@article{24b441f88cc742b6a360255549b10485,
title = "Tuber Locations Associated with Infantile Spasms Map to a Common Brain Network",
abstract = "Objective: Approximately 50\% of patients with tuberous sclerosis complex develop infantile spasms, a sudden onset epilepsy syndrome associated with poor neurological outcomes. An increased burden of tubers confers an elevated risk of infantile spasms, but it remains unknown whether some tuber locations confer higher risk than others. Here, we test whether tuber location and connectivity are associated with infantile spasms. Methods: We segmented tubers from 123 children with (n = 74) and without (n = 49) infantile spasms from a prospective observational cohort. We used voxelwise lesion symptom mapping to test for an association between spasms and tuber location. We then used lesion network mapping to test for an association between spasms and connectivity with tuber locations. Finally, we tested the discriminability of identified associations with logistic regression and cross-validation as well as statistical mediation. Results: Tuber locations associated with infantile spasms were heterogenous, and no single location was significantly associated with spasms. However, >95\% of tuber locations associated with spasms were functionally connected to the globi pallidi and cerebellar vermis. These connections were specific compared to tubers in patients without spasms. Logistic regression found that globus pallidus connectivity was a stronger predictor of spasms (odds ratio [OR] = 1.96, 95\% confidence interval [CI] = 1.10–3.50, p = 0.02) than tuber burden (OR = 1.65, 95\% CI = 0.90–3.04, p = 0.11), with a mean receiver operating characteristic area under the curve of 0.73 (±0.1) during repeated cross-validation. Interpretation: Connectivity between tuber locations and the bilateral globi pallidi is associated with infantile spasms. Our findings lend insight into spasm pathophysiology and may identify patients at risk. ANN NEUROL 2021;89:726–739.",
author = "Cohen, \{Alexander L.\} and Mulder, \{Brechtje P. F.\} and Prohl, \{Anna K.\} and Louis Soussand and Peter Davis and Kroeck, \{Mallory R.\} and Peter McManus and Ali Gholipour and Benoit Scherrer and Bebin, \{E. Martina\} and Wu, \{Joyce Y.\} and Hope Northrup and Krueger, \{Darcy A.\} and Mustafa Sahin and Warfield, \{Simon K.\} and \{Tuberous Sclerosis Complex Autism Center of Excellence Network Study Group\} and Fox, \{Michael D.\} and Peters, \{Jurriaan M.\}",
note = "Funding Information: This research was supported by awards from multiple NIH grants including NINDS U01NS082320 (M.S. and D.A.K.), NIMH T32MH112510 and NIMH K23MH120510 (A.L.C. and P.M.), NINDS U54NS092090 (M.S.), NICHD U54HD090255 (M.S.), and NINDS K23NS083741 (M.F.), as well as funding from the TS Alliance to TACERN, the Child Neurology Foundation (A.L.C. and M.R.K.), the Sidney R. Baer, Jr. Foundation (M.F.), the Dystonia Foundation (M.F.), and the Nancy Lurie Marks Foundation (M.F.). We are sincerely indebted to the generosity of the families and patients in TSC clinics across the United States who contributed their time and effort to this study. We also thank the Tuberous Sclerosis Alliance for its continued support of TSC research. Funding Information: Data were provided (in part) by the Brain Genomics Superstruct Project of Harvard University and Massachusetts General Hospital (principal investigators: Randy Buckner, Joshua Roffman, and Jordan Smoller), with support from the Center for Brain Science Neuroinformatics Research Group, the Athinoula A. Martinos Center for Biomedical Imaging, and the Center for Human Genetic Research. Twenty individual investigators at Harvard University and Massachusetts General Hospital generously contributed data to the overall project. Funding Information: Some of the data used in the preparation of this article were obtained from the ABCD study ( https://abcdstudy.org ), held in the National Institute of Mental Health Data Archive. This is a multisite, longitudinal study designed to recruit more than 10,000 children aged 9–10 years and follow them over 10 years into early adulthood. The ABCD study is supported by the NIH and additional federal partners under award numbers U01DA041048, U01DA050989, U01DA051016, U01DA041022, U01DA051018, U01DA051037, U01DA050987, U01DA041174, U01DA041106, U01DA041117, U01DA041028, U01DA041134, U01DA050988, U01DA051039, U01DA041156, U01DA041025, U01DA041120, U01DA051038, U01DA041148, U01DA041093, U01DA041089, U24DA041123, U24DA041147. A full list of supporters is available at https://abcdstudy.org/federal-partners.html . A listing of participating sites and a complete listing of the study investigators can be found at https://abcdstudy.org/scientists/workgroups/ . ABCD consortium investigators designed and implemented the study and/or provided data but did not necessarily participate in analysis or writing of this report. This article reflects the views of the authors and may not reflect the opinions or views of the NIH or ABCD consortium investigators. The ABCD data repository grows and changes over time. The ABCD data used in this report are listed at: https://nda.nih.gov/study.html?id=1054 , doi: 10.15154/1520630. Funding Information: This research was supported by awards from multiple NIH grants including NINDS U01NS082320 (M.S. and D.A.K.), NIMH T32MH112510 and NIMH K23MH120510 (A.L.C. and P.M.), NINDS U54NS092090 (M.S.), NICHD U54HD090255 (M.S.), and NINDS K23NS083741 (M.F.), as well as funding from the TS Alliance to TACERN, the Child Neurology Foundation (A.L.C. and M.R.K.), the Sidney R. Baer, Jr. Foundation (M.F.), the Dystonia Foundation (M.F.), and the Nancy Lurie Marks Foundation (M.F.). Publisher Copyright: {\textcopyright} 2021 American Neurological Association Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = apr,
doi = "10.1002/ana.26015",
language = "English",
volume = "89",
pages = "726--739",
journal = "Annals of neurology",
issn = "0364-5134",
publisher = "John Wiley and Sons Inc.",
number = "4",
}