Abstract

Background:Over the past decade, numerous studies have focused on identifying genetic factors associated with schizophrenia (SCZ). Sample variations, such as size, population, race, disease status, and data processing methods resulted in selection differences. Nevertheless, no systemic study has been completed to summarize these reports and provide an objective full list of genes with a reported association to SCZ. Methods:We conducted a literature data mining (LDM) of over 13,515 articles covering publications from 1958 to Feb. 2016. These articles reported multiple types of marker-disease associations between 1,219 genes and SCZ. Then we conducted a gene set enrichment analysis (GSEA) and a sub-network enrichment analysis (SNEA) to study the functional profile and validate the pathogenic significance of these genes to SCZ. Finally, we presented additional results from the systemic review, including publication date, quality scores, and author affiliations. Results:All of these genes have been demonstrated to present multiple mutations associating with SCZ, some of which were supported by a large number of high quality articles. Enrichment analyses showed that many psychiatric and neuropathic pathways/groups related to SCZ have been significantly enriched by these genes and that they are functionally associated with each other. Conclusion:Our results indicate that these genes may operate as a functional biomarker network influencing the development of SCZ, and that LDM together with GSEA and SNEA could serve as an effective approach in finding these potential target genes

Highlights

  • Schizophrenia (SCZ) is a mental disorder characterized by abnormal social behavior and failure to understand reality

  • Summary of literature data mining (LDM) Through the LDM approach, we discovered 13,515 articles (1958~ Feb. 2016) reporting 1,219 genes associated with SCZ

  • Some are frequently reported with huge number of article support, such as COMT (430 articles), DRD2 (394 articles) and BDNF (341articles)

Read more

Summary

Introduction

Schizophrenia (SCZ) is a mental disorder characterized by abnormal social behavior and failure to understand reality. We have noticed an increased number of articles reporting over a thousand of genes/proteins that may potentially be related to SCZ (Sacchi et al, 2013; Winchester et al, 2014; Liao et al, 2015). Numerous studies have focused on identifying genetic factors associated with schizophrenia (SCZ). Sample variations, such as size, population, race, disease status, and data processing methods resulted in selection differences.

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.