CTLA-4 expression and polymorphisms in Schizophrenia; a systematic review of literature

Mol Biol Rep. 2024 Mar 23;51(1):431. doi: 10.1007/s11033-024-09299-7.

Abstract

Schizophrenia constitutes a severe psychiatric disorder with detrimental impacts on individuals, their support systems, and the broader economy. Extensive research has revealed a notable association between variations in the Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) gene and an increased susceptibility to schizophrenia.This study represents the first systematic review of the literature investigating the impact of CTLA-4 polymorphisms and expression on the development and progression of schizophrenia.Our investigation involved a comprehensive search strategy, using a combination of title, abstract, and MESH terms in four databases, including PubMed, Scopus, Web of Science, and Google Scholar, until August 29th, 2023. The complete texts of the identified records were obtained and rigorously assessed based on predefined exclusion and inclusion criteria. Out of the numerous records, a total of 88 were identified through the databases. 10 studies met the criteria; therefore, their quality was assessed and included in this systematic study. The records were then categorized into polymorphism and expression groups. Our investigation emphasizes an association between rs3087243, rs231779, rs231777, rs16840252, rs5742909, and rs231775 polymorphisms and the development of schizophrenia. The results demonstrate a correlation between CTLA-4 polymorphisms and schizophrenia, compelling the need for further research to thoroughly examine the role of CTLA-4 in schizophrenia and other psychiatric disorders.

Keywords: CTLA-4; Polymorphism; Psychiatric disorders; Schizophrenia; Systematic review; mRNA expression.

Publication types

  • Systematic Review

MeSH terms

  • CTLA-4 Antigen* / genetics
  • Genetic Predisposition to Disease*
  • Humans
  • Polymorphism, Single Nucleotide
  • Schizophrenia* / genetics

Substances

  • CTLA-4 Antigen
  • CTLA4 protein, human