| Literature DB >> 33398325 |
Grant McQueen1, Kyra-Verena Sendt1, Amy Gillespie1, Alessia Avila1, John Lally1,2, Kalliopi Vallianatou1, Nynn Chang1, Diogo Ferreira3, Faith Borgan1, Oliver D Howes1, Gareth J Barker4, David J Lythgoe4, James M Stone1,5, Philip McGuire1, James H MacCabe1, Alice Egerton1.
Abstract
It has been suggested that the antipsychotic clozapine may modulate brain glutamate, and that this effect could contribute to its efficacy in treatment-resistant schizophrenia (TRS). The aim of this study was to examine the effects of clozapine on brain glutamate in TRS longitudinally. This study examined individuals with TRS before and 12 weeks after switching from a non-clozapine antipsychotic to treatment with clozapine as part of their normal clinical care. Proton magnetic resonance spectroscopy (1H-MRS) measured concentrations, corrected for voxel tissue content, of glutamate (Glucorr), and glutamate plus glutamine (Glxcorr) in the anterior cingulate cortex (ACC) and right caudate nucleus. Symptoms were monitored using the Positive and Negative Syndrome Scale (PANSS). Of 37 recruited patients (27 men, 39.30 years old, 84% clozapine naïve), 25 completed 1H-MRS at both timepoints. 12 weeks of clozapine was associated with a longitudinal reduction in Glucorr in the caudate (n = 23, F = 7.61 P = .01) but not in the ACC (n = 24, F = 0.02, P = .59). Percentage reduction in caudate Glucorr was positively correlated with percentage improvement in symptoms (total PANSS score, n = 23, r = .42, P = .04). These findings indicate that reductions in glutamate in the caudate nucleus may contribute to symptomatic improvement during the first months of clozapine treatment.Entities:
Keywords: zzm321990 1H-MRS; anterior cingulate cortex; antipsychotic; caudate; magnetic resonance spectroscopy; psychosis
Year: 2021 PMID: 33398325 DOI: 10.1093/schbul/sbaa156
Source DB: PubMed Journal: Schizophr Bull ISSN: 0586-7614 Impact factor: 9.306