Evidence map›Paper›PMID 39276052›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2024

[An MRI multi-sequence feature imputation and fusion mutual-aid model based on sequence deletion for differentiation of high-grade from low-grade glioma].

C Wu, W Zhong, J Xie, R Yang, Y Wu, Y Xu, L Wang, X Zhen

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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

C WuSchool of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
W ZhongSchool of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
J XieSchool of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.
R YangDepartment of Radiology, Guangzhou First People's Hospital, Guangzhou 510180, China.
Y WuDepartment of Medical Imaging, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Y XuDepartment of Medical Imaging, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
L WangGuangzhou Institute of Cancer Research, the Affiliated Cancer Hospital, Guangzhou Medical University, Guangzhou 510095, China.
X ZhenSchool of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the performance of magnetic resonance imaging (MRI) multi-sequence feature imputation and fusion mutual model based on sequence deletion in differentiating high-grade glioma (HGG) from low-grade glioma (LGG).

methodsWe retrospectively collected multi-sequence MR images from 305 glioma patients, including 189 HGG patients and 116 LGG patients. The region of interest (ROI) of T1-weighted images (T1WI), T2-weighted images (T2WI), T2 fluid attenuated inversion recovery (T2_FLAIR) and post-contrast enhancement T1WI (CE_T1WI) were delineated to extract the radiomics features. A mutual-aid model of MRI multi-sequence feature imputation and fusion based on sequence deletion was used for imputation and fusion of the feature matrix with missing data. The discriminative ability of the model was evaluated using 5-fold cross-validation method and by assessing the accuracy, balanced accuracy, area under the ROC curve (AUC), specificity, and sensitivity. The proposed model was quantitatively compared with other non-holonomic multimodal classification models for discriminating HGG and LGG. Class separability experiments were performed on the latent features learned by the proposed feature imputation and fusion methods to observe the classification effect of the samples in twodimensional plane. Convergence experiments were used to verify the feasibility of the model.

resultsFor differentiation of HGG from LGG with a missing rate of 10%, the proposed model achieved accuracy, balanced accuracy, AUC, specificity, and sensitivity of 0.777, 0.768, 0.826, 0.754 and 0.780, respectively. The fused latent features showed excellent performance in the class separability experiment, and the algorithm could be iterated to convergence with superior classification performance over other methods at the missing rates of 30% and 50%.

conclusionThe proposed model has excellent performance in classification task of HGG and LGG and outperforms other non-holonomic multimodal classification models, demonstrating its potential for efficient processing of non-holonomic multimodal data.

Indexed as

Brain NeoplasmsGliomaMagnetic Resonance ImagingAlgorithmsHumansNeoplasm GradingRetrospective StudiesROC CurveSensitivity and Specificityfeature imputationhigh-grade gliomalow-grade gliomarepresentation learningsequence deletion

Identifiers

PMID39276052
PMCPMC11378041

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.