Cargando…
Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study
Auditory cognition is impaired in schizophrenia, and typically engages a complex, distributed, hierarchical network, including both auditory and frontal input. We recently demonstrated proof of principle for the target engagement of an N-methyl-D-aspartate-type glutamate receptor (NMDAR) agonist + a...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246259/ https://www.ncbi.nlm.nih.gov/pubmed/37293030 http://dx.doi.org/10.21203/rs.3.rs-2943290/v1 |
_version_ | 1785054998091005952 |
---|---|
author | Govani, Viraj Shastry, Adithya Iosifescu, Daniel Govil, Preetika Mayer, Megan Sobeih, Tarek Choo, Tse Wall, Melanie Sehatpour, Pejman Kantrowitz, Joshua |
author_facet | Govani, Viraj Shastry, Adithya Iosifescu, Daniel Govil, Preetika Mayer, Megan Sobeih, Tarek Choo, Tse Wall, Melanie Sehatpour, Pejman Kantrowitz, Joshua |
author_sort | Govani, Viraj |
collection | PubMed |
description | Auditory cognition is impaired in schizophrenia, and typically engages a complex, distributed, hierarchical network, including both auditory and frontal input. We recently demonstrated proof of principle for the target engagement of an N-methyl-D-aspartate-type glutamate receptor (NMDAR) agonist + auditory targeted remediation (d-serine+AudRem) combination, showing significant improvement in auditory-learning induced plasticity and mismatch negativity. In this secondary analysis, we report on frontal EEG outcomes, assessing for both generalized effects and the mechanism of auditory plasticity. 21 schizophrenia or schizoaffective disorder participants were randomized to three 1x weekly AudRem + double-blind d-serine (100 mg/kg) visits. In AudRem, participants indicated which paired tone was higher in pitch. The focus of this secondary analysis was a frontally (premotor) mediated EEG outcome— event-related desynchronization in the b band (b-ERD), which was shown to be sensitive to AudRem in previous studies. d-S erine+AudRem led to significant improvement in b-ERD power across the retention and motor preparation intervals (F(1,18)=6.0, p=0.025) vs. AudRem alone. b-ERD was significantly related to baseline cognition, but not auditory-learning induced plasticity. The principal finding of this prespecified secondary analysis are that in addition to improving auditory based biomarkers, the d-serine+AudRem combination led to significant improvement in biomarkers thought to represent frontally mediated dysfunction, suggesting potential generalization of effects. Changes in auditory-learning induced plasticity were independent of these frontally mediated biomarkers. Ongoing work will assess whether d-serine+AudRem is suffi cient to remediate cognition or whether targeting frontal NMDAR deficits with higher-level remediation may also be required. TRIAL REGISTRATION: NCT03711500 |
format | Online Article Text |
id | pubmed-10246259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-102462592023-06-08 Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study Govani, Viraj Shastry, Adithya Iosifescu, Daniel Govil, Preetika Mayer, Megan Sobeih, Tarek Choo, Tse Wall, Melanie Sehatpour, Pejman Kantrowitz, Joshua Res Sq Article Auditory cognition is impaired in schizophrenia, and typically engages a complex, distributed, hierarchical network, including both auditory and frontal input. We recently demonstrated proof of principle for the target engagement of an N-methyl-D-aspartate-type glutamate receptor (NMDAR) agonist + auditory targeted remediation (d-serine+AudRem) combination, showing significant improvement in auditory-learning induced plasticity and mismatch negativity. In this secondary analysis, we report on frontal EEG outcomes, assessing for both generalized effects and the mechanism of auditory plasticity. 21 schizophrenia or schizoaffective disorder participants were randomized to three 1x weekly AudRem + double-blind d-serine (100 mg/kg) visits. In AudRem, participants indicated which paired tone was higher in pitch. The focus of this secondary analysis was a frontally (premotor) mediated EEG outcome— event-related desynchronization in the b band (b-ERD), which was shown to be sensitive to AudRem in previous studies. d-S erine+AudRem led to significant improvement in b-ERD power across the retention and motor preparation intervals (F(1,18)=6.0, p=0.025) vs. AudRem alone. b-ERD was significantly related to baseline cognition, but not auditory-learning induced plasticity. The principal finding of this prespecified secondary analysis are that in addition to improving auditory based biomarkers, the d-serine+AudRem combination led to significant improvement in biomarkers thought to represent frontally mediated dysfunction, suggesting potential generalization of effects. Changes in auditory-learning induced plasticity were independent of these frontally mediated biomarkers. Ongoing work will assess whether d-serine+AudRem is suffi cient to remediate cognition or whether targeting frontal NMDAR deficits with higher-level remediation may also be required. TRIAL REGISTRATION: NCT03711500 American Journal Experts 2023-05-19 /pmc/articles/PMC10246259/ /pubmed/37293030 http://dx.doi.org/10.21203/rs.3.rs-2943290/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Article Govani, Viraj Shastry, Adithya Iosifescu, Daniel Govil, Preetika Mayer, Megan Sobeih, Tarek Choo, Tse Wall, Melanie Sehatpour, Pejman Kantrowitz, Joshua Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title | Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title_full | Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title_fullStr | Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title_full_unstemmed | Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title_short | Augmentation of learning in schizophrenia by D-serine is related to auditory and frontally-generated biomarkers: A randomized, double-blind, placebo-controlled study |
title_sort | augmentation of learning in schizophrenia by d-serine is related to auditory and frontally-generated biomarkers: a randomized, double-blind, placebo-controlled study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246259/ https://www.ncbi.nlm.nih.gov/pubmed/37293030 http://dx.doi.org/10.21203/rs.3.rs-2943290/v1 |
work_keys_str_mv | AT govaniviraj augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT shastryadithya augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT iosifescudaniel augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT govilpreetika augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT mayermegan augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT sobeihtarek augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT chootse augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT wallmelanie augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT sehatpourpejman augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy AT kantrowitzjoshua augmentationoflearninginschizophreniabydserineisrelatedtoauditoryandfrontallygeneratedbiomarkersarandomizeddoubleblindplacebocontrolledstudy |