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Transcriptome-wide association analysis of brain structures yields insights into pleiotropy with complex neuropsychiatric traits

Structural variations of the human brain are heritable and highly polygenic traits, with hundreds of associated genes identified in recent genome-wide association studies (GWAS). Transcriptome-wide association studies (TWAS) can both prioritize these GWAS findings and also identify additional gene-t...

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Detalles Bibliográficos
Autores principales: Zhao, Bingxin, Shan, Yue, Yang, Yue, Yu, Zhaolong, Li, Tengfei, Wang, Xifeng, Luo, Tianyou, Zhu, Ziliang, Sullivan, Patrick, Zhao, Hongyu, Li, Yun, Zhu, Hongtu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128893/
https://www.ncbi.nlm.nih.gov/pubmed/34001886
http://dx.doi.org/10.1038/s41467-021-23130-y
Descripción
Sumario:Structural variations of the human brain are heritable and highly polygenic traits, with hundreds of associated genes identified in recent genome-wide association studies (GWAS). Transcriptome-wide association studies (TWAS) can both prioritize these GWAS findings and also identify additional gene-trait associations. Here we perform cross-tissue TWAS analysis of 211 structural neuroimaging and discover 278 associated genes exceeding Bonferroni significance threshold of 1.04 × 10(−8). The TWAS-significant genes for brain structures have been linked to a wide range of complex traits in different domains. Through TWAS gene-based polygenic risk scores (PRS) prediction, we find that TWAS PRS gains substantial power in association analysis compared to conventional variant-based GWAS PRS, and up to 6.97% of phenotypic variance (p-value = 7.56 × 10(−31)) can be explained in independent testing data sets. In conclusion, our study illustrates that TWAS can be a powerful supplement to traditional GWAS in imaging genetics studies for gene discovery-validation, genetic co-architecture analysis, and polygenic risk prediction.