genotype variations of rs13381800 in tcf4 gene and rs17039988 in nrxn1 gene among a sample of iranian patients with schizophrenia

Objective: schizophrenia is a complicated mental disorder that affects about 1% of the world's population. it is a complex disease and is approximately 80% inherited. one of the candidate genes in schizophrenia is transcription factor 4 (tcf4), which is positioned on chromosome 18 and is a transcription factor that plays a role in the transcription of neurexin 1(nrxn1) gene, which is one of the candidate genes for developing schizophrenia. this case-control study aimed to investigate the correlation of tcf4 rs13381800 and nrxn1 rs17039988 polymorphisms with the risk of schizophrenia in a sample of iranian patients with schizophrenia. method: a total of 200 individuals were included in this study: 100 patients with schizophrenia (65 males and 35 females), with the mean age of 40.80 ± 11.298 years, and 100 as a control group (63 males and 37 females), with the mean age 32.92 ± 7.391 years. allele specific polymerase chain reaction and restriction fragment length polymorphism (pcr-rflp) were done, respectively, for genotyping of rs13381800 (t/c) and rs17039988 (a/c) polymorphisms. results: the results showed that the frequency of c / c genotype in rs13381800 in patients’ group was 9%, while it was 13% in the control group. also, the frequency of c / c genotype in rs17039988 was 9% in patients and 7% in control groups. statistical analysis of polymorphisms showed no correlation between patients and controls in rs13381800 (or = 1.51; ci = 95%; p = 0.366) and rs17039988 (or = 0.76; ci = 95%; p = 0.602). conclusion: no significant difference was found between rs13381800 and rs17039988 genotypes between patients and control groups in terms of gender, age and education in the patients group. our study suggests that there was no correlation between desired polymorphisms with schizophrenia in the studied population.