评论“是时候与路易体分享老年痴呆症的生物标志物结果了”。

IF 4.4 Q1 CLINICAL NEUROLOGY
John T O'Brien
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引用次数: 0

摘要

许多患有路易体痴呆(DLB)的人有阿尔茨海默病(AD)共病理的证据,这可以使用生物标志物在体内进行评估。在本期杂志中,Armstrong及其同事认为,现在向DLB患者披露AD生物标志物结果是及时的。它们提供了合乎逻辑且有力的论据,包括人们的知情权以及这些信息在告知结果和管理方面的价值。然而,也有重要的注意事项需要考虑,并且需要保持谨慎的平衡,一方面,了解和传达临床有用信息的权利,另一方面,承认在DLB而不是AD临床病理综合征的个体中,AD生物标志物的真正诊断和管理意义存在真正的不确定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Commentary on "It is time to share Alzheimer biomarker results in dementia with Lewy bodies".

Many people with dementia with Lewy bodies (DLB) have evidence of Alzheimer's disease (AD) co-pathology, which can be assessed in vivo using biomarkers. In this issue, Armstrong and colleagues argue that it is now timely to disclose such AD biomarker results to people with DLB. They provide logical and powerful arguments, including the right for people to know and the value of this information in informing outcome and management. However, there are also important caveats to consider and a careful balance needs to be maintained between, on the one hand, the right to know and convey clinically useful information and, on the other, acknowledging the real uncertainty that exists regarding the true diagnostic and management implications of AD biomarkers in an individual with a DLB rather than an AD clinico-pathological syndrome.

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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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