Acute phase proteins in schizophrenia, mania and major depression: modulation by psychotropic drugs

Recently, an acute phase (AP) protein response has been reported in major depression. In order to examine whether an AP response occurs in other psychiatric disorders, such as schizophrenia and mania, the authors measured plasma AP reactants, such as haptoglobin (Hp), immunoglobulin G (IgG), IgM, fi...

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Veröffentlicht in:Psychiatry research 1997-01, Vol.66 (1), p.1-11
Hauptverfasser: Maes, Michael, Delange, Joris, Ranjan, Rakesch, Meltzer, Herbert Y., Desnyder, Roger, Cooremans, Walter, Scharpé, Simon
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container_end_page 11
container_issue 1
container_start_page 1
container_title Psychiatry research
container_volume 66
creator Maes, Michael
Delange, Joris
Ranjan, Rakesch
Meltzer, Herbert Y.
Desnyder, Roger
Cooremans, Walter
Scharpé, Simon
description Recently, an acute phase (AP) protein response has been reported in major depression. In order to examine whether an AP response occurs in other psychiatric disorders, such as schizophrenia and mania, the authors measured plasma AP reactants, such as haptoglobin (Hp), immunoglobulin G (IgG), IgM, fibrinogen (Fb), complement component 3 (C3C), C4, α 1-antitrypsin ( α 1AT), α 1-acid-glycoprotein ( α 1S) and hemopexin (Hpx), in 27 schizophrenic, 23 manic, 29 major depressed and 21 normal subjects. Schizophrenic patients had significantly higher plasma Hp, Fb, C3C, C4, α 1S and Hpx than normal controls. Manic subjects showed significantly higher plasma Hp, Fb, α 1S and Hpx than normal volunteers. Depressed subjects had significantly higher plasma Hp, Fb, C3C, C4 and α 1S than normal controls. Overall, the above disorders in AP reactants were more pronounced in schizophrenic than in depressed subjects. No significant differences in the above AP reactants could be found between normal volunteers, and schizophrenic, manic or depressed patients who underwent chronic treatment with psychotropic drugs. Plasma Hp, Fb, C3C, C4, α 1S, and Hpx were significantly higher in schizophrenic, manic and depressed patients who were non-medicated than in those who were treated with antidepressants, antipsychotics or lithium. The results suggest that not only major depression but also schizophrenia and mania are accompanied by an AP response, and that the latter may be suppressed by (sub)chronic treatment with psychotropic drugs.
doi_str_mv 10.1016/S0165-1781(96)02915-0
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In order to examine whether an AP response occurs in other psychiatric disorders, such as schizophrenia and mania, the authors measured plasma AP reactants, such as haptoglobin (Hp), immunoglobulin G (IgG), IgM, fibrinogen (Fb), complement component 3 (C3C), C4, α 1-antitrypsin ( α 1AT), α 1-acid-glycoprotein ( α 1S) and hemopexin (Hpx), in 27 schizophrenic, 23 manic, 29 major depressed and 21 normal subjects. Schizophrenic patients had significantly higher plasma Hp, Fb, C3C, C4, α 1S and Hpx than normal controls. Manic subjects showed significantly higher plasma Hp, Fb, α 1S and Hpx than normal volunteers. Depressed subjects had significantly higher plasma Hp, Fb, C3C, C4 and α 1S than normal controls. Overall, the above disorders in AP reactants were more pronounced in schizophrenic than in depressed subjects. No significant differences in the above AP reactants could be found between normal volunteers, and schizophrenic, manic or depressed patients who underwent chronic treatment with psychotropic drugs. Plasma Hp, Fb, C3C, C4, α 1S, and Hpx were significantly higher in schizophrenic, manic and depressed patients who were non-medicated than in those who were treated with antidepressants, antipsychotics or lithium. 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No significant differences in the above AP reactants could be found between normal volunteers, and schizophrenic, manic or depressed patients who underwent chronic treatment with psychotropic drugs. Plasma Hp, Fb, C3C, C4, α 1S, and Hpx were significantly higher in schizophrenic, manic and depressed patients who were non-medicated than in those who were treated with antidepressants, antipsychotics or lithium. The results suggest that not only major depression but also schizophrenia and mania are accompanied by an AP response, and that the latter may be suppressed by (sub)chronic treatment with psychotropic drugs.</description><subject>Acute phase response</subject><subject>Acute-Phase Proteins - analysis</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Biological and medical sciences</subject><subject>Bipolar Disorder - blood</subject><subject>Bipolar Disorder - drug therapy</subject><subject>Cytokines</subject><subject>Cytokines - biosynthesis</subject><subject>Depression</subject><subject>Depressive Disorder - blood</subject><subject>Depressive Disorder - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Immune disorders</subject><subject>Male</subject><subject>Mania</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Phenotype</subject><subject>Plasma - chemistry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Psychotropic Drugs - pharmacology</subject><subject>Psychotropic Drugs - therapeutic use</subject><subject>Schizophrenia</subject><subject>Schizophrenia - blood</subject><subject>Schizophrenia - drug therapy</subject><issn>0165-1781</issn><issn>1872-7123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEuLFDEQgIMo67j6ExZyEFGwNenOcy-yLL5gwYN6Dpmk2snS3WlT3cL4683sDHP1UlWkvqokHyFXnL3jjKv332uQDdeGv7bqDWstlw17RDbc6LbRvO0ek80ZeUqeId4zxlpu7QW5sExxbe2GhJuwLkDnnccaS14gTUjTRDHs0t887wpMyb-lo6-J-inW6j4XGmEugJjydE3HHNfBL7Wm2z2dcR92eSl5ToHGsv7C5-RJ7weEF6d8SX5--vjj9ktz9-3z19ubuyZIppemN8aLbRt0aCU3kQuwwEQQ3CjotBCqY5p1QqrW1HMpFSgrIrC2N7ZnUXSX5NVxb_3H7xVwcWPCAMPgJ8grOm2M5p1lFZRHMJSMWKB3c0mjL3vHmTvIdQ9y3cGcs8o9yHWHuavTBet2hHieOtms_Zenvsfgh774KSQ8Y620VmlZsQ9HDKqMPwmKw5BgChBTgbC4mNN_HvIPdFuWIw</recordid><startdate>19970115</startdate><enddate>19970115</enddate><creator>Maes, Michael</creator><creator>Delange, Joris</creator><creator>Ranjan, Rakesch</creator><creator>Meltzer, Herbert Y.</creator><creator>Desnyder, Roger</creator><creator>Cooremans, Walter</creator><creator>Scharpé, Simon</creator><general>Elsevier Ireland Ltd</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>19970115</creationdate><title>Acute phase proteins in schizophrenia, mania and major depression: modulation by psychotropic drugs</title><author>Maes, Michael ; Delange, Joris ; Ranjan, Rakesch ; Meltzer, Herbert Y. ; Desnyder, Roger ; Cooremans, Walter ; Scharpé, Simon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-f88a4b2c7c2518d14e9e04c4186e374463070345628e04556e694de02f89f0d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Acute phase response</topic><topic>Acute-Phase Proteins - analysis</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Biological and medical sciences</topic><topic>Bipolar Disorder - blood</topic><topic>Bipolar Disorder - drug therapy</topic><topic>Cytokines</topic><topic>Cytokines - biosynthesis</topic><topic>Depression</topic><topic>Depressive Disorder - blood</topic><topic>Depressive Disorder - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Immune disorders</topic><topic>Male</topic><topic>Mania</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Plasma - chemistry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Psychotropic Drugs - pharmacology</topic><topic>Psychotropic Drugs - therapeutic use</topic><topic>Schizophrenia</topic><topic>Schizophrenia - blood</topic><topic>Schizophrenia - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maes, Michael</creatorcontrib><creatorcontrib>Delange, Joris</creatorcontrib><creatorcontrib>Ranjan, Rakesch</creatorcontrib><creatorcontrib>Meltzer, Herbert Y.</creatorcontrib><creatorcontrib>Desnyder, Roger</creatorcontrib><creatorcontrib>Cooremans, Walter</creatorcontrib><creatorcontrib>Scharpé, Simon</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>Psychiatry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maes, Michael</au><au>Delange, Joris</au><au>Ranjan, Rakesch</au><au>Meltzer, Herbert Y.</au><au>Desnyder, Roger</au><au>Cooremans, Walter</au><au>Scharpé, Simon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute phase proteins in schizophrenia, mania and major depression: modulation by psychotropic drugs</atitle><jtitle>Psychiatry research</jtitle><addtitle>Psychiatry Res</addtitle><date>1997-01-15</date><risdate>1997</risdate><volume>66</volume><issue>1</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>0165-1781</issn><eissn>1872-7123</eissn><coden>PSRSDR</coden><abstract>Recently, an acute phase (AP) protein response has been reported in major depression. In order to examine whether an AP response occurs in other psychiatric disorders, such as schizophrenia and mania, the authors measured plasma AP reactants, such as haptoglobin (Hp), immunoglobulin G (IgG), IgM, fibrinogen (Fb), complement component 3 (C3C), C4, α 1-antitrypsin ( α 1AT), α 1-acid-glycoprotein ( α 1S) and hemopexin (Hpx), in 27 schizophrenic, 23 manic, 29 major depressed and 21 normal subjects. Schizophrenic patients had significantly higher plasma Hp, Fb, C3C, C4, α 1S and Hpx than normal controls. Manic subjects showed significantly higher plasma Hp, Fb, α 1S and Hpx than normal volunteers. Depressed subjects had significantly higher plasma Hp, Fb, C3C, C4 and α 1S than normal controls. Overall, the above disorders in AP reactants were more pronounced in schizophrenic than in depressed subjects. No significant differences in the above AP reactants could be found between normal volunteers, and schizophrenic, manic or depressed patients who underwent chronic treatment with psychotropic drugs. Plasma Hp, Fb, C3C, C4, α 1S, and Hpx were significantly higher in schizophrenic, manic and depressed patients who were non-medicated than in those who were treated with antidepressants, antipsychotics or lithium. The results suggest that not only major depression but also schizophrenia and mania are accompanied by an AP response, and that the latter may be suppressed by (sub)chronic treatment with psychotropic drugs.</abstract><cop>Shannon</cop><pub>Elsevier Ireland Ltd</pub><pmid>9061799</pmid><doi>10.1016/S0165-1781(96)02915-0</doi><tpages>11</tpages></addata></record>
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subjects Acute phase response
Acute-Phase Proteins - analysis
Adult
Adult and adolescent clinical studies
Biological and medical sciences
Bipolar Disorder - blood
Bipolar Disorder - drug therapy
Cytokines
Cytokines - biosynthesis
Depression
Depressive Disorder - blood
Depressive Disorder - drug therapy
Female
Humans
Immune disorders
Male
Mania
Medical sciences
Middle Aged
Phenotype
Plasma - chemistry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychoses
Psychotropic Drugs - pharmacology
Psychotropic Drugs - therapeutic use
Schizophrenia
Schizophrenia - blood
Schizophrenia - drug therapy
title Acute phase proteins in schizophrenia, mania and major depression: modulation by psychotropic drugs
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