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Predicting diseases in the early stages is extremely important. By taking advantage of advances in deep learning and fuzzy logic techniques, a new model is proposed in this paper for disease evaluation depending on the adaptive neuro-fuzzy inference system (ANFIS) with a genetic algorithm (GA) for classification, and the pre-trained DenseNet-201 model for feature extraction, in addition to the whale optimization algorithm (WOA) for feature selection. Two medical databases (chest X-ray and MRI brain tumor) for the diagnosis of two disease types were used as input in the suggested model. The optimization of ANFIS parameters was performed by GA to achieve the optimum prediction capability. DenseNet-201 for feature extraction was employed to obtain better classification accuracy. Having more features sometimes leads to lower accuracy, and this issue can be rectified using a feature selection strategy WOA which gave good results. The proposed model was evaluated utilizing statistical metrics root mean square error (RMSE), mean square error (MSE), standard deviation (STD), and coefficient of determination ( R 2 ), and it was compared with the conventional ANFIS model, with the proposed model (ANFIS-GA) showing a superior prediction capability over the ANFIS model. As a result, it can be concluded that the proposed ANFIS-GA model is efficient and has the potential for a robust diseases evaluation with good accuracy. Also, we conclude from this work that integrating optimization algorithms with ANFIS boosts its performance, resulting in a more accurate and reliable model. [ABSTRACT FROM AUTHOR]

This paper discusses the problem of detecting cancer using such biomarkers as blood protein markers. The purpose of this research is to propose an approach for making decisions in the diagnosis of cancer through the creation of cost-sensitive SVM classifiers on the basis of datasets with a variety of features of different nature. Such datasets may include compositions of known features corresponding to blood protein markers and new features constructed using methods for calculating entropy and fractal dimensions, as well as using the UMAP algorithm. Based on these datasets, multiclass SVM classifiers were developed. They use cost-sensitive learning principles to overcome the class imbalance problem, which is typical for medical datasets. When implementing the UMAP algorithm, various variants of the loss function were considered. This was performed in order to select those that provide the formation of such new features that ultimately allow us to develop the best cost-sensitive SVM classifiers in terms of maximizing the mean value of the metric M a c r o F 1 − s c o r e . The experimental results proved the possibility of applying the UMAP algorithm, approximate entropy and, in addition, Higuchi and Katz fractal dimensions to construct new features using blood protein markers. It turned out that when working with the UMAP algorithm, the most promising is the application of a loss function on the basis of fuzzy cross-entropy, and the least promising is the application of a loss function on the basis of intuitionistic fuzzy cross-entropy. Augmentation of the original dataset with either features on the basis of the UMAP algorithm, features on the basis of the UMAP algorithm and approximate entropy, or features on the basis of approximate entropy provided the creation of the three best cost-sensitive SVM classifiers with mean values of the metric M a c r o F 1 − s c o r e increased by 5.359%, 5.245% and 4.675%, respectively, compared to the mean values of this metric in the case when only the original dataset was utilized for creating the base SVM classifier (without performing any manipulations to overcome the class imbalance problem, and also without introducing new features). [ABSTRACT FROM AUTHOR]

The medical diagnosis of many critical diseases is difficult as it usually requires the combined effort of several doctors. At this time, the process of medical diagnosis is actually a group decision-making (GDM) problem. In group medical diagnosis, considering doctors' weight information and fusing the interaction relation of symptoms remain open issues. To address this problem, a group decision-making method for intuitionistic fuzzy soft environments is proposed for medical diagnosis because the intuitionistic fuzzy soft set (IFSS) integrates the advantages of the soft set and intuitionistic fuzzy set (IFS). Intuitionistic fuzzy soft weighted Muirhead mean operators are constructed by combining Einstein operations with the Muirhead mean (MM) operator, and some properties and results are revealed. A group medical diagnosis model with unknown doctor weight information and incomplete intuitionistic fuzzy soft information is proposed. Similarity measures of the intuitionistic fuzzy soft matrix (IFSM) given by the doctors are used to estimate the incomplete information. To take into account the advantages of objective weight and subjective weight, the combined weights of doctors are calculated based on the IFSMs' similarity measure and doctors' grades. The developed operators are then used to combine the evaluation information and handle the correlation of input arguments in the group medical diagnosis process. Finally, a numerical problem is selected to illustrate the superiority of the proposed approach compared to related methods. The combined weights are determined to overcome the shortcomings of the single-weight method to some extent. Meanwhile, the proposed method is more comprehensive, and can provide more flexible and reasonable choices for group medical diagnosis problems. [ABSTRACT FROM AUTHOR]

Autism Spectrum Disorder (ASD) presents significant diagnostic challenges due to its complex, heterogeneous nature. This study explores a novel approach to enhance the accuracy and reliability of ASD diagnosis by integrating resting-state functional magnetic resonance imaging with demographic data (age, gender, and IQ). This study is based on improving the spectral graph convolutional neural network (GCN). It introduces a multi-view attention fusion module to extract useful information from different views. The graph's edges are informed by demographic data, wherein an edge-building network computes weights grounded in demographic information, thereby bolstering inter-subject correlation. To tackle the challenges of oversmoothing and neighborhood explosion inherent in deep GCNs, this study introduces DropEdge regularization and residual connections, thus augmenting feature diversity and model generalization. The proposed method is trained and evaluated on the ABIDE-I and ABIDE-II datasets. The experimental results underscore the potential of integrating multi-view and multimodal data to advance the diagnostic capabilities of GCNs for ASD. [ABSTRACT FROM AUTHOR]

In the dynamic landscape of healthcare, decision support systems (DSS) confront continuous challenges, especially in the era of big data. Background: This study extends a Q&A-based medical DSS framework that utilizes semantic technologies for disease inference based on a patient's symptoms. The framework inputs "evidential symptoms" (symptoms experienced by the patient) and outputs a ranked list of hypotheses, comprising an ordered pair of a disease and a characteristic symptom. Our focus is on advancing the framework by introducing ontology integration to semantically enrich its knowledgebase and refine its outcomes, offering three key advantages: Propagation, Hierarchy, and Range Expansion of symptoms. Additionally, we assessed the performance of the fully implemented framework in Python. During the evaluation, we inspected the framework's ability to infer the patient's disease from a subset of reported symptoms and evaluated its effectiveness in ranking it prominently among hypothesized diseases. Methods: We conducted the expansion using dedicated algorithms. For the evaluation process, we defined various metrics and applied them across our knowledge base, encompassing 410 patient records and 41 different diseases. Results: We presented the outcomes of the expansion on a toy problem, highlighting the three expansion advantages. Furthermore, the evaluation process yielded promising results: With a third of patient symptoms as evidence, the framework successfully identified the disease in 94% of cases, achieving a top-ranking accuracy of 73%. Conclusions: These results underscore the robust capabilities of the framework, and the enrichment enhances the efficiency of medical experts, enabling them to provide more precise and informed diagnostics. [ABSTRACT FROM AUTHOR]

The prediction of future disease development based on past diagnosis records has gained significant attention due to the growing health awareness among individuals. Recent deep learning-based methods have successfully predicted disease development by establishing relationships for each diagnosis record and extracting features from a patient's past diagnoses in chronological order. However, most of these models have ignored the connections between identified diseases and low-risk diseases, leading to bottlenecks and limitations. In addition, the extraction of temporal characteristics is also hindered by the problem of global feature forgetting. To address these issues, we propose a global context-aware net using disease relationship reasoning and attention-based feature fusion, abbreviated as DRR. Our model incorporates a disease relationship reasoning module that enhances the model's attention to the relationship between confirmed diseases and low-risk diseases, thereby alleviating the current model's bottlenecks. Moreover, we have established a global graph-based feature fusion module that integrates global graph-based features with temporal features, mitigating the issue of global feature forgetting. Extensive experiments were conducted on two publicly available datasets, and the experiments show that our method achieves advanced performance. [ABSTRACT FROM AUTHOR]