Increased serum interleukin-6 levels in early stages of psychosis: Associations with at-risk mental states and the severity of psychotic symptoms
Summary Schizophrenia patients experience activated inflammatory responses, but little is known about the presence of such inflammatory processes at or prior to disease onset. We measured interleukin-6 (IL-6) and C-reactive protein (CRP) serum levels and plasma fibrinogen in 17 at-risk mental state...
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description | Summary Schizophrenia patients experience activated inflammatory responses, but little is known about the presence of such inflammatory processes at or prior to disease onset. We measured interleukin-6 (IL-6) and C-reactive protein (CRP) serum levels and plasma fibrinogen in 17 at-risk mental state (ARMS) subjects, 77 patients with psychotic disorder (PD) and 25 healthy control subjects (HC). ARMS subjects were followed-up, and transition to psychosis was registered. IL6 rs1800795 SNP was genotyped, as IL-6 levels may be influenced by this genetic variant. We did not observe significant differences in the IL6 rs1800795 SNP genotype frequencies between the groups. ARMS subjects exhibited significantly higher IL-6 levels than did controls ( p = 0.019). In subjects not taking cannabis, we found that patients diagnosed with ARMS or PD exhibited increased IL-6 levels when compared with HC ( p = 0.004). In both ARMS and PD subjects, IL-6 levels were positively associated with negative symptoms. However, with respect to positive psychotic symptoms, a different relationship was observed in the ARMS and PD groups (positive relationship in ARMS; negative relationship in PD). These findings could not be attributed to confounding variables, including gender, body mass index (BMI), tobacco consumption or the rs1800795 genotype. Six of 17 ARMS subjects (35%) exhibited a transition to psychosis during the follow-up period of 26 months. ARMS subjects who developed psychosis exhibited increased median IL-6 levels compared with those who did not transition (0.61 vs. 0.35 pg/mL). However, this difference was not statistically significant, which could be explained by a lack of statistical power due to the small sample size. Our results suggest that IL-6 may be a biomarker for early psychotic symptoms; however, further studies in larger samples are needed to confirm this result. |
doi_str_mv | 10.1016/j.psyneuen.2013.12.005 |
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We measured interleukin-6 (IL-6) and C-reactive protein (CRP) serum levels and plasma fibrinogen in 17 at-risk mental state (ARMS) subjects, 77 patients with psychotic disorder (PD) and 25 healthy control subjects (HC). ARMS subjects were followed-up, and transition to psychosis was registered. IL6 rs1800795 SNP was genotyped, as IL-6 levels may be influenced by this genetic variant. We did not observe significant differences in the IL6 rs1800795 SNP genotype frequencies between the groups. ARMS subjects exhibited significantly higher IL-6 levels than did controls ( p = 0.019). In subjects not taking cannabis, we found that patients diagnosed with ARMS or PD exhibited increased IL-6 levels when compared with HC ( p = 0.004). In both ARMS and PD subjects, IL-6 levels were positively associated with negative symptoms. However, with respect to positive psychotic symptoms, a different relationship was observed in the ARMS and PD groups (positive relationship in ARMS; negative relationship in PD). These findings could not be attributed to confounding variables, including gender, body mass index (BMI), tobacco consumption or the rs1800795 genotype. Six of 17 ARMS subjects (35%) exhibited a transition to psychosis during the follow-up period of 26 months. ARMS subjects who developed psychosis exhibited increased median IL-6 levels compared with those who did not transition (0.61 vs. 0.35 pg/mL). However, this difference was not statistically significant, which could be explained by a lack of statistical power due to the small sample size. Our results suggest that IL-6 may be a biomarker for early psychotic symptoms; however, further studies in larger samples are needed to confirm this result.</description><identifier>ISSN: 0306-4530</identifier><identifier>EISSN: 1873-3360</identifier><identifier>DOI: 10.1016/j.psyneuen.2013.12.005</identifier><identifier>PMID: 24495605</identifier><identifier>CODEN: PSYCDE</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Adult and adolescent clinical studies ; At-risk mental state (ARMS) ; Behavioral psychophysiology ; Biological and medical sciences ; Biomarkers - blood ; Biomarkers - metabolism ; C-reactive protein (CRP) ; C-Reactive Protein - metabolism ; Case-Control Studies ; Early Diagnosis ; Early psychosis ; Endocrinology & Metabolism ; Female ; Fibrinogen - metabolism ; Fundamental and applied biological sciences. Psychology ; Hormones and behavior ; Humans ; IL-6 ; Inflammation ; Interleukin-6 - blood ; Interleukin-6 - genetics ; Male ; Medical sciences ; Mental Disorders - blood ; Mental Disorders - complications ; Mental Disorders - microbiology ; Mental Disorders - psychology ; Polymorphism, Single Nucleotide ; Prodromal Symptoms ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychology. Psychophysiology ; Psychopathology. Psychiatry ; Psychoses ; Psychotic Disorders - blood ; Psychotic Disorders - complications ; Psychotic Disorders - metabolism ; Psychotic Disorders - psychology ; rs1800795 ; Schizophrenia ; Severity of Illness Index ; Young Adult</subject><ispartof>Psychoneuroendocrinology, 2014-03, Vol.41, p.23-32</ispartof><rights>Elsevier Ltd</rights><rights>2013 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2013 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-9c7b6f242b88124ecf585206daaa6a9a42b6a7798799f4129bdd815ab74e25a23</citedby><cites>FETCH-LOGICAL-c486t-9c7b6f242b88124ecf585206daaa6a9a42b6a7798799f4129bdd815ab74e25a23</cites><orcidid>0000-0003-2214-1886</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.psyneuen.2013.12.005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28373597$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24495605$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stojanovic, Alexander</creatorcontrib><creatorcontrib>Martorell, Lourdes</creatorcontrib><creatorcontrib>Montalvo, Itziar</creatorcontrib><creatorcontrib>Ortega, Laura</creatorcontrib><creatorcontrib>Monseny, Rosa</creatorcontrib><creatorcontrib>Vilella, Elisabet</creatorcontrib><creatorcontrib>Labad, Javier</creatorcontrib><title>Increased serum interleukin-6 levels in early stages of psychosis: Associations with at-risk mental states and the severity of psychotic symptoms</title><title>Psychoneuroendocrinology</title><addtitle>Psychoneuroendocrinology</addtitle><description>Summary Schizophrenia patients experience activated inflammatory responses, but little is known about the presence of such inflammatory processes at or prior to disease onset. We measured interleukin-6 (IL-6) and C-reactive protein (CRP) serum levels and plasma fibrinogen in 17 at-risk mental state (ARMS) subjects, 77 patients with psychotic disorder (PD) and 25 healthy control subjects (HC). ARMS subjects were followed-up, and transition to psychosis was registered. IL6 rs1800795 SNP was genotyped, as IL-6 levels may be influenced by this genetic variant. We did not observe significant differences in the IL6 rs1800795 SNP genotype frequencies between the groups. ARMS subjects exhibited significantly higher IL-6 levels than did controls ( p = 0.019). In subjects not taking cannabis, we found that patients diagnosed with ARMS or PD exhibited increased IL-6 levels when compared with HC ( p = 0.004). In both ARMS and PD subjects, IL-6 levels were positively associated with negative symptoms. However, with respect to positive psychotic symptoms, a different relationship was observed in the ARMS and PD groups (positive relationship in ARMS; negative relationship in PD). These findings could not be attributed to confounding variables, including gender, body mass index (BMI), tobacco consumption or the rs1800795 genotype. Six of 17 ARMS subjects (35%) exhibited a transition to psychosis during the follow-up period of 26 months. ARMS subjects who developed psychosis exhibited increased median IL-6 levels compared with those who did not transition (0.61 vs. 0.35 pg/mL). However, this difference was not statistically significant, which could be explained by a lack of statistical power due to the small sample size. Our results suggest that IL-6 may be a biomarker for early psychotic symptoms; however, further studies in larger samples are needed to confirm this result.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>At-risk mental state (ARMS)</subject><subject>Behavioral psychophysiology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - metabolism</subject><subject>C-reactive protein (CRP)</subject><subject>C-Reactive Protein - metabolism</subject><subject>Case-Control Studies</subject><subject>Early Diagnosis</subject><subject>Early psychosis</subject><subject>Endocrinology & Metabolism</subject><subject>Female</subject><subject>Fibrinogen - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormones and behavior</subject><subject>Humans</subject><subject>IL-6</subject><subject>Inflammation</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-6 - genetics</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mental Disorders - blood</subject><subject>Mental Disorders - complications</subject><subject>Mental Disorders - microbiology</subject><subject>Mental Disorders - psychology</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Prodromal Symptoms</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Psychotic Disorders - blood</subject><subject>Psychotic Disorders - complications</subject><subject>Psychotic Disorders - metabolism</subject><subject>Psychotic Disorders - psychology</subject><subject>rs1800795</subject><subject>Schizophrenia</subject><subject>Severity of Illness Index</subject><subject>Young Adult</subject><issn>0306-4530</issn><issn>1873-3360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkstu1DAUhiMEokPhFSpvkNgk-BYnYYGoKi6VKrEA1pbjnDCeSZzBxxmUx-CNcTRTKrHpypL9_ee3_DnLrhgtGGXq7a444OJhBl9wykTBeEFp-STbsLoSuRCKPs02VFCVy1LQi-wF4o5SqmrFn2cXXMqmVLTcZH9uvQ1gEDqCEOaROB8hDDDvnc8VGeAIA6ZNAiYMC8FofgKSqSep3m4ndPiOXCNO1pnoJo_kt4tbYmIeHO7JCD6aYU3FlDK-I3ELqegIwcXlYUx0luAyHuI04svsWW8GhFfn9TL78enj95sv-d3Xz7c313e5lbWKeWOrVvVc8rauGZdg-7IuOVWdMUaZxqQDZaqqqaum6SXjTdt1NStNW0ngpeHiMntzmnsI068ZMOrRoYVhMB6mGTUrmarSG0n5OCqbhjHFqEioOqE2TIgBen0IbjRh0Yzq1Zze6XtzejWnGdfJXApenTvmdoTuX-xeVQJenwGD1gx9MN46fOBqUYmyqRL34cQlcXB0EDRaB95C5wLYqLvJPX6X9_-NsIPzLrXuYQHcTXPwSY1mGlNAf1v_2frNmKBUSsbEX-rf0gQ</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Stojanovic, Alexander</creator><creator>Martorell, Lourdes</creator><creator>Montalvo, Itziar</creator><creator>Ortega, Laura</creator><creator>Monseny, Rosa</creator><creator>Vilella, Elisabet</creator><creator>Labad, Javier</creator><general>Elsevier 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><scope>7TK</scope><orcidid>https://orcid.org/0000-0003-2214-1886</orcidid></search><sort><creationdate>20140301</creationdate><title>Increased serum interleukin-6 levels in early stages of psychosis: Associations with at-risk mental states and the severity of psychotic symptoms</title><author>Stojanovic, Alexander ; Martorell, Lourdes ; Montalvo, Itziar ; Ortega, Laura ; Monseny, Rosa ; Vilella, Elisabet ; Labad, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-9c7b6f242b88124ecf585206daaa6a9a42b6a7798799f4129bdd815ab74e25a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>At-risk mental state (ARMS)</topic><topic>Behavioral psychophysiology</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - metabolism</topic><topic>C-reactive protein (CRP)</topic><topic>C-Reactive Protein - metabolism</topic><topic>Case-Control Studies</topic><topic>Early Diagnosis</topic><topic>Early psychosis</topic><topic>Endocrinology & Metabolism</topic><topic>Female</topic><topic>Fibrinogen - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormones and behavior</topic><topic>Humans</topic><topic>IL-6</topic><topic>Inflammation</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-6 - genetics</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mental Disorders - blood</topic><topic>Mental Disorders - complications</topic><topic>Mental Disorders - microbiology</topic><topic>Mental Disorders - psychology</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Prodromal Symptoms</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Psychotic Disorders - blood</topic><topic>Psychotic Disorders - complications</topic><topic>Psychotic Disorders - metabolism</topic><topic>Psychotic Disorders - psychology</topic><topic>rs1800795</topic><topic>Schizophrenia</topic><topic>Severity of Illness Index</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stojanovic, Alexander</creatorcontrib><creatorcontrib>Martorell, Lourdes</creatorcontrib><creatorcontrib>Montalvo, Itziar</creatorcontrib><creatorcontrib>Ortega, Laura</creatorcontrib><creatorcontrib>Monseny, Rosa</creatorcontrib><creatorcontrib>Vilella, Elisabet</creatorcontrib><creatorcontrib>Labad, Javier</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><collection>Neurosciences Abstracts</collection><jtitle>Psychoneuroendocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stojanovic, Alexander</au><au>Martorell, Lourdes</au><au>Montalvo, Itziar</au><au>Ortega, Laura</au><au>Monseny, Rosa</au><au>Vilella, Elisabet</au><au>Labad, Javier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased serum interleukin-6 levels in early stages of psychosis: Associations with at-risk mental states and the severity of psychotic symptoms</atitle><jtitle>Psychoneuroendocrinology</jtitle><addtitle>Psychoneuroendocrinology</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>41</volume><spage>23</spage><epage>32</epage><pages>23-32</pages><issn>0306-4530</issn><eissn>1873-3360</eissn><coden>PSYCDE</coden><abstract>Summary Schizophrenia patients experience activated inflammatory responses, but little is known about the presence of such inflammatory processes at or prior to disease onset. We measured interleukin-6 (IL-6) and C-reactive protein (CRP) serum levels and plasma fibrinogen in 17 at-risk mental state (ARMS) subjects, 77 patients with psychotic disorder (PD) and 25 healthy control subjects (HC). ARMS subjects were followed-up, and transition to psychosis was registered. IL6 rs1800795 SNP was genotyped, as IL-6 levels may be influenced by this genetic variant. We did not observe significant differences in the IL6 rs1800795 SNP genotype frequencies between the groups. ARMS subjects exhibited significantly higher IL-6 levels than did controls ( p = 0.019). In subjects not taking cannabis, we found that patients diagnosed with ARMS or PD exhibited increased IL-6 levels when compared with HC ( p = 0.004). In both ARMS and PD subjects, IL-6 levels were positively associated with negative symptoms. However, with respect to positive psychotic symptoms, a different relationship was observed in the ARMS and PD groups (positive relationship in ARMS; negative relationship in PD). These findings could not be attributed to confounding variables, including gender, body mass index (BMI), tobacco consumption or the rs1800795 genotype. Six of 17 ARMS subjects (35%) exhibited a transition to psychosis during the follow-up period of 26 months. ARMS subjects who developed psychosis exhibited increased median IL-6 levels compared with those who did not transition (0.61 vs. 0.35 pg/mL). However, this difference was not statistically significant, which could be explained by a lack of statistical power due to the small sample size. Our results suggest that IL-6 may be a biomarker for early psychotic symptoms; however, further studies in larger samples are needed to confirm this result.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>24495605</pmid><doi>10.1016/j.psyneuen.2013.12.005</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2214-1886</orcidid></addata></record> |
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subjects | Adolescent Adult Adult and adolescent clinical studies At-risk mental state (ARMS) Behavioral psychophysiology Biological and medical sciences Biomarkers - blood Biomarkers - metabolism C-reactive protein (CRP) C-Reactive Protein - metabolism Case-Control Studies Early Diagnosis Early psychosis Endocrinology & Metabolism Female Fibrinogen - metabolism Fundamental and applied biological sciences. Psychology Hormones and behavior Humans IL-6 Inflammation Interleukin-6 - blood Interleukin-6 - genetics Male Medical sciences Mental Disorders - blood Mental Disorders - complications Mental Disorders - microbiology Mental Disorders - psychology Polymorphism, Single Nucleotide Prodromal Symptoms Psychiatry Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Psychopathology. Psychiatry Psychoses Psychotic Disorders - blood Psychotic Disorders - complications Psychotic Disorders - metabolism Psychotic Disorders - psychology rs1800795 Schizophrenia Severity of Illness Index Young Adult |
title | Increased serum interleukin-6 levels in early stages of psychosis: Associations with at-risk mental states and the severity of psychotic symptoms |
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