A Novel Fusion Framework Combining Graph Embedding Class-Based Convolutional Recurrent Attention Network with Brown Bear Optimization Algorithm for EEG-Based Parkinson’s Disease Recognition

IF 2.7 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Neuroscience Pub Date : 2025-03-15 DOI:10.1007/s12031-025-02329-4
Nalla Shirisha, Baranitharan Kannan, Padmanaban Kuppan, Loganathan Guganathan
{"title":"A Novel Fusion Framework Combining Graph Embedding Class-Based Convolutional Recurrent Attention Network with Brown Bear Optimization Algorithm for EEG-Based Parkinson’s Disease Recognition","authors":"Nalla Shirisha,&nbsp;Baranitharan Kannan,&nbsp;Padmanaban Kuppan,&nbsp;Loganathan Guganathan","doi":"10.1007/s12031-025-02329-4","DOIUrl":null,"url":null,"abstract":"<div><p>Parkinson’s disease recognition (PDR) involves identifying Parkinson’s disease using clinical evaluations, imaging studies, and biomarkers, focusing on early symptoms like tremors, rigidity, and bradykinesia to facilitate timely treatment. However, due to noise, variability, and the non-stationary nature of EEG signals, distinguishing PD remains a challenge. Traditional deep learning methods struggle to capture the intricate temporal and spatial dependencies in EEG data, limiting their precision. To address this, a novel fusion framework called graph embedding class-based convolutional recurrent attention network with Brown Bear Optimization Algorithm (GECCR2ANet + BBOA) is introduced for EEG-based PD recognition. Preprocessing is conducted using numerical operations and noise removal with weighted guided image filtering and entropy evaluation weighting (WGIF-EEW). Feature extraction is performed via the improved VGG19 with graph triple attention network (IVGG19-GTAN), which captures spatial and temporal dependencies in EEG data. The extracted features are classified using the graph embedding class-based convolutional recurrent attention network (GECCR2ANet), further optimized through the Brown Bear Optimization Algorithm (BBOA) to enhance classification accuracy. The model achieves 99.9% accuracy, 99.4% sensitivity, and a 99.3% F1-score on the UNM dataset, and 99.8% accuracy, 99.1% sensitivity, and 99.2% F1-score on the UC San Diego dataset, significantly outperforming existing methods. Additionally, it records an error rate of 0.5% and a computing time of 0.25 s. Previous models like 2D-MDAGTS, A-TQWT, and CWCNN achieved below 95% accuracy, while the proposed model’s 99.9% accuracy underscores its superior performance in real-world clinical applications, enhancing early PD detection and improving diagnostic efficiency.</p></div>","PeriodicalId":652,"journal":{"name":"Journal of Molecular Neuroscience","volume":"75 1","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1007/s12031-025-02329-4","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Parkinson’s disease recognition (PDR) involves identifying Parkinson’s disease using clinical evaluations, imaging studies, and biomarkers, focusing on early symptoms like tremors, rigidity, and bradykinesia to facilitate timely treatment. However, due to noise, variability, and the non-stationary nature of EEG signals, distinguishing PD remains a challenge. Traditional deep learning methods struggle to capture the intricate temporal and spatial dependencies in EEG data, limiting their precision. To address this, a novel fusion framework called graph embedding class-based convolutional recurrent attention network with Brown Bear Optimization Algorithm (GECCR2ANet + BBOA) is introduced for EEG-based PD recognition. Preprocessing is conducted using numerical operations and noise removal with weighted guided image filtering and entropy evaluation weighting (WGIF-EEW). Feature extraction is performed via the improved VGG19 with graph triple attention network (IVGG19-GTAN), which captures spatial and temporal dependencies in EEG data. The extracted features are classified using the graph embedding class-based convolutional recurrent attention network (GECCR2ANet), further optimized through the Brown Bear Optimization Algorithm (BBOA) to enhance classification accuracy. The model achieves 99.9% accuracy, 99.4% sensitivity, and a 99.3% F1-score on the UNM dataset, and 99.8% accuracy, 99.1% sensitivity, and 99.2% F1-score on the UC San Diego dataset, significantly outperforming existing methods. Additionally, it records an error rate of 0.5% and a computing time of 0.25 s. Previous models like 2D-MDAGTS, A-TQWT, and CWCNN achieved below 95% accuracy, while the proposed model’s 99.9% accuracy underscores its superior performance in real-world clinical applications, enhancing early PD detection and improving diagnostic efficiency.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于图嵌入类的卷积循环注意网络与棕熊优化算法相结合的脑电图帕金森病识别融合框架
帕金森病识别(PDR)包括通过临床评估、影像学研究和生物标志物来识别帕金森病,重点关注震颤、僵硬和运动迟缓等早期症状,以促进及时治疗。然而,由于脑电图信号的噪声、可变性和非平稳性,区分PD仍然是一个挑战。传统的深度学习方法难以捕捉脑电图数据中复杂的时间和空间依赖关系,限制了它们的精度。为了解决这一问题,提出了一种新的融合框架,即基于图嵌入类的卷积循环注意网络与棕熊优化算法(GECCR2ANet + BBOA),用于基于脑电图的PD识别。预处理采用数值运算和加权引导图像滤波和熵值加权(WGIF-EEW)去噪。通过改进的VGG19和图三重注意网络(IVGG19-GTAN)进行特征提取,该网络捕获脑电数据的空间和时间依赖性。提取的特征使用基于图嵌入类的卷积循环关注网络(GECCR2ANet)进行分类,并进一步通过棕熊优化算法(BBOA)进行优化,以提高分类精度。该模型在UNM数据集上达到99.9%的准确率、99.4%的灵敏度和99.3%的f1分数,在UC San Diego数据集上达到99.8%的准确率、99.1%的灵敏度和99.2%的f1分数,显著优于现有方法。此外,它记录的错误率为0.5%,计算时间为0.25 s。之前的2D-MDAGTS、A-TQWT、CWCNN等模型准确率均在95%以下,而本文提出的模型准确率达到99.9%,在实际临床应用中表现优异,增强了PD的早期发现,提高了诊断效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
期刊最新文献
Mendelian Randomization Analysis of the Brain, Cerebrospinal Fluid, and Plasma Proteome Identifies a Potential Peripheral Biomarker for Isolated REM Sleep Behavior Disorder. LDHA as a Potential Therapeutic Target for Lactylation Regulation in Spinal Cord Injury: Integrated Bioinformatics Analysis, Experimental Validation, and Drug Prediction The Clinical Utility of Cell-Free DNA in Brain Tumor Management: A Comprehensive Review Is the Era of One-Size-Fits-All Alzheimer’s Treatment Officially Over? Acupuncture Upregulates hsa-miR-550a-3-5p Targeting PECAM1 To Reduce Transendothelial Migration of Inflammatory Cells and Alleviate Migraine
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1