Lymphocyte glucocorticoid receptor resistance and depressive symptoms severity: A preliminary report
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pan style='font-weight: bold'>Methods:pan> Eight-four out-patients aged between 18 and 70 years, who met DSMIII-Rcriteria for Major Depressive Disorder with melancholia, without psychotic symptoms, and in turn exhibited> = 6 points on the Newcastle scale. We collected data corresponding to: 1. Sociodemographic, clinical and personality variables; 2. Family antecedents; 3. Serial bimonsly dexamethasone suppression test (DST); 4. Life events and social support. A relapse was considered to have taken place when the patient attained a scoring of> = 16 points on the Hamilton Depression Rating Scale (HDRS) after a clinical recovery (HDRS < = 6) of 8 weeks. Cumulative and instantaneos probabilities of relapse were estimed using the Kaplan-Meier method and the Cox proportional hazard model was used to ascertain the prognostic variables.<p>pan style='font-weight: bold'>Results:pan> The strongest predictors of early relapse were: 1) The maintenance treatment with imipramine over 2 years; 2) High initial neuroticism; 3) The presence in two or more instance of NON-suppression in the serial DST previously to relapse (Likelihood ratio × for overall model = 26, 67, df = 6, P < 0.001).

p://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T4S-3WBPRJ7-1BB-1&_cdi=4982&_user=2795313&_orig=article&_coverDate=07 % 2F01 % 2F1997&_sk=999579998.8998&view=c&wchp=dGLzVlz-zSkWW&md5=5479f6f5045faa4000e61692f2908b1d&ie=/sdarticle.pdf"" target=""newPdfWin"" onClick=""var newWidth=((document.body.clientWidth*90)/100); var newHeight=document.body.clientHeight; var pdfWin; pdfWin=window.open('','newPdfWin','width='+newWidth+',height='+newHeight+',resizable=yes, left=50, top=50');pdfWin.focus()"">pdf"" style=""vertical-align:absmiddle;"" border=""0"" src=""http://www.sciencedirect.com/scidirimg/icon_pdf.gif"" alt=""""> PDF (123 K)
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p"" style=""padding: 5px 5px 0px 5px"">Polysomnography and criteria for the antidepressant res...
Journal of Affective Disorders

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p://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T2X-4MWGYDK-2&_user=2795313&_coverDate=08 % 2F31 % 2F2007&_rdoc=1&_fmt=high&_orig=article&_cdi=4930&_sort=v&_docanchor=&view=c&_ct=2421&_acct=C000058823&_version=1&_urlVersion=0&_userid=2795313&md5=f47003f5077c0f82ace43bc4ba02eb2b"">Polysomnography and criteria for the antidepressant response to sleep deprivation
Journal of Affective DisordersVolume 101, Issues 1-3August 2007, Pages 195-200
Camellia P. Clark, Shahrokh Golshan

Abstract

Background

One night of total or partial sleep deprivation (SD) produces a temporary remission in 40–60 % of patients with major depression. Yet no attempts to determine the optimum response criterion(a) for the antidepressant response to SD have been published.

Methods

<p>Twenty-three unmedicated major depression patients received polysomnography (PSG) on an adaptation night; a baseline night; a partial SD (PSD) night (awake after 3 a.m.); and a “recovery” night. Subjects received the Hamilton Depression Rating Scale (HDRS17) at standard times during baseline and PSD days and at 8 a.m. after the “recovery” night. Response was defined as percent decrease in the modified HDRS17 (HDRS17Mod) (omitting sleep and weight loss items) from baseline to the minimum following PSD. Using cutoffs of 30 % , 35 % , 40 % , and 50 % to dichotomize responders and nonresponders, PSG variables were analyzed for between-group differences.

Results

<p>All cutoffs differentiated responders' and nonresponders' mood response to PSD despite similar baseline values. Sleep continuity measures most consistently differed between responders and nonresponders on baseline and recovery nights. None of the response cutoffs tested were clearly “best” in terms of detecting the most PSG differences between groups.

Limitations

<p>More subjects may be needed.

Conclusions

<p>Given the increasing interest in SD for clinical and research applications, as well as its proposed use for subtyping depression, further study to determine the optimal response criterion(a) for the antidepressant response to SD is warranted. Planned pooling of multisite data on standardized SD protocols could help determine the optimal cutpoint for response.

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<p>Lymphocyte glucocorticoid receptor resistance and depressive symptoms severity: A preliminary report

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