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March 15, 2011; 76 (11) Articles

Identification of risk factors for autism spectrum disorders in tuberous sclerosis complex

A.L. Numis, P. Major, M.A. Montenegro, D.A. Muzykewicz, M.B. Pulsifer, E.A. Thiele
First published March 14, 2011, DOI: https://doi.org/10.1212/WNL.0b013e3182104347
A.L. Numis
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P. Major
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M.A. Montenegro
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D.A. Muzykewicz
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Identification of risk factors for autism spectrum disorders in tuberous sclerosis complex
A.L. Numis, P. Major, M.A. Montenegro, D.A. Muzykewicz, M.B. Pulsifer, E.A. Thiele
Neurology Mar 2011, 76 (11) 981-987; DOI: 10.1212/WNL.0b013e3182104347

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Abstract

Objective: The purpose of this study was to assess the prevalence of and to identify epidemiologic, genetic, electrophysiologic, and neuroanatomic risk factors for autism spectrum disorders (ASD) in a cohort of patients with tuberous sclerosis complex (TSC).

Methods: A total of 103 patients with TSC were evaluated for ASD. A retrospective review of patients' records was performed, including mutational analysis. EEG reports were analyzed for the presence of ictal and interictal epileptiform features. Brain MRI scans were evaluated for TSC neuropathology, including tuber burden.

Results: Of the 103 patients with TSC, 40%were diagnosed with an ASD. On univariate analysis, patients with ASD were less likely to have mutations in the TSC1 gene. Patients with ASD also had an earlier age at seizure onset and more frequent seizures. On EEG, those with ASD had a significantly greater amount of interictal epileptiform features in the left temporal lobe only. On MRI, there were no differences in the regional distribution of tuber burden, although those with TSC2 and ASD had a higher prevalence of cyst-like tubers.

Conclusions: The development of ASD in TSC is not well understood. Given our findings, ASD may be associated with persistent seizure activity early in development in particular brain regions, such as those responsible for social perception and communication in the left temporal lobe. The presence of cyst-like tubers on MRI could provide a structural basis or marker for ASD pathology in TSC, although studies assessing their effect on cortical function are needed.

Footnotes

  • Study funding: Supported by the Carol and James Herscot Center for Tuberous Sclerosis Complex, NIH 5P01NS024279, and the Doris Duke Charitable Foundation (A.L.N.).

  • ASD
    autism spectrum disorders
    DSM-IV
    Diagnostic and Statistical Manual of Mental Disorders, 4th edition
    FLAIR
    fluid attenuation inversion recovery
    GAP
    guanosine triphosphatase-activating protein
    NMI
    no mutation identified
    NP
    neurophysiologic
    SEN
    subependymal nodule
    TSC
    tuberous sclerosis complex

  • Supplemental data at www.neurology.org

  • Received January 19, 2010.
  • Accepted November 23, 2010.
  • Copyright © 2011 by AAN Enterprises, Inc.
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