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Updated: Aug 31, 2025

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A novel multi-class classification model for schizophrenia, bipolar disorder and healthy controls using comprehensive

Qingxia Yang1, Yi Li2, Bo Li3

  • 1Department of Bioinformatics, Smart Health Big Data Analysis and Location Services Engineering Lab of Jiangsu Province, School of Geographic and Biologic Information, Nanjing University of Posts and Telecommunications, Nanjing, 210023, China.

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Summary

This study identifies 341 differentially expressed genes (DEGs) to create a novel classification model for schizophrenia (SCZ) and bipolar disorder (BP). The model demonstrates strong diagnostic capabilities for these complex psychiatric disorders.

Keywords:
Bipolar disorderGene signatureMulti-class classificationPartial least squares discriminant analysisSchizophrenia

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Area of Science:

  • Neuroscience
  • Genetics
  • Psychiatry

Background:

  • Schizophrenia (SCZ) and bipolar disorder (BP) are prevalent psychiatric disorders with overlapping symptoms and genetic risk factors.
  • Current diagnostic methods rely on symptom-based assessments, highlighting the need for more objective diagnostic tools.
  • The underlying etiology and pathology of SCZ and BP remain unclear, necessitating improved classification models.

Purpose of the Study:

  • To develop a more accurate and consistent classification model for diagnosing schizophrenia (SCZ) and bipolar disorder (BP).
  • To identify a gene signature that can differentiate between SCZ, BP, and healthy individuals.
  • To assess the diagnostic capacity of a novel multi-class classification model.

Main Methods:

  • Combined transcriptomic data from five independent studies, including 120 SCZ patients, 101 BP patients, and 149 healthy controls.
  • Utilized partial least squares discriminant analysis (PLS-DA) to identify 341 differentially expressed genes (DEGs).
  • Constructed a multi-class classification model using support vector machine (SVM) with the identified gene signature.

Main Results:

  • Identified a significant gene signature comprising 341 DEGs with high disease relevance.
  • Analyzed the protein-protein interaction network and gene ontology terms, revealing key roles in psychiatric disorders.
  • The developed SVM multi-class model demonstrated strong classification ability on independent test sets.

Conclusions:

  • The identified gene signature and the novel SVM-based classification model show promise for improving the diagnosis of SCZ and BP.
  • This approach offers a potential pathway towards more objective and accurate diagnostic methods for these psychiatric conditions.
  • Further validation is warranted to translate these findings into clinical practice.