Data-driven identification of diagnostically useful extrastriatal signal in dopamine transporter SPECT using explainable AI

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Data-driven identification of diagnostically useful extrastriatal signal in dopamine transporter SPECT using explainable AI. / Nazari, Mahmood; Kluge, Andreas; Apostolova, Ivayla; Klutmann, Susanne; Kimiaei, Sharok; Schroeder, Michael; Buchert, Ralph.

In: SCI REP-UK, Vol. 11, No. 1, 22932, 25.11.2021.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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@article{dbef5b4d3e9b44a994a23c5471df1317,
title = "Data-driven identification of diagnostically useful extrastriatal signal in dopamine transporter SPECT using explainable AI",
abstract = "This study used explainable artificial intelligence for data-driven identification of extrastriatal brain regions that can contribute to the interpretation of dopamine transporter SPECT with 123I-FP-CIT in parkinsonian syndromes. A total of 1306 123I-FP-CIT-SPECT were included retrospectively. Binary classification as 'reduced' or 'normal' striatal 123I-FP-CIT uptake by an experienced reader served as standard-of-truth. A custom-made 3-dimensional convolutional neural network (CNN) was trained for classification of the SPECT images with 1006 randomly selected images in three different settings: {"}full image{"}, {"}striatum only{"} (3-dimensional region covering the striata cropped from the full image), {"}without striatum{"} (full image with striatal region removed). The remaining 300 SPECT images were used to test the CNN classification performance. Layer-wise relevance propagation (LRP) was used for voxelwise quantification of the relevance for the CNN-based classification in this test set. Overall accuracy of CNN-based classification was 97.0%, 95.7%, and 69.3% in the {"}full image{"}, {"}striatum only{"}, and {"}without striatum{"} setting. Prominent contributions in the LRP-based relevance maps beyond the striatal signal were detected in insula, amygdala, ventromedial prefrontal cortex, thalamus, anterior temporal cortex, superior frontal lobe, and pons, suggesting that 123I-FP-CIT uptake in these brain regions provides clinically useful information for the differentiation of neurodegenerative and non-neurodegenerative parkinsonian syndromes.",
author = "Mahmood Nazari and Andreas Kluge and Ivayla Apostolova and Susanne Klutmann and Sharok Kimiaei and Michael Schroeder and Ralph Buchert",
note = "{\textcopyright} 2021. The Author(s).",
year = "2021",
month = nov,
day = "25",
doi = "10.1038/s41598-021-02385-x",
language = "English",
volume = "11",
journal = "SCI REP-UK",
issn = "2045-2322",
publisher = "NATURE PUBLISHING GROUP",
number = "1",

}

RIS

TY - JOUR

T1 - Data-driven identification of diagnostically useful extrastriatal signal in dopamine transporter SPECT using explainable AI

AU - Nazari, Mahmood

AU - Kluge, Andreas

AU - Apostolova, Ivayla

AU - Klutmann, Susanne

AU - Kimiaei, Sharok

AU - Schroeder, Michael

AU - Buchert, Ralph

N1 - © 2021. The Author(s).

PY - 2021/11/25

Y1 - 2021/11/25

N2 - This study used explainable artificial intelligence for data-driven identification of extrastriatal brain regions that can contribute to the interpretation of dopamine transporter SPECT with 123I-FP-CIT in parkinsonian syndromes. A total of 1306 123I-FP-CIT-SPECT were included retrospectively. Binary classification as 'reduced' or 'normal' striatal 123I-FP-CIT uptake by an experienced reader served as standard-of-truth. A custom-made 3-dimensional convolutional neural network (CNN) was trained for classification of the SPECT images with 1006 randomly selected images in three different settings: "full image", "striatum only" (3-dimensional region covering the striata cropped from the full image), "without striatum" (full image with striatal region removed). The remaining 300 SPECT images were used to test the CNN classification performance. Layer-wise relevance propagation (LRP) was used for voxelwise quantification of the relevance for the CNN-based classification in this test set. Overall accuracy of CNN-based classification was 97.0%, 95.7%, and 69.3% in the "full image", "striatum only", and "without striatum" setting. Prominent contributions in the LRP-based relevance maps beyond the striatal signal were detected in insula, amygdala, ventromedial prefrontal cortex, thalamus, anterior temporal cortex, superior frontal lobe, and pons, suggesting that 123I-FP-CIT uptake in these brain regions provides clinically useful information for the differentiation of neurodegenerative and non-neurodegenerative parkinsonian syndromes.

AB - This study used explainable artificial intelligence for data-driven identification of extrastriatal brain regions that can contribute to the interpretation of dopamine transporter SPECT with 123I-FP-CIT in parkinsonian syndromes. A total of 1306 123I-FP-CIT-SPECT were included retrospectively. Binary classification as 'reduced' or 'normal' striatal 123I-FP-CIT uptake by an experienced reader served as standard-of-truth. A custom-made 3-dimensional convolutional neural network (CNN) was trained for classification of the SPECT images with 1006 randomly selected images in three different settings: "full image", "striatum only" (3-dimensional region covering the striata cropped from the full image), "without striatum" (full image with striatal region removed). The remaining 300 SPECT images were used to test the CNN classification performance. Layer-wise relevance propagation (LRP) was used for voxelwise quantification of the relevance for the CNN-based classification in this test set. Overall accuracy of CNN-based classification was 97.0%, 95.7%, and 69.3% in the "full image", "striatum only", and "without striatum" setting. Prominent contributions in the LRP-based relevance maps beyond the striatal signal were detected in insula, amygdala, ventromedial prefrontal cortex, thalamus, anterior temporal cortex, superior frontal lobe, and pons, suggesting that 123I-FP-CIT uptake in these brain regions provides clinically useful information for the differentiation of neurodegenerative and non-neurodegenerative parkinsonian syndromes.

U2 - 10.1038/s41598-021-02385-x

DO - 10.1038/s41598-021-02385-x

M3 - SCORING: Journal article

C2 - 34824352

VL - 11

JO - SCI REP-UK

JF - SCI REP-UK

SN - 2045-2322

IS - 1

M1 - 22932

ER -