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. 2022 Aug 22;12:14307. doi: 10.1038/s41598-022-18325-2

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© The Author(s) 2022

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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Vertex-wise point biserial correlation analysis between APOE4 status (APOE4 carrier = 1, non-carrier = 0) and the variables (tau, amyloid, and cortical thickness controlling for age and sex by FDR corrected p < 0.05). (A) Correlation between APOE4 and biomarkers in all cognitive normal participants; (B) Correlation between APOE4 and biomarkers in cognitive normal Aβ+ participants; (C) Correlation between APOE4 and biomarkers in cognitive normal Aβ− participants. Tau burden (left), amyloid burden (mid), and cortical thickness (right).