Common genetic variation influencing human white matter microstructure

• DOI: 10.1101/2020.05.23.112409
• Publication Date: 2020-05-25T17:29:32Z
• Authors: Bingxin Zhao; Tengfei Li; Yue Yang; Xifeng Wang; Tianyou Luo; Yue Shan; Ziliang Zhu; Di Xiong; Mads E. Hauberg; Jaroslav Bendl; John F. Fullard; Panagiotis Roussos; Yun Li; Jason L. Stein; Hongtu Zhu
• Keywords: Male; Multifactorial Inheritance; Quantitative Trait Loci; Cognition; Brain Diseases/genetics; Risk Factors; Neural Pathways; Humans; Brain/anatomy & histology; Mental Disorders/genetics; Neurons; Brain Diseases; Principal Component Analysis; White Matter/diagnostic imaging; Genome, Human; Mental Disorders; Brain; Genetic Variation; 3. Good health; Neuroglia/physiology; Diffusion Magnetic Resonance Imaging; Diffusion Tensor Imaging; Heart Disease Risk Factors; Female; Neurons/physiology; Neuroglia; Genome-Wide Association Study

AbstractBrain regions communicate with each other via tracts of myelinated axons, commonly referred to as white matter. White matter microstructure can be measured in the living human brain using diffusion based magnetic resonance imaging (dMRI), and has been found to be altered in patients with neuropsychiatric disorders. Although under strong genetic control, few genetic variants influencing white matter microstructure have ever been identified. Here we identified common genetic variants influencing white matter microstructure using dMRI in 42,919 individuals (35,741 in the UK Biobank). The dMRIs were summarized into 215 white matter microstructure traits, including 105 measures from tract-specific functional principal component analysis. Genome-wide association analysis identified many novel white matter microstructure associated loci (P< 2.3 × 10−10). We identified shared genetic influences through genetic correlations between white matter tracts and 62 other complex traits, including stroke, neuropsychiatric disorders (e.g., ADHD, bipolar disorder, major depressive disorder, schizophrenia), cognition, neuroticism, chronotype, as well as non-brain traits. Common variants associated with white matter microstructure alter the function of regulatory elements in glial cells, particularly oligodendrocytes. White matter associated genes were enriched in pathways involved in brain disease pathogenesis, neurodevelopment process, and repair of white matter damage (P< 1.5 × 10−8). In summary, this large-scale tract-specific study provides a big step forward in understanding the genetic architecture of white matter and its genetic links to a wide spectrum of clinical outcomes.