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 - Zhang, Xinhe
AU - Weir, Elizabeth
AU - Uzefovsky, Florina
AU - Tsompanidis, Alexandros
AU - Srivastava, Deepak
AU - Sichlinger, Laura
AU - Rowitch, David
AU - Radecki, Marcin
AU - Polit, Lucia Dutan
AU - Pavlinek, Adam
AU - Niakan, Kathy
AU - Musa, Mahmoud Koko
AU - Mill, Jonathan
AU - Martinez, Jose Gonzalez
AU - Lombardo, Michael
AU - Lancaster, Madeline
AU - Lai, Meng Chuan
AU - Khan, Yumnah
AU - Hurles, Matthew
AU - Holt, Rosemary
AU - Heazell, Alexander
AU - Havdahl, Alexandra
AU - Greenberg, David M.
AU - Geschwind, Daniel
AU - Gabis, Lidia
AU - Franklin, Alice
AU - Floris, Dori
AU - Davis, Joanna
AU - Davies, Jonathan
AU - Burton, Graham
AU - Biron-Shental, Tal
AU - Bethlehem, Richard
AU - Bamford, Rosie
AU - Ayeung, Bonnie
AU - Allison, Carrie
AU - Adhya, Deep
AU - Werge, Thomas
AU - Nordentoft, Merete
AU - Mortensen, Preben Bo
AU - Mors, Ole
AU - Hougaard, David M.
AU - Bybjerg-Grauholm, Jonas
AU - Borglum, Anders
AU - Romero-Garcia, Rafael
AU - Grove, Jakob
AU - Børglum, Anders D.
AU - Martin, Hilary
N1 - Publisher Copyright: © The Author(s) 2025.
PY - 2025/2/24
Y1 - 2025/2/24
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.
UR - http://www.scopus.com/inward/record.url?scp=85218701046&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/s41380-025-02927-z
DO - https://doi.org/10.1038/s41380-025-02927-z
M3 - مقالة
C2 - 39994426
SN - 1359-4184
JO - Molecular Psychiatry
JF - Molecular Psychiatry
M1 - 2301
ER -