• 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

利用指尖血进行分子基因表达测试,以高精度识别阿尔茨海默病。

Molecular Gene Expression Testing to Identify Alzheimer's Disease with High Accuracy from Fingerstick Blood.

机构信息

BioSpyder Technologies, Inc., Carlsbad, CA, USA.

Neurology Center of Southern California, Carlsbad, CA, USA.

出版信息

J Alzheimers Dis. 2024;101(3):813-822. doi: 10.3233/JAD-240174.

DOI:10.3233/JAD-240174
PMID:39269833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11492108/
Abstract

BACKGROUND

There is no molecular test for Alzheimer's disease (AD) using self-collected samples, nor is there a definitive molecular test for AD. We demonstrate an accurate and potentially definitive TempO-Seq® gene expression test for AD using fingerstick blood spotted and dried on filter paper, a sample that can be collected in any doctor's office or can be self-collected.

OBJECTIVE

Demonstrate the feasibility of developing an accurate test for the classification of persons with AD from a minimally invasive sample of fingerstick blood spotted on filter paper which can be obtained in any doctor's office or self-collected to address health disparities.

METHODS

Fingerstick blood samples from patients clinically diagnosed with AD, Parkinson's disease (PD), or asymptomatic controls were spotted onto filter paper in the doctor's office, dried, and shipped to BioSpyder for testing. Three independent patient cohorts were used for training/retraining and testing/retesting AD and PD classification algorithms.

RESULTS

After initially identifying a 770 gene classification signature, a minimum set of 68 genes was identified providing classification test areas under the ROC curve of 0.9 for classifying patients as having AD, and 0.94 for classifying patients as having PD.

CONCLUSIONS

These data demonstrate the potential to develop a screening and/or definitive, minimally invasive, molecular diagnostic test for AD and PD using dried fingerstick blood spot samples that are collected in a doctor's office or clinic, or self-collected, and thus, can address health disparities. Whether the test can classify patients with AD earlier then possible with cognitive testing remains to be determined.

摘要

背景

目前尚无使用自采样本的阿尔茨海默病(AD)分子检测方法,也没有明确的 AD 分子检测方法。我们通过使用指尖血斑和滤纸干燥的方法,证明了 TempO-Seq® 基因表达检测方法对 AD 的准确性和潜在确定性,这种方法可以在任何医生的办公室或自行采集样本进行采集。

目的

证明从手指血斑的微创样本中开发 AD 分类的准确测试的可行性,这种样本可以在任何医生的办公室或自行采集,以解决健康差异问题。

方法

在医生办公室中,将来自临床诊断为 AD、帕金森病(PD)或无症状对照者的指尖血样斑点在滤纸上,干燥并运送到 BioSpyder 进行检测。三个独立的患者队列用于 AD 和 PD 分类算法的培训/再培训和测试/再测试。

结果

最初确定了 770 个基因分类特征后,确定了一组最小的 68 个基因,提供了分类测试区域,ROC 曲线下面积为 0.9,用于将患者分类为 AD,为 0.94,用于将患者分类为 PD。

结论

这些数据表明,有可能使用在医生办公室或诊所采集的干燥指尖血斑样本,或自行采集的样本,开发用于 AD 和 PD 的筛查和/或明确的微创分子诊断测试,从而解决健康差异问题。该测试是否能够比认知测试更早地对 AD 患者进行分类还有待确定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/afe5a49c323f/jad-101-jad240174-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/ce5b4d3f1889/jad-101-jad240174-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/b91e51bb3a01/jad-101-jad240174-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/a0a2681ae86c/jad-101-jad240174-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/d9ee0ca136f7/jad-101-jad240174-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/d2b796488d4a/jad-101-jad240174-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/afe5a49c323f/jad-101-jad240174-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/ce5b4d3f1889/jad-101-jad240174-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/b91e51bb3a01/jad-101-jad240174-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/a0a2681ae86c/jad-101-jad240174-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/d9ee0ca136f7/jad-101-jad240174-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/d2b796488d4a/jad-101-jad240174-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5dd/11492108/afe5a49c323f/jad-101-jad240174-g006.jpg

相似文献

1
Molecular Gene Expression Testing to Identify Alzheimer's Disease with High Accuracy from Fingerstick Blood.利用指尖血进行分子基因表达测试,以高精度识别阿尔茨海默病。
J Alzheimers Dis. 2024;101(3):813-822. doi: 10.3233/JAD-240174.
2
Apolipoprotein E4 serum concentration for increased sensitivity and specificity of diagnosis of drug treated Alzheimer's disease patients vs. drug treated parkinson's disease patients vs. age-matched normal controls.载脂蛋白 E4 血清浓度可提高药物治疗的阿尔茨海默病患者与药物治疗的帕金森病患者以及年龄匹配的正常对照者诊断的灵敏度和特异性。
Curr Alzheimer Res. 2012 Dec;9(10):1149-67. doi: 10.2174/156720512804142868.
3
Multivariate analyses of peripheral blood leukocyte transcripts distinguish Alzheimer's, Parkinson's, control, and those at risk for developing Alzheimer's.
Neurobiol Aging. 2017 Oct;58:225-237. doi: 10.1016/j.neurobiolaging.2017.05.012. Epub 2017 Jun 20.
4
A molecular signature in blood identifies early Parkinson's disease.血液中的分子特征可识别早期帕金森病。
Mol Neurodegener. 2012 May 31;7:26. doi: 10.1186/1750-1326-7-26.
5
A gene expression pattern in blood for the early detection of Alzheimer's disease.用于阿尔茨海默病早期检测的血液基因表达模式。
J Alzheimers Dis. 2011;23(1):109-19. doi: 10.3233/JAD-2010-101518.
6
An investigation of microRNA-103 and microRNA-107 as potential blood-based biomarkers for disease risk and progression of Alzheimer's disease.探讨 microRNA-103 和 microRNA-107 作为阿尔茨海默病疾病风险和进展的潜在血液生物标志物。
J Clin Lab Anal. 2020 Jan;34(1):e23006. doi: 10.1002/jcla.23006. Epub 2019 Aug 16.
7
Circulatory miR-223-3p Discriminates Between Parkinson's and Alzheimer's Patients.循环 miR-223-3p 可区分帕金森病和阿尔茨海默病患者。
Sci Rep. 2019 Jun 28;9(1):9393. doi: 10.1038/s41598-019-45687-x.
8
Parkinson's and Alzheimer's diseases in Costa Rica: a feasibility study toward a national screening program.哥斯达黎加的帕金森病和阿尔茨海默病:一项全国性筛查计划的可行性研究。
Glob Health Action. 2013 Dec 27;6:23061. doi: 10.3402/gha.v6i0.23061.
9
Ultrasensitive detection of blood biomarkers of Alzheimer's and Parkinson's diseases: a systematic review.阿尔茨海默病和帕金森病血液生物标志物的超灵敏检测:一项系统综述
Biomark Med. 2021 Dec;15(17):1693-1708. doi: 10.2217/bmm-2021-0219. Epub 2021 Nov 8.
10
CYP2D6 gene polymorphism as a probable risk factor for Alzheimer's disease and Parkinson's disease with dementia.细胞色素P450 2D6基因多态性作为阿尔茨海默病和帕金森病伴痴呆症的潜在危险因素。
Neurol Neurochir Pol. 2007 Mar-Apr;41(2):113-21.

引用本文的文献

1
Identification of HIBCH and MGME1 as Mitochondrial Dynamics-Related Biomarkers in Alzheimer's Disease Via Integrated Bioinformatics Analysis.通过综合生物信息学分析鉴定HIBCH和MGME1作为阿尔茨海默病中线粒体动力学相关生物标志物
IET Syst Biol. 2025 Jan-Dec;19(1):e70018. doi: 10.1049/syb2.70018.

本文引用的文献

1
Differential diagnostic performance of a panel of plasma biomarkers for different types of dementia.一组血浆生物标志物对不同类型痴呆的鉴别诊断性能。
Alzheimers Dement (Amst). 2022 May 15;14(1):e12285. doi: 10.1002/dad2.12285. eCollection 2022.
2
2022 Alzheimer's disease facts and figures.2022 年阿尔茨海默病事实和数据。
Alzheimers Dement. 2022 Apr;18(4):700-789. doi: 10.1002/alz.12638. Epub 2022 Mar 14.
3
Whole Blood Expression Pattern of Inflammation and Redox Genes in Mild Alzheimer's Disease.轻度阿尔茨海默病中炎症和氧化还原基因的全血表达模式
J Inflamm Res. 2021 Nov 20;14:6085-6102. doi: 10.2147/JIR.S334337. eCollection 2021.
4
Performance of Plasma Amyloid β, Total Tau, and Neurofilament Light Chain in the Identification of Probable Alzheimer's Disease in South China.血浆淀粉样蛋白β、总tau蛋白和神经丝轻链在华南地区疑似阿尔茨海默病诊断中的性能
Front Aging Neurosci. 2021 Oct 27;13:749649. doi: 10.3389/fnagi.2021.749649. eCollection 2021.
5
Validation of the LUMIPULSE automated immunoassay for the measurement of core AD biomarkers in cerebrospinal fluid.验证 LUMIPULSE 自动化免疫分析系统在脑脊液中核心 AD 生物标志物测量中的应用。
Clin Chem Lab Med. 2021 Nov 15;60(2):207-219. doi: 10.1515/cclm-2021-0651. Print 2022 Jan 27.
6
DNA Methylation and Expression Profiles of Whole Blood in Parkinson's Disease.帕金森病全血的DNA甲基化与表达谱
Front Genet. 2021 Apr 26;12:640266. doi: 10.3389/fgene.2021.640266. eCollection 2021.
7
Clinical diagnosis of Alzheimer's disease: recommendations of the International Working Group.阿尔茨海默病的临床诊断:国际工作组的建议。
Lancet Neurol. 2021 Jun;20(6):484-496. doi: 10.1016/S1474-4422(21)00066-1. Epub 2021 Apr 29.
8
A Shortage of Neurologists - We Must Act Now: A Report From the AAN 2019 Transforming Leaders Program.神经科医生短缺——我们必须立即行动:美国神经病学学会2019年转型领导者计划报告
Neurology. 2021 Jun 14;96(24):1122-1134. doi: 10.1212/WNL.0000000000012111.
9
Geographic Variation in Neurologist Density and Neurologic Care in the United States.美国神经科医生密度与神经科医疗的地域差异。
Neurology. 2021 Jan 19;96(3):e309-e321. doi: 10.1212/WNL.0000000000011276. Epub 2020 Dec 23.
10
Identification of potential blood biomarkers for early diagnosis of Alzheimer's disease through RNA sequencing analysis.通过 RNA 测序分析鉴定阿尔茨海默病早期诊断的潜在血液生物标志物。
Alzheimers Res Ther. 2020 Jul 16;12(1):87. doi: 10.1186/s13195-020-00654-x.