• 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

前颞叶痴呆患者脑脊液中前体神经生长因子水平作为潜在诊断生物标志物

Cerebrospinal fluid level of proNGF as potential diagnostic biomarker in patients with frontotemporal dementia.

作者信息

Malerba Francesca, Florio Rita, Arisi Ivan, Zecca Chiara, Dell'Abate Maria Teresa, Logroscino Giancarlo, Cattaneo Antonino

机构信息

Fondazione European Brain Research Institute (EBRI) Rita Levi-Montalcini, Rome, Italy.

Institute of Translational Pharmacology - National Research Council (IFT-CNR), Rome, Italy.

出版信息

Front Aging Neurosci. 2024 Jan 25;15:1298307. doi: 10.3389/fnagi.2023.1298307. eCollection 2023.

DOI:10.3389/fnagi.2023.1298307
PMID:38332808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10850263/
Abstract

INTRODUCTION

Frontotemporal dementia (FTD) is an extremely heterogeneous and complex neurodegenerative disease, exhibiting different phenotypes, genetic backgrounds, and pathological states. Due to these characteristics, and to the fact that clinical symptoms overlap with those of other neurodegenerative diseases or psychiatric disorders, the diagnosis based only on the clinical evaluation is very difficult. The currently used biomarkers help in the clinical diagnosis, but are insufficient and do not cover all the clinical needs.

METHODS

By the means of a new immunoassay, we have measured and analyzed the proNGF levels in 43 cerebrospinal fluids (CSF) from FTD patients, and compared the results to those obtained in CSF from 84 Alzheimer's disease (AD), 15 subjective memory complaints (SMC) and 13 control subjects.

RESULTS

A statistically significant difference between proNGF levels in FTD compared to AD, SMC and controls subjects was found. The statistical models reveal that proNGF determination increases the accuracy of FTD diagnosis, if added to the clinically validated CSF biomarkers.

DISCUSSION

These results suggest that proNGF could be included in a panel of biomarkers to improve the FTD diagnosis.

摘要

引言

额颞叶痴呆(FTD)是一种极其异质性和复杂性的神经退行性疾病,表现出不同的表型、遗传背景和病理状态。由于这些特征,以及临床症状与其他神经退行性疾病或精神障碍的症状重叠这一事实,仅基于临床评估进行诊断非常困难。目前使用的生物标志物有助于临床诊断,但并不充分,无法满足所有临床需求。

方法

通过一种新的免疫测定方法,我们测量并分析了43例FTD患者脑脊液(CSF)中的前体神经生长因子(proNGF)水平,并将结果与84例阿尔茨海默病(AD)、15例主观记忆障碍(SMC)患者的脑脊液以及13例对照受试者的脑脊液结果进行比较。

结果

发现FTD患者脑脊液中的proNGF水平与AD、SMC患者及对照受试者相比存在统计学显著差异。统计模型显示,如果将proNGF测定添加到经过临床验证的脑脊液生物标志物中,可提高FTD诊断的准确性。

讨论

这些结果表明,proNGF可纳入生物标志物组合中以改善FTD诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/b589104d4867/fnagi-15-1298307-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/76d3ab7c14b6/fnagi-15-1298307-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/37e9f4b820b5/fnagi-15-1298307-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/c61766c1ef95/fnagi-15-1298307-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/4a2811b6db36/fnagi-15-1298307-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/7624ca97e06c/fnagi-15-1298307-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/a31120211522/fnagi-15-1298307-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/b589104d4867/fnagi-15-1298307-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/76d3ab7c14b6/fnagi-15-1298307-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/37e9f4b820b5/fnagi-15-1298307-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/c61766c1ef95/fnagi-15-1298307-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/4a2811b6db36/fnagi-15-1298307-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/7624ca97e06c/fnagi-15-1298307-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/a31120211522/fnagi-15-1298307-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e745/10850263/b589104d4867/fnagi-15-1298307-g007.jpg

相似文献

1
Cerebrospinal fluid level of proNGF as potential diagnostic biomarker in patients with frontotemporal dementia.前颞叶痴呆患者脑脊液中前体神经生长因子水平作为潜在诊断生物标志物
Front Aging Neurosci. 2024 Jan 25;15:1298307. doi: 10.3389/fnagi.2023.1298307. eCollection 2023.
2
proNGF Measurement in Cerebrospinal Fluid Samples of a Large Cohort of Living Patients With Alzheimer's Disease by a New Automated Immunoassay.采用新型自动化免疫测定法对大量在世阿尔茨海默病患者脑脊液样本中的前神经生长因子(proNGF)进行检测。
Front Aging Neurosci. 2021 Oct 27;13:741414. doi: 10.3389/fnagi.2021.741414. eCollection 2021.
3
Cerebrospinal Fluid YKL-40 and Chitotriosidase Levels in Frontotemporal Dementia Vary by Clinical, Genetic and Pathological Subtype.脑脊髓液 YKL-40 和壳三糖酶水平在额颞叶痴呆的临床、遗传和病理亚型中存在差异。
Dement Geriatr Cogn Disord. 2020;49(1):56-76. doi: 10.1159/000506282. Epub 2020 Apr 28.
4
Novel diagnostic cerebrospinal fluid biomarkers for pathologic subtypes of frontotemporal dementia identified by proteomics.通过蛋白质组学鉴定的额颞叶痴呆病理亚型的新型诊断性脑脊液生物标志物。
Alzheimers Dement (Amst). 2016 Jan 19;2:86-94. doi: 10.1016/j.dadm.2015.12.004. eCollection 2016.
5
Novel fluid biomarkers to differentiate frontotemporal dementia and dementia with Lewy bodies from Alzheimer's disease: A systematic review.用于鉴别额颞叶痴呆和路易体痴呆与阿尔茨海默病的新型体液生物标志物:一项系统评价
J Neurol Sci. 2020 Aug 15;415:116886. doi: 10.1016/j.jns.2020.116886. Epub 2020 May 11.
6
Cerebrospinal fluid soluble TREM2 levels in frontotemporal dementia differ by genetic and pathological subgroup.脑脊液可溶性 TREM2 水平在额颞叶痴呆的遗传和病理亚组中存在差异。
Alzheimers Res Ther. 2018 Aug 16;10(1):79. doi: 10.1186/s13195-018-0405-8.
7
Cerebrospinal Fluid proNGF: A Putative Biomarker for Early Alzheimer's Disease.脑脊液前体神经生长因子:早期阿尔茨海默病的一种潜在生物标志物。
Curr Alzheimer Res. 2016;13(7):800-8. doi: 10.2174/1567205013666160129095649.
8
Potential diagnostic value of CSF metabolism-related proteins across the Alzheimer's disease continuum.脑脊液代谢相关蛋白在阿尔茨海默病连续体中的潜在诊断价值。
Alzheimers Res Ther. 2023 Jul 15;15(1):124. doi: 10.1186/s13195-023-01269-8.
9
Comparisons of clinical symptoms in biomarker-confirmed Alzheimer's disease, dementia with Lewy bodies, and frontotemporal dementia patients in a local memory clinic.当地记忆诊所中生物标志物确诊的阿尔茨海默病、路易体痴呆和额颞叶痴呆患者临床症状的比较。
Psychogeriatrics. 2015 Dec;15(4):235-41. doi: 10.1111/psyg.12103. Epub 2014 Dec 23.
10
A Combination of Neurofilament Light, Glial Fibrillary Acidic Protein, and Neuronal Pentraxin-2 Discriminates Between Frontotemporal Dementia and Other Dementias.神经丝轻链、神经胶质纤维酸性蛋白和神经元五聚素-2 的联合检测可区分额颞叶痴呆和其他类型痴呆。
J Alzheimers Dis. 2022;90(1):363-380. doi: 10.3233/JAD-220318.

本文引用的文献

1
Frontotemporal dementia: Past, present, and future.额颞叶痴呆:过去、现在与未来。
Alzheimers Dement. 2023 Nov;19(11):5253-5263. doi: 10.1002/alz.13363. Epub 2023 Jun 28.
2
Microglia-mediated T cell infiltration drives neurodegeneration in tauopathy.小胶质细胞介导的 T 细胞浸润驱动神经退行性变在 tau 病中。
Nature. 2023 Mar;615(7953):668-677. doi: 10.1038/s41586-023-05788-0. Epub 2023 Mar 8.
3
Microglial activation in the frontal cortex predicts cognitive decline in frontotemporal dementia.额皮质中的小胶质细胞激活可预测额颞叶痴呆的认知能力下降。
Brain. 2023 Aug 1;146(8):3221-3231. doi: 10.1093/brain/awad078.
4
Genotype-phenotype correlation in the spectrum of frontotemporal dementia-parkinsonian syndromes and advanced diagnostic approaches.额颞叶痴呆-帕金森综合征谱系中的基因型-表型相关性及先进诊断方法
Crit Rev Clin Lab Sci. 2023 May;60(3):171-188. doi: 10.1080/10408363.2022.2150833. Epub 2022 Dec 12.
5
The effects of painless nerve growth factor on human microglia polarization.无痛性神经生长因子对人小胶质细胞极化的影响。
Front Cell Neurosci. 2022 Oct 21;16:969058. doi: 10.3389/fncel.2022.969058. eCollection 2022.
6
New developments of biofluid-based biomarkers for routine diagnosis and disease trajectories in frontotemporal dementia.基于生物流体的生物标志物在额颞叶痴呆的常规诊断和疾病轨迹中的新进展。
Alzheimers Dement. 2022 Nov;18(11):2292-2307. doi: 10.1002/alz.12643. Epub 2022 Mar 2.
7
Advances and controversies in frontotemporal dementia: diagnosis, biomarkers, and therapeutic considerations.额颞叶痴呆的研究进展与争议:诊断、生物标志物和治疗考虑。
Lancet Neurol. 2022 Mar;21(3):258-272. doi: 10.1016/S1474-4422(21)00341-0.
8
proNGF Measurement in Cerebrospinal Fluid Samples of a Large Cohort of Living Patients With Alzheimer's Disease by a New Automated Immunoassay.采用新型自动化免疫测定法对大量在世阿尔茨海默病患者脑脊液样本中的前神经生长因子(proNGF)进行检测。
Front Aging Neurosci. 2021 Oct 27;13:741414. doi: 10.3389/fnagi.2021.741414. eCollection 2021.
9
Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here?阿尔茨海默病中的神经炎症和小胶质细胞激活:我们的路在何方?
Nat Rev Neurol. 2021 Mar;17(3):157-172. doi: 10.1038/s41582-020-00435-y. Epub 2020 Dec 14.
10
Nerve growth factor (NGF) pathway biomarkers in Down syndrome prior to and after the onset of clinical Alzheimer's disease: A paired CSF and plasma study.唐氏综合征患者在出现临床阿尔茨海默病前后的神经生长因子(NGF)通路生物标志物:一项配对的 CSF 和血浆研究。
Alzheimers Dement. 2021 Apr;17(4):605-617. doi: 10.1002/alz.12229. Epub 2020 Nov 23.