Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications
It has been postulated that schizophrenia (SZ) is related to a lower expression of brain-derived neurotrophic factor (BDNF). In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship...
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Veröffentlicht in: | Molecular psychiatry 2015-09, Vol.20 (9), p.1108-1119 |
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description | It has been postulated that schizophrenia (SZ) is related to a lower expression of brain-derived neurotrophic factor (BDNF). In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship between BDNF levels and severity of symptoms in SZ as well as the effects of antipsychotic drugs on BDNF using meta-analysis. The aims of this study were to verify if peripheral BDNF is decreased in SZ, whether its levels are correlated with positive and negative symptomatology and if BDNF levels change after antipsychotic treatment. This report consists of two distinct meta-analyses of peripheral BDNF in SZ including a total of 41 studies and more than 7000 participants: (1) peripheral BDNF levels in serum and plasma were moderately reduced in SZ compared with controls. Notably, this decrease was accentuated with the disease duration. However, the extent of peripheral BDNF level decrease did not correlate with the severity of positive and negative symptoms. (2) In plasma, but not serum, peripheral BDNF levels are consistently increased after antipsychotic treatment irrespective of the patient’s response to medication. In conclusion, there is compelling evidence that there are decreased levels of peripheral BDNF in SZ, in parallel to previously described reduced cerebral BDNF expression. It remains unclear whether these systemic changes are causally related to the development of SZ or if they are merely a pathologic epiphenomenon. |
doi_str_mv | 10.1038/mp.2014.117 |
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In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship between BDNF levels and severity of symptoms in SZ as well as the effects of antipsychotic drugs on BDNF using meta-analysis. The aims of this study were to verify if peripheral BDNF is decreased in SZ, whether its levels are correlated with positive and negative symptomatology and if BDNF levels change after antipsychotic treatment. This report consists of two distinct meta-analyses of peripheral BDNF in SZ including a total of 41 studies and more than 7000 participants: (1) peripheral BDNF levels in serum and plasma were moderately reduced in SZ compared with controls. Notably, this decrease was accentuated with the disease duration. However, the extent of peripheral BDNF level decrease did not correlate with the severity of positive and negative symptoms. (2) In plasma, but not serum, peripheral BDNF levels are consistently increased after antipsychotic treatment irrespective of the patient’s response to medication. In conclusion, there is compelling evidence that there are decreased levels of peripheral BDNF in SZ, in parallel to previously described reduced cerebral BDNF expression. It remains unclear whether these systemic changes are causally related to the development of SZ or if they are merely a pathologic epiphenomenon.</description><identifier>ISSN: 1359-4184</identifier><identifier>EISSN: 1476-5578</identifier><identifier>DOI: 10.1038/mp.2014.117</identifier><identifier>PMID: 25266124</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>692/699/476/1799 ; Adult ; Antipsychotic Agents - therapeutic use ; Antipsychotic drugs ; Antipsychotics ; Behavioral Sciences ; Biological Psychology ; Biomarkers - blood ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - blood ; Care and treatment ; Case-Control Studies ; Emotional behavior ; Female ; Humans ; Male ; Medicine ; Medicine & Public Health ; Mental disorders ; Meta-analysis ; Middle Aged ; Neurosciences ; original-article ; Pharmacotherapy ; Physiological aspects ; Psychiatry ; Psychotropic drugs ; Risk factors ; Schizophrenia ; Schizophrenia - blood ; Schizophrenia - drug therapy ; Serum ; Systematic review ; Young Adult</subject><ispartof>Molecular psychiatry, 2015-09, Vol.20 (9), p.1108-1119</ispartof><rights>Macmillan Publishers Limited 2014</rights><rights>COPYRIGHT 2015 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Sep 2015</rights><rights>Macmillan Publishers Limited 2014.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-1a3fa9ba69eb99d268cfe48eac2088620ce67551aaff29e3fd8f28f6fe9243293</citedby><cites>FETCH-LOGICAL-c589t-1a3fa9ba69eb99d268cfe48eac2088620ce67551aaff29e3fd8f28f6fe9243293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/mp.2014.117$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/mp.2014.117$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25266124$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernandes, B S</creatorcontrib><creatorcontrib>Steiner, J</creatorcontrib><creatorcontrib>Berk, M</creatorcontrib><creatorcontrib>Molendijk, M L</creatorcontrib><creatorcontrib>Gonzalez-Pinto, A</creatorcontrib><creatorcontrib>Turck, C W</creatorcontrib><creatorcontrib>Nardin, P</creatorcontrib><creatorcontrib>Gonçalves, C-A</creatorcontrib><title>Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications</title><title>Molecular psychiatry</title><addtitle>Mol Psychiatry</addtitle><addtitle>Mol Psychiatry</addtitle><description>It has been postulated that schizophrenia (SZ) is related to a lower expression of brain-derived neurotrophic factor (BDNF). In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship between BDNF levels and severity of symptoms in SZ as well as the effects of antipsychotic drugs on BDNF using meta-analysis. The aims of this study were to verify if peripheral BDNF is decreased in SZ, whether its levels are correlated with positive and negative symptomatology and if BDNF levels change after antipsychotic treatment. This report consists of two distinct meta-analyses of peripheral BDNF in SZ including a total of 41 studies and more than 7000 participants: (1) peripheral BDNF levels in serum and plasma were moderately reduced in SZ compared with controls. Notably, this decrease was accentuated with the disease duration. However, the extent of peripheral BDNF level decrease did not correlate with the severity of positive and negative symptoms. (2) In plasma, but not serum, peripheral BDNF levels are consistently increased after antipsychotic treatment irrespective of the patient’s response to medication. In conclusion, there is compelling evidence that there are decreased levels of peripheral BDNF in SZ, in parallel to previously described reduced cerebral BDNF expression. It remains unclear whether these systemic changes are causally related to the development of SZ or if they are merely a pathologic epiphenomenon.</description><subject>692/699/476/1799</subject><subject>Adult</subject><subject>Antipsychotic Agents - therapeutic use</subject><subject>Antipsychotic drugs</subject><subject>Antipsychotics</subject><subject>Behavioral Sciences</subject><subject>Biological Psychology</subject><subject>Biomarkers - blood</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - blood</subject><subject>Care and treatment</subject><subject>Case-Control Studies</subject><subject>Emotional behavior</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mental disorders</subject><subject>Meta-analysis</subject><subject>Middle Aged</subject><subject>Neurosciences</subject><subject>original-article</subject><subject>Pharmacotherapy</subject><subject>Physiological aspects</subject><subject>Psychiatry</subject><subject>Psychotropic drugs</subject><subject>Risk factors</subject><subject>Schizophrenia</subject><subject>Schizophrenia - 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therapeutic use</topic><topic>Antipsychotic drugs</topic><topic>Antipsychotics</topic><topic>Behavioral Sciences</topic><topic>Biological Psychology</topic><topic>Biomarkers - blood</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - blood</topic><topic>Care and treatment</topic><topic>Case-Control Studies</topic><topic>Emotional behavior</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mental disorders</topic><topic>Meta-analysis</topic><topic>Middle Aged</topic><topic>Neurosciences</topic><topic>original-article</topic><topic>Pharmacotherapy</topic><topic>Physiological aspects</topic><topic>Psychiatry</topic><topic>Psychotropic drugs</topic><topic>Risk factors</topic><topic>Schizophrenia</topic><topic>Schizophrenia - blood</topic><topic>Schizophrenia - drug therapy</topic><topic>Serum</topic><topic>Systematic review</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernandes, B S</creatorcontrib><creatorcontrib>Steiner, J</creatorcontrib><creatorcontrib>Berk, M</creatorcontrib><creatorcontrib>Molendijk, M L</creatorcontrib><creatorcontrib>Gonzalez-Pinto, A</creatorcontrib><creatorcontrib>Turck, C W</creatorcontrib><creatorcontrib>Nardin, P</creatorcontrib><creatorcontrib>Gonçalves, C-A</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>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Biological Science Database</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 One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernandes, B S</au><au>Steiner, J</au><au>Berk, M</au><au>Molendijk, M L</au><au>Gonzalez-Pinto, A</au><au>Turck, C W</au><au>Nardin, P</au><au>Gonçalves, C-A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications</atitle><jtitle>Molecular psychiatry</jtitle><stitle>Mol Psychiatry</stitle><addtitle>Mol Psychiatry</addtitle><date>2015-09-01</date><risdate>2015</risdate><volume>20</volume><issue>9</issue><spage>1108</spage><epage>1119</epage><pages>1108-1119</pages><issn>1359-4184</issn><eissn>1476-5578</eissn><abstract>It has been postulated that schizophrenia (SZ) is related to a lower expression of brain-derived neurotrophic factor (BDNF). In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship between BDNF levels and severity of symptoms in SZ as well as the effects of antipsychotic drugs on BDNF using meta-analysis. The aims of this study were to verify if peripheral BDNF is decreased in SZ, whether its levels are correlated with positive and negative symptomatology and if BDNF levels change after antipsychotic treatment. This report consists of two distinct meta-analyses of peripheral BDNF in SZ including a total of 41 studies and more than 7000 participants: (1) peripheral BDNF levels in serum and plasma were moderately reduced in SZ compared with controls. Notably, this decrease was accentuated with the disease duration. However, the extent of peripheral BDNF level decrease did not correlate with the severity of positive and negative symptoms. (2) In plasma, but not serum, peripheral BDNF levels are consistently increased after antipsychotic treatment irrespective of the patient’s response to medication. In conclusion, there is compelling evidence that there are decreased levels of peripheral BDNF in SZ, in parallel to previously described reduced cerebral BDNF expression. It remains unclear whether these systemic changes are causally related to the development of SZ or if they are merely a pathologic epiphenomenon.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25266124</pmid><doi>10.1038/mp.2014.117</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 692/699/476/1799 Adult Antipsychotic Agents - therapeutic use Antipsychotic drugs Antipsychotics Behavioral Sciences Biological Psychology Biomarkers - blood Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - blood Care and treatment Case-Control Studies Emotional behavior Female Humans Male Medicine Medicine & Public Health Mental disorders Meta-analysis Middle Aged Neurosciences original-article Pharmacotherapy Physiological aspects Psychiatry Psychotropic drugs Risk factors Schizophrenia Schizophrenia - blood Schizophrenia - drug therapy Serum Systematic review Young Adult |
title | Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications |
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