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. 2020 Nov 9;2(2):fcaa192. doi: 10.1093/braincomms/fcaa192

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© The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Demographic and clinical characteristics captured by the different subtyping methods. The bar plots for sex and APOE ε4 show what percentage of patients in each subtype were females and APOE ε4 carriers, respectively. Kruskal–Wallis hypothesis testing was conducted comparing the subtypes within each method; *P < 0.05 within the subtyping method. APOE = apolipoprotein; F = female; HS = hippocampal-sparing; LP = limbic-predominant; MA = minimal atrophy; MMSE = mini mental state exam; MT = minimal tau; PET = positron emission tomography; sMRI = structural magnetic resonance imaging; TAD = typical AD.