TY - JOUR
T1 - Polygenic and developmental profiles of autism differ by age at diagnosis
AU - APEX Consortium
AU - iPSYCH-autism consortium
AU - PGC-PTSD Consortium
AU - Zhang, Xinhe
AU - Grove, Jakob
AU - Gu, Yuanjun
AU - Buus, Cornelia K.
AU - Nielsen, Lea K.
AU - Neufeld, Sharon A.S.
AU - Koko, Mahmoud
AU - Malawsky, Daniel S.
AU - Wade, Emma M.
AU - Verhoef, Ellen
AU - Gui, Anna
AU - Hegemann, Laura
AU - Del Rio, Juan Pablo
AU - Khan, Yumnah T.
AU - Uzefovsky, Florina
AU - Weir, Elizabeth
AU - Greenberg, Yeshaya David
AU - Lai, Meng Chuan
AU - Radecki, Marcin
AU - Lombardo, Michael V.
AU - Bethlehem, Richard
AU - Floris, Dorothea
AU - Gabis, Lidia V.
AU - Biron-Shental, Tal
AU - Gonzalez-Martinez, Jose
AU - Lancaster, Madeline A.
AU - Nagy, Roland
AU - Sichlinger, Laura
AU - Pavlinek, Adam
AU - Dutan-Polit, Lucia
AU - Srivastava, Deepak P.
AU - Cindrova-Davies, Tereza
AU - Burton, Graham J.
AU - Niakan, Kathy K.
AU - Rowitch, David H.
AU - Mousa, Mahmoud
AU - Hurles, Matthew E.
AU - Bamford, Rosie
AU - Franklin, Alice
AU - Mill, Jonathan
AU - Heazell, Alexander E.P.
AU - Ghoddousi, Ramin Ali Marandi
AU - Al-Rubaie, Omar
AU - Holt, Rosemary
AU - Adhya, Deep
AU - Tsompanidis, Alex
AU - Allison, Carrie
AU - Werge, Thomas
AU - Nordentoft, Merete
AU - Mortensen, Preben Bo
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/10/30
Y1 - 2025/10/30
N2 - Although autism has historically been conceptualized as a condition that emerges in early childhood1,2, many autistic people are diagnosed later in life3, 4–5. It is unknown whether earlier- and later-diagnosed autism have different developmental trajectories and genetic profiles. Using longitudinal data from four independent birth cohorts, we demonstrate that two different socioemotional and behavioural trajectories are associated with age at diagnosis. In independent cohorts of autistic individuals, common genetic variants account for approximately 11% of the variance in age at autism diagnosis, similar to the contribution of individual sociodemographic and clinical factors, which typically explain less than 15% of this variance. We further demonstrate that the polygenic architecture of autism can be broken down into two modestly genetically correlated (rg = 0.38, s.e. = 0.07) autism polygenic factors. One of these factors is associated with earlier autism diagnosis and lower social and communication abilities in early childhood, but is only moderately genetically correlated with attention deficit–hyperactivity disorder (ADHD) and mental-health conditions. Conversely, the second factor is associated with later autism diagnosis and increased socioemotional and behavioural difficulties in adolescence, and has moderate to high positive genetic correlations with ADHD and mental-health conditions. These findings indicate that earlier- and later-diagnosed autism have different developmental trajectories and genetic profiles. Our findings have important implications for how we conceptualize autism and provide a model to explain some of the diversity found in autism.
AB - Although autism has historically been conceptualized as a condition that emerges in early childhood1,2, many autistic people are diagnosed later in life3, 4–5. It is unknown whether earlier- and later-diagnosed autism have different developmental trajectories and genetic profiles. Using longitudinal data from four independent birth cohorts, we demonstrate that two different socioemotional and behavioural trajectories are associated with age at diagnosis. In independent cohorts of autistic individuals, common genetic variants account for approximately 11% of the variance in age at autism diagnosis, similar to the contribution of individual sociodemographic and clinical factors, which typically explain less than 15% of this variance. We further demonstrate that the polygenic architecture of autism can be broken down into two modestly genetically correlated (rg = 0.38, s.e. = 0.07) autism polygenic factors. One of these factors is associated with earlier autism diagnosis and lower social and communication abilities in early childhood, but is only moderately genetically correlated with attention deficit–hyperactivity disorder (ADHD) and mental-health conditions. Conversely, the second factor is associated with later autism diagnosis and increased socioemotional and behavioural difficulties in adolescence, and has moderate to high positive genetic correlations with ADHD and mental-health conditions. These findings indicate that earlier- and later-diagnosed autism have different developmental trajectories and genetic profiles. Our findings have important implications for how we conceptualize autism and provide a model to explain some of the diversity found in autism.
UR - https://www.scopus.com/pages/publications/105020633871
U2 - 10.1038/s41586-025-09542-6
DO - 10.1038/s41586-025-09542-6
M3 - Article
C2 - 41034588
AN - SCOPUS:105020633871
SN - 0028-0836
VL - 646
SP - 1146
EP - 1155
JO - Nature
JF - Nature
IS - 8087
ER -