Multimodal analysis of the hippocampus in schizophrenia using proton magnetic resonance spectroscopy and functional magnetic resonance imaging

SCHIZOPHRENIA RESEARCH

卷:140

Article

Hutcheson, Nathan L.^1,2  Reid, Meredith A.^1,3  White, David M.¹  Kraguljac, Nina V.⁷  Avsar, Kathy B.^1,4  Bolding, Mark S.^1,5  Knowlton, Robert C.⁶  den Hollander, Jan A.⁷  Lahti, Adrienne C.¹ 

[1] Univ Alabama Birmingham, Dept Psychiat & Behav Neurobiol, Birmingham, AL 35294 USA

[2] Univ Alabama Birmingham, Dept Grad Biomed Sci, Birmingham, AL 35294 USA

[3] Univ Alabama Birmingham, Dept Biomed Engn, Birmingham, AL 35294 USA

[4] Univ Alabama Birmingham, Dept Psychol, Birmingham, AL 35294 USA

[5] Univ Alabama Birmingham, Dept Vis Sci, Birmingham, AL 35294 USA

[6] Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35294 USA

[7] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA

关键词: Schizophrenia;    Hippocampus;    fMRI;    MRS;    NAA;    Glutamate;   

DOI  :  10.1016/j.schres.2012.06.039

来源: Elsevier

【 摘 要 】

Background: Studies have shown that individuals with schizophrenia suffer from memory impairments. In this study, we combined proton magnetic resonance spectroscopy (H-1-MRS) and functional magnetic resonance imaging (fMRI) to clarify the neurobiology of memory deficits in schizophrenia. Methods: We used single-voxel MRS acquired in the left hippocampus and fMRI during performance of a memory task to obtain measures of neurochemistry and functional response in 28 stable, medicated participants with schizophrenia (SZ) and 28 matched healthy controls (HC). Results: The SZ group had significantly decreased blood oxygen level-dependent (BOLD) signal in left inferior frontal gyrus (IFG) during encoding and in the anterior cingulate cortex (ACC) and superior temporal gyrus (STG) during retrieval. We did not find significant differences in N-acetylaspartate/creatine (NAA/Cr) or glutamate+glutamine (Glx/Cr) levels between the groups, but did find a significant positive correlation between NAA/Cr and Glx/Cr in the HC group thatwas absent in the SZ group. Therewere no significant correlations between BOLD and MRS measured in the hippocampus. Further analyses revealed a negative correlation between left IFG BOLD and task performance in the SZ group. Finally, in the HC group, the left IFG BOLD was positively correlated with Glx/Cr. Conclusions: We replicated findings of reduced BOLD signal in left IFG and of an altered relationship between IFG BOLD response and task performance in the SZ. The absence of correlation between NAA/Cr and Glx/Cr levels in patients might suggest underlying pathologies of the glutamate-glutamine cycle and/or mitochondria. (C) 2012 Elsevier B. V. All rights reserved.

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