Age-related temporal and parietal cortical thinning in autism spectrum disorders

• Published in: Brain (London, England : 1878) Vol. 133; no. 12; pp. 3745 - 3754
• Main Authors: Wallace, Gregory L., Dankner, Nathan, Kenworthy, Lauren, Giedd, Jay N., Martin, Alex
• Format: Journal Article
• Language: English
• Published: Oxford Oxford University Press 01.12.2010
• Subjects: Adolescent; age-related changes; Aging - pathology; Aging - psychology; autism; Autistic Disorder - drug therapy; Autistic Disorder - pathology; Autistic Disorder - psychology; Biological and medical sciences; brain; Child; cortical thickness; Frontal Lobe - pathology; Functional Laterality - physiology; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy; Humans; Image Processing, Computer-Assisted; Intelligence Tests; Magnetic Resonance Imaging; Male; Medical sciences; Mental Disorders - complications; Mental Disorders - psychology; MRI; Nervous system (semeiology, syndromes); Neurology; Neuropsychological Tests; Original; Parietal Lobe - pathology; Psychotropic Drugs - adverse effects; Psychotropic Drugs - therapeutic use; Temporal Lobe - pathology; Young Adult; Autism; Nervous system diseases; Pervasive developmental disorder; MRI; cortical thickness; Central nervous system; Parietal; Developmental disorder; age-related changes; brain; Nuclear magnetic resonance imaging; Encephalon
• ISSN: 0006-8950; 1460-2156
• DOI: 10.1093/brain/awq279

Studies of head size and brain volume in autism spectrum disorders have suggested that early cortical overgrowth may be followed by prematurely arrested growth. However, the few investigations quantifying cortical thickness have yielded inconsistent results, probably due to variable ages and/or small sample sizes. We assessed differences in cortical thickness between high-functioning adolescent and young adult males with autism spectrum disorders (n = 41) and matched typically developing males (n = 40). We hypothesized thinner cortex, particularly in frontal, parietal and temporal regions, for individuals with autism spectrum disorders in comparison with typically developing controls. Furthermore, we expected to find an age × diagnosis interaction: with increasing age, more pronounced cortical thinning would be observed in autism spectrum disorders than typically developing participants. T1-weighted magnetization prepared rapid gradient echo 3 T magnetic resonance imaging scans were acquired from high-functioning males with autism spectrum disorders and from typically developing males matched group-wise on age (range 12–24 years), intelligence quotient (≥85) and handedness. Both gyral-level and vertex-based analyses revealed significantly thinner cortex in the autism spectrum disorders group that was located predominantly in left temporal and parietal regions (i.e. the superior temporal sulcus, inferior temporal, postcentral/superior parietal and supramarginal gyri). These findings remained largely unchanged after controlling for intelligence quotient and after accounting for psychotropic medication usage and comorbid psychopathology. Furthermore, a significant age × diagnosis interaction was found in the left fusiform/inferior temporal cortex: participants with autism spectrum disorders had thinner cortex in this region with increasing age to a greater degree than did typically developing participants. Follow-up within group comparisons revealed significant age-related thinning in the autism spectrum disorders group but not in the typically developing group. Both thinner temporal and parietal cortices during adolescence and young adulthood and discrepantly accelerated age-related cortical thinning in autism spectrum disorders suggest that a second period of abnormal cortical growth (i.e. greater thinning) may be characteristic of these disorders.