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. 2014 Jun;71(6):665-71.
doi: 10.1001/jamapsychiatry.2014.179.

Mitochondrial dysfunction as a neurobiological subtype of autism spectrum disorder: evidence from brain imaging

Affiliations

Mitochondrial dysfunction as a neurobiological subtype of autism spectrum disorder: evidence from brain imaging

Suzanne Goh et al. JAMA Psychiatry. 2014 Jun.

Erratum in

  • JAMA Psychiatry. 2014 Jul;71(7):840

Abstract

Importance: Impaired mitochondrial function impacts many biological processes that depend heavily on energy and metabolism and can lead to a wide range of neurodevelopmental disorders, including autism spectrum disorder (ASD). Although evidence that mitochondrial dysfunction is a biological subtype of ASD has grown in recent years, no study, to our knowledge, has demonstrated evidence of mitochondrial dysfunction in brain tissue in vivo in a large, well-defined sample of individuals with ASD.

Objectives: To assess brain lactate in individuals with ASD and typically developing controls using high-resolution, multiplanar spectroscopic imaging; to map the distribution of lactate in the brains of individuals with ASD; and to assess correlations of elevated brain lactate with age, autism subtype, and intellectual ability.

Design, setting, and participants: Case-control study at Columbia University Medical Center and New York State Psychiatric Institute involving 75 children and adults with ASD and 96 age- and sex-matched, typically developing controls.

Main outcomes and measures: Lactate doublets (present or absent) on brain magnetic resonance spectroscopic imaging.

Results: Lactate doublets were present at a significantly higher rate in participants with ASD (13%) than controls (1%) (P = .001). In the ASD group, the presence of lactate doublets correlated significantly with age (P = .004) and was detected more often in adults (20%) than in children (6%), though it did not correlate with sex, ASD subtype, intellectual ability, or the Autism Diagnostic Observation Schedule total score or subscores. In those with ASD, lactate was detected most frequently within the cingulate gyrus but it was also present in the subcortical gray matter nuclei, corpus callosum, superior temporal gyrus, and pre- and postcentral gyri.

Conclusions and relevance: In vivo brain findings provide evidence for a possible neurobiological subtype of mitochondrial dysfunction in ASD.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr. Suzanne Goh is president of MitoMedical LLC, a nutritional supplement company. The other authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1. An example of spectra from a lactate-positive ASD participant
The localizer image shows lactate-positive voxels outlined in red. Individual spectra appear in the lower panel. One spectrum has been enlarged to clearly show the inverted doublet of lactate at 1.33 ppm.
Figure 2
Figure 2. Lactate distribution in ASD participants
Lactate-positive voxels found across all ASD participants are projected onto brain templates (downloaded from http://www.bic.mni.mcgill.ca/ServicesAtlases/ICBM152NLin2009). Voxel color indicates the number of ASD participants with a lactate doublet: Blue = 1 participant; Yellow = 2 participants; Red = 3 participants. aAC: anterior portion of the anterior cingulate gyrus mAC: mid-portion of the anterior cingulate gyrus pAC: posterior portion of the anterior cingulate gyrus CC: corpus callosum CSF: cerebrospinal fluid ST: superior temporal gyrus SC: subcortical nuclei, including putamen, globus pallidus, thalamus (and associated internal capsule) SM: sensory and motor portions of the pre- and post-central gyri

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