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. 2023 Feb 10;15:32. doi: 10.1186/s13195-023-01181-1

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© The Author(s) 2023

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — The key EEG biomarkers at parieto-occipital regions effectively recognized distinct neural patterns among six groups. Selected EEG features included a absolute theta PSD at O2 (F = 42.46, p < 0.001), b relative theta PSD at O2 (F = 50.11, p < 0.001), c Hjorth mobility at O1 (F = 51.08, p < 0.001), d Hjorth mobility at O2 (F = 50.14, p < 0.001), and e Hjorth mobility at P4 (F = 47.09, p < 0.001). “*” indicates that there is a significant between-group difference (p<0.05, FDR corrected)