The association of suicide risk with negative life events and social support according to gender in Asian patients with major depressive disorder

2015 ◽  
Vol 228 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Subin Park ◽  
Ahmad Hatim Sulaiman ◽  
Manit Srisurapanont ◽  
Sung-man Chang ◽  
Chia-Yih Liu ◽  
...  
2001 ◽  
Vol 42 (1) ◽  
pp. 57-63 ◽  
Author(s):  
Yoav Kohn ◽  
Joseph Zislin ◽  
Ofer Agid ◽  
Bella Hanin ◽  
Tristan Troudart ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Jiarun Yang ◽  
Siyuan Ke ◽  
Zhengxue Qiao ◽  
Xiuxian Yang ◽  
Xiaohui Qiu ◽  
...  

Background: Recent studies suggest that glycogen synthase kinase (GSK)-3β is involved in the development of major depressive disorder (MDD). The aim of this study was to investigate the interaction between GSK-3β polymorphism (rs6438552, rs334558, and rs2199503) and negative life events in the pathogenesis of major depressive disorder (MDD).Methods: DNA genotyping was performed on peripheral blood leukocytes in 550 patients with MDD and 552 age- and gender-matched controls. The frequency and severity of negative life events were assessed by the Life Events Scale (LES). A chi-square method was employed to assess the gene-environment interaction (G × E).Results: Differences in rs6438552, rs334558, and rs2199503 genotype distributions were observed between MDD patients and controls. Significant G × E interactions between allelic variation of rs6438552, rs334558, and rs2199503 and negative life events were observed. Individuals with negative life events and carrying genotypes of rs6438552 A+, rs334558 A+, and rs2199503G+ have increased the risk of depression.Conclusions: These results indicate that interactions between the GSK-3β rs6438552, rs334558, and rs2199503 polymorphisms and environment increases the risk of developing MDD.


2006 ◽  
Vol 36 (6) ◽  
pp. 779-788 ◽  
Author(s):  
ULLA LESKELÄ ◽  
HEIKKI RYTSÄLÄ ◽  
ERKKI KOMULAINEN ◽  
TARJA MELARTIN ◽  
PETTERI SOKERO ◽  
...  

Background. Adverse life events and social support may influence the outcome of major depressive disorder (MDD). We hypothesized that outcome would depend on the level of depressive symptoms present at the outset, with those in partial remission being particularly vulnerable.Method. In the Vantaa Depression Study (VDS), patients with DSM-IV MDD were interviewed at baseline, and at 6 and 18 months. Life events were investigated with the Interview for Recent Life Events (IRLE) and social support with the Interview Measure of Social Relationships (IMSR) and the Perceived Social Support Scale – Revised (PSSS-R). The patients were divided into three subgroups at 6 months, those in full remission (n=68), partial remission (n=75) or major depressive episode (MDE) (n=50). The influence of social support and negative life events during the next 12 months on the level of depressive symptoms, measured by the Hamilton Rating Scale for Depression (HAMD), was investigated at endpoint.Results. The severity of life events and perceived social support influenced the outcome of depression overall, even after adjusting for baseline level of depression and neuroticism. In the full remission subgroup, both severity of life events and subjective social support significantly predicted outcome. However, in the partial remission group, only the severity of events, and in the MDE group, the level of social support were significant predictors.Conclusions. Adverse life events and/or poor perceived social support influence the medium-term outcome of all psychiatric patients with MDD. These factors appear to have the strongest predictive value in the subgroup of patients currently in full remission.


2015 ◽  
Vol 61 (8) ◽  
pp. 735-742 ◽  
Author(s):  
Subin Park ◽  
Ahmad Hatim ◽  
Tian-Mei Si ◽  
Hong Jin Jeon ◽  
Manit Srisurapanont ◽  
...  

2010 ◽  
Vol 41 (4) ◽  
pp. 721-729 ◽  
Author(s):  
S. Gheyara ◽  
K. L. Klump ◽  
M. McGue ◽  
W. G. Iacono ◽  
S. A. Burt

BackgroundPrior work has suggested that genetic influences on major depressive disorder (MDD) may be activated by the experience of negative life events. However, it is unclear whether these results persist when controlling for the possibility of confounding active gene–environment correlations (rGE).MethodWe examined a sample of 1230 adopted and biological siblings between the ages of 10 and 20 years from the Sibling Interaction and Behavior Study. MDD was measured via a lifetime DSM-IV symptom count. Number of deaths experienced served as our environmental risk experience. Because this variable is largely independent of the individual's choices/behaviors, we were able to examine gene–environment interactions while circumventing possible rGE confounds.ResultsBiometric analyses revealed pronounced linear increases in the magnitude of genetic influences on symptoms of MDD with the number of deaths experienced, such that genetic influences were estimated to be near-zero for those who had experienced no deaths but were quite large in those who had experienced two or more deaths (i.e. accounting for roughly two-thirds of the phenotypic variance). By contrast, shared and non-shared environmental influences on symptoms of MDD were not meaningfully moderated by the number of deaths experienced.ConclusionsSuch results constructively replicate prior findings of genetic moderation of depressive symptoms by negative life events, thereby suggesting that this effect is not a function of active rGE confounds. Our findings are thus consistent with the notion that exposure to specific negative life events may serve to activate genetic risk for depression during adolescence.


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