Highlights from IMFAR 2008:
Friday, May 16
Convergence of behavioural dysfunction, abnormalities in functional imaging and neuropathology in the fusiform gyrus in autism
C. Schmitz
Maastricht University, School for Mental Health and Neurosciences, Div. Cellular Neuroscience, Universiteitssingel 50, Maastricht, Netherlands
S. Palmen
University Medical Center Utrecht, Utrecht, Netherlands
H. Heinsen
Morphological Brain Research Unit, University of Wuerzburg, Wuerzburg, Germany
H. Van Engeland
Child and Adolescent Psychiatry, University Medical Center-Utrecht, Postbox 85500 A01.468, Utrecht, 3508 GA, Netherlands
P. R. Hof
Department of Neuroscience, Mount Sinai School for Medicine, New York, NY 10029
H. W. M. Steinbusch
I. Van Kooten
Maastricht University, School for Mental Health and Neurosciences, Div. Cellular Neuroscience, Universiteitssingel 50, Maastricht, Netherlands
Abstract
Abnormalities in face perception are a core feature of social disabilities in autism. Recent functional magnetic resonance imaging studies showed that patients with autism can perform face perception tasks. However, the fusiform gyrus and other cortical regions supporting face processing in controls are hypoactive in patients with autism. The neurobiological basis of this phenomenon is unknown. Here, we tested the hypothesis that the fusiform gyrus shows neuropathological alterations in autism, namely alterations in neuron density, total neuron number and mean perikaryal volume. We investigated the fusiform gyrus (analyzing separately layers II, III, IV, V, and VI), in 7 postmortem brains from patients with autism and 10 controls for volume, neuron density, total neuron number and mean perikaryal volume with high-precision design-based stereology. To determine whether these results were specific for the fusiform gyrus the same analyses were also performed in the primary visual cortex and in the cortical gray matter as a whole. Compared to controls, patients with autism showed significant reductions in neuron densities in layer III, total neuron numbers in layers III, V, and VI, and mean perikaryal volumes of neurons in layers V and VI in the fusiform gyrus. None of these alterations were found in the primary visual cortex or in the whole cerebral cortex. Although based on a relatively small sample of postmortem brains from patients with autism and controls, the results of the present study may provide important insight about the cellular basis of abnormalities in face perception in autism.
Extended Abstract
Abnormalities in face perception are a core feature of social disabilities in autism. Recent functional magnetic resonance imaging studies showed that patients with autism can perform face perception tasks. However, the fusiform gyrus and other cortical regions supporting face processing in controls are hypoactive in patients with autism. The neurobiological basis of this phenomenon is unknown. Here, we tested the hypothesis that the fusiform gyrus shows neuropathological alterations in autism, namely alterations in neuron density, total neuron number and mean perikaryal volume. We investigated the fusiform gyrus (analyzing separately layers II, III, IV, V, and VI), in 7 postmortem brains from patients with autism and 10 controls for volume, neuron density, total neuron number and mean perikaryal volume with high-precision design-based stereology. To determine whether these results were specific for the fusiform gyrus the same analyses were also performed in the primary visual cortex and in the cortical gray matter as a whole. Compared to controls, patients with autism showed significant reductions in neuron densities in layer III, total neuron numbers in layers III, V, and VI, and mean perikaryal volumes of neurons in layers V and VI in the fusiform gyrus. None of these alterations were found in the primary visual cortex or in the whole cerebral cortex. Although based on a relatively small sample of postmortem brains from patients with autism and controls, the results of the present study may provide important insight about the cellular basis of abnormalities in face perception in autism.
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