| Literature DB >> 29656951 |
Joshua T Kantrowitz1, Neal R Swerdlow2, Walter Dunn3, Sophia Vinogradov4.
Abstract
Cognitive deficits are predictive of long-term social and occupational functional deficits in schizophrenia but are currently without gold-standard treatments. In particular, augmentation of auditory cortical neuroplasticity may represent a rate-limiting first step before addressing higher-order cognitive deficits. We review the rationale for N-methyl-d-aspartate-type glutamate receptor (NMDAR) modulators as treatments for auditory plasticity deficits in schizophrenia, along with potential serum and electroencephalographic target engagement biomarkers for NMDAR function. Several recently published NMDAR-modulating treatment studies are covered, involving D-serine, memantine, and transcranial direct current stimulation. While all three interventions appear to modulate auditory plasticity, direct agonists (D-serine) appear to have the largest and most consistent effects on plasticity, at least acutely. We hypothesize that there may be synergistic effects of combining procognitive NMDAR-modulating approaches with auditory cortical neuroplasticity cognitive training interventions. Future studies should assess biomarkers for target engagement and patient stratification, along with head-to-head studies comparing putative interventions and potential long-term versus acute effects.Entities:
Keywords: Biomarker; Cognition; MMN; NMDA; Plasticity; Schizophrenia; Treatment
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Year: 2018 PMID: 29656951 PMCID: PMC6062454 DOI: 10.1016/j.bpsc.2018.02.002
Source DB: PubMed Journal: Biol Psychiatry Cogn Neurosci Neuroimaging ISSN: 2451-9022