| Literature DB >> 25772786 |
Jae-Min Kim1, Robert Stewart2, Hee-Ju Kang3, Kyung-Yeol Bae3, Sung-Wan Kim3, Il-Seon Shin3, Young Joon Hong4, Youngkeun Ahn4, Myung Ho Jeong4, Sung-Woo Park5, Young-Hoon Kim5, Jin-Sang Yoon3.
Abstract
Genes coding for the serotonergic pathway have been associated with depressive disorders. However, these associations have rarely been tested in acute coronary syndrome (ACS) patients vulnerable to depression. This study aimed to investigate whether polymorphisms of serotonin transporter (5-HTT) and serotonin 2a receptor (5-HTR2a) genes are associated with occurrence of depressive disorder in ACS. 969 patients with recently developed ACS were recruited at baseline, and 711 were followed 1 year thereafter. Depressive disorder was diagnosed according to DSM-IV criteria, and analysed as an outcome at baseline (prevalence), and follow up (incidence and persistence). Genotypes were ascertained for 5-HTTLPR, STin2 VNTR, 5-HTR2a 102T/C, and 5-HTR2a 1438A/G. Logistic regression models were used to investigate associations. The 5-HTTLPR s/s genotype was independently associated with depressive disorder prevalence and persistence following ACS, but no significant associations were found with the other polymorphisms. ACS patients with the 5-HTTLPR s allele are thus potentially susceptible to depressive disorder in the early phase after ACS, and with its persistence over the subsequent year.Entities:
Keywords: Acute coronary syndrome; Depression; Genetic association study; Serotonin receptor; Serotonin transporter
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Year: 2015 PMID: 25772786 DOI: 10.1016/j.euroneuro.2015.02.006
Source DB: PubMed Journal: Eur Neuropsychopharmacol ISSN: 0924-977X Impact factor: 4.600