Title of article :
Association between IFN-γ +874 T/A (Rs2430561) Polymorphisms and Bipolar 1 Disorder: A Study in an Ethnic Iranian Population
Author/Authors :
Fatemi Nayeri, Mahdieh Psychiatry and Behavioral Sciences Research Center - Mashhad University of Medical Sciences, Iran , Talaei, Ali Psychiatry and Behavioral Sciences Research Center - Mashhad University of Medical Sciences, Iran , Tavakkol Afshari, Jalil Immunology Research Center - Mashhad University of Medical Sciences, Iran , Nikpoor, Amin Reza Department of Immunology - Faculty of Medicine - Hormozgan University of Medical Sciences, Bandar Abbas, Iran , Talaei, Andisheh Department of Biotechnology - University College of Science - University of Tehran, Iran , Ganjali, Rashin Psychiatry and Behavioral Sciences Research Center - Mashhad University of Medical Sciences, Iran
Abstract :
Background: The pathophysiology of bipolar 1 disorder (B1D), a major psychiatric disorder with
inflammatory origins and structural changes in the brain, is of great interest to researchers. Pro-inflammatory
biomarkers and specific gene expression play pivotal roles in B1D development, and IFN-γ has emerged as an
important inflammatory marker. The aim of this research was to determine whether the INF-γ +874 T/A
polymorphism is associated with B1D susceptibility in an ethnic Iranian population.
Methods: The IFN-γ +874 T/A (rs2430561) gene polymorphism was studied in 106 B1D patients and 109
control subjects using sequence specific primers (SSPs) and amplification refractory mutation systempolymerase chain reaction (ARMS-PCR).
Results:Significant statistical differences in IFN-γ +874 T/A polymorphism genotype distribution were found
between the patients and control subjects (P = 0.0006). Decreased risk of B1D was detected in the codominant
model (T/T vs T/A and A/A, or = 0.19, 95% CI = 0.07-0.49 for T/A, or = 0.38, 95% CI = 0.12-1.24 for
A/A, P value=0.0006), and in the dominant model (T/T vs T/A-A/A, or = 0.21, 95% CI = 0.08-0.54, P =
0.0005). However, no significant difference in the IFN-γ polymorphism allele distribution was found between
the two groups (P = 0.25).
Conclusions: The IFN-γ +874 T/A polymorphism may have a significant role in BID development.
Keywords :
Bipolar 1 Disorder , Gene Polymorphism , Interferon gamma
Journal title :
Reports of Biochemistry and Molecular Biology (RBMB)