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dc.contributor.authorHudson, James I.
dc.contributor.authorHudson, Margo S.
dc.contributor.authorRothschild, Anthony J.
dc.contributor.authorVignati, Louis
dc.contributor.authorSchatzberg, Alan F.
dc.contributor.authorMelby, James C.
dc.date2022-08-11T08:10:26.000
dc.date.accessioned2022-08-23T17:08:37Z
dc.date.available2022-08-23T17:08:37Z
dc.date.issued1984-11-01
dc.date.submitted2010-05-05
dc.identifier.citationArch Gen Psychiatry. 1984 Nov;41(11):1086-9.
dc.identifier.issn0003-990X (Linking)
dc.identifier.pmid6497571
dc.identifier.urihttp://hdl.handle.net/20.500.14038/45620
dc.description.abstractTo investigate the specificity of the dexamethasone suppression test (DST) for the diagnosis of major depression in patients with diabetes mellitus, we administered 1 mg of dexamethasone to 30 nondepressed diabetics and to 58 normal controls at 11 PM. Diabetic subjects received hemoglobin A1 (Hb A1) determinations, the Hamilton Rating Scale for Depression (HRSD), and five to eight blood glucose determinations during the 48 hours surrounding the DST. Results demonstrated a significantly higher rate of nonsuppression (plasma cortisol level, greater than or equal to 5 micrograms/dL) at 4 PM the following day among diabetics (43%) than among controls (7%) but no difference between these groups in the rate of nonsuppression at 8 AM. Plasma cortisol level at 4 PM correlated with Hb A1 level but not with duration of illness, HRSD score, mean blood glucose level, or maximum blood glucose excursion. These results suggest that the results of the DST used as a diagnostic test for major depression must be interpreted with caution in patients with diabetes.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=6497571&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://archpsyc.ama-assn.org/cgi/reprint/41/11/1086
dc.subjectAdult
dc.subjectAged
dc.subjectBlood Glucose
dc.subjectDepressive Disorder
dc.subjectDexamethasone
dc.subjectDiabetes Complications
dc.subjectDiabetes Mellitus
dc.subjectEvaluation Studies as Topic
dc.subjectFemale
dc.subjectHemoglobin A, Glycosylated
dc.subjectHospitalization
dc.subjectHumans
dc.subjectHydrocortisone
dc.subjectHypoglycemia
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectPsychiatric Status Rating Scales
dc.subjectResearch Design
dc.subjectPsychiatry
dc.titleAbnormal results of dexamethasone suppression tests in nondepressed patients with diabetes mellitus
dc.typeJournal Article
dc.source.journaltitleArchives of general psychiatry
dc.source.volume41
dc.source.issue11
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/psych_pp/15
dc.identifier.contextkey1299362
html.description.abstract<p>To investigate the specificity of the dexamethasone suppression test (DST) for the diagnosis of major depression in patients with diabetes mellitus, we administered 1 mg of dexamethasone to 30 nondepressed diabetics and to 58 normal controls at 11 PM. Diabetic subjects received hemoglobin A1 (Hb A1) determinations, the Hamilton Rating Scale for Depression (HRSD), and five to eight blood glucose determinations during the 48 hours surrounding the DST. Results demonstrated a significantly higher rate of nonsuppression (plasma cortisol level, greater than or equal to 5 micrograms/dL) at 4 PM the following day among diabetics (43%) than among controls (7%) but no difference between these groups in the rate of nonsuppression at 8 AM. Plasma cortisol level at 4 PM correlated with Hb A1 level but not with duration of illness, HRSD score, mean blood glucose level, or maximum blood glucose excursion. These results suggest that the results of the DST used as a diagnostic test for major depression must be interpreted with caution in patients with diabetes.</p>
dc.identifier.submissionpathpsych_pp/15
dc.contributor.departmentDepartment of Psychiatry
dc.source.pages1086-9


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