Evidence map›Paper›PMID 36840621›Full record

ArticleMedical physics2023

A neural ordinary differential equation model for visualizing deep neural network behaviors in multi-parametric MRI-based glioma segmentation.

Zhenyu Yang, Zongsheng Hu, Hangjie Ji, Kyle Lafata, Eugene Vaios, Scott Floyd, Fang-Fang Yin, Chunhao Wang

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In one paragraph

Article in Medical physics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

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14citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Zhenyu YangDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Zongsheng HuMedical Physics Graduate Program, Duke Kunshan University, Kunshan, Jiangsu, China.
Hangjie JiDepartment of Mathematics, North Carolina State University, Raleigh, North Carolina, USA.
Kyle LafataDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Eugene VaiosDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Scott FloydDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Fang-Fang YinDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.
Chunhao WangDeparment of Radiation Oncology, Duke University, Durham, North Carolina, USA.

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI JOHN N. NORTON · 1985 to 2026
$174.8M
Duke Radiation Oncology and Radiology Stimulating Access to Research in ResidencyR38CA245204 · NCI · DUKE UNIVERSITY · PI FLOYD, SCOTT R · 2020 to 2023
$1.4M
NCI NIH HHS P30 CA014236NCI NIH HHS R38 CA245204NIH HHS CA014236
6 · The paper itself

Abstract

purposeTo develop a neural ordinary differential equation (ODE) model for visualizing deep neural network behavior during multi-parametric MRI-based glioma segmentation as a method to enhance deep learning explainability.

methodsBy hypothesizing that deep feature extraction can be modeled as a spatiotemporally continuous process, we implemented a novel deep learning model, Neural ODE, in which deep feature extraction was governed by an ODE parameterized by a neural network. The dynamics of (1) MR images after interactions with the deep neural network and (2) segmentation formation can thus be visualized after solving the ODE. An accumulative contribution curve (ACC) was designed to quantitatively evaluate each MR image's utilization by the deep neural network toward the final segmentation results. The proposed Neural ODE model was demonstrated using 369 glioma patients with a 4-modality multi-parametric MRI protocol: T1, contrast-enhanced T1 (T1-Ce), T2, and FLAIR. Three Neural ODE models were trained to segment enhancing tumor (ET), tumor core (TC), and whole tumor (WT), respectively. The key MRI modalities with significant utilization by deep neural networks were identified based on ACC analysis. Segmentation results by deep neural networks using only the key MRI modalities were compared to those using all four MRI modalities in terms of Dice coefficient, accuracy, sensitivity, and specificity.

resultsAll Neural ODE models successfully illustrated image dynamics as expected. ACC analysis identified T1-Ce as the only key modality in ET and TC segmentations, while both FLAIR and T2 were key modalities in WT segmentation. Compared to the U-Net results using all four MRI modalities, the Dice coefficient of ET (0.784→0.775), TC (0.760→0.758), and WT (0.841→0.837) using the key modalities only had minimal differences without significance. Accuracy, sensitivity, and specificity results demonstrated the same patterns.

conclusionThe Neural ODE model offers a new tool for optimizing the deep learning model inputs with enhanced explainability. The presented methodology can be generalized to other medical image-related deep-learning applications.

Indexed as

GliomaHumansNeural Networks, Computerdeep learningexplainabilityglioma segmentationneural ODEvisualization

Identifiers

PMID36840621
PMCPMC10440249

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