Association of cerebrospinal fluid ciliary neurotrophic factor levels with cognitive decline and disease progression.

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Shanshan Wang, Li Han, Hong Ni, Shaofa Ke, Tengwei Pan
{"title":"Association of cerebrospinal fluid ciliary neurotrophic factor levels with cognitive decline and disease progression.","authors":"Shanshan Wang, Li Han, Hong Ni, Shaofa Ke, Tengwei Pan","doi":"10.1177/13872877251329612","DOIUrl":null,"url":null,"abstract":"<p><p>BackgroundCiliary neurotrophic factor (CNTF) has been identified as a neuroprotective cytokine that can alleviate cognitive impairment in preclinical studies, although the association of cerebrospinal fluid (CSF) CNTF levels with cognitive decline and disease progression in living humans remains unclear.ObjectiveThis study aimed to explore the association between baseline CSF CNTF levels and the rate of cognitive decline in cognitively unimpaired (CU) and cognitively impaired (CI) older people respectively.MethodsA total of 667 participants were included in the study, comprising 161 CU and 506 CI individuals, with an average follow-up time of 3.97 years (SD = 2.99). Linear mixed-effects models were fitted with the Mini-Mental State Examination (MMSE) scores as the primary outcome. As sensitivity analyses, we used another three commonly used cognitive measures as secondary outcomes to test the robustness of our findings. In addition, a Cox proportional hazards model was used to the mild cognitive impairment (MCI) subgroup to investigate the association between baseline CSF CNTF levels and the progression from MCI to dementia.ResultsWe observed that higher baseline CSF CNTF levels were linked with a slower rate of cognitive decline in the CI group, while this association was absent in the CU group. These findings were consistent across different cognitive measures. Among MCI participants, higher levels of CSF CNTF were associated with a slower rate of disease progression to dementia.ConclusionsThe association between CSF CNTF levels and both cognitive decline and disease progression highlights the potential of CNTF as a therapeutic target in the context of Alzheimer's disease and related cognitive disorders.</p>","PeriodicalId":14929,"journal":{"name":"Journal of Alzheimer's Disease","volume":" ","pages":"13872877251329612"},"PeriodicalIF":3.4000,"publicationDate":"2025-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alzheimer's Disease","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/13872877251329612","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

BackgroundCiliary neurotrophic factor (CNTF) has been identified as a neuroprotective cytokine that can alleviate cognitive impairment in preclinical studies, although the association of cerebrospinal fluid (CSF) CNTF levels with cognitive decline and disease progression in living humans remains unclear.ObjectiveThis study aimed to explore the association between baseline CSF CNTF levels and the rate of cognitive decline in cognitively unimpaired (CU) and cognitively impaired (CI) older people respectively.MethodsA total of 667 participants were included in the study, comprising 161 CU and 506 CI individuals, with an average follow-up time of 3.97 years (SD = 2.99). Linear mixed-effects models were fitted with the Mini-Mental State Examination (MMSE) scores as the primary outcome. As sensitivity analyses, we used another three commonly used cognitive measures as secondary outcomes to test the robustness of our findings. In addition, a Cox proportional hazards model was used to the mild cognitive impairment (MCI) subgroup to investigate the association between baseline CSF CNTF levels and the progression from MCI to dementia.ResultsWe observed that higher baseline CSF CNTF levels were linked with a slower rate of cognitive decline in the CI group, while this association was absent in the CU group. These findings were consistent across different cognitive measures. Among MCI participants, higher levels of CSF CNTF were associated with a slower rate of disease progression to dementia.ConclusionsThe association between CSF CNTF levels and both cognitive decline and disease progression highlights the potential of CNTF as a therapeutic target in the context of Alzheimer's disease and related cognitive disorders.

脑脊液睫状神经营养因子水平与认知能力下降和疾病进展的关系。
背景睫状神经营养因子(CNTF)已被确定为一种神经保护细胞因子,在临床前研究中可减轻认知功能障碍,但脑脊液(CSF)CNTF水平与活人认知功能衰退和疾病进展的关系仍不清楚。本研究旨在探讨认知功能未受损(CU)和认知功能受损(CI)老年人的基线 CSF CNTF 水平分别与认知功能衰退速度之间的关系。方法本研究共纳入 667 名参与者,其中包括 161 名 CU 和 506 名 CI 患者,平均随访时间为 3.97 年(SD = 2.99)。我们以迷你精神状态检查(MMSE)得分作为主要结果,建立了线性混合效应模型。作为敏感性分析,我们使用了另外三种常用的认知指标作为次要结果,以检验我们研究结果的稳健性。此外,我们还在轻度认知障碍(MCI)亚组中使用了Cox比例危险模型,以研究基线CSF CNTF水平与MCI进展为痴呆之间的关系。结果我们发现,在CI组中,较高的基线CSF CNTF水平与较慢的认知能力下降速度有关,而在CU组中则没有这种关系。这些发现在不同的认知测量中都是一致的。结论CSF CNTF水平与认知能力下降和疾病进展之间的关联凸显了CNTF作为阿尔茨海默病及相关认知障碍治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease 医学-神经科学
CiteScore
6.40
自引率
7.50%
发文量
1327
审稿时长
2 months
期刊介绍: The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信