Speech Pause Time as a Method for the Evaluation of Psychomotor Retardation in Depressive Illness

1985 ◽  
Vol 146 (5) ◽  
pp. 535-538 ◽  
Author(s):  
G. M. A. Hoffman ◽  
J. C. Gonze ◽  
J. Mendlewicz

SummaryPsychomotor retardation is important in some depressed patients. We found that speech pause time (SPT) during a counting test correlated with the reaction time of both depressed patients and controls. It also correlated with global psychomotor retardation measured on Widlocher's scale. We demonstrated increased SPT in unipolar depressives, and also in retarded depressives as a group when compared with controls and with non-retarded depressives. SPT varied diurnally in controls, but not in depressed subjects. It did not correlate with biological markers of depression (REM sleep latency and the dexamethasone suppression test). It did, however, shorten during clinical improvement with antidepressant chemotherapy.

1994 ◽  
Vol 164 (3) ◽  
pp. 316-326 ◽  
Author(s):  
Gordon Parker ◽  
Dusan Hadzi-Pavlovic ◽  
Kay Wilhelm ◽  
Ian Hickie ◽  
Henry Brodaty ◽  
...  

We hypothesised that psychomotor disturbance is specific to the melancholic subtype of depression and capable of defining melancholia more precisely than symptom-based criteria sets. We studied 413 depressed patients, and examined the utility of a refined, operationally driven set of clinician-rated signs, principally against a set of historically accepted symptoms of endogeneity. We specified items defining psychomotor disturbance generally as well as those weighted either to agitation or to retardation. We demonstrated the system's capacity to differentiate ‘melancholic’ and ‘non-melancholic’ depression (and the comparable success of DSM–III–R and Newcastle criteria systems) by reference to several patient, illness and treatment response variables, to an independent measure of psychomotor disturbance (reaction time) and to a biological marker (the dexamethasone suppression test).


1982 ◽  
Vol 140 (3) ◽  
pp. 292-304 ◽  
Author(s):  
Bernard J. Carroll

SummaryMelancholia is thought by many investigators to have a biological basis, and biological research, particularly on abnormalities of the neuroendocrine system and of the sleep electroencephalogram, is now beginning to yield results which can help in the differential diagnosis of depressive illness. This review will focus on the most widely studied neuroendocrine disturbance: disinhibition of the hypothalamus-pituitary-adrenal cortex (HPA) system as revealed by the dexamethasone suppression test (DST).


1988 ◽  
Vol 152 (4) ◽  
pp. 554-558 ◽  
Author(s):  
Sarah Watkins ◽  
Brian Harris ◽  
Nigel Cook ◽  
Roger Thomas ◽  
Diana Riad-Fahmy

The performance of the dexamethasone suppression test was assessed in 90 consecutive admissions with a diagnosis of depression, categorised according to two classification systems (DSM-III and ICD-9). Non-suppression was found in most of the diagnostic categories, but there was a highly significant association with the DSM-III classification ‘major depressive episode with melancholia’ (52%) in comparison with the ICD group ‘manic-depressive illness-depressed’ (29%).


1987 ◽  
Vol 151 (6) ◽  
pp. 780-784 ◽  
Author(s):  
I. Schweitzer ◽  
K. P. Maguire ◽  
A. H. Gee ◽  
J. W. G. Tiller ◽  
N. Biddle ◽  
...  

Forty-three depressed patients in hospital were studied with weekly dexamethasone suppression tests (DSTs) and were followed as out-patients for at least three months after discharge. The detection rate of patients with LHPA axis dysfunction increased from 41% with a single DST to 59% with serial DSTs. There was a poor correlation between weekly post-dexamethasone cortisol levels and Hamilton depression rating scores. In patients with evidence of LHPA axis dysfunction, a DST at discharge discriminated effectively between a good and a poor outcome group; persistent non-suppression was strongly linked with a relapse of depression in the first three months after discharge. In general, our results support previous claims that the DST is a state marker for depressive illness.


1984 ◽  
Vol 144 (3) ◽  
pp. 311-313 ◽  
Author(s):  
D. Ames ◽  
G. Burrows ◽  
B. Davies ◽  
K. Maguire ◽  
T. Norman

1991 ◽  
Vol 69 (3) ◽  
pp. 878-878
Author(s):  
David Lester

For 10 nations suicide rates were not correlated with the percentages of depressed patients who responded abnormally to the Dexamethasone Suppression Test.


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