4.7 Article

Heritability of brain morphology related to schizophrenia: A large-scale automated magnetic resonance imaging segmentation study

Journal

BIOLOGICAL PSYCHIATRY
Volume 63, Issue 5, Pages 475-483

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2007.06.006

Keywords

brain volume; heritability; MRI; phenotypes; schizophrenia

Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NCRR NIH HHS [P41-RR14075, R01 RR16594-01A1, U24 RR021382] Funding Source: Medline
  3. NIBIB NIH HHS [U54 EB005149, R01 EB001550] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS052585-01] Funding Source: Medline

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Background: Schizophrenia is a devastating psychiatric disorder with a strong genetic component that has been related to a number of structural brain alterations. Currently available data on the heritability of these structural changes are inconsistent. Methods: To examine heritability of morphological alterations in a large sample, we used a novel and validated fully-automated whole brain segmentation technique to study disease-related variability and heritability in anatomically defined regions of interest in 221 healthy control subjects, 169 patients with schizophrenia, and 183 unaffected siblings. Results: Compared with healthy control subjects, patients showed a bilateral decrease in hippocampal and cortical gray matter volume and increases in bilateral dorsal striatum and right lateral ventricle. No significant volumetric differences were found in unaffected siblings compared with normal control subjects in any structure. Post hoc analysis of the dorsal striatum showed the volumetric increase to be widespread, including caudate, putamen, and globus pallidus. With Risch's lambda (lambda(s)), we found strong evidence for heritability of reduced cortical volume and moderate evidence for hippocampal volume, whereas abnormal striatal and ventricle volumes showed no sign of heritability. Additional exploratory analyses were performed on amygdala, thalamus, nucleus accumbens, ventral diencephalon, and cerebral and cerebellar cortex and white matter. Of these regions, patients showed increased volume in ventral diencephalon and cerebellum. Conclusions: These findings support evidence of genetic control of brain volume even in adults, particularly of hippocampal and neocortical volume and of cortical volumetric reductions being familial, but do not support measures of subcortical volumes per se as representing intermediate biologic phenotypes.

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