{"title":"早期稳定型精神分裂症患者血清白细胞介素-6与阴性症状的关系","authors":"Peng Chen, Hai-Dong Yang, Jun-Jie Wang, Zhen-Hua Zhu, Hui-Min Zhao, Xu-Yuan Yin, Yuan Cai, Hong-Liang Zhu, Jia-Lin Fu, Xin-Zhu Zhang, Wen-Xi Sun, Li Hui, Xiao-Bin Zhang","doi":"10.5498/wjp.v14.i6.794","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Accumulating evidence suggests that the inflammatory cytokine interleukin-6 (IL-6) contributes to the pathophysiology of psychiatric disorders. However, there was no study concerning the relationship between IL-6 concentrations and clinical features in the chronic phase of early-onset schizophrenia (EOS).</p><p><strong>Aim: </strong>To investigate the relationship between serum IL-6 concentration and the clinical features of EOS.</p><p><strong>Methods: </strong>We measured serum IL-6 Levels from 74 patients with chronic schizophrenia, including 33 with age at onset < 21 years (EOS group) and 41 with onset ≥ 21 years in [adult-onset schizophrenia (AOS) group], and from 41 healthy controls. Symptom severities were evaluated using the Positive and Negative Syndrome Scale (PANSS).</p><p><strong>Results: </strong>Serum IL-6 concentrations were higher in both EOS and AOS groups than healthy controls (<i>F</i> = 22.32, <i>P</i> < 0.01), but did not differ significantly between EOS and AOS groups (<i>P</i> > 0.05) after controlling for age, body mass index, and other covariates. Negative symptom scores were higher in the EOS group than the AOS group (<i>F</i> = 6.199, <i>P</i> = 0.015). Serum IL-6 concentrations in the EOS group were negatively correlated with both total PANSS-negative symptom score (<i>r</i> = -0.389, <i>P</i> = 0.032) and avolition/asociality subscore (<i>r</i> = -0.387, <i>P</i> = 0.026).</p><p><strong>Conclusion: </strong>Patients with EOS may have more severe negative symptoms than those with adult-onset schizophrenia during the chronic phase of the illness. IL-6 signaling may regulate negative symptoms and its avolition/asociality subsymptoms among the early-onset chronic schizophrenic patients.</p>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11230098/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of serum interleukin-6 with negative symptoms in stable early-onset schizophrenia.\",\"authors\":\"Peng Chen, Hai-Dong Yang, Jun-Jie Wang, Zhen-Hua Zhu, Hui-Min Zhao, Xu-Yuan Yin, Yuan Cai, Hong-Liang Zhu, Jia-Lin Fu, Xin-Zhu Zhang, Wen-Xi Sun, Li Hui, Xiao-Bin Zhang\",\"doi\":\"10.5498/wjp.v14.i6.794\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Accumulating evidence suggests that the inflammatory cytokine interleukin-6 (IL-6) contributes to the pathophysiology of psychiatric disorders. However, there was no study concerning the relationship between IL-6 concentrations and clinical features in the chronic phase of early-onset schizophrenia (EOS).</p><p><strong>Aim: </strong>To investigate the relationship between serum IL-6 concentration and the clinical features of EOS.</p><p><strong>Methods: </strong>We measured serum IL-6 Levels from 74 patients with chronic schizophrenia, including 33 with age at onset < 21 years (EOS group) and 41 with onset ≥ 21 years in [adult-onset schizophrenia (AOS) group], and from 41 healthy controls. Symptom severities were evaluated using the Positive and Negative Syndrome Scale (PANSS).</p><p><strong>Results: </strong>Serum IL-6 concentrations were higher in both EOS and AOS groups than healthy controls (<i>F</i> = 22.32, <i>P</i> < 0.01), but did not differ significantly between EOS and AOS groups (<i>P</i> > 0.05) after controlling for age, body mass index, and other covariates. Negative symptom scores were higher in the EOS group than the AOS group (<i>F</i> = 6.199, <i>P</i> = 0.015). Serum IL-6 concentrations in the EOS group were negatively correlated with both total PANSS-negative symptom score (<i>r</i> = -0.389, <i>P</i> = 0.032) and avolition/asociality subscore (<i>r</i> = -0.387, <i>P</i> = 0.026).</p><p><strong>Conclusion: </strong>Patients with EOS may have more severe negative symptoms than those with adult-onset schizophrenia during the chronic phase of the illness. IL-6 signaling may regulate negative symptoms and its avolition/asociality subsymptoms among the early-onset chronic schizophrenic patients.</p>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-06-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11230098/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.5498/wjp.v14.i6.794\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5498/wjp.v14.i6.794","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
Association of serum interleukin-6 with negative symptoms in stable early-onset schizophrenia.
Background: Accumulating evidence suggests that the inflammatory cytokine interleukin-6 (IL-6) contributes to the pathophysiology of psychiatric disorders. However, there was no study concerning the relationship between IL-6 concentrations and clinical features in the chronic phase of early-onset schizophrenia (EOS).
Aim: To investigate the relationship between serum IL-6 concentration and the clinical features of EOS.
Methods: We measured serum IL-6 Levels from 74 patients with chronic schizophrenia, including 33 with age at onset < 21 years (EOS group) and 41 with onset ≥ 21 years in [adult-onset schizophrenia (AOS) group], and from 41 healthy controls. Symptom severities were evaluated using the Positive and Negative Syndrome Scale (PANSS).
Results: Serum IL-6 concentrations were higher in both EOS and AOS groups than healthy controls (F = 22.32, P < 0.01), but did not differ significantly between EOS and AOS groups (P > 0.05) after controlling for age, body mass index, and other covariates. Negative symptom scores were higher in the EOS group than the AOS group (F = 6.199, P = 0.015). Serum IL-6 concentrations in the EOS group were negatively correlated with both total PANSS-negative symptom score (r = -0.389, P = 0.032) and avolition/asociality subscore (r = -0.387, P = 0.026).
Conclusion: Patients with EOS may have more severe negative symptoms than those with adult-onset schizophrenia during the chronic phase of the illness. IL-6 signaling may regulate negative symptoms and its avolition/asociality subsymptoms among the early-onset chronic schizophrenic patients.