Ambulatory emotional reactivity to negative daily life events predicts remission from major depressive disorder

2010 ◽  
Vol 48 (8) ◽  
pp. 754-760 ◽  
Author(s):  
Frenk Peeters ◽  
Johannes Berkhof ◽  
Jonathan Rottenberg ◽  
Nancy A. Nicolson
2020 ◽  
Vol 29 ◽  
Author(s):  
C. E. Lloyd ◽  
N. Sartorius ◽  
H. U. Ahmed ◽  
A. Alvarez ◽  
S. Bahendeka ◽  
...  

Abstract Aims To examine the factors that are associated with changes in depression in people with type 2 diabetes living in 12 different countries. Methods People with type 2 diabetes treated in out-patient settings aged 18–65 years underwent a psychiatric assessment to diagnose major depressive disorder (MDD) at baseline and follow-up. At both time points, participants completed the Patient Health Questionnaire (PHQ-9), the WHO five-item Well-being scale (WHO-5) and the Problem Areas in Diabetes (PAID) scale which measures diabetes-related distress. A composite stress score (CSS) (the occurrence of stressful life events and their reported degree of ‘upset’) between baseline and follow-up was calculated. Demographic data and medical record information were collected. Separate regression analyses were conducted with MDD and PHQ-9 scores as the dependent variables. Results In total, there were 7.4% (120) incident cases of MDD with 81.5% (1317) continuing to remain free of a diagnosis of MDD. Univariate analyses demonstrated that those with MDD were more likely to be female, less likely to be physically active, more likely to have diabetes complications at baseline and have higher CSS. Mean scores for the WHO-5, PAID and PHQ-9 were poorer in those with incident MDD compared with those who had never had a diagnosis of MDD. Regression analyses demonstrated that higher PHQ-9, lower WHO-5 scores and greater CSS were significant predictors of incident MDD. Significant predictors of PHQ-9 were baseline PHQ-9 score, WHO-5, PAID and CSS. Conclusion This study demonstrates the importance of psychosocial factors in addition to physiological variables in the development of depressive symptoms and incident MDD in people with type 2 diabetes. Stressful life events, depressive symptoms and diabetes-related distress all play a significant role which has implications for practice. A more holistic approach to care, which recognises the interplay of these psychosocial factors, may help to mitigate their impact on diabetes self-management as well as MDD, thus early screening and treatment for symptoms is recommended.


2020 ◽  
Vol 285 ◽  
pp. 112847 ◽  
Author(s):  
Bryce J. M. Bogie ◽  
Flávio P. Kapczinski ◽  
Randi E. McCabe ◽  
Margaret C. McKinnon ◽  
Benicio N. Frey

2001 ◽  
Vol 42 (1) ◽  
pp. 57-63 ◽  
Author(s):  
Yoav Kohn ◽  
Joseph Zislin ◽  
Ofer Agid ◽  
Bella Hanin ◽  
Tristan Troudart ◽  
...  

2015 ◽  
Vol 228 (3) ◽  
pp. 277-282 ◽  
Author(s):  
Subin Park ◽  
Ahmad Hatim Sulaiman ◽  
Manit Srisurapanont ◽  
Sung-man Chang ◽  
Chia-Yih Liu ◽  
...  

2020 ◽  
Author(s):  
Stevan Nikolin ◽  
Nicholas Chand ◽  
Donel Martin ◽  
Jacqueline Rushby ◽  
Colleen Loo ◽  
...  

Background: Individuals with major depressive disorder present with deficits in emotional reactivity. Conflicting models have been proposed to characterise the direction of this effect. Previous studies mostly support the emotional context insensitivity model, which suggests that reactivity to positive and negatively-valenced emotional stimuli is blunted in depression. We sought to test the emotional context insensitivity hypothesis in a preregistered study. Methods: Forty-one depressed participants and 41 age- and gender-matched healthy controls were shown a series of unpleasant and neutrally-valenced pictures in a passive view paradigm while acquiring electroencephalography (EEG). The late positive potential (LPP), an EEG marker of emotional reactivity, was compared between groups using mixed-effects repeated-measures models and exploratory cluster-based permutation tests. Results: We found no difference in LPP amplitudes between MDD and healthy individuals using the preregistered analysis plan. However, exploratory permutation analysis revealed a significant reduction in the LPP for MDD participants while viewing unpleasant pictures in EEG electrodes marginally more posterior and within a narrower time interval than specified in our original analysis plan. Secondary analyses found that emotion regulation strategy use and anxiety comorbidity did not influence the LPP. Conclusions: We found significantly reduced LPP amplitudes to unpleasant pictures in MDD, in support of the emotional context insensitivity hypothesis. However, the parameters used to estimate the LPP deviated from the preregistered analysis plan, suggesting that methodological differences between studies may result in variability in the cortical response to emotional stimuli. 


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.


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