S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications

With the success of U-Net or its variants in automatic medical image segmentation, building a fully convolutional network (FCN) based on an encoder-decoder structure has become an effective end-to-end learning approach. However, the intrinsic property of FCNs is that as the encoder deepens, higher-l...

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Main Authors: Nan Mu, Zonghan Lyu, Mostafa Rezaeitaleshmahalleh, Cassie Bonifas, Jordan Gosnell, Marcus Haw, Joseph Vettukattil, Jingfeng Jiang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-11-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2023.1209659/full
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author Nan Mu
Nan Mu
Zonghan Lyu
Zonghan Lyu
Mostafa Rezaeitaleshmahalleh
Mostafa Rezaeitaleshmahalleh
Cassie Bonifas
Cassie Bonifas
Jordan Gosnell
Marcus Haw
Joseph Vettukattil
Joseph Vettukattil
Jingfeng Jiang
Jingfeng Jiang
author_facet Nan Mu
Nan Mu
Zonghan Lyu
Zonghan Lyu
Mostafa Rezaeitaleshmahalleh
Mostafa Rezaeitaleshmahalleh
Cassie Bonifas
Cassie Bonifas
Jordan Gosnell
Marcus Haw
Joseph Vettukattil
Joseph Vettukattil
Jingfeng Jiang
Jingfeng Jiang
author_sort Nan Mu
collection DOAJ
description With the success of U-Net or its variants in automatic medical image segmentation, building a fully convolutional network (FCN) based on an encoder-decoder structure has become an effective end-to-end learning approach. However, the intrinsic property of FCNs is that as the encoder deepens, higher-level features are learned, and the receptive field size of the network increases, which results in unsatisfactory performance for detecting low-level small/thin structures such as atrial walls and small arteries. To address this issue, we propose to keep the different encoding layer features at their original sizes to constrain the receptive field from increasing as the network goes deeper. Accordingly, we develop a novel S-shaped multiple cross-aggregation segmentation architecture named S-Net, which has two branches in the encoding stage, i.e., a resampling branch to capture low-level fine-grained details and thin/small structures and a downsampling branch to learn high-level discriminative knowledge. In particular, these two branches learn complementary features by residual cross-aggregation; the fusion of the complementary features from different decoding layers can be effectively accomplished through lateral connections. Meanwhile, we perform supervised prediction at all decoding layers to incorporate coarse-level features with high semantic meaning and fine-level features with high localization capability to detect multi-scale structures, especially for small/thin volumes fully. To validate the effectiveness of our S-Net, we conducted extensive experiments on the segmentation of cardiac wall and intracranial aneurysm (IA) vasculature, and quantitative and qualitative evaluations demonstrated the superior performance of our method for predicting small/thin structures in medical images.
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spelling doaj.art-cc4892c94c644972a65e0810bdcb55732023-11-03T06:08:44ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2023-11-011410.3389/fphys.2023.12096591209659S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applicationsNan Mu0Nan Mu1Zonghan Lyu2Zonghan Lyu3Mostafa Rezaeitaleshmahalleh4Mostafa Rezaeitaleshmahalleh5Cassie Bonifas6Cassie Bonifas7Jordan Gosnell8Marcus Haw9Joseph Vettukattil10Joseph Vettukattil11Jingfeng Jiang12Jingfeng Jiang13Department of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesCenter for Biocomputing and Digital Health, Health Research Institute, Institute of Computing and Cybernetics, Michigan Technological University, Houghton, MI, United StatesDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesCenter for Biocomputing and Digital Health, Health Research Institute, Institute of Computing and Cybernetics, Michigan Technological University, Houghton, MI, United StatesDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesCenter for Biocomputing and Digital Health, Health Research Institute, Institute of Computing and Cybernetics, Michigan Technological University, Houghton, MI, United StatesDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesCenter for Biocomputing and Digital Health, Health Research Institute, Institute of Computing and Cybernetics, Michigan Technological University, Houghton, MI, United StatesBetz Congenital Health Center, Helen DeVos Children’s Hospital, Grand Rapids, MI, United StatesBetz Congenital Health Center, Helen DeVos Children’s Hospital, Grand Rapids, MI, United StatesDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesBetz Congenital Health Center, Helen DeVos Children’s Hospital, Grand Rapids, MI, United StatesDepartment of Biomedical Engineering, Michigan Technological University, Houghton, MI, United StatesCenter for Biocomputing and Digital Health, Health Research Institute, Institute of Computing and Cybernetics, Michigan Technological University, Houghton, MI, United StatesWith the success of U-Net or its variants in automatic medical image segmentation, building a fully convolutional network (FCN) based on an encoder-decoder structure has become an effective end-to-end learning approach. However, the intrinsic property of FCNs is that as the encoder deepens, higher-level features are learned, and the receptive field size of the network increases, which results in unsatisfactory performance for detecting low-level small/thin structures such as atrial walls and small arteries. To address this issue, we propose to keep the different encoding layer features at their original sizes to constrain the receptive field from increasing as the network goes deeper. Accordingly, we develop a novel S-shaped multiple cross-aggregation segmentation architecture named S-Net, which has two branches in the encoding stage, i.e., a resampling branch to capture low-level fine-grained details and thin/small structures and a downsampling branch to learn high-level discriminative knowledge. In particular, these two branches learn complementary features by residual cross-aggregation; the fusion of the complementary features from different decoding layers can be effectively accomplished through lateral connections. Meanwhile, we perform supervised prediction at all decoding layers to incorporate coarse-level features with high semantic meaning and fine-level features with high localization capability to detect multi-scale structures, especially for small/thin volumes fully. To validate the effectiveness of our S-Net, we conducted extensive experiments on the segmentation of cardiac wall and intracranial aneurysm (IA) vasculature, and quantitative and qualitative evaluations demonstrated the superior performance of our method for predicting small/thin structures in medical images.https://www.frontiersin.org/articles/10.3389/fphys.2023.1209659/fullautomatic segmentationcardiac wallintracranial aneurysm (IA)small/thin structurefully convolutional network (FCN)
spellingShingle Nan Mu
Nan Mu
Zonghan Lyu
Zonghan Lyu
Mostafa Rezaeitaleshmahalleh
Mostafa Rezaeitaleshmahalleh
Cassie Bonifas
Cassie Bonifas
Jordan Gosnell
Marcus Haw
Joseph Vettukattil
Joseph Vettukattil
Jingfeng Jiang
Jingfeng Jiang
S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
Frontiers in Physiology
automatic segmentation
cardiac wall
intracranial aneurysm (IA)
small/thin structure
fully convolutional network (FCN)
title S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
title_full S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
title_fullStr S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
title_full_unstemmed S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
title_short S-Net: a multiple cross aggregation convolutional architecture for automatic segmentation of small/thin structures for cardiovascular applications
title_sort s net a multiple cross aggregation convolutional architecture for automatic segmentation of small thin structures for cardiovascular applications
topic automatic segmentation
cardiac wall
intracranial aneurysm (IA)
small/thin structure
fully convolutional network (FCN)
url https://www.frontiersin.org/articles/10.3389/fphys.2023.1209659/full
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