4.7 Article

Altered Integrity of Perisylvian Language Pathways in Schizophrenia: Relationship to Auditory Hallucinations

Journal

BIOLOGICAL PSYCHIATRY
Volume 70, Issue 12, Pages 1143-1150

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2011.06.013

Keywords

Arcuate fasciculus; auditory verbal hallucinations; diffusion tensor imaging; language; schizophrenia; tractography; white matter

Funding

  1. Guy's and St. Thomas' Charity
  2. Wellcome Trust
  3. Medical Research Council, United Kingdom Autism Multi-Centre Imaging Study Network
  4. National Division of the South London and Maudsley National Health Service Foundation Trust
  5. Lilly
  6. AstraZeneca
  7. Bristol-Myers Squibb
  8. Roche
  9. Lundbeck
  10. Janssen Cilag
  11. Novartis
  12. Sanofi Synthelabo
  13. Pfizer
  14. Eli-Lilly
  15. Medical Research Council [G0901868] Funding Source: researchfish
  16. MRC [G0901868] Funding Source: UKRI

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Background: Functional neuroimaging supports the hypothesis that auditory verbal hallucinations (AVH) in schizophrenia result from altered functional connectivity between perisylvian language regions, although the extent to which AVH are also associated with an altered tract anatomy is less clear. Methods: Twenty-eight patients with schizophrenia subdivided into 17 subjects with a history of AVH and 11 without a history of hallucinations and 59 age- and IQ-matched healthy controls were recruited. The number of streamlines, fractional anisotropy (FA), and mean diffusivity were measured along the length of the arcuate fasciculus and its medial and lateral components. Results: Patients with schizophrenia had bilateral reduction of FA relative to controls in the arcuate fasciculi (p < .001). Virtual dissection of the subcomponents of the arcuate fasciculi revealed that these reductions were specific to connections between posterior temporal and anterior regions in the inferior frontal and parietal lobe. Also, compared with controls, the reduction in FA of these tracts was highest, and bilateral, in patients with AVH, but in patients without AVH, this reduction was reported only on the left. Conclusions: These findings point toward a supraregional network model of AVH in schizophrenia. They support the hypothesis that there may be selective vulnerability of specific anatomical connections to posterior temporal regions in schizophrenia and that extensive bilateral damage is associated with a greater vulnerability to AVH. If confirmed by further studies, these findings may advance our understanding of the anatomical factors that are protective against AVH and predictive of a treatment response.

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