英国生物库中精神分裂症、大脑结构和环境风险的多基因风险

Xingxing Zhu, J. Ward, B. Cullen, D. Lyall, R. Strawbridge, L. Lyall, Danny J. Smith
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引用次数: 9

摘要

精神分裂症是一种以大脑神经解剖改变为特征的遗传性神经发育障碍,但精神分裂症的遗传负担增加究竟如何影响大脑结构尚不清楚。同样,精神分裂症的环境风险因素对大脑结构的影响也不完全清楚。我们调查了来自UK Biobank的18147名白人英国血统参与者的精神分裂症遗传负担(由多基因风险评分,PRS-SCZ索引)如何与皮质厚度(CT)、皮质表面积(SA)、皮质体积(CV)和多个皮质下结构相关。我们还探讨了精神分裂症的环境危险因素(大麻使用、童年创伤、低出生体重和Townsend社会剥夺指数)是否加剧了PRS-SCZ对脑结构的影响。我们发现,PRS-SCZ与额叶、岛叶、外侧眶额皮质、内侧眶额皮质、后扣带皮质和额下皮质的CT降低以及边缘上皮质和颞上皮质的SA和CV降低显著相关,但与皮质下体积差异不显著。当模型将环境风险因素作为协变量时,PRS-SCZ仅与边缘上皮层、颞上皮层和额下皮层内较低的SA/CV相关。此外,PRS-SCZ与各环境危险因素对脑结构的影响没有相互作用。总的来说,我们确定了PRS-SCZ的大脑结构相关性主要在额叶和颞叶区域。其中一些关联独立于环境风险因素,表明它们可能代表精神分裂症遗传风险的生物标志物。
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Polygenic Risk for Schizophrenia, Brain Structure and Environmental Risk in UK Biobank
Schizophrenia is a heritable neurodevelopmental disorder characterized by neuroanatomical changes in the brain but exactly how increased genetic burden for schizophrenia influences brain structure is unknown. Similarly, the impact of environmental risk factors for schizophrenia on brain structure is not fully understood. We investigated how genetic burden for schizophrenia (indexed by a polygenic risk score, PRS-SCZ) was associated with cortical thickness (CT), cortical surface area (SA), cortical volume (CV) and multiple subcortical structures within 18,147 White British ancestry participants from UK Biobank. We also explored whether environmental risk factors for schizophrenia (cannabis use, childhood trauma, low birth weight and Townsend social deprivation index) exacerbated the impact of PRS-SCZ on brain structure. We found that PRS-SCZ was significantly associated with lower CT in the frontal lobe, insula lobe, lateral orbitofrontal cortex, medial orbitofrontal cortex, posterior cingulate cortex and inferior frontal cortex, as well as reduced SA and CV in the supramarginal cortex and superior temporal cortex, but not with differences in subcortical volumes. When models included environmental risk factors as covariates, PRS-SCZ was only associated with lower SA/CV within the supramarginal cortex, superior temporal cortex and inferior frontal cortex. Moreover, no interactions were observed between PRS-SCZ and each of the environmental risk factors on brain structure. Overall, we identified brain structural correlates of PRS-SCZ predominantly within frontal and temporal regions. Some of these associations were independent of environmental risk factors, suggesting that they may represent biomarkers of genetic risk for schizophrenia.
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