TY - JOUR
T1 - Polygenic scores for autism are associated with reduced neurite density in adults and children from the general population
AU - Gu, Yuanjun
AU - Maria-Stauffer, Eva
AU - Bedford, Saashi A
AU - Romero-Garcia, Rafael
AU - Grove, Jakob
AU - Børglum, Anders D
AU - Martin, Hilary
AU - Baron-Cohen, Simon
AU - Bethlehem, Richard A I
AU - Warrier, Varun
AU - APEX consortium
AU - iPSYCH-autism consortium
A2 - Werge, Thomas Mears
A2 - Nordentoft, Merete
N1 - © 2025. The Author(s).
PY - 2025/8
Y1 - 2025/8
N2 - Genetic variants linked to autism are thought to change cognition and behaviour by altering the structure and function of the brain. Although a substantial body of literature has identified structural brain differences in autism, it is unknown whether autism-associated common genetic variants are linked to changes in cortical macro- and micro-structure. We investigated this using neuroimaging and genetic data from adults (UK Biobank, N = 31,748) and children (ABCD, N = 4928). Using polygenic scores and genetic correlations we observe a robust negative association between common variants for autism and a magnetic resonance imaging derived phenotype for neurite density (intracellular volume fraction) in the general population. This result is consistent across both children and adults, in both the cortex and in white matter tracts, and confirmed using polygenic scores and genetic correlations. There were no sex differences in this association. Mendelian randomisation analyses provide no evidence for a causal relationship between autism and intracellular volume fraction, although this should be revisited using better powered instruments. Overall, this study provides evidence for shared common variant genetics between autism and cortical neurite density.
AB - Genetic variants linked to autism are thought to change cognition and behaviour by altering the structure and function of the brain. Although a substantial body of literature has identified structural brain differences in autism, it is unknown whether autism-associated common genetic variants are linked to changes in cortical macro- and micro-structure. We investigated this using neuroimaging and genetic data from adults (UK Biobank, N = 31,748) and children (ABCD, N = 4928). Using polygenic scores and genetic correlations we observe a robust negative association between common variants for autism and a magnetic resonance imaging derived phenotype for neurite density (intracellular volume fraction) in the general population. This result is consistent across both children and adults, in both the cortex and in white matter tracts, and confirmed using polygenic scores and genetic correlations. There were no sex differences in this association. Mendelian randomisation analyses provide no evidence for a causal relationship between autism and intracellular volume fraction, although this should be revisited using better powered instruments. Overall, this study provides evidence for shared common variant genetics between autism and cortical neurite density.
KW - Adult
KW - Autism Spectrum Disorder/genetics
KW - Autistic Disorder/genetics
KW - Brain/metabolism
KW - Cerebral Cortex
KW - Child
KW - Female
KW - Genetic Predisposition to Disease/genetics
KW - Genome-Wide Association Study/methods
KW - Humans
KW - Magnetic Resonance Imaging/methods
KW - Male
KW - Mendelian Randomization Analysis
KW - Middle Aged
KW - Multifactorial Inheritance/genetics
KW - Neurites/metabolism
KW - Polymorphism, Single Nucleotide/genetics
KW - United Kingdom
KW - White Matter
UR - https://www.scopus.com/pages/publications/85218701046
U2 - 10.1038/s41380-025-02927-z
DO - 10.1038/s41380-025-02927-z
M3 - Journal article
C2 - 39994426
SN - 1359-4184
VL - 30
SP - 3393
EP - 3403
JO - Molecular Psychiatry
JF - Molecular Psychiatry
IS - 8
M1 - 2301
ER -