The dexamethasone suppression test in schizophrenia

Background. Cortisol non-suppression following the dexamethasone suppression test (DST) has been found to a variable extent in schizophrenia. The aetiology is unclear but may be related to depression or negative symptoms. Methods. The DST was administered to 64 patients with DSM-IV schizophrenia. Al...

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Veröffentlicht in:Psychological medicine 1998-03, Vol.28 (2), p.311-317, Article S0033291797006521
Hauptverfasser: ISMAIL, K., MURRAY, R. M., WHEELER, M. J., O'KEANE, V.
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container_end_page 317
container_issue 2
container_start_page 311
container_title Psychological medicine
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creator ISMAIL, K.
MURRAY, R. M.
WHEELER, M. J.
O'KEANE, V.
description Background. Cortisol non-suppression following the dexamethasone suppression test (DST) has been found to a variable extent in schizophrenia. The aetiology is unclear but may be related to depression or negative symptoms. Methods. The DST was administered to 64 patients with DSM-IV schizophrenia. All patients were screened for DSM-IV major depression and rated on the Hamilton Rating Scale for Depression (HRSD), Scale for Assessment of Negative Symptoms (SANS) and the Brief Psychiatric Rating Scale (BPRS). Results. DSM-IV criteria for major depression was fulfilled by 36% of the patients and 42% of patients had a history of parasuicide. Four patients had undetectable levels of dexamethasone and were excluded from the endocrine analyses. Only one remaining patient had a cortisol level above the cut-off point (>138 nmol/l), indicating escape from dexamethasone suppression. The post-dexamethasone cortisol level correlated significantly with HRSD and BPRS scores but not with the SANS. The SANS and HRSD scores were not correlated, but they were independently correlated with the BPRS score. Conclusions. In contrast to some other work, rates of dexamethasone non-suppression were very low; together with the high rates of depression, this suggests that depression in schizophrenia may have a different neuroendocrine profile from major depressive disorders. Failure to measure dexamethasone levels can be misleading.
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Only one remaining patient had a cortisol level above the cut-off point (&gt;138 nmol/l), indicating escape from dexamethasone suppression. The post-dexamethasone cortisol level correlated significantly with HRSD and BPRS scores but not with the SANS. The SANS and HRSD scores were not correlated, but they were independently correlated with the BPRS score. Conclusions. In contrast to some other work, rates of dexamethasone non-suppression were very low; together with the high rates of depression, this suggests that depression in schizophrenia may have a different neuroendocrine profile from major depressive disorders. 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M.</creatorcontrib><creatorcontrib>WHEELER, M. J.</creatorcontrib><creatorcontrib>O'KEANE, V.</creatorcontrib><title>The dexamethasone suppression test in schizophrenia</title><title>Psychological medicine</title><addtitle>Psychol. Med</addtitle><description>Background. Cortisol non-suppression following the dexamethasone suppression test (DST) has been found to a variable extent in schizophrenia. The aetiology is unclear but may be related to depression or negative symptoms. Methods. The DST was administered to 64 patients with DSM-IV schizophrenia. All patients were screened for DSM-IV major depression and rated on the Hamilton Rating Scale for Depression (HRSD), Scale for Assessment of Negative Symptoms (SANS) and the Brief Psychiatric Rating Scale (BPRS). Results. DSM-IV criteria for major depression was fulfilled by 36% of the patients and 42% of patients had a history of parasuicide. Four patients had undetectable levels of dexamethasone and were excluded from the endocrine analyses. Only one remaining patient had a cortisol level above the cut-off point (&gt;138 nmol/l), indicating escape from dexamethasone suppression. The post-dexamethasone cortisol level correlated significantly with HRSD and BPRS scores but not with the SANS. The SANS and HRSD scores were not correlated, but they were independently correlated with the BPRS score. Conclusions. In contrast to some other work, rates of dexamethasone non-suppression were very low; together with the high rates of depression, this suggests that depression in schizophrenia may have a different neuroendocrine profile from major depressive disorders. 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J. ; O'KEANE, V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-16c1bf1dff928b4c66c7f274390822deaffda04184b65444f7792e3cb5f6cf1f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Biological and medical sciences</topic><topic>Chi-Square Distribution</topic><topic>Confidence Intervals</topic><topic>Depression</topic><topic>Depression - complications</topic><topic>Depression - diagnosis</topic><topic>Depression - physiopathology</topic><topic>Dexamethasone</topic><topic>Dexamethasone Suppression Test</topic><topic>Female</topic><topic>Glucocorticoids</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Patients</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Schizophrenia</topic><topic>Schizophrenia, Paranoid - complications</topic><topic>Schizophrenia, Paranoid - physiopathology</topic><topic>Severity of Illness Index</topic><topic>Suicide, Attempted</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ISMAIL, K.</creatorcontrib><creatorcontrib>MURRAY, R. M.</creatorcontrib><creatorcontrib>WHEELER, M. 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Four patients had undetectable levels of dexamethasone and were excluded from the endocrine analyses. Only one remaining patient had a cortisol level above the cut-off point (&gt;138 nmol/l), indicating escape from dexamethasone suppression. The post-dexamethasone cortisol level correlated significantly with HRSD and BPRS scores but not with the SANS. The SANS and HRSD scores were not correlated, but they were independently correlated with the BPRS score. Conclusions. In contrast to some other work, rates of dexamethasone non-suppression were very low; together with the high rates of depression, this suggests that depression in schizophrenia may have a different neuroendocrine profile from major depressive disorders. Failure to measure dexamethasone levels can be misleading.</abstract><cop>Cambridge</cop><pub>Cambridge University Press</pub><pmid>9572089</pmid><doi>10.1017/S0033291797006521</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Applied Social Sciences Index & Abstracts (ASSIA); Cambridge University Press Journals Complete
subjects Adult
Adult and adolescent clinical studies
Biological and medical sciences
Chi-Square Distribution
Confidence Intervals
Depression
Depression - complications
Depression - diagnosis
Depression - physiopathology
Dexamethasone
Dexamethasone Suppression Test
Female
Glucocorticoids
Humans
Male
Medical sciences
Patients
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychoses
Schizophrenia
Schizophrenia, Paranoid - complications
Schizophrenia, Paranoid - physiopathology
Severity of Illness Index
Suicide, Attempted
title The dexamethasone suppression test in schizophrenia
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