A HybridConformerNet network to identify structural biomarkers in the dystonia

Poster No:

89 

Submission Type:

Abstract Submission 

Authors:

Xu Jinping1, Qinxiu Cheng2, Lin Wang3, Gang liu4

Institutions:

1Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, shenzhen, Guangdong, 2Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, shenzhem, Guangdong, 3Aviation General Hospital, China Medical University, shenzhen, Guangdong, 4Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial, shenzhen, Guangdong

First Author:

Xu Jinping  
Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences
shenzhen, Guangdong

Co-Author(s):

Qinxiu Cheng  
Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences
shenzhem, Guangdong
Lin Wang  
Aviation General Hospital, China Medical University
shenzhen, Guangdong
Gang liu  
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangdong Provincial
shenzhen, Guangdong

Introduction:

Isolated dystonia is a neurological disorder marked by abnormal muscle contractions, leading to significant functional impairment.[1] Diagnosis remains challenging due to its reliance on subjective clinical evaluations and the absence of reliable biomarkers.[2] Recent studies suggest structural brain alterations, particularly in the basal ganglia and sensorimotor networks,[3] could serve as potential biomarkers. In this study, we proposed the use of a novel deep learning architecture, HybridConformerNet, to identify structural biomarkers associated with isolated dystonia using structural magnetic resonance imaging (sMRI). The model integrated Convolutional Neural Networks[4][5] for local feature extraction and Vision Transformers[6] for global contextual analysis. The approach achieved an accuracy of 0.97 on the training dataset and 0.96 on the test dataset in two-way classification. To gain insights into the model's predictions, we employed techniques for interpreting deep learning models, identifying four key clusters of structural biomarkers:(1). right inferior temporal gyrus/right cerebellar. (2).bilateral middle cingulate cortex /supplementary motor area. (3).left precentral gyrus. (4).left fusiform gyrus. These findings offer a robust solution for the early diagnosis of this complex disorder and contribute to advancing our understanding of its underlying structural brain changes.

Methods:

We collected sMRI data from three centers. First Affiliated Hospital of Sun Yat-sen University (SYU): 74 patients with BSP, 31 with BOM, 42 with CD, and 136 HCs were included. Aviation General Hospital of China Medical University (AGH):31 patients with BSP, 92 with BOM, and 36 with CCD were included in the second center, Additionally, we obtained T1-weighted MRI images of 405 HCs from the IXI database.
Preprocessing: T1-weighted images were segmented into gray matter, white matter, and CSF, then transformed into MNI space and cropped.
Data Alignment: VQ-VAE model aligned gray matter images from different centers to a common space, ensuring robustness.
Model Framework
A hybrid framework combining 3D CNNs (local feature extraction) and ViTs (modeling long-range dependencies) was developed. The model used a linear attention mechanism for efficiency.
3D CNN Branch: Extracts local features using convolution layers and max-pooling, followed by fully connected layers for feature vector generation. Dropout and batch normalization prevent overfitting.
Vision Transformer (ViT) Branch: Uses a patch-embedding module to process images into non-overlapping patches, with DenseNet for extracting 512 local features. Applies spatial reduction and feature transformation for improved efficiency. The workflow is illustrated in Fig. 1.
Supporting Image: Fig1.png
   ·Flowchart of the Proposed Framework. (A) Data Preprocessing Steps for sMRI Data: 1) Head motion correction, 2) Skull stripping, 3) Segmentation into gray matter, white matter, and cerebrospinal fluid,
 

Results:

The results revealed that our deep learning model accurately classified dystonia in multicenter sMRI scans (Fig. 2). The proposed method outperformed other 3D methods in almost all metrics. In SYU, the ACC values were 0.960/0.863/0.903, AUC values were 0.978/0.960/0.972, recall values were 0.958/0.855/0.896, precision values were 0.980/0.893/0.924, and F1-scores were 0.938/ 0.872/0.907 for the three tasks, respectively. In AGH, the recall values were 0.977, 0.982, and 0.977 for the three tasks, respectively, while the precision was 0.950. Our approach demonstrated a superior balance between high performance and stability, thus enhancing its utility in clinical settings where reliability is crucial. All the results of the proposed method surpassed those of the other models, which demonstrate the optimal generalizability of the proposed model.
Supporting Image: Fig3.png
   ·The accuracy of three centers
 

Conclusions:

Four clusters were identified in the model interpretation, including the right inferior temporal gyrus (ITG.R)/right cerebellum (CERE.R), bilateral middle cingulate cortex (MCG)/supplementary motor area (SMA), the left precentral gyrus (PreCG.L), and the left fusiform gyrus (FG.L)

Disorders of the Nervous System:

Neurodegenerative/ Late Life (eg. Parkinson’s, Alzheimer’s) 1

Modeling and Analysis Methods:

Classification and Predictive Modeling 2

Keywords:

MRI
Neurological

1|2Indicates the priority used for review

Abstract Information

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Please indicate below if your study was a "resting state" or "task-activation” study.

Resting state

Healthy subjects only or patients (note that patient studies may also involve healthy subjects):

Healthy subjects

Was this research conducted in the United States?

No

Were any human subjects research approved by the relevant Institutional Review Board or ethics panel? NOTE: Any human subjects studies without IRB approval will be automatically rejected.

Yes

Were any animal research approved by the relevant IACUC or other animal research panel? NOTE: Any animal studies without IACUC approval will be automatically rejected.

No

Please indicate which methods were used in your research:

Structural MRI
Computational modeling

For human MRI, what field strength scanner do you use?

3.0T

Which processing packages did you use for your study?

SPM

Provide references using APA citation style.

1.Albanese A, Bhatia K, Bressman SB, et al. Phenomenology and classification of dystonia: a consensus update. Mov Disord. Jun 15 2013;28(7):863-873.
2.Kaur M, Sharma U, Solanki RK. Anesthetic nuances in Segawa's syndrome: A case report and review of the literature. Saudi J Anaesth. Oct-Dec 2020;14(4):524-527.
3.Gao, Z., et al., Activation likelihood estimation identifies brain regions activated during puncturing at Hegu in healthy volunteers: A meta-analysis. Front Neurosci, 2022. 16: p. 1084362.
4.He K, Zhang X, Ren S, Sun J. Deep residual learning for image recognition, 2016.
5.Valeriani D, Simonyan K. A microstructural neural network biomarker for dystonia diagnosis identified by a DystoniaNet deep learning platform. Proc Natl Acad Sci U S A. Oct 20 2020;117(42):26398-26405.
6.Vaswani A. Attention is all you need. Advances in Neural Information Processing Systems. 2017.

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