Depression, self-focused attention, and the negative memory bias.

1989 ◽  
Vol 57 (2) ◽  
pp. 351-357 ◽  
Author(s):  
Tom Pyszczynski ◽  
James C. Hamilton ◽  
Fred H. Herring ◽  
Jeff Greenberg
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Hiroaki Hori ◽  
Mariko Itoh ◽  
Fuyuko Yoshida ◽  
Mingming Lin ◽  
Madoka Niwa ◽  
...  

2018 ◽  
Vol 8 (12) ◽  
pp. e01181 ◽  
Author(s):  
Janna N. Vrijsen ◽  
Camiel T. van Amen ◽  
Bauke Koekkoek ◽  
Iris van Oostrom ◽  
Aart H. Schene ◽  
...  

2018 ◽  
Vol 74 (9) ◽  
pp. 1509-1525 ◽  
Author(s):  
Samuel M.Y. Ho ◽  
Joseph Cheng ◽  
Darren Wai Tong Dai ◽  
Titian Tam ◽  
Otilia Hui

2017 ◽  
Vol 7 (6) ◽  
pp. e00693 ◽  
Author(s):  
Janna N. Vrijsen ◽  
Camiel T. van Amen ◽  
Bauke Koekkoek ◽  
Iris van Oostrom ◽  
Aart H. Schene ◽  
...  

2014 ◽  
Vol 40 ◽  
pp. 181-190 ◽  
Author(s):  
Susanne Vogel ◽  
Lotte Gerritsen ◽  
Iris van Oostrom ◽  
Alejandro Arias-Vásquez ◽  
Mark Rijpkema ◽  
...  

Author(s):  
Johannes Michalak ◽  
Lanre Aranmolate ◽  
Antonia Bonn ◽  
Karen Grandin ◽  
Robert Schleip ◽  
...  

Abstract Background The myofascial system plays a fundamental role in the mechanics of the body, in body tension regulation and the etiology of pathological states like chronic pain. Moreover, it contains contractile elements and preliminary evidence suggests that its properties are linked to psychological factors. The aim of the present research was to investigate characteristics of the myofascial tissue in patients with Major Depressive Disorder (MDD) and to examine whether the state of the myofascial tissue causally affects pathopsychological processes in MDD. Methods In Study 1, stiffness and elasticity of the myofascial tissue of 40 inpatients suffering from MDD measured with a tissue compliance meter were compared with those of 40 matched never-depressed participants. In Study 2, 69 MDD patients were randomly assigned to single-session self-myofascial release intervention (SMRI) or a placebo intervention. Effects on memory bias and affect were investigated. Results Results showed that MDD patients displayed heightened stiffness and reduced elasticity of the myofascial tissue and that patients in the SMRI group showed a reduced negative memory bias and more positive affect compared to patients in the placebo condition. Conclusions The preliminary results of our studies indicate that the myofascial tissue might be part of a dysfunctional body-mind dynamic that maintains MDD.


2015 ◽  
Vol 25 (3) ◽  
pp. 99-105 ◽  
Author(s):  
Janna N. Vrijsen ◽  
Susanne Vogel ◽  
Alejandro Arias-Vásquez ◽  
Barbara Franke ◽  
Guillén Fernández ◽  
...  

2011 ◽  
Vol 42 (2) ◽  
pp. 335-343 ◽  
Author(s):  
L. Gerritsen ◽  
M. Rijpkema ◽  
I. van Oostrom ◽  
J. Buitelaar ◽  
B. Franke ◽  
...  

BackgroundNegative memory bias is thought to be one of the main cognitive risk and maintenance factors for depression, but its neural substrates are largely unknown. Here, we studied whether memory bias is related to amygdala and hippocampal volume, two structures that are critical for emotional memory processes and that show consistent volume alterations in depression.MethodStructural magnetic resonance imaging (MRI) was carried out in 272 healthy participants (62% female, 18–50 years old). All images were acquired on 1.5 T Siemens MRI scanners. Automatic segmentation of amygdala and hippocampus was performed using the FIRST module of FSL. Negative memory bias was assessed by the self-referent encoding/evaluation test.ResultsNegative memory bias was associated with larger amygdala (p=0.042) and smaller hippocampal (p=0.029) volumes. In additional analyses, we found that, compared with the associations found with hippocampus and amygdala volume separately, a stronger association was found between negative memory bias and the ratio of amygdala:hippocampus volume (p=0.021).ConclusionsIn non-depressed subjects we found that larger amygdala and smaller hippocampal volumes are associated with negative memory bias. This suggests that an increased amygdala:hippocampus volume ratio plays a role in cognitive vulnerability often seen in individuals with high risk for depression and that these structural brain differences may pre-date the onset of depression.


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