In Vivo ¹ H-Magnetic Resonance Spectroscopy Study of Amygdala-Hippocampal and Parietal Regions in Autism

We used ¹ H-MRS to investigate the neuronal integrity of the amygdala-hippocampal complex and a parietal region in 25 normal-intelligence adults with autistic spectrum disorders (full-scale IQ>70, measured using Wechsler Adult Intelligence Scale-III) and 21 healthy comparison subjects who did not differ significantly in age or sex. We obtained measures of the amygdala-hippocampal region in 20 subjects, the parietal region in 17 subjects, and both regions in 12 subjects with autistic spectrum disorders. All volunteers were diagnosed using ICD-10 criteria and the Autism Diagnostic Interview-Revised where possible. Seven (28%) subjects with an autistic spectrum disorder did not have an Autism Diagnostic Interview-Revised score. Exclusion criteria were a history of physical or psychiatric disorder affecting brain function (e.g., epilepsy or psychosis), a genetic disorder putatively associated with autistic spectrum disorders (e.g., Fragile X syndrome), or use of psychotropic medication. The study had ethical approval, and written informed consent was obtained from all subjects.

Volunteers were scanned using a 1.5-T GE Signa neurovascular magnetic resonance system. Initially, a coronal three-dimensional spoiled-gradient-recalled acquisition in a steady-state pulse sequence was acquired with whole-brain coverage. A voxel of interest was positioned in the right amygdala-hippocampal complex (6 ml) and in the right parietal lobe (8 ml) using a standard protocol, and a PRESS spectrum (time to repetition/time to echo=3000/35 msec, 160 data averages) was obtained after chemical shift selective water suppression.

MRS metabolite concentrations may be confounded by differences in the proportion of gray and white matter and by CSF contained in the voxel of interest. Thus, the three-dimensional spoiled-gradient-recalled volume was segmented into white matter, gray matter, and CSF using statistical parametric mapping software and the tissue composition of the voxels determined. Metabolite concentrations were corrected for the proportion of cerebral spinal fluid within the voxel. We measured concentrations of Glu+Gln, NAA, myo -inositol, Cho, and Cr+PCr using LC-model and in-house software. Some spectra did not yield significant fits and were discarded. Between-group differences in demographic factors, tissue volumes, and mean metabolite concentrations were assessed using a Student’s t test (two-tailed), while equality of variance was assessed using an F value. Gender differences were assessed using chi-square tests.

The voxel of interest proportions of gray and white matter did not differ between groups in either brain region. However, people with an autistic spectrum disorder had significantly higher concentrations of Cr+PCr and Glu+Gln than comparison subjects in the amygdala-hippocampal complex ( Table 1 ). This corresponds to an effect size of 0.71 for Cr+PCr and 0.95 for Glu+Gln. There were no significant differences in any metabolite in the parietal region. There were no significant correlations between metabolite concentrations and IQ or Autism Diagnostic Interview-Revised subscores. The analysis was then repeated, excluding the seven subjects without an Autism Diagnostic Interview-Revised score. There was no longer a significant between-group difference in Cr+PCr (p=0.22, effect size reduced from 0.71 to 0.50); however, the significant between-group difference remained for Glu+Gln (p=0.02, effect size increased from 0.95 to 1.00).

People with autistic spectrum disorders had a significantly higher concentration of Glu+Gln and Cr+PCr in amygdala-hippocampal complex than comparison subjects. Our findings may be confounded by type I error; however, they cannot be fully explained by differences in physical health or voxel proportion of gray/white matter. In addition, our negative findings in the parietal lobe are consistent with previous ¹ H-MRS studies. One possible interpretation is that people with autistic spectrum disorders have regionally specific differences in Glu+Gln and Cr+PCr. We were unable to acquire voxels of interest in both regions in all subjects, but after restricting our analysis to those in whom we obtained both voxels of interest, the results remained significant for Glu+Gln but not for Cr+PCr.

At 1.5-T, it is not possible to examine which compound (i.e., glutamate or glutamine) is contributing most to the elevation in Glu+Gln. However, glutamate is the most abundant central neurotransmitter and is crucial for many neurodevelopmental processes, including synapse induction, cell migration, and synapse elimination. We suggest that neurodevelopmental differences in autistic spectrum disorders may be partially explained by differences in the glutamatergic system. This proposal is supported by recent postmortem reports of glutamatergic abnormalities in cerebellum (12) of people with autistic spectrum disorders and reports of an association between autistic spectrum disorders and a number of glutamate receptor genes (5, 7 – 9) . In addition, postmortem studies of autistic spectrum disorders have reported abnormalities in neuronal migration in the amygdala-hippocampal region (13), and functional brain imaging studies found differences in limbic anatomy and function (3) .

By demonstrating increased Cr+PCr in amygdala-hippocampal regions, this study augments prior work showing that normal-intelligence adults with Asperger’s syndrome have increased Cr+PCr in frontal regions (11) . It is not known whether the changes that we report are caused by the same underlying abnormality, nor is it clear if our findings represent a primary (causal) abnormality or are secondary to the disorder. In summary, differences in amygdala-hippocampal Cr+PCr and Glu+Gln occur in normal-intelligence adults with autistic spectrum disorders, and this may be linked to some of the pathological features of these disorders. Further developmental studies in children are required.

The results of this study were presented at the International Meeting for Autism Research (IMFAR), Boston, May 2005. Received June 3, 2005; revision received Sept. 1, 2005; accepted Oct. 19, 2005. From the Section of Brain Maturation, Institute of Psychiatry, London; Department of Radiology, Leiden University Medical Centre, Leiden, the Netherlands; Neuroimaging Research Group, Institute of Psychiatry, London; Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Republic of Ireland; and the Department of Psychiatry, University of Hong Kong, Hong Kong, S.A.R. China. Address correspondence and reprint requests to Professor Murphy, Division of Psychological Medicine, P.O. Box 50, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF; [email protected] (e-mail).All authors report no competing interests.This study was funded by the Medical Research Council (U.K.) [AIMS Network] and South London & Maudsley NHS Trust, neither of which had a role in the study design, data collection, analysis, or decision to submit for publication. The corresponding author has full access to all the data and had the final decision to submit for publication.