Egyszerű nézet

dc.contributor.author Fountoulakis KN
dc.contributor.author Gonda Xénia
dc.contributor.author Rihmer Zoltán
dc.contributor.author Fokas C
dc.contributor.author Iacovides A
dc.date.accessioned 2014-12-12T08:44:45Z
dc.date.available 2014-12-12T08:44:45Z
dc.date.issued 2008
dc.identifier 57149127231
dc.identifier.citation pagination=22; journalVolume=7; journalTitle=ANNALS OF GENERAL PSYCHIATRY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/768
dc.identifier.uri doi:10.1186/1744-859X-7-22
dc.description.abstract Background: Important methodological questions still exist concerning the Dexamethasone Suppression Test (DST), including the possibility of a better way of interpreting it. The aim of the present study was to explore the feasibility of an alternative way of interpreting DST results. Methods: A total of 50 patients with major depression aged 41.0 ± 11.4 years old participated in the study. Past and present suicide attempts were recorded. Psychometric assessment included the Hamilton Depression Rating Scale (HDRS), the Hamilton Anxiety Scale (HAS), the Newcastle Depression Diagnostic Scale (NDDS), the Diagnostic Melancholia Scale (DMS) and the General Assessment of Functioning (GAF) scale. The 1 mg DST protocol was used. Analysis methods included the chi square test and analysis of covariance (ANCOVA) with Fisher least significant difference (LSD) as post hoc tests. Results: In all, 34 patients (68%) were suppressors, 16 (32%) were non-suppressors and 14 patients had cortisol values above 5 μg/dl at baseline. Baseline cortisol level did not influence the classical DST interpretation. A total of 18 patients (36%) showed an increase of their cortisol levels after dexamethasone administration and 32 patients (64%) showed a decrease. Reducers had less melancholic features, similar levels of depression, better sleep and less suicidal thoughts in comparison to increasers. No relationship of DST to suicidality was found. Discussion: The present study explored the pattern of cortisol response to dexamethasone suppression and suggested an alternative way of coding and interpreting the DST on the basis of whether the cortisol levels remain stable or increase vs decrease after the administration of cortisol. The results put forward a complex way of understanding the relationship of the DST results with clinical symptoms. © 2008 Fountoulakis et al; licensee BioMed Central Ltd.
dc.relation.ispartof urn:issn:1744-859X
dc.title Revisiting the Dexamethasone Suppression Test in unipolar major depression: An exploratory study
dc.type Journal Article
dc.date.updated 2014-12-11T14:13:50Z
dc.language.rfc3066 en
dc.identifier.mtmt 1801044
dc.identifier.pubmed 19014558
dc.contributor.department SE/ÁOK/I/Farmakológiai és Farmakoterápiás Intézet
dc.contributor.department SE/ÁOK/K/Kútvölgyi Klinikai Tömb egyéb osztályok
dc.contributor.institution Semmelweis Egyetem


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