Genetic Polymorphism of 1019C/G (rs6295) Promoter of Serotonin 1A Receptor and Catechol-O-Methyltransferase in Panic Disorder.
- Author:
Takashi WATANABE
1
;
Shin ISHIGURO
;
Akiko AOKI
;
Mikito UEDA
;
Yuki HAYASHI
;
Kazufumi AKIYAMA
;
Kazuko KATO
;
Kazutaka SHIMODA
Author Information
- Publication Type:Twin Study ; Original Article
- Keywords: Panic disorder; Serortonin transporter gene linked polymorphic region; Serotonin 1A receptor; Catechol-O-methyltransferase
- MeSH: Agoraphobia; Asian Continental Ancestry Group; Case-Control Studies; Catechol O-Methyltransferase*; Gene Frequency; Genotype; Humans; Panic Disorder*; Panic*; Polymorphism, Genetic*; Receptor, Serotonin, 5-HT1A*; Serotonin Plasma Membrane Transport Proteins; Serotonin*
- From:Psychiatry Investigation 2017;14(1):86-92
- CountryRepublic of Korea
- Language:English
- Abstract: OBJECTIVE: Family and twin studies have suggested genetic liability for panic disorder (PD) and therefore we sought to determine the role of noradrenergic and serotonergic candidate genes for susceptibility for PD in a Japanese population. METHODS: In this age- and gender-matched case-control study involving 119 PD patients and 119 healthy controls, we examined the genotype distributions and allele frequencies of the serotonin transporter gene linked polymorphic region (5-HTTLPR), −1019C/G (rs6295) promoter polymorphism of the serotonin receptor 1A (5-HT1A), and catechol-O-methyltransferase (COMT) gene polymorphism (rs4680) and their association with PD. RESULTS: No significant differences were evident in the allele frequencies or genotype distributions of the COMT (rs4680), 5-HTTLPR polymorphisms or the −1019C/G (rs6295) promoter polymorphism of 5-HT1A between PD patients and controls. Although there were no significant associations of these polymorphisms with in subgroups of PD patients differentiated by gender or in subgroup comorbid with agoraphobia (AP), significant difference was observed in genotype distributions of the −1019C/G (rs6295) promoter polymorphism of 5-HT1A between PD patients without AP and controls (p=0.047). CONCLUSION: In this association study, the 1019C/G (rs6295) promoter polymorphism of the 5-HT1A receptor G/G genotype was associated with PD without AP in a Japanese population.
