Muhammad Hassan, Jieqong Lin, Ahmed Ameen Fateh, Wei Pang, Luning Zhang, Wang Di, Guojun Yun, Hongwu Zeng
{"title":"关注与脑瘫障碍和生物标记相关的易受损脑区","authors":"Muhammad Hassan, Jieqong Lin, Ahmed Ameen Fateh, Wei Pang, Luning Zhang, Wang Di, Guojun Yun, Hongwu Zeng","doi":"10.1016/j.jare.2024.11.015","DOIUrl":null,"url":null,"abstract":"<h3><strong>Introduction</strong>:</h3>Cerebral palsy (CP) is a neurological disorder caused by cerebral ischemia and hypoxia during fetal brain development. Early intervention in CP favors medications and therapy; however, detecting early brain development with CP is critical. It is inevitable to thoroughly examine brain-vulnerable regions associated with biological traits (BTs). Variations in BTs were evident in children with CP; however, it is critical to explore the BTs’ impact on the brains of health controls (HC) and CP-disordered children.<h3><strong>Objective</strong>:</h3>This study associates BTs with HC and CP children. This study investigates the neurodevelopment of HC and CP underlying BTs. This study establishes a benchmark of BT’s association and HC and CP children.<h3><strong>Method</strong>:</h3>The introduced AWG-Net is composed of customized spatial-channel (CSC) and multi-head self (MHA) attentions, where CSC blocks are incorporated at the first few stages, MAH at later stages, and cumulative-dense structures to propagate susceptible regions to deeper layers. The training samples include T1-w, T2-w, Flair, and Sag, annotated with age, gender, and weight.<h3><strong>Results</strong>:</h3>The significant results for HC and CP are Age (HC: MAE=1.05, MCS<sub>10</sub>=85.63, R<sub>2</sub>=0.844; CP: MAE=1.16, MCS<sub>10</sub>=84.79, R<sub>2</sub>=0.717), gender (HC: Acc=82.98%, CP: Acc= 82.00%), and weight (HC: MAE=4.65, MCS<sub>10</sub>=56.30, R<sub>2</sub>=0.78; CP: MAE=2.85, MCS<sub>10</sub>=70.24, R<sub>2</sub>=0.82). Vulnerable regions for age are the cerebellar hemisphere, frontal, occipital, and parietal bones in OC and inconsistent in CP. HC and OP commonalities are in the frontal bone and cerebellar hemisphere with HC and discrepant in the occipital and temporal bones for CP. Similarly, gender differences are found for HC and CP.<h3><strong>Conclusion</strong>:</h3>Age and gender are marginally less affected by the brain regions vulnerable to CP than weight estimation. T1-w is appropriate for age, weight, and gender. The learned trends are different for HC and CP in brain development and gender while slightly different in the case of weight.","PeriodicalId":14952,"journal":{"name":"Journal of Advanced Research","volume":null,"pages":null},"PeriodicalIF":11.4000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Attention Over Vulnerable Brain Regions Associating Cerebral Palsy Disorder and Biological Markers\",\"authors\":\"Muhammad Hassan, Jieqong Lin, Ahmed Ameen Fateh, Wei Pang, Luning Zhang, Wang Di, Guojun Yun, Hongwu Zeng\",\"doi\":\"10.1016/j.jare.2024.11.015\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3><strong>Introduction</strong>:</h3>Cerebral palsy (CP) is a neurological disorder caused by cerebral ischemia and hypoxia during fetal brain development. Early intervention in CP favors medications and therapy; however, detecting early brain development with CP is critical. It is inevitable to thoroughly examine brain-vulnerable regions associated with biological traits (BTs). Variations in BTs were evident in children with CP; however, it is critical to explore the BTs’ impact on the brains of health controls (HC) and CP-disordered children.<h3><strong>Objective</strong>:</h3>This study associates BTs with HC and CP children. This study investigates the neurodevelopment of HC and CP underlying BTs. This study establishes a benchmark of BT’s association and HC and CP children.<h3><strong>Method</strong>:</h3>The introduced AWG-Net is composed of customized spatial-channel (CSC) and multi-head self (MHA) attentions, where CSC blocks are incorporated at the first few stages, MAH at later stages, and cumulative-dense structures to propagate susceptible regions to deeper layers. The training samples include T1-w, T2-w, Flair, and Sag, annotated with age, gender, and weight.<h3><strong>Results</strong>:</h3>The significant results for HC and CP are Age (HC: MAE=1.05, MCS<sub>10</sub>=85.63, R<sub>2</sub>=0.844; CP: MAE=1.16, MCS<sub>10</sub>=84.79, R<sub>2</sub>=0.717), gender (HC: Acc=82.98%, CP: Acc= 82.00%), and weight (HC: MAE=4.65, MCS<sub>10</sub>=56.30, R<sub>2</sub>=0.78; CP: MAE=2.85, MCS<sub>10</sub>=70.24, R<sub>2</sub>=0.82). Vulnerable regions for age are the cerebellar hemisphere, frontal, occipital, and parietal bones in OC and inconsistent in CP. HC and OP commonalities are in the frontal bone and cerebellar hemisphere with HC and discrepant in the occipital and temporal bones for CP. Similarly, gender differences are found for HC and CP.<h3><strong>Conclusion</strong>:</h3>Age and gender are marginally less affected by the brain regions vulnerable to CP than weight estimation. T1-w is appropriate for age, weight, and gender. 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Attention Over Vulnerable Brain Regions Associating Cerebral Palsy Disorder and Biological Markers
Introduction:
Cerebral palsy (CP) is a neurological disorder caused by cerebral ischemia and hypoxia during fetal brain development. Early intervention in CP favors medications and therapy; however, detecting early brain development with CP is critical. It is inevitable to thoroughly examine brain-vulnerable regions associated with biological traits (BTs). Variations in BTs were evident in children with CP; however, it is critical to explore the BTs’ impact on the brains of health controls (HC) and CP-disordered children.
Objective:
This study associates BTs with HC and CP children. This study investigates the neurodevelopment of HC and CP underlying BTs. This study establishes a benchmark of BT’s association and HC and CP children.
Method:
The introduced AWG-Net is composed of customized spatial-channel (CSC) and multi-head self (MHA) attentions, where CSC blocks are incorporated at the first few stages, MAH at later stages, and cumulative-dense structures to propagate susceptible regions to deeper layers. The training samples include T1-w, T2-w, Flair, and Sag, annotated with age, gender, and weight.
Results:
The significant results for HC and CP are Age (HC: MAE=1.05, MCS10=85.63, R2=0.844; CP: MAE=1.16, MCS10=84.79, R2=0.717), gender (HC: Acc=82.98%, CP: Acc= 82.00%), and weight (HC: MAE=4.65, MCS10=56.30, R2=0.78; CP: MAE=2.85, MCS10=70.24, R2=0.82). Vulnerable regions for age are the cerebellar hemisphere, frontal, occipital, and parietal bones in OC and inconsistent in CP. HC and OP commonalities are in the frontal bone and cerebellar hemisphere with HC and discrepant in the occipital and temporal bones for CP. Similarly, gender differences are found for HC and CP.
Conclusion:
Age and gender are marginally less affected by the brain regions vulnerable to CP than weight estimation. T1-w is appropriate for age, weight, and gender. The learned trends are different for HC and CP in brain development and gender while slightly different in the case of weight.
期刊介绍:
Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences.
The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.