Correlation between variants of the CREB1 and GRM7 genes and risk of depression

BMC Psychiatry. 2023 Jan 3;23(1):3. doi: 10.1186/s12888-022-04458-1.

Abstract

The pathogenesis of depression involves cAMP-response element binding protein1 (CREB1) and metabotropic glutamate receptor 7 (GRM7), and their genetic polymorphisms may affect susceptibility to depression. The purpose of this study was to investigate whether the CREB1 polymorphisms rs2253206 and rs10932201 and the GRM7 polymorphism rs162209 are associated with the risk of depression. Using polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing, we analyzed the rs2253206, rs10932201, and rs162209 frequencies in 479 patients with depression and 329 normal controls. The results showed that the rs2253206 and rs10932201 polymorphisms were significantly associated with an increased risk of depression. However, no association was found between rs162209 and depression risk. When the data were stratified for several disease-related variables, none of the three polymorphisms were found to be correlated to onset, disease severity, family history, or suicidal tendency. Thus, the present findings indicate that the CREB1 polymorphisms rs2253206 and rs10932201 may be related to the occurrence of depression.

Keywords: Depression; Glutamate receptor 7; Polymorphism; cAMP-response element-binding protein 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Cyclic AMP Response Element-Binding Protein / genetics
  • Depression* / genetics
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Polymorphism, Single Nucleotide*

Substances

  • CREB1 protein, human
  • Cyclic AMP Response Element-Binding Protein