Psychiatry and Clinical Psychopharmacology
Original Article

Investigating the eNOS and IFN-γ Gene Variants Susceptible to Bipolar Disorder or Schizophrenia in a Turkish Cohort

1.

Istanbul University, Istanbul Faculty of Medicine, Department of Medical Biology, Istanbul Faculty of Medicine, Istanbul University, Istanbul;Turkey

2.

Malazgirt State Hospital, Psychiatry Unit, Mus

3.

Gaziantep University, Department of Internal Medicine Division of Hematology, Gaziantep

4.

Hitit University, Department of Medical Genetics, Faculty of Medicine, Corum, Turkey

Psychiatry and Clinical Psychopharmacology 2020; 30: 354-361
DOI: 10.5455/PCP.20200807083153
Read: 1981 Downloads: 773 Published: 20 January 2021

Background: Schizophrenia (Sch) and bipolar disorder (BD) are debilitating chronic psychiatric disorders that are both etiologically and clinically heterogeneous. According to the gathered evidence, multiple mental disorders are accompanied by inflammation. Interferon-γ (IFN-γ), as a regulatory cytokine, is involved in the immune response as a proinflammatory mediator. Several critical physiological functions are regulated and governed by nitric oxide (NO) in the central nervous system. This study aimed to investigate the association between IFN-γ +874T/A and eNOS 894G/T variants and Sch or BD susceptibility.

Methods: Blood samples were collected from patients and healthy subjects. IFN-γ +874T/A and eNOS 894G/T variants were genotyped with the PCR-RFLP. We evaluated the patients with some clinical parameters (the duration of the disorder, age of onset, number of hospitalizations, family history, tobacco smoking or drug, alcohol usage). Statistical analyses were performed using the SPSS version.

Results: When the genotype distributions and allele frequencies of the IFN-γ +874T/A and eNOS 894G/T in the patients diagnosed with Sch or BD were compared with the control group, there were not found to be significant differences between the groups. When comparing IFN-γ +874T/A and eNOS 894G/T genotype distributions and allele frequencies of Sch or BD patients due to clinical parameters, the genotype distribution of IFN-γ +874T/A in BD patients was significantly different between the groups due to the presence of tobacco smoking (OR: 0.217, 95%Cl: 0.054–0.878; p = 0.032).

Conclusions: To the best of our knowledge, this is the first study that examines the association between the IFN-γ and eNOS gene variants and Sch or BD in a Turkish population. Although IFN-γ +874T/A and eNOS 894G/T variants are not considered as candidate genes for Sch or BD, the results indicated that the BD patients carrying IFN-γ +874T/A AA genotype were less susceptible to tobacco smoking in a Turkish population.

To cite this article: Pehlivan S, Aytac HM, Ciftci Senturk H, Oyaci Y, Pehlivan M, Nursal AF. Investigating the eNOS and IFN-γ Gene Variants Susceptible to Bipolar Disorder or Schizophrenia in a Turkish Cohort. Psychiatry and Clinical Psychopharmacology 2020;30(4):354-361

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