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Medial Frontal Lobe Neurochemistry in Autism Spectrum Disorder is Marked by Reduced N-Acetylaspartate and Unchanged Gamma-Aminobutyric Acid and Glutamate + Glutamine Levels
被引:0
|作者:
Andreia Carvalho Pereira
Inês R. Violante
Susana Mouga
Guiomar Oliveira
Miguel Castelo-Branco
机构:
[1] University of Coimbra,Institute for Biomedical Imaging and Life Sciences (CNC.IBILI), Faculty of Medicine
[2] King’s College London,Sackler Institute for Translational Neurodevelopment, Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience
[3] Imperial College London,The Computational, Cognitive and Clinical Neuroimaging Laboratory, Department of Medicine
[4] Centro Hospitalar e Universitário de Coimbra,Unidade de Neurodesenvolvimento e Autismo do Serviço do Centro de Desenvolvimento da Criança, Pediatric Hospital
[5] Hospital Pediátrico – Centro Hospitalar e Universitário de Coimbra,Centro de Investigação e Formação Clínica
[6] University of Coimbra,University Clinic of Pediatrics, Faculty of Medicine
[7] University of Coimbra,Institute of Nuclear Sciences Applied to Health (ICNAS), CiBIT, Brain Imaging Network of Portugal
来源:
关键词:
Autism spectrum disorder;
-acetylaspartate;
Gamma-aminobutyric acid;
Glutamate + glutamine;
Creatine;
Autism diagnostic interview—revised;
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摘要:
The nature of neurochemical changes in autism spectrum disorder (ASD) remains controversial. We compared medial prefrontal cortex (mPFC) neurochemistry of twenty high-functioning children and adolescents with ASD without associated comorbidities and fourteen controls. We observed reduced total N-acetylaspartate (tNAA) and total creatine, increased Glx/tNAA but unchanged glutamate + glutamine (Glx) and unchanged absolute or relative gamma-aminobutyric acid (GABA+) in the ASD group. Importantly, both smaller absolute and relative GABA+ levels were associated with worse communication skills and developmental delay scores assessed by the autism diagnostic interview—revised (ADI-R). We conclude that tNAA is reduced in the mPFC in ASD and that glutamatergic metabolism may be altered due to unbalanced Glx/tNAA. Moreover, GABA+ is related to autistic symptoms assessed by the ADI-R.
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页码:1467 / 1482
页数:15
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