» Articles » PMID: 23692933

NMDA Receptor Antagonists Interventions in Schizophrenia: Meta-analysis of Randomized, Placebo-controlled Trials

Overview
Journal J Psychiatr Res
Specialty Psychiatry
Date 2013 May 23
PMID 23692933
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Background: We examined whether N-methyl d-aspartate (NMDA) receptor antagonists as adjunctive therapy have therapeutic potential for schizophrenia treatment.

Method: Systematic review of PubMed, Cochrane Library, PsycINFO and Google Scholar up until October 2012 and meta-analysis of randomized placebo-controlled trials were performed. Risk ratio (RR), 95% confidence intervals (CI), numbers-needed-to-harm (NNH), and standardized mean difference (SMD) were calculated.

Results: Results were across 8 studies and 406 patients (85.5% schizophrenia related disorder and 14.5% bipolar disorder) were included (amantadine: 5 trials and 220 patients, memantine: 3 trials and 186 patients). NMDA receptor antagonists (NMDAR-ANTs) as adjunctive therapy were not superior to placebo in overall (SMD = -0.25, CI = -0.72, 0.23, p = 0.31, N = 6, n = 347), positive symptoms (SMD = -0.20, CI = -0.70, 0.31, p = 0.44, N = 4, n = 205), and negative symptoms (SMD = -0.69, CI = -1.65, 0.27, p = 0.16, N = 4, n = 205), and Clinical Global Impression Severity scale (SMD = -0.27, CI = -1.20, 0.65, p = 0.56, N = 3, n = 177). There was also no significant difference in discontinuation rate between NMDAR-ANTs and placebo treatments (all cause: RR = 1.23, CI = 0.89-1.70, p = 0.20, N = 8, n = 396, side effects: RR = 1.86, CI = 0.84-4.13, p = 0.13, N = 6, n = 359, inefficacy/worsening psychosis: RR = 0.70, CI = 0.20-2.38, p = 0.56, N = 7, n = 380). However, memantine was favorable compared with placebo in Mini-Mental State Examination in schizophrenia (SMD = -0.77, CI = -1.27, -0.28, p = 0.002, N = 3, n = 71). While NMDAR-ANTs caused weight loss compared with placebo (SMD = -0.42, CI = -0.73, -0.11, p = 0.008, N = 3, n = 165), amantadine caused more frequent insomnia than placebo (RR = 3.83, CI = 1.41-10.38, p = 0.008, NNH = 9, p = 0.002, N = 2, n = 147).

Conclusion: Our results indicate that NMDAR-ANTs as adjunctive therapy may improve cognitive function in patients with schizophrenia. Because the included studies were small, a replication study using larger samples is needed.

Citing Articles

Pharmacological Treatments of Negative Symptoms in Schizophrenia-An Update.

Tsapakis E, Treiber M, Mitkani C, Drakaki Z, Cholevas A, Spanaki C J Clin Med. 2024; 13(18).

PMID: 39337126 PMC: 11432821. DOI: 10.3390/jcm13185637.


Chemical Probes to Investigate Central Nervous System Disorders: Design, Synthesis and Mechanism of Action of a Potent Human Serine Racemase Inhibitor.

Marchesani F, Rebecchi F, Pieroni M, Faggiano S, Annunziato G, Spaggiari C ACS Med Chem Lett. 2024; 15(8):1298-1305.

PMID: 39140049 PMC: 11318019. DOI: 10.1021/acsmedchemlett.4c00174.


The Effect of Memantine Versus Folic Acid on Cognitive Impairment in Patients with Schizophrenia: A Randomized Clinical Trial.

Hosseini S, Sepehrmanesh Z, Gilasi H, Ghoraishi F Iran J Psychiatry. 2023; 18(3):258-265.

PMID: 37575608 PMC: 10422942. DOI: 10.18502/ijps.v18i3.13002.


Refractory Methamphetamine-Induced Psychosis: An Emerging Crisis in Rural America and the Role of Amantadine in Therapeutics.

Gupta M, Gupta N, Esang M, Antai A, Moll J Cureus. 2022; 14(3):e22871.

PMID: 35392446 PMC: 8979574. DOI: 10.7759/cureus.22871.


Amantadine: reappraisal of the timeless diamond-target updates and novel therapeutic potentials.

Danysz W, Dekundy A, Scheschonka A, Riederer P J Neural Transm (Vienna). 2021; 128(2):127-169.

PMID: 33624170 PMC: 7901515. DOI: 10.1007/s00702-021-02306-2.