Abstract
Background: Genome-wide association studies have identified numerous genetic variants that predispose to neuropsychiatric traits. Identification of mechanisms in the brain that underlie these associations is essential for understanding manifestations of genetic predisposition within the general population. Here, we investigated the association between polygenic scores (PGSs) for seven neuropsychiatric traits and white matter microstructure of the brain on diffusion tensor imaging in the pediatric population. Methods: Participants from the Generation R Study who had genotype and diffusion tensor imaging data available (n = 1138, mean age = 10.2 years, range = 8.7–12.0) were included. PGSs were calculated for five psychiatric disorders (attention-deficit/hyperactivity disorder, bipolar disorder, autism, major depressive disorder, and schizophrenia) and two cognitive traits (intelligence and educational attainment) and were tested for associations with global and tract-specific fractional anisotropy (FA) and mean diffusivity. Results: Significant positive associations with global FA were observed for the PGSs of intelligence (β =.109, SE =.029, p <.001, ΔR 2 =.012) and educational attainment (β =.118, SE =.029, p <.001, ΔR 2 =.014). No significant associations were observed with FA for the PGSs of psychiatric disorders. Tract-specific analysis showed that the PGSs for intelligence and educational attainment were associated with FA of several association and projection fibers of the brain. Conclusions: Our results show that genetic predisposition for cognition-related traits, but not for psychiatric disorders, is associated with microstructural diffusion measures of white matter tracts at an early age. These results suggest a shared genetic etiology among structural connectivity, intelligence, and educational achievement.
Original language | English |
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Pages (from-to) | 243-250 |
Number of pages | 8 |
Journal | Biological Psychiatry : Cognitive Neuroscience and Neuroimaging |
Volume | 4 |
Issue number | 3 |
Early online date | 3 Aug 2018 |
DOIs | |
Publication status | Published - Mar 2019 |
Funding
This research was supported by the Sophia Foundation for Scientific Research (“Stiching Vrienden van Sophia,” Grant No. S14-27 [to DP and TW]) and the Netherlands Organisation for Scientific Research (NWO) (Grant Nos. VICI 453-14-005 [to DP], 645-000-003 [to DP], and 016.VICI.170.200 [to HT]). Neuroimaging data collection and infrastructure was supported by the Netherlands Organization for Health Research and Development (ZonMw) TOP project number 91211021 (to TW). Supercomputing computations were supported by the NWO Physical Sciences Division (Exacte Wetenschappen) and SURFsara (Lisa computer cluster; http://www.surfsara.nl ). The general design of the Generation R Study is made possible by financial support from the Erasmus Medical Center (Rotterdam, The Netherlands), Erasmus University Rotterdam, ZonMw, NWO, and Ministry of Health, Welfare and Sport . We thank all parents and children who participate in the Generation R Study and the investigators who were involved in data collection procedures. All authors report no biomedical financial interests or potential conflicts of interest.
Funders | Funder number |
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NWO Physical Sciences Division | |
Sophia Foundation for Scientific Research | S14-27 |
ZonMw | 91211021 |
Erasmus Universiteit Rotterdam | |
Ministerie van Volksgezondheid, Welzijn en Sport | |
Erasmus Medisch Centrum | |
Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 645-000-003, VICI 453-14-005 |
Keywords
- Children
- Cognition
- DTI
- Polygenic scores
- Psychiatric disorders
- White matter