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      Assessing Brain Metabolism With 7-T Proton Magnetic Resonance Spectroscopy in Patients With First-Episode Psychosis

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          Key Points

          Question

          Can localized magnetic resonance spectroscopy performed at 7 T detect metabolic changes early in the course of a first-episode psychosis, and are these associated with neuropsychological performance?

          Findings

          Eighty-one patients with first-episode psychosis were compared to 91 age-matched control participants; decreased levels of N-acetylaspartate were found in several brain regions, as well as selective regional decreases in glutamate, glutathione and γ-aminobutyric acid.

          Meaning

          Multiple metabolic abnormalities can be detected by 7-T magnetic resonance spectroscopy in patients with first-episode psychosis, which correlated with performance on neuropsychological tests.

          Abstract

          Importance

          The use of high-field magnetic resonance spectroscopy (MRS) in multiple brain regions of a large population of human participants facilitates in vivo study of localized or diffusely altered brain metabolites in patients with first-episode psychosis (FEP) compared to healthy participants.

          Objective

          To compare metabolite levels in 5 brain regions between patients with FEP (evaluated within 2 years of onset) and healthy controls, and to explore possible associations between targeted metabolite levels and neuropsychological test performance.

          Design, Setting, and Participants

          Cross-sectional design used 7-T MRS at a research MR imaging facility in participants recruited from clinics at the Johns Hopkins Schizophrenia Center and the local population. Eighty-one patients who had received a DSM-IV diagnosis of FEP within the last 2 years and 91 healthy age-matched (but not sex-matched) volunteers participated.

          Main Outcomes and Measures

          Brain metabolite levels including glutamate, glutamine, γ-aminobutyric acid (GABA), N-acetylaspartate, N-acetylaspartyl glutamate, and glutathione, as well as performance on neuropsychological tests.

          Results

          The mean (SD) age of 81 patients with FEP was 22.3 (4.4) years and 57 were male, while the mean (SD) age of 91 healthy participants was 23.3 (3.9) years and 42 were male. Compared with healthy participants, patients with FEP had lower levels of glutamate ( F 1,162= 8.63, P = .02), N-acetylaspartate ( F 1,161= 5.93, P = .03), GABA ( F 1,163= 6.38, P = .03), and glutathione ( F 1,162= 4.79, P = .04) in the anterior cingulate (all P values are corrected for multiple comparisons); lower levels of N-acetylaspartate in the orbitofrontal region ( F 1,136= 7.23, P = .05) and thalamus ( F 1,133= 6.78, P = .03); and lower levels of glutathione in the thalamus ( F 1,135= 7.57, P = .03). Among patients with FEP, N-acetylaspartate levels in the centrum semiovale white matter were significantly correlated with performance on neuropsychological tests, including processing speed ( r = 0.48; P < .001), visual ( r = 0.33; P = .04) and working ( r = 0.38; P = .01) memory, and overall cognitive performance ( r = 0.38; P = .01).

          Conclusions and Relevance

          Seven-tesla MRS offers insights into biochemical changes associated with FEP and may be a useful tool for probing brain metabolism that ranges from neurotransmission to stress-associated pathways in participants with psychosis.

          Abstract

          This cross-sectional study evaluates whether 7-T magnetic resonance spectroscopy is a useful tool for assessing brain metabolite levels in regions salient to psychosis, and explores the association exists between regional metabolite levels and neuropsychological test performance among healthy participants and patients with first-episode psychosis.

          Related collections

          Most cited references53

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          Cortical inhibitory neurons and schizophrenia.

          Impairments in certain cognitive functions, such as working memory, are core features of schizophrenia. Convergent findings indicate that a deficiency in signalling through the TrkB neurotrophin receptor leads to reduced GABA (gamma-aminobutyric acid) synthesis in the parvalbumin-containing subpopulation of inhibitory GABA neurons in the dorsolateral prefrontal cortex of individuals with schizophrenia. Despite both pre- and postsynaptic compensatory responses, the resulting alteration in perisomatic inhibition of pyramidal neurons contributes to a diminished capacity for the gamma-frequency synchronized neuronal activity that is required for working memory function. These findings reveal specific targets for therapeutic interventions to improve cognitive function in individuals with schizophrenia.
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            Autism spectrum disorder (ASD), characterized by both impaired communication and social interaction, and by stereotypic behavior, affects about 1 in 68, predominantly males. The medico-economic burdens of ASD are enormous, and no recognized treatment targets the core features of ASD. In a placebo-controlled, double-blind, randomized trial, young men (aged 13-27) with moderate to severe ASD received the phytochemical sulforaphane (n = 29)--derived from broccoli sprout extracts--or indistinguishable placebo (n = 15). The effects on behavior of daily oral doses of sulforaphane (50-150 µmol) for 18 wk, followed by 4 wk without treatment, were quantified by three widely accepted behavioral measures completed by parents/caregivers and physicians: the Aberrant Behavior Checklist (ABC), Social Responsiveness Scale (SRS), and Clinical Global Impression Improvement Scale (CGI-I). Initial scores for ABC and SRS were closely matched for participants assigned to placebo and sulforaphane. After 18 wk, participants receiving placebo experienced minimal change (<3.3%), whereas those receiving sulforaphane showed substantial declines (improvement of behavior): 34% for ABC (P < 0.001, comparing treatments) and 17% for SRS scores (P = 0.017). On CGI-I, a significantly greater number of participants receiving sulforaphane had improvement in social interaction, abnormal behavior, and verbal communication (P = 0.015-0.007). Upon discontinuation of sulforaphane, total scores on all scales rose toward pretreatment levels. Dietary sulforaphane, of recognized low toxicity, was selected for its capacity to reverse abnormalities that have been associated with ASD, including oxidative stress and lower antioxidant capacity, depressed glutathione synthesis, reduced mitochondrial function and oxidative phosphorylation, increased lipid peroxidation, and neuroinflammmation.
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                Author and article information

                Journal
                JAMA Psychiatry
                JAMA Psychiatry
                JAMA Psychiatry
                JAMA Psychiatry
                American Medical Association
                2168-622X
                2168-6238
                9 January 2019
                March 2019
                9 January 2020
                : 76
                : 3
                : 314-323
                Affiliations
                [1 ]Russell H. Morgan Department of Radiology and Radiological Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland
                [2 ]Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland
                [3 ]Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland
                [4 ]Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, Maryland
                [5 ]Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland
                [6 ]Kennedy Krieger Institute, Baltimore, Maryland
                Author notes
                Article Information
                Accepted for Publication: August 29, 2018.
                Corresponding Authors: Akira Sawa, MD, PhD, Department of Psychiatry and Behavioral Sciences ( asawa1@ 123456jhmi.edu ), and Peter B. Barker, DPhil, Russell H. Morgan Department of Radiology and Radiological Sciences ( pbarker2@ 123456jhmi.edu ), Johns Hopkins University School of Medicine, 600 N Wolfe St, Baltimore, MD 21287.
                Published Online: January 9, 2019. doi:10.1001/jamapsychiatry.2018.3637
                Author Contributions: Drs Sawa and Barker had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Sedlak, Schretlen, Sawa, Barker.
                Acquisition, analysis, or interpretation of data: All authors.
                Drafting of the manuscript: Wang, Coughlin, DuBois, Sawa, Barker.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Wang, Crawford, Schretlen, Sawa.
                Obtained funding: Sawa.
                Administrative, technical, or material support: Pradhan, Trivedi, DuBois, Sedlak, F. Nucifora, L. Nucifora, Sawa, Barker.
                Supervision: Pradhan, Nestadt, Schretlen, Sawa, Barker.
                Conflict of Interest Disclosures: Dr Schretlen reported receiving royalties on sales of a test used in the present study under an agreement with Psychological Assessment Resources, Inc, which has been reviewed and approved by Johns Hopkins University in accordance with its conflict of interest policies. No other disclosures were reported.
                Funding/Support: This work was supported by grants MH-094268, MH-092443 Silvio O. Conte Center, MH-105660, and MH-107730 from the National Institute of Mental Health and by awards from the Stanley Foundation and S/R Foundation (Dr Sawa); and by grant EB015909 from the National Institute of Biomedical Imaging and Bioengineering and grant MH-096263 from the National Institute of Mental Health (Dr Barker). Participant recruitment was partially supported by the Mitsubishi Tanabe Pharma Corporation.
                Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; or the decision to submit the manuscript for publication.
                Article
                PMC6439827 PMC6439827 6439827 yoi180090
                10.1001/jamapsychiatry.2018.3637
                6439827
                30624573
                40d10d6a-a164-47fa-bf48-a8cc28c59a0d
                Copyright 2019 American Medical Association. All Rights Reserved.
                History
                : 9 May 2018
                : 28 August 2018
                : 29 August 2018
                Funding
                Funded by: Silvio O. Conte Center
                Funded by: National Institute of Mental Health
                Funded by: Stanley Foundation
                Funded by: National Institute of Biomedical Imaging and Bioengineering
                Funded by: Mitsubishi Tanabe Pharma Corporation
                Categories
                Research
                Research
                Original Investigation
                Online First

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