| Literature DB >> 29202425 |
T V Zhilyaeva1, A V Sergeeva2, A S Blagonravova3, L N Kasimova4, K V Kuznetsov5, V I Golovanova5, T B Shebolkova5, E A Korshunova5.
Abstract
The purpose of the research was to investigate the association of methylenetetrahydrofolate reductase (hereinafter MTHFR) genetic polymorphism 677C>T with schizophrenia in the Russian population in comparison with the control group of healthy blood donors. Also some characteristics of schizophrenia were examined in patients with/without defective T-allele of MTHFR677C>T polymorphism. 500 patients with schizophrenia and 499 blood donors were examined for T-allele carriage of polymorphism MTHFR677C>T by PCR method. 150 archival medical records were studied (in the first patients included in the study). The carriage of T-allele of genetic polymorphism MTHFR677C>T was significantly more common in patients than in healthy donors: 255/500 versus 219/499 (p=0,0287, χ2=4,79; OR=1,33, 95%CI [1037; 1707]). The number of patients with chronic type of schizophrenia onset was significantly more among T-allele carriers (n=77) than among normal CC-genotype carriers (n=73): р=0.038. The number of "incapacitated" persons in the group of patients with defective T-allele (n=77) was significantly higher than in patients with normal genotype (n=73, p=0.0439; OR=2.878, 95%CI=1.111-7.456). The results suggest that T-allele of genetic polymorphism MTHFR677C>T in the population of European Russia may increase the risk of developing schizophrenia and its unfavorable prognosis, which requires further investigation.Entities:
Keywords: Folate deficiency; MTHFR 677C>T; Methylenetetrahydrofolate reductase genetic polymorphism 677C>T; Schizophrenia
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Year: 2017 PMID: 29202425 DOI: 10.1016/j.ajp.2017.11.027
Source DB: PubMed Journal: Asian J Psychiatr ISSN: 1876-2018