Scientific Library of Tomsk State University

   E-catalog        

Normal view MARC view

CYP1A2 and CYP2D6 gene polymorphisms in schizophrenic patients with neuroleptic drug-induced side effects S. A. Ivanova, M. L. Filipenko, N. M. Vyalova [et.al.]

Contributor(s): Ivanova, Svetlana A | Vyalova, Natalya M | Voronina, E. N | Pozhidaev, Ivan V | Osmanova, D. Z | Ivanov, M. V | Fedorenko, Olga Yu | Semke, Arkadiy V | Bokhan, Nikolay A | Filipenko, M. LMaterial type: ArticleArticleSubject(s): шизофрения | тардивная дискинезия | полиморфизмы генов | цитохромыGenre/Form: статьи в журналах Online resources: Click here to access online In: Bulletin of experimental biology and medicine Vol. 160, № 5. P. 687-690Abstract: Polymorphic variants of CYP1A2 and CYP2D6 genes of the cytochrome P450 system were studied in patients with schizophrenia with drug-induced motor disorders and hyperprolactinemia against the background of long-term neuroleptic therapy. We revealed an association of polymorphic variant C-163A CYP1A2*1F of CYP1A2 gene with tardive dyskinesia and association of polymorphic variant 1846G>A CY2D6*4 and genotype A/A of CYP2D6 gene (responsible for debrisoquin-4-hydroxylase synthesis) with limbotruncal tardive dyskinesia in patients with schizophrenia receiving neuroleptics for a long time.
Tags from this library: No tags from this library for this title. Log in to add tags.
No physical items for this record

Библиогр.: 15 назв.

Polymorphic variants of CYP1A2 and CYP2D6 genes of the cytochrome P450 system were studied in patients with schizophrenia with drug-induced motor disorders and hyperprolactinemia against the background of long-term neuroleptic therapy. We revealed an association of polymorphic variant C-163A CYP1A2*1F of CYP1A2 gene with tardive dyskinesia and association of polymorphic variant 1846G>A CY2D6*4 and genotype A/A of CYP2D6 gene (responsible for debrisoquin-4-hydroxylase synthesis) with limbotruncal tardive dyskinesia in patients with schizophrenia receiving neuroleptics for a long time.

There are no comments on this title.

to post a comment.
Share