| Literature DB >> 33009551 |
J Zhang1, K Xia2, M Ahn3, S C Jha4, R Blanchett5, J J Crowley2,6,7, J P Szatkiewicz2,6, F Zou8, H Zhu8, M Styner2, J H Gilmore2, R C Knickmeyer2,9,10.
Abstract
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.Entities:
Keywords: diffusion tensor imaging; genome-wide association study; infant; magnetic resonance imaging
Mesh:
Substances:
Year: 2021 PMID: 33009551 PMCID: PMC7786356 DOI: 10.1093/cercor/bhaa266
Source DB: PubMed Journal: Cereb Cortex ISSN: 1047-3211 Impact factor: 5.357