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1
Plasma and CSF biomarkers in a memory clinic: Head-to-head comparison of phosphorylated tau immunoassays.在记忆诊所中进行的血浆和脑脊液生物标志物检测:磷酸化tau 免疫分析的头对头比较。
Alzheimers Dement. 2023 May;19(5):1913-1924. doi: 10.1002/alz.12841. Epub 2022 Nov 12.
2
Head-to-head comparison of 10 plasma phospho-tau assays in prodromal Alzheimer's disease.在阿尔茨海默病前驱期,对 10 种血浆磷酸化 tau 检测方法进行头对头比较。
Brain. 2023 Apr 19;146(4):1592-1601. doi: 10.1093/brain/awac333.
3
Plasma p-tau231 and p-tau217 as state markers of amyloid-β pathology in preclinical Alzheimer's disease.血浆 p-tau231 和 p-tau217 作为临床前阿尔茨海默病淀粉样β病理的状态标志物。
Nat Med. 2022 Sep;28(9):1797-1801. doi: 10.1038/s41591-022-01925-w. Epub 2022 Aug 11.
4
The Alzheimer's Association appropriate use recommendations for blood biomarkers in Alzheimer's disease.阿尔茨海默病协会关于阿尔茨海默病血液生物标志物的合理使用建议。
Alzheimers Dement. 2022 Dec;18(12):2669-2686. doi: 10.1002/alz.12756. Epub 2022 Jul 31.
5
Hepatic and renal function impact concentrations of plasma biomarkers of neuropathology.肝脏和肾脏功能会影响神经病理学血浆生物标志物的浓度。
Alzheimers Dement (Amst). 2022 Jul 12;14(1):e12321. doi: 10.1002/dad2.12321. eCollection 2022.
6
Performance of plasma phosphorylated tau 181 and 217 in the community.社区人群中血浆磷酸化 tau181 和 tau217 的检测性能。
Nat Med. 2022 Jul;28(7):1398-1405. doi: 10.1038/s41591-022-01822-2. Epub 2022 May 26.
7
Two Randomized Phase 3 Studies of Aducanumab in Early Alzheimer's Disease.两项早期阿尔茨海默病中阿杜卡努单抗的随机 3 期研究。
J Prev Alzheimers Dis. 2022;9(2):197-210. doi: 10.14283/jpad.2022.30.
8
Effect of Race on Prediction of Brain Amyloidosis by Plasma Aβ42/Aβ40, Phosphorylated Tau, and Neurofilament Light.血浆 Aβ42/Aβ40、磷酸化 tau 和神经丝轻链对脑淀粉样变预测的种族影响。
Neurology. 2022 Jul 19;99(3):e245-e257. doi: 10.1212/WNL.0000000000200358. Epub 2022 Apr 21.
9
Serum Beta-Synuclein Is Higher in Down Syndrome and Precedes Rise of pTau181.血清β-突触核蛋白在唐氏综合征中升高,并先于 pTau181 的升高。
Ann Neurol. 2022 Jul;92(1):6-10. doi: 10.1002/ana.26360. Epub 2022 Apr 12.
10
The accuracy and robustness of plasma biomarker models for amyloid PET positivity.血浆生物标志物模型对淀粉样 PET 阳性的准确性和稳健性。
Alzheimers Res Ther. 2022 Feb 7;14(1):26. doi: 10.1186/s13195-021-00942-0.

神经退行性疾病中的血液生物标志物:对临床神经科医生的影响。

Blood Biomarkers in Neurodegenerative Diseases: Implications for the Clinical Neurologist.

机构信息

From the Sant Pau Memory Unit (D.A., A.L.), Department of Neurology, Hospital de la Santa Creu i Sant Pau, IIB SANT PAU, Universitat Autònoma de Barcelona; Centro de Investigación Biomédica en Red en Enfermedades Neurodegenerativas (D.A., A.L.), CIBERNED, Madrid, Spain; Department of Psychiatry (M.S.B.), Icahn School of Medicine at Mount Sinai, New York, NY; The Joseph Sagol Neuroscience (M.S.B., R.C.G.), Center Sheba Medical Center, Tel-Hashomer, Israel; and Department of Neurology (J.C.R.), Weill Institute for Neurosciences, UCSF Memory and Aging Center, San Francisco, CA.

出版信息

Neurology. 2023 Jul 25;101(4):172-180. doi: 10.1212/WNL.0000000000207193. Epub 2023 Mar 6.

DOI:10.1212/WNL.0000000000207193
PMID:36878698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10435056/
Abstract

Blood-based biomarkers offer a major advance in the clinical evaluation of neurodegenerative diseases. Currently, research studies have reported robust assays of blood markers for the detection of amyloid and tau pathologies specific to Alzheimer disease (amyloid-β peptides, and p-tau) and nonspecific blood markers of neuronal (neurofilament light, β-synuclein, and ubiquitin-C-terminal-hydrolase-L1) and glial degeneration (glial fibrillary acidic protein) that can measure key pathophysiologic processes in several neurodegenerative diseases. In the near future, these markers may be used for screening, diagnosis, or disease and treatment response monitoring. Blood-based biomarkers for neurodegenerative diseases have been rapidly implemented in research, and they have the potential to enter clinical use soon in different clinical settings. In this review, we will describe the main developments and their potential implications for the general neurologist.

摘要

基于血液的生物标志物在神经退行性疾病的临床评估中取得了重大进展。目前,研究报告已经发现了针对阿尔茨海默病(淀粉样β肽和 p-tau)的淀粉样蛋白和 tau 病理的血液标志物以及神经元(神经丝轻链、β-突触核蛋白和泛素 C 端水解酶 L1)和神经胶质变性(神经胶质纤维酸性蛋白)的非特异性血液标志物的可靠检测方法,这些标志物可以测量几种神经退行性疾病中的关键病理生理过程。在不久的将来,这些标志物可能用于筛选、诊断或疾病和治疗反应监测。用于神经退行性疾病的基于血液的生物标志物已经在研究中迅速实施,并且它们有可能在不同的临床环境中很快进入临床应用。在这篇综述中,我们将描述主要的进展及其对一般神经科医生的潜在影响。