Abstract

Schizophrenia is well-known to be associated with hippocampal structural abnormalities. We used 1H-MR spectroscopy to test the hypothesis that these abnormalities are accompanied by NAA deficits, reflecting neuronal dysfunction, in patients compared with healthy controls. Nineteen patients with schizophrenia (11 men; mean age, 40.6 ± 10.1 years; mean disease duration, 19.5 ± 10.5 years) and 11 matched healthy controls (5 men; mean age, 33.7 ± 10.1 years) underwent MR imaging and multivoxel point-resolved spectroscopy (TE/TR, 35/1400 ms) 1H-MRS at 3T to obtain their hippocampal GM absolute NAA, Cr, Cho, and mIns concentrations. Unequal variance t tests and ANCOVA were used to compare patients with controls. Bilateral volumes from manually outlined hippocampal masks were compared by using unequal variance t tests. Patients' average hippocampal GM Cr concentrations were 19% higher than that of controls, 8.7 ± 2.2 versus 7.4 ± 1.2 mmol/L (P < .05); showing no differences, concentrations in NAA were 8.8 ± 1.6 versus 8.7 ± 1.2 mmol/L; in Cho, 2.3 ± 0.7 versus 2.1 ± 0.3 mmol/L; and in mIns, 6.1 ± 1.5 versus 5.2 ± 0.9 (all P > .1). There was a positive correlation between mIns and Cr in patients (r = 0.57, P = .05) but not in controls. The mean bilateral hippocampal volume was ∼10% lower in patients: 7.5 ± 0.9 versus 8.4 ± 0.7 cm3 (P < .05). These findings suggest that the hippocampal volume deficit in schizophrenia is not due to net loss of neurons, in agreement with histopathology studies but not with prior 1H-MR spectroscopy reports. Elevated Cr is consistent with hippocampal hypermetabolism, and its correlation with mIns may also suggest an inflammatory process affecting some cases; these findings may suggest treatment targets and markers to monitor them.

Highlights

  • BACKGROUND AND PURPOSESchizophrenia is well-known to be associated with hippocampal structural abnormalities

  • The mean bilateral hippocampal volume was ϳ10% lower in patients: 7.5 Ϯ 0.9 versus 8.4 Ϯ 0.7 cm[3] (P Ͻ .05). These findings suggest that the hippocampal volume deficit in schizophrenia is not due to net loss of neurons, in agreement with histopathology studies but not with prior 1H-MR spectroscopy reports

  • Elevated Cr is consistent with hippocampal hypermetabolism, and its correlation with mIns may suggest an inflammatory process affecting some cases; these findings may suggest treatment targets and markers to monitor them

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Summary

Methods

Nineteen patients with schizophrenia (11 men; mean age, 40.6 Ϯ 10.1 years; mean disease duration, 19.5 Ϯ 10.5 years) and 11 matched healthy controls (5 men; mean age, 33.7 Ϯ 10.1 years) underwent MR imaging and multivoxel point-resolved spectroscopy (TE/TR, 35/1400 ms) 1H-MRS at 3T to obtain their hippocampal GM absolute NAA, Cr, Cho, and mIns concentrations. Age-matched controls recruited from hospital postings memory tasks, decreased neurogenesis in the dentate gyrus, and met the criteria of no personal or family history of psychosis, no reduced connectivity with cortical and subcortical regions.[4,5,6,7,8,9] Re- axis I disorder in the past 2 years, and no known neurologic discent findings show that conversion to psychosis in high-risk sub- order Exclusion criteria for both patients and controls included jects is predicted by hypermetabolism in the hippocampal CA1 uncontrolled medical illness, MR imaging contraindication or insubregion.[4] Psychosis may be conceptualized as a disruption in ability to tolerate an MR imaging examination, and substance learning and memory involving impaired habituation and “run- (except tobacco) use in the past 6 months. Tissue segmenfor underlying physiologic processes, most prominently: NAA tation, and 1H-MRSI VOI guidance, T1-weighted 3D MPRAGE (NAA and N-acetyl aspartylglutamate) for neuronal integrity, Cr images were obtained from each subject: TE/TI/TR, 2.6/800/1360

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