A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia
Despite 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 i...
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Veröffentlicht in: | International journal of molecular sciences 2017-03, Vol.18 (4), p.734-734 |
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description | Despite 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 γ-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. |
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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 γ-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.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms18040734</identifier><identifier>PMID: 28358303</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animals ; Antipsychotic Agents - adverse effects ; Antipsychotic Agents - pharmacology ; Antipsychotic Agents - therapeutic use ; Behavior Therapy - methods ; Brain - drug effects ; Brain - metabolism ; Brain - physiopathology ; Dopamine ; Drug therapy ; Humans ; Neurodevelopment ; Neurogenesis ; Neurotransmitter Agents - metabolism ; Psychotropic drugs ; Review ; Schizophrenia ; Schizophrenia - drug therapy ; Schizophrenia - metabolism ; Schizophrenia - physiopathology ; Schizophrenia - therapy</subject><ispartof>International journal of molecular sciences, 2017-03, Vol.18 (4), p.734-734</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-2fb4e0596f685155a3d8f15d66964b98b066075b167d1da41a7ad3e3e48b830d3</citedby><cites>FETCH-LOGICAL-c511t-2fb4e0596f685155a3d8f15d66964b98b066075b167d1da41a7ad3e3e48b830d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412320/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412320/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28358303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Yong-Ku</creatorcontrib><creatorcontrib>Choi, Joonho</creatorcontrib><creatorcontrib>Park, Seon-Cheol</creatorcontrib><title>A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Despite 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 γ-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.</description><subject>Animals</subject><subject>Antipsychotic Agents - adverse effects</subject><subject>Antipsychotic Agents - pharmacology</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Behavior Therapy - methods</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain - physiopathology</subject><subject>Dopamine</subject><subject>Drug therapy</subject><subject>Humans</subject><subject>Neurodevelopment</subject><subject>Neurogenesis</subject><subject>Neurotransmitter Agents - metabolism</subject><subject>Psychotropic drugs</subject><subject>Review</subject><subject>Schizophrenia</subject><subject>Schizophrenia - drug therapy</subject><subject>Schizophrenia - metabolism</subject><subject>Schizophrenia - physiopathology</subject><subject>Schizophrenia - therapy</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkUtLAzEUhYMotlZ3rmXAjQtHk8ljko3Q1ifUB1jXITOTcVJmJjVpC_XXG2kt1Y2LSy7k43DuOQAcI3iBsYCXZtJ4xCGBKSY7oItIksQQsnR3a--AA-8nECY4oWIfdBKOKccQd8F1P3qyC11HA2PjF7_MK-ttblQdD3SlFsY6VUdjp9Ws0e0serRFYE0bveaV-bTTyunWqEOwV6ra66P12wNvtzfj4X08er57GPZHcU4RmsVJmRENqWAl4xRRqnDBS0QLxgQjmeAZZAymNEMsLVChCFKpKrDGmvAsuC1wD1ytdKfzrNFFHhwFe3LqTKPcUlpl5O-f1lTy3S4kJSicDoPA2VrA2Y-59jPZGJ_rulattnMvkYAopViE-RflPKEhW4IDevoHndi5a0MSgRKCh9hJEqjzFZU7673T5cY3gvK7SbndZMBPtm_dwD_V4S9ef5hY</recordid><startdate>20170330</startdate><enddate>20170330</enddate><creator>Kim, Yong-Ku</creator><creator>Choi, Joonho</creator><creator>Park, Seon-Cheol</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20170330</creationdate><title>A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia</title><author>Kim, Yong-Ku ; Choi, Joonho ; Park, Seon-Cheol</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-2fb4e0596f685155a3d8f15d66964b98b066075b167d1da41a7ad3e3e48b830d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Antipsychotic Agents - adverse effects</topic><topic>Antipsychotic Agents - pharmacology</topic><topic>Antipsychotic Agents - therapeutic use</topic><topic>Behavior Therapy - methods</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain - physiopathology</topic><topic>Dopamine</topic><topic>Drug therapy</topic><topic>Humans</topic><topic>Neurodevelopment</topic><topic>Neurogenesis</topic><topic>Neurotransmitter Agents - metabolism</topic><topic>Psychotropic drugs</topic><topic>Review</topic><topic>Schizophrenia</topic><topic>Schizophrenia - drug therapy</topic><topic>Schizophrenia - metabolism</topic><topic>Schizophrenia - physiopathology</topic><topic>Schizophrenia - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Yong-Ku</creatorcontrib><creatorcontrib>Choi, Joonho</creatorcontrib><creatorcontrib>Park, Seon-Cheol</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Yong-Ku</au><au>Choi, Joonho</au><au>Park, Seon-Cheol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2017-03-30</date><risdate>2017</risdate><volume>18</volume><issue>4</issue><spage>734</spage><epage>734</epage><pages>734-734</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Despite 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 γ-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. 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subjects | Animals Antipsychotic Agents - adverse effects Antipsychotic Agents - pharmacology Antipsychotic Agents - therapeutic use Behavior Therapy - methods Brain - drug effects Brain - metabolism Brain - physiopathology Dopamine Drug therapy Humans Neurodevelopment Neurogenesis Neurotransmitter Agents - metabolism Psychotropic drugs Review Schizophrenia Schizophrenia - drug therapy Schizophrenia - metabolism Schizophrenia - physiopathology Schizophrenia - therapy |
title | A Novel Bio-Psychosocial-Behavioral Treatment Model in Schizophrenia |
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