Finding effective and objective biomarkers to inform the diagnosis of schizophrenia is of great importance yet remains challenging. Relatively little work has been conducted on multi-biological data for the diagnosis of schizophrenia. In this cross-sectional study, we extracted multiple features from three types of biological data, including gut microbiota data, blood data, and electroencephalogram data. Then, an integrated framework of machine learning consisting of five classifiers, three feature selection algorithms, and four cross validation methods was used to discriminate patients with schizophrenia from healthy controls. Our results show that the support vector machine classifier without feature selection using the input features of multi-biological data achieved the best performance, with an accuracy of 91.7% and an AUC of 96.5% (p < 0.05). These results indicate that multi-biological data showed better discriminative capacity for patients with schizophrenia than single biological data. The top 5% discriminative features selected from the optimal model include the gut microbiota features (Lactobacillus, Haemophilus, and Prevotella), the blood features (superoxide dismutase level, monocyte-lymphocyte ratio, and neutrophil count), and the electroencephalogram features (nodal local efficiency, nodal efficiency, and nodal shortest path length in the temporal and frontal-parietal brain areas). The proposed integrated framework may be helpful for understanding the pathophysiology of schizophrenia and developing biomarkers for schizophrenia using multi-biological data.
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http://dx.doi.org/10.1038/s41598-021-94007-9 | DOI Listing |
Front Endocrinol (Lausanne)
June 2024
Department of Urology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China.
Prostate cancer (PCa) is commonly occurred with high incidence in men worldwide, and many patients will be eventually suffered from the dilemma of castration-resistance with the time of disease progression. Castration-resistant PCa (CRPC) is an advanced subtype of PCa with heterogeneous carcinogenesis, resulting in poor prognosis and difficulties in therapy. Currently, disorders in androgen receptor (AR)-related signaling are widely acknowledged as the leading cause of CRPC development, and some non-AR-based strategies are also proposed for CRPC clinical analyses.
View Article and Find Full Text PDFJ Dermatol Sci
January 2022
L'Oréal Research and Innovation, Shanghai, PR China. Electronic address:
Background: Ultraviolet exposure has profound effect on the dermal connective tissue of human skin.
Objective: We aimed to develop and validate an evaluation method/methodology using a full-thickness reconstructed skin model, to assess the anti-photoaging efficacy of cosmetic ingredients and sunscreen formulas by blending multi relevant biological endpoints including the newly developed dermal collagen quantification method with Multi-photon microscopy.
Methods: The response of ex vivo human skin to UVA exposure was first characterized with multiphoton microscopy.
IEEE/ACM Trans Comput Biol Bioinform
October 2022
The important role of microRNA (miRNA) in human diseases has been confirmed by some studies. However, only using biological experiments has greater blindness, leading to higher experimental costs. In this paper a high-efficiency algorithm based on a variety of biological source information and applying a combination of a convolutional neural network (CNN) feature extractor and an extreme learning machine (ELM) classifier is proposed.
View Article and Find Full Text PDFSci Rep
July 2021
Department of Biomedical Engineering, School of Material Science and Engineering, South China University of Technology, Guangzhou, 510006, Guangdong, China.
Finding effective and objective biomarkers to inform the diagnosis of schizophrenia is of great importance yet remains challenging. Relatively little work has been conducted on multi-biological data for the diagnosis of schizophrenia. In this cross-sectional study, we extracted multiple features from three types of biological data, including gut microbiota data, blood data, and electroencephalogram data.
View Article and Find Full Text PDFIEEE/ACM Trans Comput Biol Bioinform
August 2022
With the advances in gene sequencing technologies, millions of somatic mutations have been reported in the past decades, but mining cancer driver genes with oncogenic mutations from these data remains a critical and challenging area of research. In this study, we proposed a network-based classification method for identifying cancer driver genes with merging the multi-biological information. In this method, we construct a cancer specific genetic network from the human protein-protein interactome (PPI) to mine the network structure attributes, and combine biological information such as mutation frequency and differential expression of genes to achieve accurate prediction of cancer driver genes.
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