Working memory deficits in schizophrenia are associated with the rs34884856 variant and expression levels of the NR4A2 gene in a sample Mexican population: a case control study

• Published in: BMC psychiatry Vol. 21; no. 1; pp. 86 - 13
• Main Authors: Ruiz-Sánchez, Elizabeth, Jiménez-Genchi, Janet, Alcántara-Flores, Yessica M., Castañeda-González, Carlos J., Aviña-Cervantes, Carlos L., Yescas, Petra, del Socorro González-Valadez, María, Martínez-Rodríguez, Nancy, Ríos-Ortiz, Antonio, González-González, Martha, López-Navarro, María E., Rojas, Patricia
• Format: Journal Article
• Language: English
• Published: London BioMed Central 09.02.2021; BioMed Central Ltd; BMC
• Subjects: Analysis; Animal models; Biomarkers; Case-Control Studies; Clinical trials; Cognition; Cognition & reasoning; Cognitive ability; Complications and side effects; Demographic aspects; Diagnosis; Disease; Endophenotype; Gene expression; Genetic aspects; Genetic diversity; Genomics; Genotype & phenotype; Genotypes; Genotyping; Humans; Leukocytes (mononuclear); Medicine; Medicine & Public Health; Memory; Memory Disorders; Memory, Disorders of; Memory, Short-Term; Mental disorders; Mexico; Neuropsychological Tests; NR4A2 genetic variants; NR4A2 mRNA levels; Nuclear Receptor Subfamily 4, Group A, Member 2; Population; Population studies; Psychiatric molecular genetics; Psychiatrists; Psychiatry; Psychotherapy; Research Article; Risk factors; Schizophrenia; Schizophrenia - complications; Schizophrenia - genetics; Short term memory; Working memory; Mexico; genetic variants; Schizophrenia; mRNA levels; Cognition; Working memory; Endophenotype; NR4A2 genetic variants; NR4A2 mRNA levels
• ISSN: 1471-244X; 1471-244X
• DOI: 10.1186/s12888-021-03081-w

Background Cognitive functions represent useful endophenotypes to identify the association between genetic variants and schizophrenia. In this sense, the NR4A2 gene has been implicated in schizophrenia and cognition in different animal models and clinical trials. We hypothesized that the NR4A2 gene is associated with working memory performance in schizophrenia. This study aimed to analyze two variants and the expression levels of the NR4A2 gene with susceptibility to schizophrenia, as well as to evaluate whether possession of NR4A2 variants influence the possible correlation between gene expression and working memory performance in schizophrenia. Methods The current study included 187 schizophrenia patients and 227 controls genotyped for two of the most studied NR4A2 genetic variants in neurological and neuropsychiatric diseases. Genotyping was performed using High Resolution Melt and sequencing techniques. In addition, mRNA expression of NR4A2 was performed in peripheral mononuclear cells of 112 patients and 118 controls. A group of these participants, 54 patients and 87 controls, performed the working memory index of the WAIS III test. Results Both genotypic frequencies of the two variants and expression levels of the NR4A2 gene showed no significant difference when in patients versus controls. However, patients homozygous for the rs34884856 promoter variant showed a positive correlation between expression levels and auditory working memory. Conclusions Our finding suggested that changes in expression levels of the NR4A2 gene could be associated with working memory in schizophrenia depending on patients’ genotype in a sample from a Mexican population.