4.6 Article

Morphometric Brain Abnormalities in Schizophrenia in a Population-Based Sample: Relationship to Duration of Illness

期刊

SCHIZOPHRENIA BULLETIN
卷 36, 期 4, 页码 766-777

出版社

OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbn141

关键词

schizophrenia; magnetic resonance imaging; birth cohort; gray matter; white matter; voxel-based morphometry

资金

  1. Academy of Finland [110 143, 120 479, 214 273]
  2. Sigrid Juselius Foundation
  3. Stanley Medical Research Institute
  4. Radiological Society of Finland
  5. Lundbeck Foundation
  6. AstraZeneca Oy
  7. National Institute of Mental Health
  8. National Institute of Biomedical Imaging and Bioengineering
  9. Medical Research Council [G0001354, G0701911, G0001354B] Funding Source: researchfish
  10. MRC [G0701911] Funding Source: UKRI

向作者/读者索取更多资源

Biased recruitment and sample selection may cause variability in neuroimaging studies. Epidemiologically principled population-based magnetic resonance imaging (MRI) studies of schizophrenia are very rare. We gathered structural MRI data on 154 subjects from the Northern Finland 1966 Birth Cohort, aged 33-35 (100 controls, 54 schizophrenia patients). Regional differences in density of gray matter, white matter, and cerebrospinal fluid (CSF) were identified between groups using nonparametric statistical analysis, and the relationship of the regional differences to duration of illness was explored. Gray matter reductions were found bilaterally in the cerebellum, thalamus, basal ganglia, middle frontal gyrus, inferior frontal gyrus, precentral gyrus, insula, superior temporal gyrus, fusiform gyrus, parahippocampal gyrus, cuneus, and lingual gyrus; in the left posterior cingulate, superior frontal gyrus, transverse temporal gyrus, and precuneus; and in the right postcentral gyrus. Gray matter excesses were observed bilaterally in the basal ganglia, anterior cingulate, and medial orbitofrontal cortices. There were white matter deficits in an extensive network including inter- and intrahemispheric tracts bilaterally in the frontal, temporal, parietal, and occipital lobes, subcortical structures, cerebellum, and brain stem. CSF excesses were found bilaterally in the lateral ventricles, third ventricle, interhemispheric, and left Sylvian fissure. We replicated the previous findings of structural brain abnormalities in schizophrenia on a general population level. Gray and white matter deficits were associated with duration of illness suggesting either that developmental brain deficits relate to an earlier age of onset or that brain abnormalities in schizophrenia are progressive in nature.

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