University of Western Ontario, London, Ontario, Canada
Roberts Research Institute, London, Ontario, Canada
University of Western Ontario, London, Ontario, Canada
St Joseph's Health Centre, London, Ontario, Canada
Correspondence: Professor P.C.Williamson, Department of Psychiatry, London Health Science Centre, University Campus, Rm IONI5, London, Ontario, Canada N6A 5A5
Declaration of interest This work was funded by the Canadian Institute of Health Research Grant MT-1078.
Background Membrane phospholipid abnormalities in people with schizophrenia, measured with 31P magnetic resonance spectroscopy (31P-MRS), have been previously reported in brain regions involved in this disorder.
Aims In this 4.0 Tesla 31P-MRS study of people with schizophrenia, membrane phospholipid metabolism was examined in brain regions previously inaccessible due to their small volumes.
Method Three-dimensional chemical-shift imaging (3DCSI) examined 15 cc volumes in 12 brain regions in 11 people with chronic schizophrenia and 11 healthy control volunteers.
Results Glycerophosphoethanolamine was decreased in the anterior cingulate, right prefrontal cortex and left thalamus, but increased in the left hippocampus and cerebellum in those with schizophrenia. Phosphoethanolamine and glycerophosphocholine were decreased in the right prefrontal region and phosphocholine was decreased in the anterior cingulate. No significant difference in membrane phospholipid levels existed between groups in the parieto-occipital and posterior cingulate regions.
Conclusions Altered membrane phospholipid metabolism was demonstrated in all regions implicated in schizophrenia.
This article has been cited by other articles:
![]() |
P. Fusar-Poli, M.R. Broome, P. Matthiasson, J.B. Woolley, A. Mechelli, L.C. Johns, P. Tabraham, E. Bramon, L. Valmaggia, S.C. Williams, et al. Prefrontal Function at Presentation Directly Related to Clinical Outcome in People at Ultrahigh Risk of Psychosis Schizophr Bull, August 7, 2009; (2009) sbp074v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Konrad and G. Winterer Disturbed Structural Connectivity in Schizophrenia Primary Factor in Pathology or Epiphenomenon? Schizophr Bull, January 1, 2008; 34(1): 72 - 92. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. S. J. Rands, J. E. Jensen, J. Miller, P. C. Williamson, R. W. J. Neufeld, R. S. Menon, A. Malla, R. Manchanda, B. Schaefer, M. Densmore, et al. Memantine as a neuroprotective treatment in schizophrenia * Authors' reply The British Journal of Psychiatry, January 1, 2005; 186(1): 77 - 78. [Full Text] [PDF] |
||||
![]() |
J. E. Jensen, J. Miller, P. C. Williamson, R. W. J. Neufeld, R. S. Menon, A. Malla, R. Manchanda, B. Schaefer, M. Densmore, and D. J. Drost Focal changes in brain energy and phospholipid metabolism in first-episode schizophrenia: 31P-MRS chemical shift imaging study at 4 Tesla The British Journal of Psychiatry, May 1, 2004; 184(5): 409 - 415. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Paradiso, N. C. Andreasen, B. Crespo-Facorro, D. S. O'Leary, G. L. Watkins, L. L. Boles Ponto, and R. D. Hichwa Emotions in Unmedicated Patients With Schizophrenia During Evaluation With Positron Emission Tomography Am J Psychiatry, October 1, 2003; 160(10): 1775 - 1783. [Abstract] [Full Text] [PDF] |
||||