4.6 Article

Mapping cortical thickness and gray matter concentration in first episode schizophrenia

Journal

CEREBRAL CORTEX
Volume 15, Issue 6, Pages 708-719

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cercor/bhh172

Keywords

brain structure; heteromodal association cortices; imaging; prefrontal cortices; superior temporal gyrus

Categories

Funding

  1. NCRR NIH HHS [2 M01 RR00865, 2 P41 RR13642, R21 RR19771] Funding Source: Medline
  2. NIBIB NIH HHS [EB 001561] Funding Source: Medline
  3. NIMH NIH HHS [MH14584, R01-MH-60374] Funding Source: Medline
  4. NLM NIH HHS [5 R01 LM05639] Funding Source: Medline

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We mapped regional changes in cortical thickness and intensity-based cortical gray matter concentration in first episode schizophrenia. High-resolution magnetic resonance images were obtained from 72 (51 male, 21 female) first episode patients and 78 (37 male, 41 female) healthy subjects similar in age. Cortical pattern matching methods allowed comparisons of cortical thickness and gray matter concentration at thousands of homologous cortical locations between subjects in three dimensions. Principal components analyses reduced measures obtained across the cortex to identify global differences in cortical thickness/gray matter concentration. First principal component factor scores showed significant effects of diagnosis, sex and age for both cortical measures. Diagnosis and age effects remained significant after brain size correction. Cortical thickness and gray matter concentration values were highly correlated. Statistical maps showed significant regional gray matter thinning in frontal, temporal and parietal heteromodal association cortices bilaterally in first episode patients. Regional reductions in cortical gray matter concentration were similar but pronounced in the superior temporal lobe. Regional reductions in cortical thickness and gray matter concentration are present at disease onset in brain regions linked with functional disturbances in schizophrenia. Cortical thickness and gray matter concentration mapping produce similar results, although the concentration metric may be influenced by diagnostic differences in extra-cortical cerebrospinal fluid and surface curvature/complexity.

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