Parkinson's Disease Classification Research Articles

Explainable hypergraphs for gait based Parkinson classification

Parkinson Disease (PD) classification using Vertical Ground Reaction Force (VGRF) sensors can help in unobtrusive detection and monitoring of PD patients. State-of-the-art (SOTA) research in PD classification reveals that Deep Learning (DL), at the expense of explainability, performs better than Shallow Learning (SL). In this paper, we introduce a novel explainable weighted hypergraph, where the interconnections of the SOTA features are exploited, leading to more discriminative derived features, and thereby, forming an SL arm. In parallel, we create a DL arm consisting of ResNet architecture to learn the spatio-temporal patterns of the VGRF signals. Probabilities of PD classification scores from the SL and the DL arms are adaptively fused to create a hybrid pipeline. The pipeline achieves an AUC value of 0.979 on the Physionet Parkinson Dataset. This AUC value is found to be superior to the SL as well as the DL arm used in isolation, yielding respective AUCs of 0.878 and 0.852. The proposed pipeline demonstrates explainability through improved permutation feature importance and contrasting examples of use cases, where incorrect misclassification of the DL arm gets rectified by the SL arm and vice versa. We further demonstrate that our solution achieves comparable performance with SOTA methods. To the best of our knowledge, this is the first approach to analyze PD classification with a hypergraph based xAI (Explainable Artificial Intelligence).

The combination of 18F-fluorodeoxyglucose and 18F 9-fluoropropyl-(+)-dihydrotetrabenazine positron emission tomography for distinguishing between early-onset and late-onset idiopathic Parkinson disease and analyzing influencing factors.

The classification of Parkinson disease by age of onset has proven to be a valuable method for subtyping, given its practical application in clinical settings. However, the interactions between the metabolic brain changes, dopaminergic dysfunction, and clinical manifestations in patients with early-onset (early-iPD) and late-onset (late-iPD) idiopathic Parkinson disease have not been adequately evaluated. Therefore, this study aimed to investigate the difference in cerebral metabolism and presynaptic dopaminergic function between patients with early-iPD and those with late-onset disease using 18F-fluorodeoxyglucose (18F-FDG) and [18F] 9-fluoropropyl-(+)-dihydrotetrabenazine (18F-FP-DTBZ) positron emission tomography (PET). Furthermore, the goal was to further explore the correlation between imaging measurements and clinical manifestations in the early and late idiopathic patients with Parkinson disease. This cross-sectional study included 80 patients with idiopathic Parkinson disease and 29 healthy control participants who underwent 18F-FDG and18F-FP-DTBZ PET imaging at Xuanwu Hospital, Capital Medical University from August 2022 to August 2023. The patients were categorized into early-iPD (n=27) and late-iPD (n=53) groups based on an age threshold of 50 years. The mean standardized uptake value of 18F-FDG and the standardized uptake value ratio (SUVR) of 18F-FP-DTBZ were compared between the early-iPD and late-iPD groups using unpaired Student t-tests. Furthermore, pairwise correlations among cerebral metabolism, dopaminergic function, and corresponding clinical ratings in all patients were conducted using Pearson correlation analysis. Patients with late-iPD exhibited a significant metabolic decrease in the frontal, parietal, and temporal cortex, along with the globus pallidus, putamen, thalamus, and cerebellum, compared to those with early-iPD in 18F-FDG PET imaging (all P values <0.05). Furthermore, the 18F-FP-DTBZ binding potential was significantly lower in the contralateral caudate and anterior putamen of patients with late-iPD compared to those with early-iPD (contralateral caudate: 3.16±1.2 vs. 2.63±0.7, P=0.020; contralateral anterior putamen: 2.49±1.2 vs. 2.05±0.7, P=0.040). Further analysis of the correlations between imaging clinical features revealed that glucose metabolism increases and dopaminergic function decreases with higher motor ratings. 18F-FDG and 18F-FP-DTBZ PET offer an objective molecular imaging basis for distinguishing between early-onset and late-onset idiopathic with Parkinson disease. Additionally, correlation analysis between imaging and clinical data represents a new approach for exploring the potential applications in future studies involving patients with early-iPD and late-iPD.

Late feature fusion using neural network with voting classifier for Parkinson’s disease detection

Parkinson’s disease (PD) is classified as a neurological, progressive illness brought on by cell death in the posterior midbrain. Early PD detection will assist doctors in reducing the disease’s consequences. A collection of skilled models that may be applied to regression as well as classification is known as artificial intelligence (AI). PD can be detected using a variety of dataset formats, including text, speech, and picture datasets. For the purpose of classifying Parkinson’s disease, this study suggests merging deep with machine learning recognition approaches. The three primary components of the suggested approach are designed to enhance the accuracy of Parkinson’s disease early diagnosis. These sections cover the topics of categorising, combining, and separating. Convolutional Neural Networks (CNN) as well as attention procedures are used to create feature extractors. The related motion signals are fed to a combination of convolutional neural network and long-short-memory model for feature extraction. Besides, for the classification of patients from non-suffers of Parkinson’s disease, Random Forest, Logistic Regression, Support Vector Machine, Extreme Boot Classifier, and voting classifier were used. Our result shows that for the PD handwriting and related motion datasets, using the proposed CNN with an attention and voting classifier yields 99.95% accuracy, 99.99% precision, 99.98% sensitivity, and 99.95% F1-score. Based on these results, it is warranted to conclude that the proposed methodology of feature extraction from photos of handwriting and relating motor symptoms, fusing of those features, and following it with a voting classifier yields excellent results for PD classification.

An efficient ranking-based ensembled multiclassifier for neurodegenerative diseases classification using deep learning.

Neurodegenerative diseases are group of debilitating and progressive disorders that primarily affect the structure and functions of nervous system, leading to gradual loss of neurons and subsequent decline in cognitive, and behavioral activities. The two frequent diseases affecting the world's significant population falling in the above category are Alzheimer's disease (AD) and Parkinson's disease (PD). These disorders substantially impact the quality of life and burden healthcare systems and society. The demographic characteristics, and machine learning approaches have now been employed to diagnose these illnesses; however, they possess accuracy limitations. Therefore, the authors have developed ranking-based ensemble approach based on the weighted strategy of deep learning classifiers. The whole modeling procedure of the proposed approach incorporates three phases. In phase I, preprocessing techniques are applied to clean the noise in datasets to make it standardized according to deep learning models as it significantly impacts their performance. In phase II, five deep learning models are selected for classification and calculation of prediction results. In phase III, a ranking-based ensemble approach is proposed to ensemble the results of the five models after calculating the ranks and weights of them. In addition, the Magnetic Resonance Imaging (MRI) datasets named Alzheimer's Disease Neuroimaging Initiative (ADNI) for AD classification and Parkinson's Progressive Marker Initiative (PPMI) for PD classification are selected to validate the proposed approach. Furthermore, the proposed method achieved the classification accuracy on AD- Cognitive Normals (CN) at 97.89%, AD- Mild Cognitive Impairment (MCI) at 99.33% and CN-MCI at 99.44% and on PD-CN at 99.22%, PD- Scans Without Evidence of Dopaminergic Effect (SWEDD) at 97.56% and CN-SWEDD at 98.22% respectively. Also, the multi-class classification shows the promising accuracy of 97.18% for AD and 97.85% for PD for the proposed framework. The findings of the study show that the proposed deep learning-based ensemble technique is competitive for AD and PD prediction in both multiclass and binary class classification. Furthermore, the proposed approach enhances generalization performance in diagnosing neurodegenerative diseases and performs better than existing approaches.

Utilizing deep learning models in an intelligent spiral drawing classification system for Parkinson's disease classification.

Parkinson's disease (PD) is a neurodegenerative illness that impairs normal human movement. The primary cause of PD is the deficiency of dopamine in the human brain. PD also leads to several other challenges, including insomnia, eating disturbances, excessive sleepiness, fluctuations in blood pressure, sexual dysfunction, and other issues. The suggested system is an extremely promising technological strategy that may help medical professionals provide accurate and unbiased disease diagnoses. This is accomplished by utilizing significant and unique traits taken from spiral drawings connected to Parkinson's disease. While PD cannot be cured, early administration of drugs may significantly improve the condition of a patient with PD. An expeditious and accurate clinical classification of PD ensures that efficacious therapeutic interventions can commence promptly, potentially impeding the advancement of the disease and enhancing the quality of life for both patients and their caregivers. Transfer learning models have been applied to diagnose PD by analyzing important and distinctive characteristics extracted from hand-drawn spirals. The studies were carried out in conjunction with a comparison analysis employing 102 spiral drawings. This work enhances current research by analyzing the effectiveness of transfer learning models, including VGG19, InceptionV3, ResNet50v2, and DenseNet169, for identifying PD using hand-drawn spirals. Transfer machine learning models demonstrate highly encouraging outcomes in providing a precise and reliable classification of PD. Actual results demonstrate that the InceptionV3 model achieved a high accuracy of 89% when learning from spiral drawing images and had a superior receiver operating characteristic (ROC) curve value of 95%. The comparison results suggest that PD identification using these models is currently at the forefront of PD research. The dataset will be enlarged, transfer learning strategies will be investigated, and the system's integration into a comprehensive Parkinson's monitoring and evaluation platform will be looked into as future research areas. The results of this study could lead to a better quality of life for Parkinson's sufferers, individualized treatment, and an early classification.

HarmonyTM: multi-center data harmonization applied to distributed learning for Parkinson's disease classification.

Distributed learning is widely used to comply with data-sharing regulations and access diverse datasets for training machine learning (ML) models. The traveling model (TM) is a distributed learning approach that sequentially trains with data from one center at a time, which is especially advantageous when dealing with limited local datasets. However, a critical concern emerges when centers utilize different scanners for data acquisition, which could potentially lead models to exploit these differences as shortcuts. Although data harmonization can mitigate this issue, current methods typically rely on large or paired datasets, which can be impractical to obtain in distributed setups. We introduced HarmonyTM, a data harmonization method tailored for the TM. HarmonyTM effectively mitigates bias in the model's feature representation while retaining crucial disease-related information, all without requiring extensive datasets. Specifically, we employed adversarial training to "unlearn" bias from the features used in the model for classifying Parkinson's disease (PD). We evaluated HarmonyTM using multi-center three-dimensional (3D) neuroimaging datasets from 83 centers using 23 different scanners. Our results show that HarmonyTM improved PD classification accuracy from 72% to 76% and reduced (unwanted) scanner classification accuracy from 53% to 30% in the TM setup. HarmonyTM is a method tailored for harmonizing 3D neuroimaging data within the TM approach, aiming to minimize shortcut learning in distributed setups. This prevents the disease classifier from leveraging scanner-specific details to classify patients with or without PD-a key aspect for deploying ML models for clinical applications.

Assessing gait dysfunction severity in Parkinson’s Disease using 2-Stream Spatial-Temporal Neural Network

Parkinson’s Disease (PD), a neurodegenerative disorder, significantly impacts the quality of life for millions of people worldwide. PD primarily impacts dopaminergic neurons in the brain’s substantia nigra, resulting in dopamine deficiency and gait impairments such as bradykinesia and rigidity. Currently, several well-established tools, such as the Movement Disorder Society-Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) and Hoehn and Yahr (H&Y) Scale, are used for evaluating gait dysfunction in PD. While insightful, these methods are subjective, time-consuming, and often ineffective in early-stage diagnosis. Other methods using specialized sensors and equipment to measure movement disorders are cumbersome and expensive, limiting their accessibility. This study introduces a hierarchical approach to evaluating gait dysfunction in PD through videos. The novel 2-Stream Spatial-Temporal Neural Network (2S-STNN) leverages the spatial–temporal features from the skeleton and silhouette streams for PD classification. This approach achieves an accuracy rate of 89% and outperforms other state-of-the-art models. The study also employs saliency values to highlight critical body regions that significantly influence model decisions and are severely affected by the disease. For a more detailed analysis, the study investigates 21 specific gait attributes for a more nuanced quantification of gait disorders. Parameters such as walking pace, step length, and neck forward angle are found to be strongly correlated with PD gait severity categories. This approach offers a comprehensive and convenient solution for PD management in clinical settings, enabling patients to receive a more precise evaluation and monitoring of their gait impairments.

Automatic Transcranial Sonography-Based Classification of Parkinson's Disease Using a Novel Dual-Channel CNXV2-DANet.

Transcranial sonography (TCS) has been introduced to assess hyper-echogenicity in the substantia nigra of the midbrain for Parkinson's disease (PD); however, its subjective and resource-demanding nature has impeded its widespread application. An AI-empowered TCS-based PD classification tool is greatly demanding, yet relevant research is severely scarce. Therefore, we proposed a novel dual-channel CNXV2-DANet for TCS-based PD classification using a large cohort. A total of 1176 TCS images from 588 subjects were retrospectively enrolled from Beijing Tiantan Hospital, encompassing both the left and right side of the midbrain for each subject. The entire dataset was divided into a training/validation/testing set at a ratio of 70%/15%/15%. Development of the proposed CNXV2-DANet was performed on the training set with comparisons between the single-channel and dual-channel input settings; model evaluation was conducted on the independent testing set. The proposed dual-channel CNXV2-DANet was compared against three state-of-the-art networks (ConvNeXtV2, ConvNeXt, Swin Transformer). The results demonstrated that both CNXV2-DANet and ConvNeXt V2 performed more superiorly under dual-channel inputs than the single-channel input. The dual-channel CNXV2-DANet outperformed the single-channel, achieving superior average metrics for accuracy (0.839 ± 0.028), precision (0.849 ± 0.014), recall (0.845 ± 0.043), F1-score (0.820 ± 0.038), and AUC (0.906 ± 0.013) compared with the single channel metrics for accuracy (0.784 ± 0.037), precision (0.817 ± 0.090), recall (0.748 ± 0.093), F1-score (0.773 ± 0.037), and AUC (0.861 ± 0.047). Furthermore, the dual-channel CNXV2-DANet outperformed all other networks (all p-values < 0.001). These findings suggest that the proposed dual-channel CNXV2-DANet may provide the community with an AI-empowered TCS-based tool for PD assessment.

Classification of Parkinson's disease by deep learning on midbrain MRI.

Susceptibility map weighted imaging (SMWI), based on quantitative susceptibility mapping (QSM), allows accurate nigrosome-1 (N1) evaluation and has been used to develop Parkinson's disease (PD) deep learning (DL) classification algorithms. Neuromelanin-sensitive (NMS) MRI could improve automated quantitative N1 analysis by revealing neuromelanin content. This study aimed to compare classification performance of four approaches to PD diagnosis: (1) N1 quantitative "QSM-NMS" composite marker, (2) DL model for N1 morphological abnormality using SMWI ("Heuron IPD"), (3) DL model for N1 volume using SMWI ("Heuron NI"), and (4) N1 SMWI neuroradiological evaluation. PD patients (n = 82; aged 65 ± 9 years; 68% male) and healthy-controls (n = 107; 66 ± 7 years; 48% male) underwent 3 T midbrain MRI with T2*-SWI multi-echo-GRE (for QSM and SMWI), and NMS-MRI. AUC was used to compare diagnostic performance. We tested for correlation of each imaging measure with clinical parameters (severity, duration and levodopa dosing) by Spearman-Rho or Kendall-Tao-Beta correlation. Classification performance was excellent for the QSM-NMS composite marker (AUC = 0.94), N1 SMWI abnormality (AUC = 0.92), N1 SMWI volume (AUC = 0.90), and neuroradiologist (AUC = 0.98). Reasons for misclassification were right-left asymmetry, through-plane re-slicing, pulsation artefacts, and thin N1. In the two DL models, all 18/189 (9.5%) cases misclassified by Heuron IPD were controls with normal N1 volumes. We found significant correlation of the SN QSM-NMS composite measure with levodopa dosing (rho = -0.303, p = 0.006). Our data demonstrate excellent performance of a quantitative QSM-NMS marker and automated DL PD classification algorithms based on midbrain MRI, while suggesting potential further improvements. Clinical utility is supported but requires validation in earlier stage PD cohorts.

Application of Deep Learning in the Classification of EEG Signals of Parkinson's Disease Patients

This article summarizes research on classifying electroencephalogram (EEG) signals of Parkinson's disease (PD) patients using deep learning technologies. Parkinson's disease is a common neurodegenerative disorder that severely affects quality of life. EEG signals provide valuable information about brain activity. Therefore, analyzing and classifying the EEG signals of PD patients can aid in early diagnosis and treatment. The paper outlines the assessment metrics and cross-validation methods in the diagnosis of Parkinson's disease, highlighting the effectiveness of deep learning in diagnosis. The key technologies reviewed in the article include Wavelet Packet Transform (WPT) and Deep Residual Neural Networks (DRSN), with the WPT-DRSN method achieving up to 99.92% prediction accuracy in the binary classification task of PD patients. Furthermore, this method has also been applied to more complex classweweification tasks, such as categorizing PD patients, REM sleep behavior disorder patients, and healthy controls, maintaining high accuracy. When analyzing Parkinson's disease EEG with the CRNN model, the accuracy is high, but the sample size is small and the model interpretability is limited, necessitating further validation and improvement. For EEG-based PD diagnosis and classification methods, high accuracy was achieved through ICA preprocessing, CSP feature extraction, and ensemble learning classifiers. Future research should consider the integration of multimodal data fusion, deep learning, and NLP technologies, as well as the development of personalized models to enhance the accuracy of PD diagnosis.

Genetics of Parkinson's Disease: From Causes to Treatment.

The genetic architecture of Parkinson's disease (PD) comprises five autosomal dominantly inherited forms with a clinical picture overall resembling idiopathic disease (PARK-SNCA, PARK-LRRK2, PARK-VPS35, PARK-CHCHD2, and PARK-RAB32) and three recessive types (PARK-PRKN, PARK-PINK1, and PARK-PARK7), several monogenic forms causing atypical parkinsonism, as well as a plethora of known genetic risk factors, most notably SNCA and GBA1 including a recently discovered risk variant unique to individuals of African descent, as well as polygenic scores. The Movement Disorder Society Genetic mutation database (MDSGene) (www.mdsgene.org) provides PD genotype-phenotype relationships, whereas global PD genetics networks, such as the Global Parkinson's Genetics Program (www.gp2.org) elucidate PD genetic factors at an unprecedented scale. Two large studies in relatively unselected, multicenter PD samples estimate the frequency of genetic forms, including PARK-GBA1, at ∼15%. PD genetics are becoming increasingly actionable, with the first gene-targeted clinical trials underway. Furthermore, PD genetics has recently been incorporated into a new biological classification of PD.

A unified approach for Parkinson's disease recognition: imbalance mitigation and grid search optimized boosting with LightGBM.

The work elucidates the importance of accurate Parkinson's disease classification within medical diagnostics and introduces a novel framework for achieving this goal. Specifically, the study focuses on enhancing disease identification accuracy utilizing boosting methods. A standout contribution of this work lies in the utilization of a light gradient boosting machine (LGBM) coupled with hyperparameter tuning through grid search optimization (GSO) on the Parkinson's disease dataset derived from speech recording signals. In addition, the Synthetic Minority Over-sampling Technique (SMOTE) has also been employed as a pre-processing technique to balance the dataset, enhancing the robustness and reliability of the analysis. This approach is a novel addition to the study and underscores its potential to enhance disease identification accuracy. The datasets employed in this work include both gender-specific and combined cases, utilizing several distinctive feature subsets including baseline, Mel-frequency cepstral coefficients (MFCC), time-frequency, wavelet transform (WT), vocal fold, and tunable-Q-factor wavelet transform (TQWT). Comparative analyses against state-of-the-art boosting methods, such as AdaBoost and XG-Boost, reveal the superior performance of our proposed approach across diverse datasets and metrics. Notably, on the male cohort dataset, our method achieves exceptional results, demonstrating an accuracy of 0.98, precision of 1.00, sensitivity of 0.97, F1-Score of 0.98, and specificity of 1.00 when utilizing all features with GSO-LGBM. In comparison to AdaBoost and XGBoost, the proposed framework utilizing LGBM demonstrates superior accuracy, achieving an average improvement of 5% in classification accuracy across all feature subsets and datasets. These findings underscore the potential of the proposed methodology to enhance disease identification accuracy and provide valuable insights for further advancements in medical diagnostics.

SS-DRPL: self-supervised deep representation pattern learning for voice-based Parkinson's disease detection.

Parkinson's disease (PD) is a globally significant health challenge, necessitating accurate and timely diagnostic methods to facilitate effective treatment and intervention. In recent years, self-supervised deep representation pattern learning (SS-DRPL) has emerged as a promising approach for extracting valuable representations from data, offering the potential to enhance the efficiency of voice-based PD detection. This research study focuses on investigating the utilization of SS-DRPL in conjunction with deep learning algorithms for voice-based PD classification. This study encompasses a comprehensive evaluation aimed at assessing the accuracy of various predictive models, particularly deep learning methods when combined with SS-DRPL. Two deep learning architectures, namely hybrid Long Short-Term Memory and Recurrent Neural Networks (LSTM-RNN) and Deep Neural Networks (DNN), are employed and compared in terms of their ability to detect voice-based PD cases accurately. Additionally, several traditional machine learning models are also included to establish a baseline for comparison. The findings of the study reveal that the incorporation of SS-DRPL leads to improved model performance across all experimental setups. Notably, the LSTM-RNN architecture augmented with SS-DRPL achieves the highest F1-score of 0.94, indicating its superior ability to detect PD cases using voice-based data effectively. This outcome underscores the efficacy of SS-DRPL in enabling deep learning models to learn intricate patterns and correlations within the data, thereby facilitating more accurate PD classification.

An interpretable deep learning Bayesian optimized random forest framework for the diagnosis of Parkinson's disease in structural magnetic resonance images

AbstractAs one of the fastest‐growing neurological disorders, Parkinson's disease is a neurodegenerative, cardinally motor ailment. Associated with the late onset of symptoms and often misdiagnosed, it inflicts massive life handicaps. To aid in its early detection, the research community is seeking alternative in‐vivo biomarkers, mainly in the field of neuroimaging. This study aimed to build a computer‐aided diagnosis system to distinguish between healthy controls (HC) and early Parkinsonian patients (PD). Our classification paradigm encompasses a Convolutional Neural Network built from scratch to extract discriminatory features, followed by a Bayesian‐optimized Random Forest classifier (CNN_RF). We trained and validated our customized model on the MRI images of 178 PD and 124 HC, taken from the benchmark Parkinson's Progression Markers Initiative (PPMI) dataset, as well as their brain tissue segments and Jacobian determinant maps. The classification was evaluated using seven performance metrics. For visual interpretation, we employed Grad‐CAM to generate saliency maps. Our findings demonstrate the robustness of the proposed method, as it outperformed deep‐tuned ResNet18, VGG16, and SqueezeNet, implemented for comparison. Furthermore, it resulted in 98.9% accuracy, 98.6% specificity, 99.0% precision, 99.5% F1‐score, a 97.7% Matthews correlation coefficient (MCC), and an AUC of 99.6% for the classification of fused gray matter and Jacobian map features. This indicates that the tailored CNN_RF possesses superior adaptability to identify intrinsic characteristics linked to the disease, as highlighted in the salient maps showcasing pertinent regions in the striatum, thalamus, frontal, temporal, and insular cortices for Parkinson's disease classification. Moreover, it offers a single modality and cost‐effective CAD, which could pave the way for a feasible early PD diagnosis. As data availability and AI robustness increase, PD diagnosis will no longer be a challenging task in the future.

EVALUATING SPEECH ANALYSIS TECHNIQUES FOR PARKINSONS DISEASE DETECTION: A COMPARISON OF MACHINE LEARNING AND DEEP LEARNING ALGORITHMS

Parkinsons disease (PD) presents a diagnostic challenge due to its often subtle and gradual onset. Speech analysis offers a promising avenue for early detection, enabling intervention before the disease significantly progresses. This study investigates the efficacy of supervised machine learning algorithms in identifying PD using speech features. We compared the performance of Logistic Regression (LR), Decision Tree (DT), Random Forest (RF), Support Vector Machine (SVM), Naive Bayes (NB), K-Nearest Neighbors (KNN), and Artificial Neural Networks (ANN) for PD classification. Our findings demonstrate the superiority of ANNs, achieving a test accuracy of 97.44%, which surpasses existing benchmarks and highlights their potential for PD diagnosis. This approach leverages readily available speech data, potentially reducing reliance on expensive and time-consuming clinical procedures. This research contributes to the development of non-invasive, speech-based diagnostic tools for PD, paving the way for earlier intervention and improved patient management.

PARKINSON'S DISEASE CLASSIFICATION USING CONTRASTIVE GRAPH CROSS-VIEW LEARNING WITH MULTIMODAL FUSION OF SPECT IMAGES AND CLINICAL FEATURES.

Parkinson's Disease (PD) affects millions globally, impacting movement. Prior research utilized deep learning for PD prediction, primarily focusing on medical images, neglecting the data's underlying manifold structure. This work proposes a multimodal approach encompassing both image and non-image features, leveraging contrastive cross-view graph fusion for PD classification. We introduce a novel multimodal co-attention module, integrating embeddings from separate graph views derived from low-dimensional representations of images and clinical features. This enables more robust and structured feature extraction for improved multi-view data analysis. Additionally, a simplified contrastive loss-based fusion method is devised to enhance cross-view fusion learning. Our graph-view multimodal approach achieves an accuracy of 91% and an area under the receiver operating characteristic curve (AUC) of 92.8% in five-fold cross-validation. It also demonstrates superior predictive capabilities on non-image data compared to solely machine learning-based methods.

Machine Learning Models for Parkinson Disease: Systematic Review.

With the increasing availability of data, computing resources, and easier-to-use software libraries, machine learning (ML) is increasingly used in disease detection and prediction, including for Parkinson disease (PD). Despite the large number of studies published every year, very few ML systems have been adopted for real-world use. In particular, a lack of external validity may result in poor performance of these systems in clinical practice. Additional methodological issues in ML design and reporting can also hinder clinical adoption, even for applications that would benefit from such data-driven systems. To sample the current ML practices in PD applications, we conducted a systematic review of studies published in 2020 and 2021 that used ML models to diagnose PD or track PD progression. We conducted a systematic literature review in accordance with PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines in PubMed between January 2020 and April 2021, using the following exact string: "Parkinson's" AND ("ML" OR "prediction" OR "classification" OR "detection" or "artificial intelligence" OR "AI"). The search resulted in 1085 publications. After a search query and review, we found 113 publications that used ML for the classification or regression-based prediction of PD or PD-related symptoms. Only 65.5% (74/113) of studies used a holdout test set to avoid potentially inflated accuracies, and approximately half (25/46, 54%) of the studies without a holdout test set did not state this as a potential concern. Surprisingly, 38.9% (44/113) of studies did not report on how or if models were tuned, and an additional 27.4% (31/113) used ad hoc model tuning, which is generally frowned upon in ML model optimization. Only 15% (17/113) of studies performed direct comparisons of results with other models, severely limiting the interpretation of results. This review highlights the notable limitations of current ML systems and techniques that may contribute to a gap between reported performance in research and the real-life applicability of ML models aiming to detect and predict diseases such as PD.

Efficient feature fusion model withmodified bidirectional LSTM for automatic Parkinson's disease classification

Efficient feature fusion model withmodified bidirectional LSTM for automatic Parkinson's disease classification

Bridging Modalities: A Multimodal Machine Learning Approach for Parkinson’s Disease Diagnosis Using EEG and MRI Data

Parkinson’s disease (PD) is a slowly progressing neurological disorder with symptoms that overlap with those of other conditions, making early detection and accurate diagnosis vital for effective treatment and a patient’s quality of life. Symptoms such as tremors, stiffness, slow movements, and balance issues, along with psychiatric manifestations, are typical of PD. This study introduces a groundbreaking approach to PD diagnosis, utilizing a multimodal machine learning framework that integrates Electroencephalography (EEG) and Magnetic Resonance Imaging (MRI) data. Focusing on the early detection and accurate classification of PD, the proposed research leverages the distinct yet complementary nature of EEG and MRI datasets to enhance diagnostic precision. We employed a robust algorithmic strategy, including LightGBM and machine learning techniques, to analyze the complex patterns inherent in neurological data. The key steps of the proposed research are preprocessing and feature extraction from both EEG and MRI modalities, followed by their fusion using Principal Component Analysis (PCA) for dimensionality reduction. The fused dataset was then analyzed using a LightGBM model and validated through a 10-fold cross-validation process to ensure reliability and stability. The model’s efficacy was further tested on independent datasets, demonstrating its robustness across diverse patient demographics. The obtained results showcased an accuracy of 97.17%, sensitivity of 96.58%, and specificity of 96.82% in PD classification, outperforming traditional multimodal as well as single-modality diagnostic methods. The integration of EEG and MRI data provided a more comprehensive view of the neurophysiological and neuroanatomical changes associated with PD. Additionally, the use of advanced machine learning algorithms allowed for a nuanced analysis, capturing subtle patterns indicative of early PD stages.

Optimized wavelet and feature set of EEG signal for Parkinson disease classification

Parkinson disease (PD) is a type of neurodegenerative disorder that affects the motor movement of the patient. But each technique has its own advantages or disadvantages. In gene, speech and handwriting data model, the feature extraction and reduction is an important step for efficient classification. These two steps require proper attention for selection and also require high processing time as compared to other data model like images. Because in image modality, the deep learning algorithm can be applied that can perform all process and automate the classification. As compared to these domains, the signal produces better and best results. Because the electroencephalogram (EEG) signal are taken from the brain using electrodes and it helps to observe the brain signals effectively and immediately as compared to the other data modals. Hence, in this paper, the wavelet transform will be used to decompose the signals and statistical features will be extracted from the transformed signal. Here, the satin bower bird optimization will be used for both type of wavelet selection and feature reduction process for final classification. The reduced feature set will be classified using Ensemble Neural Network type including InceptionV3, DenseNet, MobileNet, Xception, and NasNet) recently proposed for medical image classification. The whole process will be realized using MATLAB R2021a software and its performance will be evaluated in terms of Accuracy and is compared against Automated Tunable Q-wavelet transform performance. The proposed ensemble method, employing EEG signal processing and neural networks, achieved a 97% success rate in discriminating PD datasets, surpassing Convolutional Neural Network (CNN) and Machine Learning (ML) classifications (88% –92%). Utilizing MATLAB R2021a, its superiority over Q-wavelet transform was evident, signifying improved PD dataset discrimination.