Adenosine hypothesis in schizophrenia and bipolar disorder: A systematic review and meta-analysis of randomized controlled trial of adjuvant purinergic modulators
Abstract Objective Adenosine has been reported to interact with dopamine and glutamate of which are currently central pathophysiology of schizophrenia. Further, there have been emerging reports that patients with bipolar disorder (BD) have pathophysiological changes of the purinergic system. Thus, w...
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description | Abstract Objective Adenosine has been reported to interact with dopamine and glutamate of which are currently central pathophysiology of schizophrenia. Further, there have been emerging reports that patients with bipolar disorder (BD) have pathophysiological changes of the purinergic system. Thus, we performed a systematic review and meta-analysis of adenosine modulators in these disorders. Method We searched PubMed, EMBASE, the Cochrane Library databases, CINAHL, and PsycINFO up to April 25, 2013. Randomized controlled trials comparing adenosine modulator adjuvant therapy with placebo in patients with schizophrenia and BD were included. Primary outcome measures were Positive and Negative Syndrome Scale (PANSS) and Young Mania Rating Scales (YMRS). The risk ratio, 95% confidence interval, and standardized mean differences (SMD) were used. Results Nine studies, including six studies in schizophrenia (total n = 457) and three studies in BD (total n = 289) were included. Overall, adenosine modulators were superior to placebo in PANSS total scores (SMD = − 1.07, p = 0.01) and positive and general but not negative symptom subscale scores in schizophrenia. Individually, allopurinol failed to show its superiority to placebo in all primary outcome measures in schizophrenia. In BD, data from pooled adenosine modulators indicated significant reduction of YMRS scores in comparison to placebo (SMD = − 0.39, p = 0.004). Conclusions Our results suggest that adenosine modulator adjuvant therapy is more beneficial in overall psychopathology (especially positive symptoms) in schizophrenia and in treating mania episodes of BD in comparison to placebo. The limited sample size of available studies suggests that more research should be done to evaluate both efficacy and tolerability of these medications. |
doi_str_mv | 10.1016/j.schres.2013.06.038 |
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Further, there have been emerging reports that patients with bipolar disorder (BD) have pathophysiological changes of the purinergic system. Thus, we performed a systematic review and meta-analysis of adenosine modulators in these disorders. Method We searched PubMed, EMBASE, the Cochrane Library databases, CINAHL, and PsycINFO up to April 25, 2013. Randomized controlled trials comparing adenosine modulator adjuvant therapy with placebo in patients with schizophrenia and BD were included. Primary outcome measures were Positive and Negative Syndrome Scale (PANSS) and Young Mania Rating Scales (YMRS). The risk ratio, 95% confidence interval, and standardized mean differences (SMD) were used. Results Nine studies, including six studies in schizophrenia (total n = 457) and three studies in BD (total n = 289) were included. Overall, adenosine modulators were superior to placebo in PANSS total scores (SMD = − 1.07, p = 0.01) and positive and general but not negative symptom subscale scores in schizophrenia. Individually, allopurinol failed to show its superiority to placebo in all primary outcome measures in schizophrenia. In BD, data from pooled adenosine modulators indicated significant reduction of YMRS scores in comparison to placebo (SMD = − 0.39, p = 0.004). Conclusions Our results suggest that adenosine modulator adjuvant therapy is more beneficial in overall psychopathology (especially positive symptoms) in schizophrenia and in treating mania episodes of BD in comparison to placebo. The limited sample size of available studies suggests that more research should be done to evaluate both efficacy and tolerability of these medications.</description><identifier>ISSN: 0920-9964</identifier><identifier>EISSN: 1573-2509</identifier><identifier>DOI: 10.1016/j.schres.2013.06.038</identifier><identifier>PMID: 23870805</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adenosine - metabolism ; Adult and adolescent clinical studies ; Allopurinol ; Antipsychotic Agents ; Biological and medical sciences ; Bipolar Disorder - drug therapy ; Bipolar disorders ; Databases, Factual - statistics & numerical data ; Dipyridamole ; Humans ; Mania ; Medical sciences ; Mood disorders ; Propentofylline ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; Psychosis ; Purine ; Purinergic Agents - therapeutic use ; Randomized Controlled Trials as Topic ; Schizophrenia ; Schizophrenia - drug therapy</subject><ispartof>Schizophrenia research, 2013-09, Vol.149 (1), p.88-95</ispartof><rights>Elsevier B.V.</rights><rights>2013 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>2013.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-b55e264eca473ea1940e8742fdb3c95f86876b0dad186c6979f31304cbe132fa3</citedby><cites>FETCH-LOGICAL-c513t-b55e264eca473ea1940e8742fdb3c95f86876b0dad186c6979f31304cbe132fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0920996413003381$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27653322$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23870805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hirota, Tomoya</creatorcontrib><creatorcontrib>Kishi, Taro</creatorcontrib><title>Adenosine hypothesis in schizophrenia and bipolar disorder: A systematic review and meta-analysis of randomized controlled trial of adjuvant purinergic modulators</title><title>Schizophrenia research</title><addtitle>Schizophr Res</addtitle><description>Abstract Objective Adenosine has been reported to interact with dopamine and glutamate of which are currently central pathophysiology of schizophrenia. Further, there have been emerging reports that patients with bipolar disorder (BD) have pathophysiological changes of the purinergic system. Thus, we performed a systematic review and meta-analysis of adenosine modulators in these disorders. Method We searched PubMed, EMBASE, the Cochrane Library databases, CINAHL, and PsycINFO up to April 25, 2013. Randomized controlled trials comparing adenosine modulator adjuvant therapy with placebo in patients with schizophrenia and BD were included. Primary outcome measures were Positive and Negative Syndrome Scale (PANSS) and Young Mania Rating Scales (YMRS). The risk ratio, 95% confidence interval, and standardized mean differences (SMD) were used. Results Nine studies, including six studies in schizophrenia (total n = 457) and three studies in BD (total n = 289) were included. Overall, adenosine modulators were superior to placebo in PANSS total scores (SMD = − 1.07, p = 0.01) and positive and general but not negative symptom subscale scores in schizophrenia. Individually, allopurinol failed to show its superiority to placebo in all primary outcome measures in schizophrenia. In BD, data from pooled adenosine modulators indicated significant reduction of YMRS scores in comparison to placebo (SMD = − 0.39, p = 0.004). Conclusions Our results suggest that adenosine modulator adjuvant therapy is more beneficial in overall psychopathology (especially positive symptoms) in schizophrenia and in treating mania episodes of BD in comparison to placebo. The limited sample size of available studies suggests that more research should be done to evaluate both efficacy and tolerability of these medications.</description><subject>Adenosine - metabolism</subject><subject>Adult and adolescent clinical studies</subject><subject>Allopurinol</subject><subject>Antipsychotic Agents</subject><subject>Biological and medical sciences</subject><subject>Bipolar Disorder - drug therapy</subject><subject>Bipolar disorders</subject><subject>Databases, Factual - statistics & numerical data</subject><subject>Dipyridamole</subject><subject>Humans</subject><subject>Mania</subject><subject>Medical sciences</subject><subject>Mood disorders</subject><subject>Propentofylline</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Psychosis</subject><subject>Purine</subject><subject>Purinergic Agents - therapeutic use</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Schizophrenia</subject><subject>Schizophrenia - drug therapy</subject><issn>0920-9964</issn><issn>1573-2509</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks2OFCEUhStG47Sjb2AMGxM31V6K-nVh0pn4l0ziQl0TCm7ZlBSUQM2k5nF8Uim71cSNKwh895zLPWTZUwp7CrR-Oe6DPHoM-wIo20O9B9bey3a0alheVNDdz3bQFZB3XV1eZI9CGAGAVtA8zC4K1jbQQrXLfhwUWhe0RXJcZxePGHQg2pIkru_cnBysFkRYRXo9OyM8UTo4r9C_IgcS1hBxElFL4vFG4-0vcsIocmGFWTcxNxCfTt2k71AR6Wz0zpi0jV4Ls10LNS43wkYyLz514r8mucmpxYjofHicPRiECfjkvF5mX96--Xz1Pr_--O7D1eE6lxVlMe-rCou6RCnKhqGgXQnYNmUxqJ7Jrhraum3qHpRQtK1l3TXdwCiDUvZIWTEIdpm9OOnO3n1fMEQ-6SDRGGHRLYHTkra07BitElqeUOldCB4HPns9Cb9yCnxLh4_8lA7f0uFQ85ROKnt2dlj6CdWfot9xJOD5GRBBCjOkuUkd_nJNXTFWFIl7feIwzSON3Sc3jVai0h5l5Mrp_3Xyr4A02urk-Q1XDKNbfIovvZmHggP_tP2k7SOlgQFjLWU_AcltyOY</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Hirota, Tomoya</creator><creator>Kishi, Taro</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20130901</creationdate><title>Adenosine hypothesis in schizophrenia and bipolar disorder: A systematic review and meta-analysis of randomized controlled trial of adjuvant purinergic modulators</title><author>Hirota, Tomoya ; Kishi, Taro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-b55e264eca473ea1940e8742fdb3c95f86876b0dad186c6979f31304cbe132fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adenosine - metabolism</topic><topic>Adult and adolescent clinical studies</topic><topic>Allopurinol</topic><topic>Antipsychotic Agents</topic><topic>Biological and medical sciences</topic><topic>Bipolar Disorder - drug therapy</topic><topic>Bipolar disorders</topic><topic>Databases, Factual - statistics & numerical data</topic><topic>Dipyridamole</topic><topic>Humans</topic><topic>Mania</topic><topic>Medical sciences</topic><topic>Mood disorders</topic><topic>Propentofylline</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Psychosis</topic><topic>Purine</topic><topic>Purinergic Agents - therapeutic use</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Schizophrenia</topic><topic>Schizophrenia - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirota, Tomoya</creatorcontrib><creatorcontrib>Kishi, Taro</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Schizophrenia research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirota, Tomoya</au><au>Kishi, Taro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adenosine hypothesis in schizophrenia and bipolar disorder: A systematic review and meta-analysis of randomized controlled trial of adjuvant purinergic modulators</atitle><jtitle>Schizophrenia research</jtitle><addtitle>Schizophr Res</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>149</volume><issue>1</issue><spage>88</spage><epage>95</epage><pages>88-95</pages><issn>0920-9964</issn><eissn>1573-2509</eissn><abstract>Abstract Objective Adenosine has been reported to interact with dopamine and glutamate of which are currently central pathophysiology of schizophrenia. Further, there have been emerging reports that patients with bipolar disorder (BD) have pathophysiological changes of the purinergic system. Thus, we performed a systematic review and meta-analysis of adenosine modulators in these disorders. Method We searched PubMed, EMBASE, the Cochrane Library databases, CINAHL, and PsycINFO up to April 25, 2013. Randomized controlled trials comparing adenosine modulator adjuvant therapy with placebo in patients with schizophrenia and BD were included. Primary outcome measures were Positive and Negative Syndrome Scale (PANSS) and Young Mania Rating Scales (YMRS). The risk ratio, 95% confidence interval, and standardized mean differences (SMD) were used. Results Nine studies, including six studies in schizophrenia (total n = 457) and three studies in BD (total n = 289) were included. Overall, adenosine modulators were superior to placebo in PANSS total scores (SMD = − 1.07, p = 0.01) and positive and general but not negative symptom subscale scores in schizophrenia. Individually, allopurinol failed to show its superiority to placebo in all primary outcome measures in schizophrenia. In BD, data from pooled adenosine modulators indicated significant reduction of YMRS scores in comparison to placebo (SMD = − 0.39, p = 0.004). Conclusions Our results suggest that adenosine modulator adjuvant therapy is more beneficial in overall psychopathology (especially positive symptoms) in schizophrenia and in treating mania episodes of BD in comparison to placebo. The limited sample size of available studies suggests that more research should be done to evaluate both efficacy and tolerability of these medications.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23870805</pmid><doi>10.1016/j.schres.2013.06.038</doi><tpages>8</tpages></addata></record> |
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subjects | Adenosine - metabolism Adult and adolescent clinical studies Allopurinol Antipsychotic Agents Biological and medical sciences Bipolar Disorder - drug therapy Bipolar disorders Databases, Factual - statistics & numerical data Dipyridamole Humans Mania Medical sciences Mood disorders Propentofylline Psychiatry Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Psychosis Purine Purinergic Agents - therapeutic use Randomized Controlled Trials as Topic Schizophrenia Schizophrenia - drug therapy |
title | Adenosine hypothesis in schizophrenia and bipolar disorder: A systematic review and meta-analysis of randomized controlled trial of adjuvant purinergic modulators |
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