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Investigation of possible epistatic interactions between GRIA2 and GRIA4 variants on clinical outcomes in patients with major depressive disorder

Authors
Chiesa, AlbertoLia, LoredanaLia, ClaudiaLee, Soo-JungHan, ChangsuPatkar, Ashwin A.Pae, Chi-UnSerretti, Alessandro
Issue Date
6월-2013
Publisher
SAGE PUBLICATIONS LTD
Keywords
Glutamate receptor; ionotropic; AMPA 2 (GRIA2); glutamate receptor; ionotropic; AMPA 4 (GRIA4); epistasis; major depression; glutamatergic; single nucleotide polymorphism
Citation
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, v.41, no.3, pp.809 - 815
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
Volume
41
Number
3
Start Page
809
End Page
815
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/103063
DOI
10.1177/0300060513477295
ISSN
0300-0605
Abstract
<sec id="sec11-0300060513477295">Objectives To investigate the effects of glutamate receptor, ionotropic, alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) 2 (GRIA2) rs4260586 and glutamate receptor, ionotropic, AMPA 4 (GRIA4) rs10736648 single nucleotide polymorphisms (SNPs) on response to antidepressants in Korean patients with major depressive disorder (MDD), and to ascertain whether epistatic interactions might exist between these SNPs. <sec id="sec12-0300060513477295">Methods In this retrospective analysis, patients were assessed at hospital admission and discharge using the Montgomery-angstrom sberg depression rating scale (MADRS). A multiple regression model was employed to investigate the effects of the two SNP variants on clinical/sociodemographic outcomes relating to MDD. <sec id="sec13-0300060513477295">Results Out of 145 Korean patients, the presence of both GRIA2 rs4260586 and GRIA4 rs10736648 polymorphisms had no significant association with MADRS improvement scores or other clinical/sociodemographic variables. <sec id="sec14-0300060513477295">Conclusions These data potentially suggest a lack of epistatic interaction between GRIA2 and GRIA4 variants, regarding clinical outcomes in patients with MDD. The study was limited by small sample size, use of different antidepressants and incomplete coverage of genes under investigation. Future research should include larger patient samples treated with different antidepressants, analysis of different SNPs and/or investigation of different gene-gene interactions within the glutamatergic system.
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