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Neurobiological Substrate of Autism Spectrum Disorder - Cerebral Blood Flow Distribution of 11C-butanol as Assessed by PET/CT

Published online by Cambridge University Press:  16 April 2020

M. Pagani
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden ISTC, CNR, Rome & Padua, Italy
I. Manouilenko
Affiliation:
Psychiatry, St. Göran's Hospital, Stockholm, Sweden
S. Stone-Elander
Affiliation:
Karolinska Pharmacy and Dept Clin Neurosciences, Karolinska Institutet, Stockholm, Sweden
R. Odh
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden
D. Salmaso
Affiliation:
ISTC, CNR, Rome & Padua, Italy
A.-M. Danielsson
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden
R. Hatherly
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden
H. Jacobsson
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden
S.A. Larsson
Affiliation:
Nuclear Medicine, Karolinska Hospital, Stockholm, Sweden
S. Bejerot
Affiliation:
Psychiatry, St. Göran's Hospital, Stockholm, Sweden

Abstract

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Background:

Functional studies in Autism Spectrum Disorder (ASD) have shown localised focal hypoperfusion and abnormalities in the anatomo-functional connectivity of limbic-striatal “social” brain. However, no common regional abnormalities have been found across studies.

The aim of this study was to investigate the cerebral blood flow (CBF) at rest in subjects with ASD as compared to a group of healthy controls.

Methods:

In this preliminary investigation six normal intelligence patients with ASD and 5 age and sex matched healthy controls (HC) were examined using PET/CT camera and, as CBF tracer, 11C-butanol, a radiopharmaceutical produced on-site. The combination of these two methodologies reduced the whole examination time to less than 10 minutes. Statistical Parametric Mapping was implemented to analyse the data.

Results:

As compared to HC, ASD showed a highly significant CBF increase (height threshold p=0.001, p< 0.0001 at voxel-level), bilaterally, in large portions of the cerebellum, of the visual associative cortex and of the posterior parietal lobe.

Conclusions:

This preliminary study was performed by the state-of-the-art neuroimaging methodologies that reduced considerably the examination time and resulted in less stress and more reliable investigations. The occipital and parietal associative cortex as well as the cerebellum showed an increased CBF in ASD, underscoring their involvement in the disease and raising methodological and diagnostic issues to be considered when exploring the neuroanatomy of ASD.

Type
P02-07
Copyright
Copyright © European Psychiatric Association 2009
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