TY - JOUR
T1 - Machine learning-based decision tree classifier for the diagnosis of progressive supranuclear palsy and corticobasal degeneration
AU - Koga, Shunsuke
AU - Zhou, Xiaolai
AU - Dickson, Dennis W.
N1 - Funding Information:
The authors thank the patients and their families who donated brains to help further the scientific understanding of neurodegeneration. The authors also thank Virginia Phillips, Jo A. Landino Garcia, and Ariston L. Librero (Mayo Clinic, Jacksonville) for histologic support, Monica Castanedes‐Casey (Mayo Clinic, Jacksonville) for immunohistochemistry support. This work is supported by a Karin & Sten Mortstedt CBD Solutions Research Grant, and CurePSP, the Rainwater Charitable Trust, and the Jaye F. and Betty F. Dyer Foundation Fellowship in progressive supranuclear palsy research, as well as NINDS Tau Center without Walls (U54‐NS100693).
Funding Information:
The authors thank the patients and their families who donated brains to help further the scientific understanding of neurodegeneration. The authors also thank Virginia Phillips, Jo A. Landino Garcia, and Ariston L. Librero (Mayo Clinic, Jacksonville) for histologic support, Monica Castanedes-Casey (Mayo Clinic, Jacksonville) for immunohistochemistry support. This work is supported by a Karin & Sten Mortstedt CBD Solutions Research Grant, and CurePSP, the Rainwater Charitable Trust, and the Jaye F. and Betty F. Dyer Foundation Fellowship in progressive supranuclear palsy research, as well as NINDS Tau Center without Walls (U54-NS100693).
Publisher Copyright:
© 2021 The Authors. Neuropathology and Applied Neurobiology published by John Wiley & Sons Ltd on behalf of British Neuropathological Society.
PY - 2021/12
Y1 - 2021/12
N2 - Aims: This study aimed to clarify the different topographical distribution of tau pathology between progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) and establish a machine learning-based decision tree classifier. Methods: Paraffin-embedded sections of the temporal cortex, motor cortex, caudate nucleus, globus pallidus, subthalamic nucleus, substantia nigra, red nucleus, and midbrain tectum from 1020 PSP and 199 CBD cases were assessed by phospho-tau immunohistochemistry. The severity of tau lesions (i.e., neurofibrillary tangle, coiled body, tufted astrocyte or astrocytic plaque, and tau threads) was semi-quantitatively scored in each region. Hierarchical cluster analysis was performed using tau pathology scores. A decision tree classifier was made with tau pathology scores using 914 cases. Cross-validation was done using 305 cases. An additional ten cases were used for a validation study. Results: Cluster analysis displayed two distinct clusters; the first cluster included only CBD, and the other cluster included all PSP and six CBD cases. We built a decision tree, which used only seven decision nodes. The scores of tau threads in the caudate nucleus were the most decisive factor for predicting CBD. In a cross-validation, 302 out of 305 cases were correctly diagnosed. In the pilot validation study, three investigators made a correct diagnosis in all cases using the decision tree. Conclusion: Regardless of the morphology of astrocytic tau lesions, semi-quantitative tau pathology scores in select brain regions are sufficient to distinguish PSP and CBD. The decision tree simplifies neuropathologic differential diagnosis of PSP and CBD.
AB - Aims: This study aimed to clarify the different topographical distribution of tau pathology between progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) and establish a machine learning-based decision tree classifier. Methods: Paraffin-embedded sections of the temporal cortex, motor cortex, caudate nucleus, globus pallidus, subthalamic nucleus, substantia nigra, red nucleus, and midbrain tectum from 1020 PSP and 199 CBD cases were assessed by phospho-tau immunohistochemistry. The severity of tau lesions (i.e., neurofibrillary tangle, coiled body, tufted astrocyte or astrocytic plaque, and tau threads) was semi-quantitatively scored in each region. Hierarchical cluster analysis was performed using tau pathology scores. A decision tree classifier was made with tau pathology scores using 914 cases. Cross-validation was done using 305 cases. An additional ten cases were used for a validation study. Results: Cluster analysis displayed two distinct clusters; the first cluster included only CBD, and the other cluster included all PSP and six CBD cases. We built a decision tree, which used only seven decision nodes. The scores of tau threads in the caudate nucleus were the most decisive factor for predicting CBD. In a cross-validation, 302 out of 305 cases were correctly diagnosed. In the pilot validation study, three investigators made a correct diagnosis in all cases using the decision tree. Conclusion: Regardless of the morphology of astrocytic tau lesions, semi-quantitative tau pathology scores in select brain regions are sufficient to distinguish PSP and CBD. The decision tree simplifies neuropathologic differential diagnosis of PSP and CBD.
KW - Machine learning
KW - corticobasal degeneration
KW - corticobasal syndrome
KW - decision tree classifier
KW - hierarchical cluster analysis
KW - progressive supranuclear palsy
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UR - http://www.scopus.com/inward/citedby.url?scp=85103620336&partnerID=8YFLogxK
U2 - 10.1111/nan.12710
DO - 10.1111/nan.12710
M3 - Article
C2 - 33763863
AN - SCOPUS:85103620336
SN - 0305-1846
VL - 47
SP - 931
EP - 941
JO - Neuropathology and Applied Neurobiology
JF - Neuropathology and Applied Neurobiology
IS - 7
ER -