%A Tantawy, Ashraf
%A Al-Yahia, Abduhamid
%A Raya, Yasser
%A Al-Mohaimeed, Abdurrahman
%A Settin, Ahmad
%T Catechol-O-methyltransferase gene polymorphisms in Saudi cases with schizophrenia
%9 Original Article
%D 2015
%J Egyptian Journal of Psychiatry
%P 118-123
%V 36
%N 3
%U https://new.ejpsy.eg.net//article.asp?issn=1110-1105;year=2015;volume=36;issue=3;spage=118;epage=123;aulast=Tantawy
%8 September 1, 2015
%X Background
This work was conducted to test for the association of genetic polymorphisms of catechol-O-methyltransferase (COMT) with the susceptibility and clinical patterns of schizophrenia among Saudi patients.
Participants and methods
This is a case-control study involving 79 patients fulfilling the ICD-10 criteria of schizophrenia and 82 healthy controls. Patients were interviewed by different tools, which included the Diagnostic Interview for Genetic Studies (DIGS/V4.0), the Positive and Negative Symptoms Scale (PANSS), and the World Health Organization Disability Assessment Schedule (version 2.0) (WHO/DAS II). All patients and controls were screened for COMT G >A gene polymorphisms using the real-time PCR technique.
Results
Frequencies of all genetic variants of COMT G >A [V158M] did not show a significant difference on comparing cases with controls (P > 0.05). Comparing the frequencies of genetic variants in cases having positive parental consanguinity and a family history of schizophrenia or other mental illnesses with those without a history also showed nonsignificant results (P > 0.05). A stratified analysis related to severity scores and associated clinical illnesses also showed a nonsignificant difference (P > 0.05).
Conclusion
Polymorphism related to COMT G >A was not associated with the susceptibility and the severity of schizophrenia among Saudi cases.
%0 Journal Article
%I Wolters Kluwer Medknow Publications
%@ 1110-1105