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Impaired response inhibition and excess cortical thickness as candidate endophenotypes for trichotillomania
Institution:1. Department of Psychiatry, Massachusetts General Hospital, 185 Cambridge St., Suite 2200, Boston, MA, 02114, USA;2. Department of Psychology, Kent State University, 600 Hilltop Drive, Kent, OH, 44242, USA;3. Department of Psychiatry & Behavioral Neuroscience, University of Chicago, 5841 S. Maryland Avenue, MC 3077, Chicago, IL 60637, USA;1. UCLA Jane and Terry Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA 90095, United States;2. University of Denver, Denver, CO 80208, United States;3. California State University Long Beach, Long Beach, CA 90840, United States;4. Vanderbilt University, Nashville, TN 37235, United States
Abstract:Trichotillomania is characterized by repetitive pulling out of one's own hair. Impaired response inhibition has been identified in patients with trichotillomania, along with gray matter density changes in distributed neural regions including frontal cortex. The objective of this study was to evaluate impaired response inhibition and abnormal cortical morphology as candidate endophenotypes for the disorder. Subjects with trichotillomania (N = 12), unaffected first-degree relatives of these patients (N = 10), and healthy controls (N = 14), completed the Stop Signal Task (SST), a measure of response inhibition, and structural magnetic resonance imaging scans. Group differences in SST performance and cortical thickness were explored using permutation testing. Groups differed significantly in response inhibition, with patients demonstrating impaired performance versus controls, and relatives occupying an intermediate position. Permutation cluster analysis revealed significant excesses of cortical thickness in patients and their relatives compared to controls, in right inferior/middle frontal gyri (Brodmann Area, BA 47 & 11), right lingual gyrus (BA 18), left superior temporal cortex (BA 21), and left precuneus (BA 7). No significant differences emerged between groups for striatum or cerebellar volumes. Impaired response inhibition and an excess of cortical thickness in neural regions germane to inhibitory control, and action monitoring, represent vulnerability markers for trichotillomania. Future work should explore genetic and environmental associations with these biological markers.
Keywords:Cognition  Compulsivity  Imaging  Impulsivity  Trichotillomania  Endophenotype
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