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. 2024 Sep 10;271(10):6991–6999. doi: 10.1007/s00415-024-12647-z

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — NfL and GFAP as biomarkers in MSA, PD and HC. A Biomarkers for differential diagnosis. NfL levels are significantly increased in both CSF and plasma of MSA compared to PD and HC. GFAP levels in CSF are significantly higher in MSA compared to HC. ****p < 0.0001. No significant changes in GFAP plasma levels were observed between the three groups. B Receiver operating characteristic (ROC) curve analysis for NfL in CSF and plasma show high AUC values for discrimination of MSA from PD patients (CSF: AUC = 0.97; plasma: AUC = 0.90)