Journal of Affective Disorders
Volume 76, Issue 1 , Pages 49-54, September 2003

A neuropathological study of periventricular white matter hyperintensities in major depression

  • Alan J. Thomas

      Affiliations

    • Department of Psychiatry and Institute for Ageing and Health, University of Newcastle upon Tyne, Newcastle upon Tyne NE4 6BE, UK
    • Corresponding Author InformationCorresponding author. Wolfson Research Centre, Institute for Ageing and Health, Newcastle General Hospital, Newcastle upon Tyne NE4 6BE, UK. Tel.: +44-191-2563-323; fax: +44-191-2195-051
  • ,
  • John T. O’Brien

      Affiliations

    • Department of Psychiatry and Institute for Ageing and Health, University of Newcastle upon Tyne, Newcastle upon Tyne NE4 6BE, UK
  • ,
  • Robert Barber

      Affiliations

    • Department of Psychiatry and Institute for Ageing and Health, University of Newcastle upon Tyne, Newcastle upon Tyne NE4 6BE, UK
  • ,
  • William McMeekin

      Affiliations

    • Department of Pathology, Newcastle General Hospital, Newcastle upon Tyne, Newcastle upon Tyne NE4 6BE, UK
  • ,
  • Robert Perry

      Affiliations

    • Department of Pathology, Newcastle General Hospital and Institute for Ageing and Health, University of Newcastle upon Tyne, Newcastle upon Tyne NE4 6BE, UK

Received 24 November 2001; received in revised form 25 January 2002; accepted 4 February 2002.

Abstract 

Background: Signal hyperintensities on magnetic resonance imaging (MRI) are increased in major depression but their pathological basis has never been assessed. We carried out a study of the neuropathological basis of periventricular hyperintensities (PVHs) in major depression. We hypothesised that different pathologies would be associated with the same MRI appearance of PVH and that such causes would be similar in depressed and control subjects. Methods: In vitro MRI was carried out on coronal slices of brain tissue from 20 elderly subjects with major depression and 20 matched control subjects. PVHs were identified and blindly rated on the films and the tissue was subsequently prepared for neuropathological analysis. Conventional histopathological stains and immunocytochemical stains for glia and macrophages, to identify ischaemic tissue damage, were used. PVHs identified on MRI films were microscopically assessed blind to diagnosis. Results: PVHs were found to be due to one of three main causes: ependymal loss, differing degrees of myelination in adjacent fibre tracts and cerebral ischaemia with associated demyelination. The causes were similar in depressed and control subjects. Limitations: All depressed subjects had been hospitalised and in spite of scanning 20 subjects only a small number of PVHs were able to be examined in depressed subjects. Conclusions: The neuropathological basis of PVH was similar in depressed and control subjects, and to previous reports in other diseases. Identical PVHs on MRI can have different causes in depression and this includes cerebral ischaemia.

Keywords:  Depression, White matter, Hyperintensities, Neuropathology, MRI

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0165-0327(02)00064-2

doi:10.1016/S0165-0327(02)00064-2

Journal of Affective Disorders
Volume 76, Issue 1 , Pages 49-54, September 2003