Abnormalities in connectivity of white-matter tracts in patients with familial and non-familial schizophrenia

• Published in: Psychological medicine Vol. 41; no. 8; pp. 1691 - 1700
• Main Authors: Wang, Q., Deng, W., Huang, C., Li, M., Ma, X., Wang, Y., Jiang, L., Lui, S., Huang, X., Chua, S. E., Cheung, C., McAlonan, G. M., Sham, P. C., Murray, R. M., Collier, D. A., Gong, Q., Li, T.
• Format: Journal Article
• Language: English
• Published: Cambridge, UK Cambridge University Press 01.08.2011
• Subjects: Adult; Adult and adolescent clinical studies; Analysis of Variance; Biological and medical sciences; Brain; Brain - pathology; Case-Control Studies; Chi-Square Distribution; Diffusion Tensor Imaging; Families & family life; Family; Family histories; Female; First time; Humans; Integrity; Magnetic Resonance Imaging; Male; Matter & antimatter; Medical sciences; Psychiatric disorders; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychoses; Schizophrenia; Schizophrenia - genetics; Schizophrenia - pathology; Young Adult; DTI; fractional anisotropy; first episode; schizophrenia; voxel-based analysis; family history; Psychosis; Human; Family story; First episode; Anisotropy; Schizophrenia; White matter
• ISSN: 0033-2917; 1469-8978
• DOI: 10.1017/S0033291710002412

Abnormalities in the connectivity of white-matter (WM) tracts in schizophrenia are supported by evidence from post-mortem investigations, functional and structural magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI). The aims of this study were to explore the microstructural changes in first-episode schizophrenia in a Han Chinese population and to investigate whether a family history of psychiatric disorder is related to the severity of WM tract integrity abnormalities in these patients. T1-weighted MR and DT images were collected in 68 patients with first-episode schizophrenia [22 with a positive family history (PFH) and 46 with a negative family history (NFH)] and 100 healthy controls. Voxel-based analysis was performed and WM integrity was quantified by fractional anisotropy (FA). Cluster- and voxel-level analyses were performed by using two-sample t tests between patients and controls and/or using a full factorial model with one factor and three levels among the three sample groups (patients with PFH or NFH, and controls), as appropriate. FA deficits were observed in the patient group, especially in the left temporal lobe and right corpus callosum. This effect was more severe in the non-familial schizophrenia than in the familial schizophrenia subgroup. Overall, these findings support the hypothesis that loss of WM integrity may be an important pathophysiological feature of schizophrenia, with particular implications for brain dysmaturation in non-familial and familial schizophrenia.