TY - JOUR
T1 - Dimensions of delusions in major depression
T2 - Socio-demographic and clinical correlates in an unipolar-bipolar sample
AU - Zaninotto, Leonardo
AU - Souery, Daniel
AU - Calati, Raffaella
AU - Camardese, Giovanni
AU - Janiri, Luigi
AU - Montgomery, Stuart
AU - Kasper, Siegfried
AU - Zohar, Joseph
AU - DeRonchi, Diana
AU - Mendlewicz, Julien
AU - Serretti, Alessandro
N1 - Publisher Copyright:
Copyright © 2015, Korean College of Neuropsychopharmacology.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Objective: The present study aims at exploring associations between a continuous measure of distorted thought contents and a set of demographic and clinical features in a sample of unipolar/bipolar depressed patients. Methods: Our sample included 1,833 depressed subjects. Severity of mood symptoms was assessed by the 21 items Hamilton Depression Rating Scale (HAM-D). The continuous outcome measure was represented by a delusion (DEL) factor, extracted from HAM-D items and including items: 2 ("Feelings of guilt"), 15 (" Hypochondriasis"), and 20 ("Paranoid symptoms"). Each socio-demographic and clinical variable was tested by a generalized linear model test, having depressive severity (HAM-D score-DEL score) as the covariate. Results: A family history of major depressive disorder (MDD; p=0.0006), a diagnosis of bipolar disorder, type I (p=0.0003), a comorbid general anxiety disorder (p<.0001), and a higher number of manic episodes during lifetime (p<.0001), were all associated to higher DEL scores. Conversely, an older age at onset (p<.0001) and a longer duration of hospitalization for depression over lifetime (p=0.0003) had a negative impact over DEL scores. On secondary analyses, only the presence of psychotic features (p<.0001) and depressive severity (p<.0001) were found to be independently associated to higher DEL scores. Conclusion: The retrospective design and a non validated continuous measure for distorted thought contents were the main limitations of our study. Excluding the presence of psychotic features and depressive severity, no socio-demographic or clinical variable was found to be associated to our continuous measure of distorted thinking in depression.
AB - Objective: The present study aims at exploring associations between a continuous measure of distorted thought contents and a set of demographic and clinical features in a sample of unipolar/bipolar depressed patients. Methods: Our sample included 1,833 depressed subjects. Severity of mood symptoms was assessed by the 21 items Hamilton Depression Rating Scale (HAM-D). The continuous outcome measure was represented by a delusion (DEL) factor, extracted from HAM-D items and including items: 2 ("Feelings of guilt"), 15 (" Hypochondriasis"), and 20 ("Paranoid symptoms"). Each socio-demographic and clinical variable was tested by a generalized linear model test, having depressive severity (HAM-D score-DEL score) as the covariate. Results: A family history of major depressive disorder (MDD; p=0.0006), a diagnosis of bipolar disorder, type I (p=0.0003), a comorbid general anxiety disorder (p<.0001), and a higher number of manic episodes during lifetime (p<.0001), were all associated to higher DEL scores. Conversely, an older age at onset (p<.0001) and a longer duration of hospitalization for depression over lifetime (p=0.0003) had a negative impact over DEL scores. On secondary analyses, only the presence of psychotic features (p<.0001) and depressive severity (p<.0001) were found to be independently associated to higher DEL scores. Conclusion: The retrospective design and a non validated continuous measure for distorted thought contents were the main limitations of our study. Excluding the presence of psychotic features and depressive severity, no socio-demographic or clinical variable was found to be associated to our continuous measure of distorted thinking in depression.
KW - Delusions
KW - Depression
KW - Dimensional model
KW - Psychotic disorders
UR - https://www.scopus.com/pages/publications/84929472134
U2 - 10.9758/cpn.2015.13.1.48
DO - 10.9758/cpn.2015.13.1.48
M3 - Article
AN - SCOPUS:84929472134
SN - 1738-1088
VL - 13
SP - 48
EP - 52
JO - Clinical Psychopharmacology and Neuroscience
JF - Clinical Psychopharmacology and Neuroscience
IS - 1
ER -