Face processing occurs outside the fusiform `face area' in autism: evidence from functional MRI

Processing the human face is at the focal point of most social interactions, yet this simple perceptual task is difficult for individuals with autism, a population that spends limited amounts of time engaged in face-to-face eye contact or social interactions in general. Thus, the study of face proce...

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Published inBrain (London, England : 1878) Vol. 124; no. 10; pp. 2059 - 2073
Main Authors Pierce, Karen, Müller, R.-A., Ambrose, J., Allen, G., Courchesne, E.
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.10.2001
Oxford Publishing Limited (England)
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Abstract Processing the human face is at the focal point of most social interactions, yet this simple perceptual task is difficult for individuals with autism, a population that spends limited amounts of time engaged in face-to-face eye contact or social interactions in general. Thus, the study of face processing in autism is not only important because it may be integral to understanding the social deficits of this disorder, but also, because it provides a unique opportunity to study experiential factors related to the functional specialization of normal face processing. In short, autism may be one of the only disorders where affected individuals spend reduced amounts of time engaged in face processing from birth. Using functional MRI, haemodynamic responses during a face perception task were compared between adults with autism and normal control subjects. Four regions of interest (ROIs), the fusiform gyrus (FG), inferior temporal gyrus, middle temporal gyrus and amygdala were manually traced on non-spatially normalized images and the percentage ROI active was calculated for each subject. Analyses in Talairach space were also performed. Overall results revealed either abnormally weak or no activation in FG in autistic patients, as well as significantly reduced activation in the inferior occipital gyrus, superior temporal sulcus and amygdala. Anatomical abnormalities, in contrast, were present only in the amygdala in autistic patients, whose mean volume was significantly reduced as compared with normals. Reaction time and accuracy measures were not different between groups. Thus, while autistic subjects could perform the face perception task, none of the regions supporting face processing in normals were found to be significantly active in the autistic subjects. Instead, in every autistic patient, faces maximally activated aberrant and individual-specific neural sites (e.g. frontal cortex, primary visual cortex, etc.), which was in contrast to the 100% consistency of maximal activation within the traditional fusiform face area (FFA) for every normal subject. It appears that, as compared with normal individuals, autistic individuals `see' faces utilizing different neural systems, with each patient doing so via a unique neural circuitry. Such a pattern of individual-specific, scattered activation seen in autistic patients in contrast to the highly consistent FG activation seen in normals, suggests that experiential factors do indeed play a role in the normal development of the FFA.
AbstractList Processing the human face is at the focal point of most social interactions, yet this simple perceptual task is difficult for individuals with autism, a population that spends limited amounts of time engaged in face-to-face eye contact or social interactions in general. Thus, the study of face processing in autism is not only important because it may be integral to understanding the social deficits of this disorder, but also, because it provides a unique opportunity to study experiential factors related to the functional specialization of normal face processing. In short, autism may be one of the only disorders where affected individuals spend reduced amounts of time engaged in face processing from birth. Using functional MRI, haemodynamic responses during a face perception task were compared between adults with autism and normal control subjects. Four regions of interest (ROIs), the fusiform gyrus (FG), inferior temporal gyrus, middle temporal gyrus and amygdala were manually traced on non-spatially normalized images and the percentage ROI active was calculated for each subject. Analyses in Talairach space were also performed. Overall results revealed either abnormally weak or no activation in FG in autistic patients, as well as significantly reduced activation in the inferior occipital gyrus, superior temporal sulcus and amygdala. Anatomical abnormalities, in contrast, were present only in the amygdala in autistic patients, whose mean volume was significantly reduced as compared with normals. Reaction time and accuracy measures were not different between groups. Thus, while autistic subjects could perform the face perception task, none of the regions supporting face processing in normals were found to be significantly active in the autistic subjects. Instead, in every autistic patient, faces maximally activated aberrant and individual-specific neural sites (e.g. frontal cortex, primary visual cortex, etc.), which was in contrast to the 100% consistency of maximal activation within the traditional fusiform face area (FFA) for every normal subject. It appears that, as compared with normal individuals, autistic individuals `see' faces utilizing different neural systems, with each patient doing so via a unique neural circuitry. Such a pattern of individual-specific, scattered activation seen in autistic patients in contrast to the highly consistent FG activation seen in normals, suggests that experiential factors do indeed play a role in the normal development of the FFA.
Author Allen, G.
Courchesne, E.
Müller, R.-A.
Pierce, Karen
Ambrose, J.
Author_xml – sequence: 1
  givenname: Karen
  surname: Pierce
  fullname: Pierce, Karen
  organization: Departments of Neurosciences and
– sequence: 2
  givenname: R.-A.
  surname: Müller
  fullname: Müller, R.-A.
  organization: Cognitive Science, University of California, San Diego
– sequence: 3
  givenname: J.
  surname: Ambrose
  fullname: Ambrose, J.
  organization: Laboratory for the Neurosciences of Autism, Children's Hospital Research Center, La Jolla, California and
– sequence: 4
  givenname: G.
  surname: Allen
  fullname: Allen, G.
  organization: Long Island Jewish Medical Center, Glen Oaks, New York, USA
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  givenname: E.
  surname: Courchesne
  fullname: Courchesne, E.
  organization: Departments of Neurosciences and
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14071942$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/11571222$$D View this record in MEDLINE/PubMed
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Keywords Human
Autism
Cartography
Central nervous system
Medical imagery
Exploration
Perception
Developmental disorder
Face
Nuclear magnetic resonance imaging
Recognition
Brain (vertebrata)
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Snippet Processing the human face is at the focal point of most social interactions, yet this simple perceptual task is difficult for individuals with autism, a...
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SubjectTerms Adult
amygdala
Amygdala - physiopathology
Autism
Autistic Disorder - physiopathology
Autistic Disorder - psychology
Biological and medical sciences
Brain Mapping - methods
Cerebral Cortex - physiopathology
Child clinical studies
Developmental disorders
EPI = echo-planar image
Face
face perception
FFA = fusiform face area
FG = fusiform gyrus
fMRI
fMRI = functional MRI
fusiform gyrus
Humans
Infantile autism
ITG = inferior temporal gyrus
Magnetic Resonance Imaging - methods
Male
Medical sciences
MTG = middle temporal gyrus
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Reaction Time - physiology
ROI = region of interest
Visual Perception - physiology
Title Face processing occurs outside the fusiform `face area' in autism: evidence from functional MRI
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