4.6 Article

Striatal glutamate, subcortical structure and clinical response to first-line treatment in first-episode psychosis patients

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pnpbp.2021.110473

关键词

First episode; Schizophrenia; Glutamate; Magnetic resonance spectroscopy; Brain volume analysis; Antipsychotic treatment

资金

  1. Consejo Nacional de Ciencia y Tecnologia, Mexico, (CONACyT) [182279, 261895]
  2. CONACyT's Sistema Nacional de Investigadores
  3. National Institutes of Health [R01 MH110270, R21 MH117434]

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This study found that in patients with schizophrenia, non-responders had higher levels of striatal glutamate compared to responders both before and after treatment. Combining anatomic measures with glutamate levels has the potential to improve classification of responders and non-responders to antipsychotic medications, and to provide mechanistic understanding of the interplay between neuroanatomical and neurochemical changes induced by these medications.
Introduction: Recent studies have observed that patients with treatment-resistant schizophrenia as well as patients with schizophrenia who do not respond within a medication trial exhibit excess activity of the glutamate system. In this study we sought to replicate the within-trial glutamate abnormality and to investigate the potential for structural differences and treatment-induced changes to improve identification of medication responders and non-responders. Methods: We enrolled 48 medication-naive patients in a 4-week trial of risperidone and classified them retrospectively into responders and non-responders using clinical criteria. Proton magnetic resonance spectroscopy and T1-weighted structural MRI were acquired pre- and post-treatment to quantify striatal glutamate levels and several measures of subcortical brain structure. Results: Patients were classified as 29 responders and 19 non-responders. Striatal glutamate was higher in the non-responders than responders both pre- and post-treatment (F1,39 = 7.15, p = .01). Volumetric measures showed a significant group x time interaction (t = 5.163, <1%FDR), and group x time x glutamate interaction (t = 4.23, <15%FDR) were seen in several brain regions. Striatal volumes increased at trend level with treatment in both groups, and a positive association of striatal volumes with glutamate levels was seen in the non-responders. Conclusions: Combining anatomic measures with glutamate levels offers the potential to enhance classification of responders and non-responders to antipsychotic medications as well as to provide mechanistic understanding of the interplay between neuroanatomical and neurochemical changes induced by these medications. Ethical statement The study was approved by the Ethics and Scientific committees of the Instituto Nacional de Neurologia y Neurocirugia in Mexico City. All participants over 18 years fully understood and signed the informed consent; in case the patient was under 18 years, informed consent was obtained from both parents. Participants did not receive a stipend.

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