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A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia

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dc.contributor.authorKim, Yong-Ku-
dc.contributor.authorChoi, Joonho-
dc.contributor.authorPark, Seon-Cheol-
dc.date.accessioned2021-09-03T07:49:52Z-
dc.date.available2021-09-03T07:49:52Z-
dc.date.created2021-06-16-
dc.date.issued2017-04-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/83970-
dc.description.abstractDespite the substantial burden of illness in schizophrenia, there has been a discrepancy between the beneficial effects of an increased use of antipsychotic medications and achieving limited recovery or remission. Because the focus of the most common antipsychotic medications is on dopamine, which is associated with positive symptoms, there is an unmet need for patients with negative symptoms. Since cognitive and negative symptoms rather than positive symptoms are more closely associated with psychosocial impairments in patients with schizophrenia, the non-dopaminergic systems including glutamate and gamma-aminobutyric acid (GABA) of the prefrontal cortex should be of concern as well. The balance of excitation and inhibition has been associated with epigenetic modifications and thus can be analyzed in terms of a neurodevelopmental and neural circuitry perspective. Hence, a novel bio-psychosocial-behavioral model for the treatment of schizophrenia is needed to account for the non-dopaminergic systems involved in schizophrenia, rather than dopaminergic mechanisms. This model can be understood from the viewpoint of neurodevelopment and neural circuitry and should include the staging care, personalized care, preventive care, reducing the cognitive deficits, and reducing stigma. Thomas R. Insel proposed this as a goal for schizophrenia treatment to be achieved by 2030.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI-
dc.subjectNMDA RECEPTOR SUBUNITS-
dc.subjectPREFRONTAL CORTEX-
dc.subjectCOGNITIVE NEUROSCIENCE-
dc.subjectGENE-EXPRESSION-
dc.subjectPSYCHOTIC DISORDERS-
dc.subjectGABA NEURONS-
dc.subjectDOUBLE-BLIND-
dc.subjectSYMPTOMS-
dc.subjectMECHANISMS-
dc.subjectNEUROINFLAMMATION-
dc.titleA Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Yong-Ku-
dc.identifier.doi10.3390/ijms18040734-
dc.identifier.scopusid2-s2.0-85016951410-
dc.identifier.wosid000402639400060-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.18, no.4-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume18-
dc.citation.number4-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusNMDA RECEPTOR SUBUNITS-
dc.subject.keywordPlusPREFRONTAL CORTEX-
dc.subject.keywordPlusCOGNITIVE NEUROSCIENCE-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusPSYCHOTIC DISORDERS-
dc.subject.keywordPlusGABA NEURONS-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusSYMPTOMS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusNEUROINFLAMMATION-
dc.subject.keywordAuthorschizophrenia-
dc.subject.keywordAuthorbio-psychosocial-behavioral-
dc.subject.keywordAuthormodel-
dc.subject.keywordAuthorneurodevelopment-
dc.subject.keywordAuthorneural circuitry-
dc.subject.keywordAuthorcognitive-
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