Neuroimaging studies of GABA in schizophrenia: a systematic review with meta-analysis

被引:100
|
作者
Egerton, A. [1 ]
Modinos, G. [1 ]
Ferrera, D. [1 ,2 ]
McGuire, P. [1 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Psychosis Studies, 16 De Crespigny Pk,Denmark Hill, London SE5 8AF, England
[2] Hosp Santa Maria EPE, Dept Neurociencias & Saude Mental, Serv Psiquiatria & Saude Mental, Lisbon, Portugal
来源
基金
英国惠康基金; 英国医学研究理事会;
关键词
GAMMA-AMINOBUTYRIC-ACID; MAGNETIC-RESONANCE-SPECTROSCOPY; BENZODIAZEPINE-RECEPTOR-BINDING; MESSENGER-RNA EXPRESSION; ULTRA-HIGH RISK; PREFRONTAL CORTEX; IN-VIVO; CINGULATE CORTEX; GENE-EXPRESSION; PARVALBUMIN NEURONS;
D O I
10.1038/tp.2017.124
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Data from animal models and from postmortem studies suggest that schizophrenia is associated with brain GABAergic dysfunction. The extent to which this is reflected in data from in vivo studies of GABA function in schizophrenia is unclear. The Medline database was searched to identify articles published until 21 October 2016. The search terms included GABA, proton magnetic resonance spectroscopy (H-1-MRS), positron emission tomography (PET), single photon emission computed tomography (SPECT), schizophrenia and psychosis. Sixteen GABA H-1-MRS studies (538 controls, 526 patients) and seven PET/SPECT studies of GABA(A)/benzodiazepine receptor (GABA(A)/BZR) availability (118 controls, 113 patients) were identified. Meta-analyses of H-1-MRS GABA in the medial prefrontal cortex (mPFC), parietal/occipital cortex (POC) and striatum did not show significant group differences (mFC: g = -0.3, 409 patients, 495 controls, 95% confidence interval (CI): -0.6 to 0.1; POC: g = -0.3, 139 patients, 111 controls, 95% CI: -0.9 to 0.3; striatum: g = -0.004, 123 patients, 95 controls, 95% CI: -0.7 to 0.7). Heterogeneity across studies was high (I-2 > 50%), and this was not explained by subsequent moderator or meta-regression analyses. There were insufficient PET/SPECT receptor availability studies for meta-analyses, but a systematic review did not suggest replicable group differences in regional GABA(A)/BZR availability. The current literature does not reveal consistent alterations in in vivo GABA neuroimaging measures in schizophrenia, as might be hypothesized from animal models and postmortem data. The analysis highlights the need for further GABA neuroimaging studies with improved methodology and addressing potential sources of heterogeneity.
引用
收藏
页码:e1147 / e1147
页数:10
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