Are GRIK3 (T928G) gene variants in schizophrenia patients different from those intheir first-degree relatives?

• Published in: Psychiatry research Vol. 175; no. 1; pp. 43 - 46
• Main Authors: Kilic, Gamze, Ismail Kucukali, Cem, Orhan, Nurcan, Ozkok, Elif, Zengin, Asli, Aydin, Makbule, Kara, Ihsan
• Format: Journal Article
• Language: English
• Published: Elsevier Ireland Ltd 2010
• Subjects: AMPA receptor; GRIK3; Kainate receptor; Polymorphism; Psychiatry; Relatives; Schizophrenia; GRIK3; Schizophrenia; AMPA receptor; Relatives; Kainate receptor; Polymorphism
• ISSN: 0165-1781; 1872-7123
• DOI: 10.1016/j.psychres.2008.10.001

Abstract We examined whether the GRIK3 (T928G) polymorphic variants in patients with schizophrenia are different from those of their first-degree relatives and healthy controls. The study population was composed of 256 patients with schizophrenia, 305 first-degree relatives of schizophrenia patients and 242 healthy control subjects. The GRIK3 (T928G) polymorphism was determined by restriction fragment length polymorphism. The frequency of the TT genotype was predominant, whereas the GG genotype was rare among all groups. The frequencies of GRIK3 (T928G) genotype distributions in the patients with schizophrenia were similar to those of their relatives. The frequency of the GG genotype was significantly higher in patients than in healthy controls. Similarly, GG genotype distribution in relatives was elevated compared with that in controls, but this value did not reach statistical significance. On the other hand, the subgroups of schizophrenia patients did not show a significant association with the GRIK3 (T928G) gene. It appears that the patients share the same (GRIK3) T928G gene variants with their relatives. One interpretation of our findings is that the relatives are at risk for the development of schizophrenia in the future.