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帕金森病和痴呆生物标志物的当前和未来临床应用:它们能帮助我们攻克疾病吗?

Current and future clinical utilities of Parkinson's disease and dementia biomarkers: can they help us conquer the disease?

机构信息

PCND Neuroscience Research Institute , Poway , CA , USA.

Tokyo Metropolitan Institute of Medical Science , Tokyo , Japan.

出版信息

Expert Rev Neurother. 2019 Nov;19(11):1149-1161. doi: 10.1080/14737175.2019.1649141. Epub 2019 Aug 9.

DOI:10.1080/14737175.2019.1649141
PMID:31359797
Abstract

: Biomarkers for Parkinson's disease and Alzheimer's disease are essential, not only for disease detection, but also provide insight into potential disease relationships leading to better detection and therapy. As metabolic disease is known to increase neurodegeneration risk, such mechanisms may reveal such novel targets for PD and AD. Moreover, metabolic disease, including insulin resistance, offer novel biomarker and therapeutic targets for neurodegeneration, including glucagon-like-peptide-1, dipeptidyl peptidase-4 and adiponectin. : The authors reviewed PubMed-listed research articles, including ours, on a number of putative PD, AD and neurodegenerative disease targets of interest, focusing on the relevance of metabolic syndrome and insulin resistance mechanisms, especially type II diabetes, to PD and AD. We highlighted various issues surrounding the current state of knowledge and propose avenues for future development. : Biomarkers for PD and AD are indispensable for disease diagnosis, prognostication and tracking disease severity, especially for clinical therapy trials. Although no validated PD biomarkers exist, their potential utility has generated tremendous interest. Combining insulin-resistance biomarkers with other core biomarkers or using them to predict non-motor symptoms of PD may be clinically useful. Collectively, although still unclear, potential biomarkers and therapies can aid in shedding new light on novel aspects of both PD and AD.

摘要

帕金森病和阿尔茨海默病的生物标志物不仅对于疾病的检测至关重要,而且还可以深入了解潜在的疾病关系,从而实现更好的检测和治疗。由于代谢性疾病已知会增加神经退行性疾病的风险,因此这些机制可能为 PD 和 AD 揭示新的靶标。此外,代谢性疾病(包括胰岛素抵抗)为神经退行性疾病提供了新的生物标志物和治疗靶标,包括胰高血糖素样肽-1、二肽基肽酶-4 和脂联素。

作者综述了包括我们的研究在内的一些关于 PD、AD 和神经退行性疾病的潜在靶点的文献,重点关注代谢综合征和胰岛素抵抗机制,特别是 2 型糖尿病与 PD 和 AD 的相关性。我们强调了当前知识状态的各种问题,并提出了未来发展的途径。

PD 和 AD 的生物标志物对于疾病的诊断、预后和跟踪疾病的严重程度是不可或缺的,尤其是对于临床治疗试验。尽管目前还没有经过验证的 PD 生物标志物,但它们的潜在应用价值引起了极大的兴趣。将胰岛素抵抗生物标志物与其他核心生物标志物结合使用,或者用它们来预测 PD 的非运动症状,可能具有临床应用价值。总的来说,尽管还不清楚,但潜在的生物标志物和治疗方法可以帮助我们深入了解 PD 和 AD 的新方面。

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Front Endocrinol (Lausanne). 2020 Mar 4;11:108. doi: 10.3389/fendo.2020.00108. eCollection 2020.