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基于超高效液相色谱-串联质谱法的莱姆病神经伯氏疏螺旋体病非靶向代谢物谱分析。

UHPLC-MS/MS-based untargeted metabolite profiling of Lyme neuroborreliosis.

作者信息

Kuukkanen Ilari, Pietikäinen Annukka, Rissanen Tiia, Hurme Saija, Kortela Elisa, Kanerva Mari J, Oksi Jarmo, Hytönen Jukka, Karonen Maarit

机构信息

Department of Chemistry, University of Turku, Turku, Finland.

TBD Turku, University of Turku, Turku, Finland.

出版信息

Sci Rep. 2025 Mar 11;15(1):8442. doi: 10.1038/s41598-025-92189-0.

Abstract

The diagnosis of Lyme neuroborreliosis (LNB) requires the demonstration of intrathecal synthesis of Borrelia antibodies in a patient's cerebrospinal fluid (CSF), which involves the invasive procedure of a lumbar puncture. This study serves as a feasibility study aimed at exploring the potential of using serum samples, which are easily obtainable routine clinical samples, for LNB diagnostics via advanced metabolomics techniques. Serum samples were collected from confirmed LNB patients before and after treatment, with post-treatment samples serving as controls. The objective of the study was to find stable biomarkers for acute LNB through untargeted metabolomics analysis using ultrahigh-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). The study focused on biomarkers that could be reliably detected in serum samples stored under typical clinical conditions, without the need for special handling, ensuring consistent detection over time. The analysis revealed 26,978 molecular features (MFs), of which 1,746 were statistically significant (p < 0.001). Further manual investigation into 91 of the most prominent MFs revealed 53 potential biomarkers for LNB, individually or in combination. The workflow developed provides a comprehensive platform for biomarker detection, with potential applications in both research and clinical settings for LNB and other infections. This minimally invasive diagnostic approach is promising, and additional validation and future studies are needed for it to be considered as a practical alternative or a complement to CSF-based diagnostics of LNB in everyday clinical practice.

摘要

莱姆病神经疏螺旋体病(LNB)的诊断需要证明患者脑脊液(CSF)中存在鞘内合成的疏螺旋体抗体,这涉及腰椎穿刺这一侵入性操作。本研究作为一项可行性研究,旨在探索通过先进的代谢组学技术,利用血清样本(一种易于获取的常规临床样本)进行LNB诊断的潜力。从确诊的LNB患者治疗前后采集血清样本,治疗后的样本作为对照。该研究的目的是通过使用超高效液相色谱-串联质谱(UHPLC-MS/MS)的非靶向代谢组学分析,寻找急性LNB的稳定生物标志物。该研究聚焦于在典型临床条件下储存的血清样本中能够可靠检测到的生物标志物,无需特殊处理,确保随时间的一致检测。分析揭示了26978个分子特征(MFs),其中1746个具有统计学意义(p < 0.001)。对91个最显著的MFs进行进一步人工研究,发现了53个LNB的潜在生物标志物,单个或组合使用。所开发的工作流程为生物标志物检测提供了一个综合平台,在LNB和其他感染的研究和临床环境中均有潜在应用。这种微创诊断方法很有前景,需要进行额外的验证和未来研究,以便在日常临床实践中被视为基于脑脊液的LNB诊断的实用替代方法或补充方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7329/11897164/a421a253577a/41598_2025_92189_Fig1_HTML.jpg

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