2016 Oct 19.

DOI:10.1212/WNL.0000000000003326
PMID:27760874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5109943/
Abstract

OBJECTIVE

We investigated differences in regional cortical thickness between previously identified empirically derived mild cognitive impairment (MCI) subtypes (amnestic MCI, dysnomic MCI, dysexecutive/mixed MCI, and cluster-derived normal) in order to determine whether these cognitive subtypes would show different patterns of cortical atrophy.

METHODS

Participants were 485 individuals diagnosed with MCI and 178 cognitively normal individuals from the Alzheimer's Disease Neuroimaging Initiative. Cortical thickness estimates were computed for 32 regions of interest per hemisphere. Statistical group maps compared each MCI subtype to cognitively normal participants and to one another.

RESULTS

The pattern of cortical thinning observed in each MCI subtype corresponded to their cognitive profile. No differences in cortical thickness were found between the cluster-derived normal MCI subtype and the cognitively normal group. Direct comparison between MCI subtypes suggested that the cortical thickness patterns reflect increasing disease severity.

CONCLUSIONS

There is an ordered pattern of cortical atrophy among patients with MCI that coincides with their profiles of increasing cognitive dysfunction. This heterogeneity is not captured when patients are grouped by conventional diagnostic criteria. Results in the cluster-derived normal group further support the premise that the conventional MCI diagnostic criteria are highly susceptible to false-positive diagnostic errors. Findings suggest a need to (1) improve the diagnostic criteria by reducing reliance on conventional screening measures, rating scales, and a single memory measure in order to avoid false-positive errors; and (2) divide MCI samples into meaningful subgroups based on cognitive and biomarkers profiles-a method that may provide better staging of MCI and inform prognosis.

摘要

目的

我们研究了先前通过经验确定的轻度认知障碍(MCI)亚型(遗忘型MCI、命名性MCI、执行功能障碍/混合型MCI以及聚类衍生正常组)之间区域皮质厚度的差异,以确定这些认知亚型是否会表现出不同的皮质萎缩模式。

方法

参与者包括来自阿尔茨海默病神经影像倡议组织的485名被诊断为MCI的个体和178名认知正常的个体。计算每个半球32个感兴趣区域的皮质厚度估计值。统计组图比较了每种MCI亚型与认知正常参与者以及相互之间的差异。

结果

在每种MCI亚型中观察到的皮质变薄模式与其认知特征相对应。聚类衍生正常MCI亚型与认知正常组之间未发现皮质厚度差异。MCI亚型之间的直接比较表明,皮质厚度模式反映了疾病严重程度的增加。

结论

MCI患者中存在一种有序的皮质萎缩模式,与他们认知功能障碍加重的特征相吻合。当根据传统诊断标准对患者进行分组时,这种异质性并未被捕捉到。聚类衍生正常组的结果进一步支持了传统MCI诊断标准极易出现假阳性诊断错误这一前提。研究结果表明需要:(1)通过减少对传统筛查措施、评定量表和单一记忆测量的依赖来改进诊断标准,以避免假阳性错误;(2)根据认知和生物标志物特征将MCI样本分为有意义的亚组——这种方法可能会为MCI提供更好的分期并为预后提供信息。