• 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

轻度认知障碍数据驱动亚型中一般认知和日常功能的纵向轨迹:一项针对老年人的纵向队列分析。

Longitudinal trajectories of general cognitive and daily functions in data-driven subtypes of MCI: A longitudinal cohort analysis of older adults.

作者信息

Long Xianxian, Yuan Manqiong, Zhang Zeyun, Fang Ya

机构信息

Key Laboratory of Health Technology Assessment of Fujian Province, School of Public Health, Xiamen University, Xiamen, China; Center for Aging and Health Research, School of Public Health, Xiamen University, Xiamen, China.

Key Laboratory of Health Technology Assessment of Fujian Province, School of Public Health, Xiamen University, Xiamen, China; Center for Aging and Health Research, School of Public Health, Xiamen University, Xiamen, China.

出版信息

Arch Gerontol Geriatr. 2025 Feb;129:105659. doi: 10.1016/j.archger.2024.105659. Epub 2024 Oct 13.

DOI:10.1016/j.archger.2024.105659
PMID:39454276
Abstract

OBJECTIVES

To derive data-driven subtypes of mild cognitive impairment (MCI) and characterize the complicated changes of general cognitive and daily functions over time in MCI subtypes.

METHODS

A total of 813 subjects diagnosed as MCI at baseline from the Alzheimer's Disease Neuroimaging Initiative (ADNI) were included. Data-driven MCI subtypes were derived from group-based multi-trajectory modeling (GBMTM) analyses using longitudinal measurement scores in the cognitive domains of visuospatial function, language, and executive function. General cognitive and daily functions were measured by the Mini-Mental State Examination (MMSE) and the Functional Assessment Questionnaire (FAQ), respectively, whose longitudinal trajectory changes were depicted by Linear mixed models.

RESULTS

Three MCI subtypes were derived, which were defined as "Cognitive decline group", "Mild cognitive decline group" and "No cognitive decline group". The "Mild cognitive decline group" had the highest percentage in the sample (46.2 %), followed by the "No cognitive decline group" (35.2 %). Patients in the "Cognitive decline group" had the highest mean age (74.69 years) at baseline, the highest APOE ε4 carriers (63.2 %), and the greatest dementia conversion rate (77.0 %). The changes in MMSE and FAQ score trajectories were fastest in the "Cognitive decline group" in the first 36 months and most slowly in the "No cognitive decline group".

CONCLUSION

MCI individuals could be subdivided into more fine-grained cognitive subtypes, and identifying these distinct MCI subtypes and their different trajectories of cognitive decline may have important prognostic value for improving clinical course prediction.

摘要

目的

推导数据驱动的轻度认知障碍(MCI)亚型,并描述MCI亚型中一般认知和日常功能随时间的复杂变化。

方法

纳入了阿尔茨海默病神经影像学倡议(ADNI)中813名在基线时被诊断为MCI的受试者。数据驱动的MCI亚型通过基于组的多轨迹建模(GBMTM)分析得出,该分析使用了视觉空间功能、语言和执行功能等认知领域的纵向测量分数。一般认知和日常功能分别通过简易精神状态检查表(MMSE)和功能评估问卷(FAQ)进行测量,其纵向轨迹变化通过线性混合模型进行描述。

结果

得出了三种MCI亚型,分别定义为“认知衰退组”、“轻度认知衰退组”和“无认知衰退组”。“轻度认知衰退组”在样本中的比例最高(46.2%),其次是“无认知衰退组”(35.2%)。“认知衰退组”的患者在基线时平均年龄最高(74.69岁),APOE ε4携带者比例最高(63.2%),痴呆转化率也最高(77.0%)。MMSE和FAQ评分轨迹的变化在“认知衰退组”的前36个月最快,在“无认知衰退组”最慢。

结论

MCI个体可细分为更精细的认知亚型,识别这些不同的MCI亚型及其不同的认知衰退轨迹可能对改善临床病程预测具有重要的预后价值。

相似文献

1
Longitudinal trajectories of general cognitive and daily functions in data-driven subtypes of MCI: A longitudinal cohort analysis of older adults.轻度认知障碍数据驱动亚型中一般认知和日常功能的纵向轨迹:一项针对老年人的纵向队列分析。
Arch Gerontol Geriatr. 2025 Feb;129:105659. doi: 10.1016/j.archger.2024.105659. Epub 2024 Oct 13.
2
Longitudinal trajectory effects of different MCI subtypes on general cognitive and daily functions in a population-based cohort of older adults.不同轻度认知障碍亚型对基于人群的老年队列中一般认知和日常功能的纵向轨迹影响。
J Psychiatr Res. 2024 Mar;171:296-305. doi: 10.1016/j.jpsychires.2024.01.038. Epub 2024 Jan 23.
3
Longitudinal Trajectories of Informant-Reported Daily Functioning in Empirically Defined Subtypes of Mild Cognitive Impairment.经验性定义的轻度认知障碍亚型中由 informant 报告的日常功能的纵向轨迹。
J Int Neuropsychol Soc. 2017 Jul;23(6):521-527. doi: 10.1017/S1355617717000285. Epub 2017 May 10.
4
Predicting Cognitive Decline in Amyloid-Positive Patients With Mild Cognitive Impairment or Mild Dementia.预测伴有轻度认知障碍或轻度痴呆的淀粉样蛋白阳性患者的认知能力下降。
Neurology. 2024 Aug 13;103(3):e209605. doi: 10.1212/WNL.0000000000209605. Epub 2024 Jul 10.
5
Trajectories of cognitive decline in different domains prior to AD onset in persons with mild cognitive impairment.在轻度认知障碍患者出现 AD 前,不同认知领域认知下降的轨迹。
Arch Gerontol Geriatr. 2024 Jul;122:105375. doi: 10.1016/j.archger.2024.105375. Epub 2024 Feb 20.
6
Relationship between the Montreal Cognitive Assessment and Mini-mental State Examination for assessment of mild cognitive impairment in older adults.蒙特利尔认知评估量表与简易精神状态检查表在评估老年人轻度认知障碍中的关系。
BMC Geriatr. 2015 Sep 7;15:107. doi: 10.1186/s12877-015-0103-3.
7
Longitudinal trajectories of cognitive, functional, and neuropsychiatric decline in Alzheimer's disease during COVID-19 lockdown in South Korea.韩国新冠疫情封锁期间阿尔茨海默病患者认知、功能及神经精神衰退的纵向轨迹
Sci Rep. 2025 Mar 8;15(1):8081. doi: 10.1038/s41598-025-92497-5.
8
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.
9
[Research on predicting the risk of mild cognitive impairment in the elderly based on the joint model].基于联合模型预测老年人轻度认知障碍风险的研究
Zhonghua Liu Xing Bing Xue Za Zhi. 2022 Feb 10;43(2):269-276. doi: 10.3760/cma.j.cn112338-20210620-00484.
10
Classification, Prediction, and Concordance of Cognitive and Functional Progression in Patients with Mild Cognitive Impairment in the United States: A Latent Class Analysis.美国轻度认知障碍患者认知和功能进展的分类、预测和一致性:潜在类别分析。
J Alzheimers Dis. 2021;82(4):1667-1682. doi: 10.3233/JAD-210305.