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帕金森病患者体液中的脑-生物标志物变化。

Brain-Biomarker Changes in Body Fluids of Patients with Parkinson's Disease.

机构信息

Department of Biomedical Sciences, University of Cagliari, 09042 Monserrato, Italy.

出版信息

Int J Mol Sci. 2023 Jun 30;24(13):10932. doi: 10.3390/ijms241310932.

Abstract

Parkinson's disease (PD) is an incurable neurodegenerative disease that is rarely diagnosed at an early stage. Although the understanding of PD-related mechanisms has greatly improved over the last decade, the diagnosis of PD is still based on neurological examination through the identification of motor symptoms, including bradykinesia, rigidity, postural instability, and resting tremor. The early phase of PD is characterized by subtle symptoms with a misdiagnosis rate of approximately 16-20%. The difficulty in recognizing early PD has implications for the potential use of novel therapeutic approaches. For this reason, it is important to discover PD brain biomarkers that can indicate early dopaminergic dysfunction through their changes in body fluids, such as saliva, urine, blood, or cerebrospinal fluid (CSF). For the CFS-based test, the invasiveness of sampling is a major limitation, whereas the other body fluids are easier to obtain and could also allow population screening. Following the identification of the crucial role of alpha-synuclein (α-syn) in the pathology of PD, a very large number of studies have summarized its changes in body fluids. However, methodological problems have led to the poor diagnostic/prognostic value of this protein and alternative biomarkers are currently being investigated. The aim of this paper is therefore to summarize studies on protein biomarkers that are alternatives to α-syn, particularly those that change in nigrostriatal areas and in biofluids, with a focus on blood, and, eventually, saliva and urine.

摘要

帕金森病(PD)是一种无法治愈的神经退行性疾病,很少在早期被诊断出来。尽管过去十年对 PD 相关机制的理解有了很大的提高,但 PD 的诊断仍然基于通过识别运动症状(包括运动迟缓、僵硬、姿势不稳和静止性震颤)进行的神经学检查。PD 的早期阶段以微妙的症状为特征,误诊率约为 16-20%。早期 PD 的识别困难对潜在的新型治疗方法的应用具有重要意义。因此,发现可以通过其在体液(如唾液、尿液、血液或脑脊液(CSF)中的变化来指示早期多巴胺能功能障碍的 PD 脑生物标志物非常重要。对于基于 CSF 的测试,采样的侵入性是一个主要限制,而其他体液更容易获得,也可以进行人群筛查。在确定α-突触核蛋白(α-syn)在 PD 病理中的关键作用后,大量研究总结了其在体液中的变化。然而,方法学问题导致该蛋白的诊断/预后价值不佳,目前正在研究替代生物标志物。因此,本文的目的是总结替代 α-syn 的蛋白生物标志物的研究,特别是那些在黑质纹状体区域和生物体液中发生变化的标志物,重点是血液,最终是唾液和尿液。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef64/10341952/9aef998c65f0/ijms-24-10932-g001.jpg

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