Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Department of Psychiatry, University of North Carolina, Chapel Hill, NC, USA.
Cereb Cortex. 2021 Jan 5;31(2):933-948. doi: 10.1093/cercor/bhaa266.
A better understanding of genetic influences on early white matter development could significantly advance our understanding of neurological and psychiatric conditions characterized by altered integrity of axonal pathways. We conducted a genome-wide association study (GWAS) of diffusion tensor imaging (DTI) phenotypes in 471 neonates. We used a hierarchical functional principal regression model (HFPRM) to perform joint analysis of 44 fiber bundles. HFPRM revealed a latent measure of white matter microstructure that explained approximately 50% of variation in our tractography-based measures and accounted for a large proportion of heritable variation in each individual bundle. An intronic SNP in PSMF1 on chromosome 20 exceeded the conventional GWAS threshold of 5 x 10-8 (p = 4.61 x 10-8). Additional loci nearing genome-wide significance were located near genes with known roles in axon growth and guidance, fasciculation, and myelination.
更好地理解遗传对早期白质发育的影响,可以显著增进我们对神经和精神疾病的认识,这些疾病的特征是轴突通路的完整性发生改变。我们对 471 名新生儿的弥散张量成像(DTI)表型进行了全基因组关联研究(GWAS)。我们使用分层功能主回归模型(HFPRM)对 44 个纤维束进行联合分析。HFPRM 揭示了一种潜在的白质微观结构衡量标准,该标准可以解释我们基于轨迹测量的约 50%的变异性,并解释了每个个体束中很大一部分可遗传性变异。20 号染色体上 PSMF1 内含子中的一个 SNP 超过了传统 GWAS 5 x 10-8 的阈值(p=4.61 x 10-8)。接近全基因组显著水平的其他基因座位于已知在轴突生长和导向、纤维束形成和髓鞘形成中起作用的基因附近。