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

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-06-01 Epub Date: 2025-05-02 DOI:10.1212/CPJ.0000000000200481
Verónica Alheia Cabreira, Jeremy D Isaacs
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引用次数: 0

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.

神经认知障碍的生物标志物驱动诊断:一个临床医生对还原论风险的看法。
最近发布的阿尔茨海默病协会工作组阿尔茨海默病诊断标准和基于共识的神经认知障碍诊断生物标志物使用工作流程促进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,我们反思了缺乏可靠的科学证据和经证实的成本效益效益的生物还原论立场的危险,特别是它无法为大量功能性认知障碍患者提供有意义的方案。这一点,再加上目前缺乏标准化、准确性有限和环境后果,意味着生物标志物作为所有神经认知表现的标准治疗测试的正常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公式继续被接受为认知评估的健全基础。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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