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联合唾液α-突触核蛋白种作为帕金森病的诊断生物标志物。

Combined measure of salivary alpha-synuclein species as diagnostic biomarker for Parkinson's disease.

机构信息

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

CNR Institute of Translational Pharmacology, Unit of Cagliari, Cagliari, Italy.

出版信息

J Neurol. 2023 Nov;270(11):5613-5621. doi: 10.1007/s00415-023-11893-x. Epub 2023 Aug 8.

Abstract

Parkinson's disease (PD) diagnosis is still vulnerable to bias, and a definitive diagnosis often relies on post-mortem neuropathological diagnosis. In this regard, alpha-synuclein (αsyn)-specific in vivo biomarkers remain a critical unmet need, based on its relevance in the neuropathology. Specifically, content changes in αsyn species such as total (tot-αsyn), oligomeric (o-αsyn), and phosphorylated (p-αsyn) within the cerebrospinal fluid (CSF) and peripheral fluids (i.e., blood and saliva) have been proposed as PD biomarkers possibly reflecting the neuropathological outcome. Here, we measured the p-αsyn levels in the saliva from 15 PD patients along with tot-αsyn, o-αsyn and their ratios, and compared the results with those from 23 healthy subjects (HS), matched per age and sex. We also calculated the optimal cutoff values for different αsyn species to provide information about their capability to discriminate PD from HS. We found that p-αsyn was the most abundant alpha-synuclein species in the saliva. While p-αsyn concentration did not differ between PD and HS when adjusted for total salivary proteins, the ratio p-αsyn/tot-αsyn was largely lower in PD patients than in HS. Moreover, the concentration of o-αsyn was increased in the saliva of PD patients, and tot-αsyn did not differ between PD and HS. The ROC curves indicated that no single αsyn form or ratio could provide an accurate diagnosis of PD. On the other hand, the ratio of different items, namely p-αsyn/tot-αsyn and o-αsyn, yielded more satisfactory diagnostic accuracy, suggesting that the combined measure of different species in the saliva may show more promises as a diagnostic means for PD.

摘要

帕金森病(PD)的诊断仍然容易受到影响,明确的诊断通常依赖于死后神经病理学诊断。在这方面,基于其在神经病理学中的相关性,α-突触核蛋白(αsyn)特异性的体内生物标志物仍然是一个关键的未满足需求。具体而言,脑脊液(CSF)和外周液(即血液和唾液)中αsyn 种的含量变化,如总(tot-αsyn)、寡聚体(o-αsyn)和磷酸化(p-αsyn),已被提出作为 PD 生物标志物,可能反映神经病理学结果。在这里,我们测量了 15 名 PD 患者和 23 名健康对照者(HS)唾液中的 p-αsyn 水平以及 tot-αsyn、o-αsyn 及其比值,并将结果与 HS 进行了比较。我们还计算了不同 αsyn 物种的最佳截断值,以提供有关其区分 PD 与 HS 的能力的信息。我们发现 p-αsyn 是唾液中最丰富的α-突触核蛋白。虽然在调整总唾液蛋白后,PD 和 HS 之间的 p-αsyn 浓度没有差异,但 PD 患者的 p-αsyn/tot-αsyn 比值明显低于 HS。此外,PD 患者唾液中 o-αsyn 的浓度增加,而 tot-αsyn 在 PD 和 HS 之间没有差异。ROC 曲线表明,没有单一的 αsyn 形式或比值可以提供 PD 的准确诊断。另一方面,不同项目的比值,即 p-αsyn/tot-αsyn 和 o-αsyn,可提供更令人满意的诊断准确性,表明唾液中不同种的联合测量可能更有希望作为 PD 的诊断手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba80/10576686/c041d0d9ee8f/415_2023_11893_Fig1_HTML.jpg

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