Abstract
Objective: Tuberous sclerosis complex (TSC) is associated with focal brain “tubers” and a high incidence of autism spectrum disorder (ASD). The location of brain tubers associated with autism may provide insight into the neuroanatomical substrate of ASD symptoms. Methods: We delineated tuber locations for 115 TSC participants with ASD (n = 31) and without ASD (n = 84) from the Tuberous Sclerosis Complex Autism Center of Excellence Research Network. We tested for associations between ASD diagnosis and tuber burden within the whole brain, specific lobes, and at 8 regions of interest derived from the ASD neuroimaging literature, including the anterior cingulate, orbitofrontal and posterior parietal cortices, inferior frontal and fusiform gyri, superior temporal sulcus, amygdala, and supplemental motor area. Next, we performed an unbiased data-driven voxelwise lesion symptom mapping (VLSM) analysis. Finally, we calculated the risk of ASD associated with positive findings from the above analyses. Results: There were no significant ASD-related differences in tuber burden across the whole brain, within specific lobes, or within a priori regions derived from the ASD literature. However, using VLSM analysis, we found that tubers involving the right fusiform face area (FFA) were associated with a 3.7-fold increased risk of developing ASD. Interpretation: Although TSC is a rare cause of ASD, there is a strong association between tuber involvement of the right FFA and ASD diagnosis. This highlights a potentially causative mechanism for developing autism in TSC that may guide research into ASD symptoms more generally. ANN NEUROL 2023;93:577–590.
Original language | English (US) |
---|---|
Pages (from-to) | 577-590 |
Number of pages | 14 |
Journal | Annals of neurology |
Volume | 93 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2023 |
Funding
This research was supported by awards from multiple NIH grants including K23MH120510 (A.L.C. and P.M.), U54NS092090 (M.S.), P50HD105351 (M.S.), the Child Neurology Foundation (A.L.C., M.R.K., and J.W.). M.D.F. was supported by the Nancy Lurie Marks Foundation, the Kaye Family Research Endowment, the Ellison/Baszucki Foundation, and the NIH (R01MH113929, R21MH126271, R56AG069086, R01MH115949, and R01AG060987). J.M.P. was additionally supported by the MacPherson Fund. Research reported in this publication was supported by NIH award number U01NS082320: Tuberous Sclerosis Complex Autism Center of Excellence Network (TACERN). The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.
ASJC Scopus subject areas
- Neurology
- Clinical Neurology