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本文引用的文献

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Alzheimer Disease as a Clinical-Biological Construct-An International Working Group Recommendation.作为一种临床生物学概念的阿尔茨海默病——国际工作组建议
JAMA Neurol. 2024 Dec 1;81(12):1304-1311. doi: 10.1001/jamaneurol.2024.3770.
2
Influence of Different Diagnostic Criteria on Alzheimer Disease Clinical Research.不同诊断标准对阿尔茨海默病临床研究的影响。
Neurology. 2024 Sep 10;103(5):e209753. doi: 10.1212/WNL.0000000000209753. Epub 2024 Aug 21.
3
Revised criteria for diagnosis and staging of Alzheimer's disease: Alzheimer's Association Workgroup.修订的阿尔茨海默病诊断和分期标准:阿尔茨海默病协会工作组。
Alzheimers Dement. 2024 Aug;20(8):5143-5169. doi: 10.1002/alz.13859. Epub 2024 Jun 27.
4
Diagnosing Preclinical and Prodromal Neurodegenerative Diseases-The Clinical Is Political.诊断临床前和前驱神经退行性疾病——临床即政治。
JAMA Neurol. 2024 May 1;81(5):439-440. doi: 10.1001/jamaneurol.2023.5684.
5
European intersocietal recommendations for the biomarker-based diagnosis of neurocognitive disorders.基于生物标志物的神经认知障碍诊断的欧洲协会间推荐意见。
Lancet Neurol. 2024 Mar;23(3):302-312. doi: 10.1016/S1474-4422(23)00447-7.
6
Biological variation estimates of Alzheimer's disease plasma biomarkers in healthy individuals.健康个体阿尔茨海默病血浆生物标志物的生物学变异估计。
Alzheimers Dement. 2024 Feb;20(2):1284-1297. doi: 10.1002/alz.13518. Epub 2023 Nov 20.
7
Prevalence and Clinical Implications of a β-Amyloid-Negative, Tau-Positive Cerebrospinal Fluid Biomarker Profile in Alzheimer Disease.阿尔茨海默病中β淀粉样蛋白阴性、tau蛋白阳性脑脊液生物标志物谱的患病率及临床意义
JAMA Neurol. 2023 Jul 31;80(9):969-79. doi: 10.1001/jamaneurol.2023.2338.
8
Analysis of Psychological Symptoms Following Disclosure of Amyloid-Positron Emission Tomography Imaging Results to Adults With Subjective Cognitive Decline.主观认知下降成人接受淀粉样蛋白正电子发射断层扫描成像结果披露后的心理症状分析。
JAMA Netw Open. 2023 Jan 3;6(1):e2250921. doi: 10.1001/jamanetworkopen.2022.50921.
9
Climate Change, Carbon Dioxide Emissions, and Medical Imaging Contribution.气候变化、二氧化碳排放与医学成像贡献
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10
Subjective Cognitive Decline Is Associated with Health-Related Quality of Life in the Middle-Aged to Elderly Population.主观认知衰退与中老年人群健康相关生活质量有关。
J Alzheimers Dis. 2023;91(1):427-436. doi: 10.3233/JAD-220659.

神经认知障碍中基于生物标志物的诊断:临床医生对还原论风险的看法

Biomarker-Driven Diagnosis in Neurocognitive Disorders: A Clinician's Perspective on the Risks of Reductionism.

作者信息

Cabreira Verónica Alheia, Isaacs Jeremy D

机构信息

Centre for Clinical Brain Sciences, University of Edinburgh, United Kingdom.

Department of Clinical Neurosciences, University of Porto, Portugal.

出版信息

Neurol Clin Pract. 2025 Jun;15(3):e200481. doi: 10.1212/CPJ.0000000000200481. Epub 2025 May 2.

DOI:10.1212/CPJ.0000000000200481
PMID:40336928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12054741/
Abstract

The recently published Alzheimer's Association Workgroup diagnostic criteria for Alzheimer disease and consensus-based workflows for the use of diagnostic biomarkers in neurocognitive disorders promote further normalization of purely biological approaches to neurocognitive disorders. In this commentary, we reflect on the dangers of biological reductionist positions lacking solid scientific evidence and proven cost-effectiveness benefits, in particular its inability to offer a meaningful formulation for the large number of people with functional cognitive disorders. This, alongside the current lack of standardization, limited accuracy, and environmental consequences, means that the normalization of biomarkers as standard-of-care tests in all neurocognitive presentations does not represent responsible innovation. We emphasize the need for pluralism when considering technological developments, such that clinical judgment and biopsychosocial formulation continue to be accepted as a sound foundation for cognitive assessment.

摘要

阿尔茨海默病协会工作组最近发布的阿尔茨海默病诊断标准以及基于共识的神经认知障碍诊断生物标志物使用工作流程,推动了神经认知障碍纯生物学方法的进一步规范化。在这篇评论中,我们反思了缺乏坚实科学证据和已证实成本效益优势的生物还原论立场的危险性,特别是其无法为大量功能性认知障碍患者提供有意义的表述。这一点,再加上目前缺乏标准化、准确性有限以及环境影响,意味着将生物标志物作为所有神经认知表现的标准护理测试进行规范化并不代表负责任的创新。我们强调在考虑技术发展时需要多元化,以便临床判断和生物心理社会表述继续被视为认知评估的坚实基础。