TY - JOUR
T1 - Discovering the gene-brain-behavior link in autism via generative machine learning
AU - Kundu, Shinjini
AU - Sair, Haris
AU - Sherr, Elliott H.
AU - Mukherjee, Pratik
AU - Rohde, Gustavo K.
N1 - Publisher Copyright:
© 2024 the Authors, some rights reserved.
PY - 2024/6
Y1 - 2024/6
N2 - Autism is traditionally diagnosed behaviorally but has a strong genetic basis. A genetics-first approach could transform understanding and treatment of autism. However, isolating the gene-brain-behavior relationship from confounding sources of variability is a challenge. We demonstrate a novel technique, 3D transport-based morphometry (TBM), to extract the structural brain changes linked to genetic copy number variation (CNV) at the 16p11.2 region. We identified two distinct endophenotypes. In data from the Simons Variation in Individuals Project, detection of these endophenotypes enabled 89 to 95% test accuracy in predicting 16p11.2 CNV from brain images alone. Then, TBM enabled direct visualization of the endophenotypes driving accurate prediction, revealing dose-dependent brain changes among deletion and duplication carriers. These endophenotypes are sensitive to articulation disorders and explain a portion of the intelligence quotient variability. Genetic stratification combined with TBM could reveal new brain endophenotypes in many neurodevelopmental disorders, accelerating precision medicine, and understanding of human neurodiversity.
AB - Autism is traditionally diagnosed behaviorally but has a strong genetic basis. A genetics-first approach could transform understanding and treatment of autism. However, isolating the gene-brain-behavior relationship from confounding sources of variability is a challenge. We demonstrate a novel technique, 3D transport-based morphometry (TBM), to extract the structural brain changes linked to genetic copy number variation (CNV) at the 16p11.2 region. We identified two distinct endophenotypes. In data from the Simons Variation in Individuals Project, detection of these endophenotypes enabled 89 to 95% test accuracy in predicting 16p11.2 CNV from brain images alone. Then, TBM enabled direct visualization of the endophenotypes driving accurate prediction, revealing dose-dependent brain changes among deletion and duplication carriers. These endophenotypes are sensitive to articulation disorders and explain a portion of the intelligence quotient variability. Genetic stratification combined with TBM could reveal new brain endophenotypes in many neurodevelopmental disorders, accelerating precision medicine, and understanding of human neurodiversity.
UR - http://www.scopus.com/inward/record.url?scp=85196102305&partnerID=8YFLogxK
U2 - 10.1126/sciadv.adl5307
DO - 10.1126/sciadv.adl5307
M3 - Article
C2 - 38865470
AN - SCOPUS:85196102305
SN - 2375-2548
VL - 10
JO - Science Advances
JF - Science Advances
IS - 24
M1 - eadl5307
ER -