No statistically robust evidence of global genetic correlations between externalizing and individual UK Biobank brain imaging phenotypes was found and small, localized, mixed-direction, or developmentally specific genetic effects remain possible.
Abstract
Externalizing has been associated with differences in brain structure and function; however, it remains unclear whether these associations reflect shared common-variant genetic influences. Cross-trait linkage disequilibrium score regression was used to estimate genome-wide genetic correlations between externalizing GWAS results and 3,935 brain imaging-derived phenotypes from the UK Biobank BIG40 resource. Imaging phenotypes covered structural MRI, diffusion MRI, susceptibility-weighted imaging, resting-state functional MRI, and task functional MRI. Analyses were included in the primary dataset when the imaging phenotype had positive SNP heritability, a heritability Z statistic of at least 1.96, a mean GWAS chi-square statistic of at least 1.02, at least 200,000 regression SNPs, and a complete LDSC result without a fatal error. Technical imaging quality-control phenotypes were excluded from biological inference. Individual results were corrected using the Benjamini-Hochberg false discovery rate procedure. Aggregated Cauchy association tests were used to evaluate evidence across all imaging phenotypes and within predefined imaging categories. Power, simultaneous confidence bounds, and alternative quality-control definitions were examined in sensitivity analyses. Of 3,935 imaging phenotypes, 3,716 produced estimable genetic correlations, 2,980 met the primary LDSC quality-control criteria, and 2,967 were biological imaging phenotypes. No individual phenotype survived false discovery rate correction; the smallest unadjusted P value was 0.0005, and the minimum adjusted q value was 0.486. The distribution of genetic correlations was centered near zero, with a median genetic correlation of 0.0014 and a median absolute correlation of 0.0338. There was no aggregate evidence across all biological imaging phenotypes using ACAT (P = 0.302), and no predefined imaging category survived correction. The median minimum detectable genetic correlation at 80% power was 0.216. Bonferroni-adjusted simultaneous confidence intervals were contained within [-0.30, 0.30] for 80.0% of phenotypes in the primary analysis and 88.0% under stringent heritability quality control. Broad and stringent sensitivity analyses produced the same overall conclusions. In this study, no statistically robust evidence of global genetic correlations between externalizing and individual UK Biobank brain imaging phenotypes was found. Small, localized, mixed-direction, or developmentally specific genetic effects remain possible.
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Wenzhuo Yang, Lin Pan, Haoqun Xie et al.· BMC Medicine· 0 citations
Although several associations reached nominal significance, none remained significant after correction for multiple comparisons and the precision of the estimates was constrained by the available imaging GWAS sample size, uncertainty in SNP-heritability estimates, and the large number of regional comparisons.
Genome-wide association studies (GWAS) have identified hundreds of common genetic variants associated with regional brain volumes, enabling the construction of polygenic scores (PGS) that summarize genetic predisposition for variation in specific neuroanatomical traits. To investigate how these genetic influences are exerted spatially throughout the brain, we computed PGS for ten brain volume phenotypes, including nine major subcortical structures and intracranial volume. Each locus was weighted by its estimated GWAS effect size on regional volume in the original GWAS. In an independent, non-overlapping sample of 2,830 UK Biobank participants, we performed whole-brain voxel-based morphometry (VBM) analyses of 3D volumetric brain MRI to reveal voxel-wise associations between each PGS and modulated gray matter volume (GMV). To probe genetic effects across multiple spatial scales, analyses were repeated across Gaussian smoothing kernels ranging from 2-mm to 12-mm full-width at half-maximum (FWHM). Several PGS demonstrated highly significant associations with GMV, including localized effects in the hippocampus, amygdala, thalamus, and basal ganglia, whereas the brainstem PGS showed more widespread associations throughout the brain. For most of the PGS, the fraction of voxels surviving the false discovery rate (FDR) correction increased with increasing FWHM. Peak voxel-wise significance was often strongest at intermediate smoothing levels. Hippocampal significance maps showed progressively larger regions of significant signal at higher smoothing levels, and subsampling showed that detectable signal remained present even with substantial reductions in sample size. These findings suggest that genetic influences on brain morphology are expressed across multiple spatial scales, with consequences that may help to guide the design of deep learning methods to discover genomic loci associated with brain structure and brain diseases.
Emma J Gleave, L. García-Marín, Z. Ceja et al.· bioRxiv· 0 citations
Genome-wide association studies (GWAS) have advanced the quest to understand how specific genetic variants influence human brain structure and function. Recent work has identified hundreds of common variants associated with subcortical brain volumes, sparking interest in how these genetic markers overlap across brain networks. While this can be estimated by hierarchical clustering of the genetic correlation matrix to identify modular patterns of shared architecture, no brain-wide maps of these effects are available. To address this, we computed polygenic scores (PGS) from loci associated with ten brain volume regions of interest (ROIs): nine major subcortical structures and intracranial volume, with each locus weighted by its association with regional volume. In an independent sample from the discovery GWAS, we performed large-scale segmentation of 3D volumetric T1-weighted MRI scans using voxel-based morphometry (VBM) to map 3D profile of regions where gray matter volume (GMV) was associated with each PGS. We found statistically significant, localized effects for PGS defined for the amygdala, thalamus, and basal ganglia, but PGS for brainstem volume was associated with widespread differences throughout the brain. These brain-wide maps reveal patterns consistent with both localized and distributed genetic influences, offering a novel approach to interpret the genomic architecture of brain structure.
Emma J Gleave, L. García-Marín, Z. Ceja et al.· bioRxiv· 0 citations
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