TY - JOUR
T1 - The effect of antipsychotics on glutamate levels in the anterior cingulate cortex and clinical response
T2 - A 1H-MRS study in first-episode psychosis patients
AU - Zahid, Uzma
AU - McCutcheon, Robert A.
AU - Borgan, Faith
AU - Jauhar, Sameer
AU - Pepper, Fiona
AU - Nour, Matthew M.
AU - Rogdaki, Maria
AU - Osugo, Martin
AU - Murray, Graham K.
AU - Hathway, Pamela
AU - Murray, Robin M.
AU - Howes, Oliver D.
N1 - Funding Information:
This study was funded by Medical Research Council-UK (no. MC_U120097115), Maudsley Charity (no. 666), and Wellcome Trust (no. 094849/Z/10/Z) grants to OH and the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. UZ was supported by funding from the Lord Leverhulme Charitable Trust. MN was funded by a UCL Welcome Ph.D. Fellowship for Clinicians (102186/B/13/Z). MN was pre-doctoral fellow of the International Max Planck Research School on Computational Methods in Psychiatry and Ageing Research ( https://www.mps-ucl-centre.mpg.de/en/comp2psych . Participating institutions: Max Planck Institute for Human Development, Berlin and UCL). The Max Planck UCL Centre was supported by UCL and the Max Planck Society.
Publisher Copyright:
Copyright © 2022 Zahid, McCutcheon, Borgan, Jauhar, Pepper, Nour, Rogdaki, Osugo, Murray, Hathway, Murray and Howes.
PY - 2022/8/11
Y1 - 2022/8/11
N2 - Introduction: Glutamatergic dysfunction is implicated in the pathophysiology of schizophrenia. It is unclear whether glutamatergic dysfunction predicts response to treatment or if antipsychotic treatment influences glutamate levels. We investigated the effect of antipsychotic treatment on glutamatergic levels in the anterior cingulate cortex (ACC), and whether there is a relationship between baseline glutamatergic levels and clinical response after antipsychotic treatment in people with first episode psychosis (FEP). Materials and methods: The sample comprised 25 FEP patients; 22 completed magnetic resonance spectroscopy scans at both timepoints. Symptoms were assessed using the Positive and Negative Syndrome Scale (PANSS). Results: There was no significant change in glutamate [baseline 13.23 ± 2.33; follow-up 13.89 ± 1.74; t(21) = −1.158, p = 0.260], or Glx levels [baseline 19.64 ± 3.26; follow-up 19.66 ± 2.65; t(21) = −0.034, p = 0.973]. There was no significant association between glutamate or Glx levels at baseline and the change in PANSS positive (Glu r = 0.061, p = 0.777, Glx r = −0.152, p = 0.477), negative (Glu r = 0.144, p = 0.502, Glx r = 0.052, p = 0.811), general (Glu r = 0.110, p = 0.607, Glx r = −0.212, p = 0.320), or total scores (Glu r = 0.078, p = 0.719 Glx r = −0.155, p = 0.470). Conclusion: These findings indicate that treatment response is unlikely to be associated with baseline glutamatergic metabolites prior to antipsychotic treatment, and there is no major effect of antipsychotic treatment on glutamatergic metabolites in the ACC.
AB - Introduction: Glutamatergic dysfunction is implicated in the pathophysiology of schizophrenia. It is unclear whether glutamatergic dysfunction predicts response to treatment or if antipsychotic treatment influences glutamate levels. We investigated the effect of antipsychotic treatment on glutamatergic levels in the anterior cingulate cortex (ACC), and whether there is a relationship between baseline glutamatergic levels and clinical response after antipsychotic treatment in people with first episode psychosis (FEP). Materials and methods: The sample comprised 25 FEP patients; 22 completed magnetic resonance spectroscopy scans at both timepoints. Symptoms were assessed using the Positive and Negative Syndrome Scale (PANSS). Results: There was no significant change in glutamate [baseline 13.23 ± 2.33; follow-up 13.89 ± 1.74; t(21) = −1.158, p = 0.260], or Glx levels [baseline 19.64 ± 3.26; follow-up 19.66 ± 2.65; t(21) = −0.034, p = 0.973]. There was no significant association between glutamate or Glx levels at baseline and the change in PANSS positive (Glu r = 0.061, p = 0.777, Glx r = −0.152, p = 0.477), negative (Glu r = 0.144, p = 0.502, Glx r = 0.052, p = 0.811), general (Glu r = 0.110, p = 0.607, Glx r = −0.212, p = 0.320), or total scores (Glu r = 0.078, p = 0.719 Glx r = −0.155, p = 0.470). Conclusion: These findings indicate that treatment response is unlikely to be associated with baseline glutamatergic metabolites prior to antipsychotic treatment, and there is no major effect of antipsychotic treatment on glutamatergic metabolites in the ACC.
KW - CSF-correction
KW - glutamate
KW - imaging and schizophrenia
KW - longitudinal
KW - NMDA
KW - spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85136963959&partnerID=8YFLogxK
U2 - 10.3389/fpsyt.2022.967941
DO - 10.3389/fpsyt.2022.967941
M3 - Article
AN - SCOPUS:85136963959
SN - 1664-0640
VL - 13
JO - Frontiers in Psychiatry
JF - Frontiers in Psychiatry
M1 - 967941
ER -