TY - JOUR
T1 - Glutamate in schizophrenia
T2 - Neurodevelopmental perspectives and drug development
AU - Egerton, Alice
AU - Grace, Anthony A
AU - Stone, James
AU - Bossong, Matthijs G
AU - Sand, Michael
AU - McGuire, Philip
N1 - Funding Information:
Editorial support was provided by Lisa Auker, PhD, of Fishawack Communications Ltd., and was funded by Boehringer Ingelheim International GmbH.
Funding Information:
This article is based on a symposium, which was funded by Boehringer Ingelheim International GmbH and presented at the 6th European Conference on Schizophrenia Research. The sponsor was given the opportunity to review the manuscript for medical and scientific accuracy as well as intellectual property considerations.
Funding Information:
The authors met the criteria for authorship as recommended by the International Committee of Medical Journal Editors. AE has previously received funding from Hoffman la Roche and a study-related consultancy payment from Heptares Therapeutics Ltd. AAG has previously received consultancy payment from Lundbeck, Pfizer, Otsuka, Takeda, Newron, Alkermes, and Janssen and has also received honoraria from Lilly, Roche, Asubio, Abbott and Autofony. JS has previously received honoraria from Roche and Janssen and has received a study-related consultancy payment from Takeda. MGB has nothing to disclose. MS is an employee of Boehringer Ingelheim, but received no direct compensation related to the development of this manuscript. PM has previously received research funding from GW Pharmaceuticals and attended advisory boards with Boehringer Ingelheim.
Publisher Copyright:
© 2020 The Authors
PY - 2020/9
Y1 - 2020/9
N2 - Research into the neurobiological processes that may lead to the onset of schizophrenia places growing emphasis on the glutamatergic system and brain development. Preclinical studies have shown that neurodevelopmental, genetic, and environmental factors contribute to glutamatergic dysfunction and schizophrenia-related phenotypes. Clinical research has suggested that altered brain glutamate levels may be present before the onset of psychosis and relate to outcome in those at clinical high risk. After psychosis onset, glutamate dysfunction may also relate to the degree of antipsychotic response and clinical outcome. These findings support ongoing efforts to develop pharmacological interventions that target the glutamate system and could suggest that glutamatergic compounds may be more effective in specific patient subgroups or illness stages. In this review, we consider the updated glutamate hypothesis of schizophrenia, from a neurodevelopmental perspective, by reviewing recent preclinical and clinical evidence, and discuss the potential implications for novel therapeutics.
AB - Research into the neurobiological processes that may lead to the onset of schizophrenia places growing emphasis on the glutamatergic system and brain development. Preclinical studies have shown that neurodevelopmental, genetic, and environmental factors contribute to glutamatergic dysfunction and schizophrenia-related phenotypes. Clinical research has suggested that altered brain glutamate levels may be present before the onset of psychosis and relate to outcome in those at clinical high risk. After psychosis onset, glutamate dysfunction may also relate to the degree of antipsychotic response and clinical outcome. These findings support ongoing efforts to develop pharmacological interventions that target the glutamate system and could suggest that glutamatergic compounds may be more effective in specific patient subgroups or illness stages. In this review, we consider the updated glutamate hypothesis of schizophrenia, from a neurodevelopmental perspective, by reviewing recent preclinical and clinical evidence, and discuss the potential implications for novel therapeutics.
KW - Glutamate
KW - N-methyl-D-aspartate receptor
KW - Psychosis
UR - http://www.scopus.com/inward/record.url?scp=85092689168&partnerID=8YFLogxK
U2 - 10.1016/j.schres.2020.09.013
DO - 10.1016/j.schres.2020.09.013
M3 - Review article
C2 - 33071070
SN - 0920-9964
VL - 223
SP - 59
EP - 70
JO - Schizophrenia Research
JF - Schizophrenia Research
ER -