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J Neurol Neurosurg Psychiatry 2005;76:1510-1515 doi:10.1136/jnnp.2004.057612
  • Paper

Possible structural abnormality of the brainstem in unipolar depressive illness: a transcranial ultrasound and diffusion tensor magnetic resonance imaging study

  1. J D Steele1,
  2. M E Bastin2,
  3. J M Wardlaw3,
  4. K P Ebmeier4
  1. 1Department of Mental Health, University of Aberdeen, Block A, Royal Cornhill Hospital, Aberdeen AB25 2ZH, UK
  2. 2Medical and Radiological Sciences (Medical Physics), University of Edinburgh, Edinburgh, UK
  3. 3Clinical Neurosciences, University of Edinburgh, Edinburgh, UK
  4. 4Division of Psychiatry, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Edinburgh EH10 5HF, UK
  1. Correspondence to:
 J D Steele
 Block A, Royal Cornhill Hospital, Aberdeen, AB25 2ZH, UK; jds333dsteele.demon.co.uk
  • Received 30 October 2004
  • Accepted 7 March 2005
  • Revised 5 March 2005

Abstract

Background: Most empirically derived antidepressants increase monoamine levels. The nuclei of cells synthesising these monoamines are located in the brainstem, and projection tracts such as the medial forebrain bundle reach virtually all other brain areas. Two studies of unipolar depressive illness using transcranial ultrasound have reported reduced echogenicity of the brainstem midline in unipolar depressed patients. This may be consistent with disruption of white matter tracts, including the medial forebrain bundle, and it has been suggested that the effect of such disruption could be reversed by antidepressants.

Objective: To replicate these findings in a group of unipolar depressed patients and controls.

Methods: Fifteen unipolar depressed patients and 15 controls were studied using transcranial ultrasound imaging and diffusion tensor magnetic resonance imaging (DT-MRI).

Results: No difference in echogenicity of the brainstem midline of unipolar depressed patients was found. A possible trend (Cohen’s d = 0.39) in the direction of previous studies was found. Although the echogenicity of the brainstem midline of the control group was found to be similar to previous reports, there was no reduction in the patient group. Additionally, no structural abnormality of the brainstem was identified using DT-MRI.

Conclusions: While these data do not replicate the findings of previous studies reporting a significant reduction in the echogenicity of the brainstem midline in unipolar depressed patients, the ultrasound investigation indicated that there may be a trend in this direction. Given the importance of identifying the causes of depressive illness, it is important that other groups attempt similar studies.

Footnotes

  • Financial support was provided by the Gordon Small Charitable Trust.

  • Competing interests: none declared

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