Heritable anisotropy associated with cognitive impairments among patients with schizophrenia and their non-psychotic relatives in multiplex families. Issue 5 (3rd April 2022)

• Record Type: Journal Article
• Authors: Prasad, K. M.; Gertler, J.; Tollefson, S.; Wood, J. A.; Roalf, D.; Gur, R. C.; Gur, R. E.; Almasy, L.; Pogue-Geile, M. F.; Nimgaonkar, V. L.
• Is Part Of: Psychological medicine. Volume 52:Issue 5(2022)
• Page Start: 989
• Page End: 1000
• Publication Date: 2022-04-03
• Subjects: Brain connectivity -- diffusion tensor imaging -- familial risk -- heritability -- schizophrenia -- neuroimaging -- white matter fibers; Psychiatry -- Periodicals; Medicine and psychology -- Periodicals; Clinical psychology -- Periodicals; 616.89
• DOI: 10.1017/S0033291720002883
• Languages: English
• ISSNs: 0033-2917

Abstract

Abstract: Background: To test the functional implications of impaired white matter (WM) connectivity among patients with schizophrenia and their relatives, we examined the heritability of fractional anisotropy (FA) measured on diffusion tensor imaging data acquired in Pittsburgh and Philadelphia, and its association with cognitive performance in a unique sample of 175 multigenerational non-psychotic relatives of 23 multiplex schizophrenia families and 240 unrelated controls (total = 438). Methods: We examined polygenic inheritance ( h 2 r ) of FA in 24 WM tracts bilaterally, and also pleiotropy to test whether heritability of FA in multiple WM tracts is secondary to genetic correlation among tracts using the Sequential Oligogenic Linkage Analysis Routines. Partial correlation tests examined the correlation of FA with performance on eight cognitive domains on the Penn Computerized Neurocognitive Battery, controlling for age, sex, site and mother's education, followed by multiple comparison corrections. Results: Significant total additive genetic heritability of FA was observed in all three-categories of WM tracts (association, commissural and projection fibers), in total 33/48 tracts. There were significant genetic correlations in 40% of tracts. Diagnostic group main effects were observed only in tracts with significantly heritable FA. Correlation of FA with neurocognitive impairments was observed mainly in heritable tracts. Conclusions: Our data show significant heritability of all three-types of tracts among relatives of schizophrenia. Significant heritability of FA of multiple tracts was not entirely due to genetic correlations among the tracts. Diagnostic group main effect and correlation with neurocognitive performance were mainly restricted to tracts with heritable FA suggesting shared genetic effects on these traits.