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Authors' reply

Published online by Cambridge University Press:  02 January 2018

S. M. MacHale
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
S. M. Lawrie
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
J. T. Cavanagh
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
M. F. Glabus
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
C. L. Marray
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
K. P. Ebmeier
Affiliation:
Department of Psychiatry and MRC Brain Metabolism Unit, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF
G. M. Goodwin
Affiliation:
University Department of Psychiatry, Warneford Hospital, Oxford OX3 7JX
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Abstract

Type
Columns
Copyright
Copyright © 2000 The Royal College of Psychiatrists 

As explained in the method section, the potential participants were screened by excluding those scoring above case threshold in the Hospital Anxiety and Depression (HAD) scale, a self-rating scale that does not require a detailed interview. The remaining participants were then interviewed using the Schedule for Affective Disorders and Schizophrenia to further exclude any current mental illness.

First, in the discussion we say: “The main limitation of the present study is that our CFS subjects had high levels of depression: almost half were on psychotropic medication and five had a previous history of depression”. “Had high levels of depression” is defined by what follows after the colon. There is, therefore, no contradiction. Participants were not currently depressed, but some were receiving antidepressant medication and some had previously been depressed.

Second, regarding that point made relating to our comment that “ thalamic overactivity in CFS (and depression) may, therefore, reflect increased attention to motor and cognitive tasks…”. The perceived contradiction is that participants were at rest during uptake of the tracer, i.e. not currently engaged in motor or cognitive tasks. It is clearly speculative that increased thalamic activity at rest will also mean increased thalamic activity during tasks. What was implied, however, was that increased baseline or resting activity of the thalamus may be an underlying brain marker that is related to patients being more attentive to motor and cognitive activity, as they occur.

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