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 |
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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. |
doi_str_mv | 10.1017/S0033291797006521 |
format | Article |
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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.</description><identifier>ISSN: 0033-2917</identifier><identifier>EISSN: 1469-8978</identifier><identifier>DOI: 10.1017/S0033291797006521</identifier><identifier>PMID: 9572089</identifier><identifier>CODEN: PSMDCO</identifier><language>eng</language><publisher>Cambridge: Cambridge University Press</publisher><subject>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</subject><ispartof>Psychological medicine, 1998-03, Vol.28 (2), p.311-317, Article S0033291797006521</ispartof><rights>1998 Cambridge University Press</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-16c1bf1dff928b4c66c7f274390822deaffda04184b65444f7792e3cb5f6cf1f3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0033291797006521/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,777,781,27905,27906,30981,55609</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2233871$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9572089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ISMAIL, K.</creatorcontrib><creatorcontrib>MURRAY, R. 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 (>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.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Biological and medical sciences</subject><subject>Chi-Square Distribution</subject><subject>Confidence Intervals</subject><subject>Depression</subject><subject>Depression - complications</subject><subject>Depression - diagnosis</subject><subject>Depression - physiopathology</subject><subject>Dexamethasone</subject><subject>Dexamethasone Suppression Test</subject><subject>Female</subject><subject>Glucocorticoids</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Patients</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Schizophrenia</subject><subject>Schizophrenia, Paranoid - complications</subject><subject>Schizophrenia, Paranoid - physiopathology</subject><subject>Severity of Illness Index</subject><subject>Suicide, Attempted</subject><issn>0033-2917</issn><issn>1469-8978</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqFkEtLxDAUhYMoOj5-gAuhC3FXzTvNUgdHRUHEisuQpokTnT5MWhj99XaYMhtBV3fxffdwOAAcI3iOIBIXzxASgiUSUkDIGUZbYIIol2kmRbYNJiucrvge2I_xHUJEEMW7YFcygWEmJ4Dkc5uUdqkr2811bGqbxL5tg43RN3XS2dglvk6imfvvpp0HW3t9CHacXkR7NN4D8DK7zqe36cPjzd308iE1DNIuRdygwqHSOYmzghrOjXBYUCJhhnFptXOlhhRltOCMUuqEkNgSUzDHjUOOHICzdW4bms9-aKIqH41dLHRtmz4qITNCJUP_imxIZoLyQURr0YQmxmCdaoOvdPhSCKrVourXosPPyRjeF5UtNx_jhAM_HbmORi9c0LXxcaNhTEgmVjHpWvOxs8sN1uFDcUEEU_zmSYlcvF7N7nNFBp-MVXVVBF--WfXe9KEeBv-j7A9NwptJ</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>ISMAIL, K.</creator><creator>MURRAY, R. M.</creator><creator>WHEELER, M. J.</creator><creator>O'KEANE, V.</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7X8</scope></search><sort><creationdate>19980301</creationdate><title>The dexamethasone suppression test in schizophrenia</title><author>ISMAIL, K. ; MURRAY, R. M. ; WHEELER, M. 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. J.</creatorcontrib><creatorcontrib>O'KEANE, V.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><jtitle>Psychological medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ISMAIL, K.</au><au>MURRAY, R. M.</au><au>WHEELER, M. J.</au><au>O'KEANE, V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The dexamethasone suppression test in schizophrenia</atitle><jtitle>Psychological medicine</jtitle><addtitle>Psychol. Med</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>28</volume><issue>2</issue><spage>311</spage><epage>317</epage><pages>311-317</pages><artnum>S0033291797006521</artnum><issn>0033-2917</issn><eissn>1469-8978</eissn><coden>PSMDCO</coden><abstract>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.</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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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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