Profiling brain morphology for autism spectrum disorder with two cross-culture large-scale consortia

Xue Ru Fan, Ye He, Yin Shan Wang, Lei Li, Xi Nian Zuo*, Andre Zugman, Dabriel Zimmerman, Hisham Ziauddeen, Juan H. Zhou, Anna Zettergren, Heather J. Zar, Andrew Zalesky, Hyuk Jin Yun, B. T.Thomas Yeo, Ning Yang, A. Veronica Witte, Simon R. White, Heather C. Whalley, Margaret L. Westwater, Eric WestmanVarun Warrier, Simon K. Warfield, Konrad Wagstyl, Jacob W. Vogel, Arno Villringer, Sylvia Villeneuve, Lindsay W. Victoria, Petra E. Vértes, Lana Vasung, Simon N. Vandekar, Therese van Amelsvoort, Sofie L. Valk, Pedro A. Valdes-Sosa, Mitchell J. Valdes-Sosa, Étienne Vachon-Presseau, Christophe Tzourio, Jetro J. Tuulari, Nicholas B. Turk-Browne, Kamen A. Tsvetanov, Nicolas Traut, Roberto Toro, Benjamin Thyreau, Gemma Sullivan, John Suckling, Aleks Stolicyn, Dan J. Stein, Reisa A. Sperling, Christopher D. Smyser, Ingmar Skoog, Machteld Marcelis, China Autism Brain Imaging Consortium (CABIC), Lifespan Brain Chart Consortium (LBCC)

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

We explore neurodevelopmental heterogeneity in Autism Spectrum Disorder (ASD) through normative modeling of cross-cultural cohorts. By leveraging large-scale datasets from Autism Brain Imaging Data Exchange (ABIDE) and China Autism Brain Imaging Consortium (CABIC), our model identifies two ASD subgroups with distinct brain morphological abnormalities: subgroup “L” is characterized by generally smaller brain region volumes and higher rates of abnormality, while subgroup “H” exhibits larger volumes with less pronounced deviations in specific areas. Key areas, such as the isthmus cingulate and transverse temporal gyrus, were identified as critical for subgroup differentiation and ASD trait correlations. In subgroup H, the regional volume of the isthmus cingulate cortex showed a direct correlation with individuals’ autistic mannerisms, potentially corresponding to its slower post-peak volumetric declines during development. These findings offer insights into the biological mechanisms underlying ASD and support the advancement of subgroup-driven precision clinical practices.
Original languageEnglish
Article number1157
Number of pages16
JournalCommunications Biology
Volume8
Issue number1
DOIs
Publication statusPublished - 1 Dec 2025

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