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阿尔茨海默病的特定蛋白质生物标志物模式:诊断方法正在改进。

Specific protein biomarker patterns for Alzheimer's disease: improved diagnostics in progress.

作者信息

Gozes Illana

机构信息

The Lily and Avraham Gildor Chair for the Investigation of Growth Factors, Elton Laboratory for Neuroendocrinology, Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Adams Super Center for Brain Studies and Sagol School of Neuroscience, Tel Aviv University, 69978 Tel Aviv, Israel.

出版信息

EPMA J. 2017 Sep 4;8(3):255-259. doi: 10.1007/s13167-017-0110-x. eCollection 2017 Sep.

DOI:10.1007/s13167-017-0110-x
PMID:29021836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5607150/
Abstract

This short review looks at Alzheimer's disease (AD) diagnosis through my own point of view, going from imaging through cerebrospinal fluid to blood proteins. Over the last couple of years, we have published two papers targeted at Alzheimer's diagnosis. In one paper, we took an approach of selecting a specific target, namely, activity-dependent neuroprotective protein (ADNP), and our results tightened the association of ADNP blood expression with intelligence. In another paper, we took an unbiased approach of analysis of all genes expressed in lymphoblastoid cells lines and discovered changes in expression of the regulator of G-protein signaling 2 (RGS2) as a potential AD predictor. This review will assess our data in comparison to selected independent studies focusing on blood protein biomarkers as well as assessing saliva and urine samples with potential predictive value for AD. Furthermore, the review will provide directions for a combination of innovative markers, stratifying the population toward disease prevention and personalized medicine.

摘要

这篇简短的综述从我的视角审视了阿尔茨海默病(AD)的诊断,涵盖了从影像学检查到脑脊液分析再到血液蛋白检测的各个方面。在过去几年里,我们发表了两篇针对阿尔茨海默病诊断的论文。在其中一篇论文中,我们采用了选择特定靶点的方法,即活性依赖的神经保护蛋白(ADNP),我们的研究结果进一步强化了ADNP血液表达与智力之间的关联。在另一篇论文中,我们采用了对淋巴母细胞系中所有表达基因进行无偏分析的方法,并发现G蛋白信号调节因子2(RGS2)的表达变化可作为AD的潜在预测指标。本综述将把我们的数据与其他一些专注于血液蛋白生物标志物的独立研究进行比较,同时评估唾液和尿液样本对AD的潜在预测价值。此外,本综述还将为创新标志物的组合提供指导方向,以便对人群进行分层,实现疾病预防和个性化医疗。

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本文引用的文献

1
Self-reported traumatic brain injury and in vivo measure of AD-vulnerable cortical thickness and AD-related biomarkers in the ADNI cohort.阿尔茨海默病神经影像学计划(ADNI)队列中自我报告的创伤性脑损伤以及AD易损皮质厚度和AD相关生物标志物的活体测量。
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Early diagnosis of mild cognitive impairment and Alzheimer's disease based on salivary lactoferrin.基于唾液乳铁蛋白的轻度认知障碍和阿尔茨海默病的早期诊断
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Genome-wide association and interaction studies of CSF T-tau/Aβ ratio in ADNI cohort.ADNI队列中脑脊液T-tau/Aβ比值的全基因组关联和相互作用研究。
Neurobiol Aging. 2017 Sep;57:247.e1-247.e8. doi: 10.1016/j.neurobiolaging.2017.05.007. Epub 2017 May 15.
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The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings.未确诊的阿尔茨海默病八年半历程:基因测序与先进基因检测的资金支持带来了希望和新的开端。
Front Endocrinol (Lausanne). 2017 May 19;8:107. doi: 10.3389/fendo.2017.00107. eCollection 2017.
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Cadmium and Alzheimer's disease mortality in U.S. adults: Updated evidence with a urinary biomarker and extended follow-up time.美国成年人中镉与阿尔茨海默病死亡率:基于尿生物标志物及延长随访时间的最新证据
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6
Longitudinal changes of tau PET imaging in relation to hypometabolism in prodromal and Alzheimer's disease dementia.tau PET 显像与前驱期和阿尔茨海默病痴呆代谢减退的关系的纵向变化。
Mol Psychiatry. 2018 Jul;23(7):1666-1673. doi: 10.1038/mp.2017.108. Epub 2017 May 16.
7
Diagnostic Biomarkers of Alzheimer's Disease as Identified in Saliva using 1H NMR-Based Metabolomics.基于1H NMR代谢组学在唾液中鉴定出的阿尔茨海默病诊断生物标志物
J Alzheimers Dis. 2017;58(2):355-359. doi: 10.3233/JAD-161226.
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Monoamine oxidase B inhibitor, selegiline, reduces F-THK5351 uptake in the human brain.单胺氧化酶B抑制剂司来吉兰可降低人脑中F-THK5351的摄取。
Alzheimers Res Ther. 2017 Mar 31;9(1):25. doi: 10.1186/s13195-017-0253-y.
9
Can Salivary Acetylcholinesterase be a Diagnostic Biomarker for Alzheimer?唾液乙酰胆碱酯酶能否作为阿尔茨海默病的诊断生物标志物?
J Clin Diagn Res. 2017 Jan;11(1):ZC58-ZC60. doi: 10.7860/JCDR/2017/21715.9192. Epub 2017 Jan 1.
10
Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children.认知/运动发育迟缓的ADNP基因突变儿童乳牙过早萌出。
Transl Psychiatry. 2017 Feb 21;7(2):e1043. doi: 10.1038/tp.2017.27.