Alterations in brain structures underlying language function in young adults at high familial risk for schizophrenia
Jabbar, Gul A.
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CitationFrancis AN, Seidman LJ, Jabbar GA, Mesholam-Gately R, Thermenos HW, Juelich R, Proal AC, Shenton M, Kubicki M, Mathew I, Keshavan M, Delisi LE. 2012. Alterations in brain structures underlying language function in young adults at high familial risk for schizophrenia. Schizophr Res. 141, no. 1:65-71. doi:10.1016/j.schres.2012.07.015
AbstractIntroduction—Neuroanatomical and cognitive alterations typical of schizophrenia (SZ) patients are observed to a lesser extent in their adolescent and adult first-degree relatives, likely reflecting neurodevelopmental abnormalities associated with genetic risk for the illness. The anatomical pathways for language are hypothesized to be abnormal and to underlie the positive symptoms of schizophrenia. Examining non-psychotic relatives at high familial risk (FHR) for schizophrenia may clarify if these deficits represent trait markers associated with genetic vulnerability, rather than specific markers resulting from the pathological process underlying schizophrenia. Methods—T1 MRI scans from a 3T Siemens scanner of young adult FHR subjects (N=46) and controls with no family history of illness (i.e. at low genetic risk LRC; N=31) were processed using FreeSurfer 5.0. We explored volumetric and lateralization alterations in regions associated with language processing. An extensive neuropsychological battery of language measures was administered. Results—No significant differences were observed between groups on any language measures. Controlling Intracranial volume, significantly smaller center Pars Triangularis (PT) (p<0.01) and right Pars Orbitalis (PO) (p < 0.01) volumes and reversal of the L > R Pars Orbitalis (p < 0.001) lateralization were observed in FHR subjects. In addition, the L Pars Triangularis and R Pars Orbitalis correlated with performance on tests of linguistic function in the FHR group. Conclusions—Reduced volume and reversed structural asymmetry in language-related regions hypothesized to be altered in SZ are also found in first degree relatives at FHR, despite normal language performance. To clarify if these findings are endophenotypes for Sz, future studied would need to be performed of ill and well family members no longer within the age range of risk for illness to show these deficits segregate with schizophrenia within families. Moreover, measures of complex language need to be studied to determine if FHR individuals manifest impairments in some aspects of language function.
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