Qi Zhang , Li Li , Zheng Gao , Xue Li , Peng Zhang , Yujing Yang , Caiyi Zhang
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The results showed that the plasma IL-33 levels were elevated in SCZ-Ag compared with NSCZ-Ag and HCs, with no significant difference between NSCZ-Ag and HCs. In the patient group, partial correlation analysis indicated a positive correlation between IL-33 levels and PANSS total scores, positive symptom subscores, and MOAS total scores. Regression analysis showed that a higher likelihood of aggression in SCZ was associated with elevated plasma IL-33 levels (OR = 1.075, 95 % <em>CI</em>: 1.023–1.129). ROC curve analysis showed that IL-33 (AUC = 0.713, 95 % <em>CI</em>: 0.582–0.844) demonstrated moderate performance in distinguishing SCZ-Ag from NSCZ-Ag. These findings suggest that elevated plasma IL-33 levels are a potential risk factor for aggression in patients with SCZ and are implicated in the clinical symptoms of patients. Increased plasma IL-33 levels may serve as a potential marker for aggression in SCZ. These findings require further validation in future studies.</div></div>","PeriodicalId":16671,"journal":{"name":"Journal of neuroimmunology","volume":"406 ","pages":"Article 578680"},"PeriodicalIF":2.5000,"publicationDate":"2025-06-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of plasma IL-33 levels with aggression in schizophrenia: A clinical study\",\"authors\":\"Qi Zhang , Li Li , Zheng Gao , Xue Li , Peng Zhang , Yujing Yang , Caiyi Zhang\",\"doi\":\"10.1016/j.jneuroim.2025.578680\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Aggression in schizophrenia (SCZ) poses a serious risk to others and complicates treatment. Inflammation has been confirmed to be associated with aggression in SCZ, but specific biomarkers remain unidentified. This study aimed to measure plasma interleukin-33 (IL-33) levels and explore their association with aggression in SCZ for the first time. The enzyme-linked immunosorbent assay (ELISA) was used to measure the levels of IL-33 in SCZ with aggression (SCZ-Ag, <em>n</em> = 31) and non-aggression (NSCZ-Ag, <em>n</em> = 32), and healthy controls (HCs, <em>n</em> = 26). Aggression was measured using the Modified Overt Aggression Scale (MOAS), and clinical symptoms were assessed with the Positive and Negative Syndrome Scale (PANSS). The results showed that the plasma IL-33 levels were elevated in SCZ-Ag compared with NSCZ-Ag and HCs, with no significant difference between NSCZ-Ag and HCs. In the patient group, partial correlation analysis indicated a positive correlation between IL-33 levels and PANSS total scores, positive symptom subscores, and MOAS total scores. Regression analysis showed that a higher likelihood of aggression in SCZ was associated with elevated plasma IL-33 levels (OR = 1.075, 95 % <em>CI</em>: 1.023–1.129). ROC curve analysis showed that IL-33 (AUC = 0.713, 95 % <em>CI</em>: 0.582–0.844) demonstrated moderate performance in distinguishing SCZ-Ag from NSCZ-Ag. These findings suggest that elevated plasma IL-33 levels are a potential risk factor for aggression in patients with SCZ and are implicated in the clinical symptoms of patients. Increased plasma IL-33 levels may serve as a potential marker for aggression in SCZ. 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引用次数: 0
摘要
精神分裂症(SCZ)的攻击行为对他人构成严重威胁,并使治疗复杂化。炎症已被证实与SCZ的攻击性有关,但具体的生物标志物仍未确定。本研究旨在首次检测血浆白细胞介素-33 (IL-33)水平,探讨其与SCZ患者攻击行为的关系。采用酶联免疫吸附试验(ELISA)检测侵袭性(SCZ- ag, n = 31)、非侵袭性(NSCZ-Ag, n = 32)和健康对照(hc, n = 26)中IL-33的水平。采用改良外显攻击量表(MOAS)测量攻击行为,采用阳性和阴性症状量表(PANSS)评估临床症状。结果显示,SCZ-Ag组血浆IL-33水平较NSCZ-Ag组和hc组升高,但与hc组差异无统计学意义。在患者组中,偏相关分析显示IL-33水平与PANSS总分、阳性症状亚分、MOAS总分呈正相关。回归分析显示,SCZ患者较高的攻击倾向与血浆IL-33水平升高相关(OR = 1.075, 95% CI: 1.023-1.129)。ROC曲线分析显示,IL-33 (AUC = 0.713, 95% CI: 0.582-0.844)在区分SCZ-Ag和NSCZ-Ag方面表现中等。这些发现表明,血浆IL-33水平升高是SCZ患者攻击行为的潜在危险因素,并与患者的临床症状有关。血浆IL-33水平升高可能是SCZ侵袭的潜在标志。这些发现需要在未来的研究中进一步验证。
Association of plasma IL-33 levels with aggression in schizophrenia: A clinical study
Aggression in schizophrenia (SCZ) poses a serious risk to others and complicates treatment. Inflammation has been confirmed to be associated with aggression in SCZ, but specific biomarkers remain unidentified. This study aimed to measure plasma interleukin-33 (IL-33) levels and explore their association with aggression in SCZ for the first time. The enzyme-linked immunosorbent assay (ELISA) was used to measure the levels of IL-33 in SCZ with aggression (SCZ-Ag, n = 31) and non-aggression (NSCZ-Ag, n = 32), and healthy controls (HCs, n = 26). Aggression was measured using the Modified Overt Aggression Scale (MOAS), and clinical symptoms were assessed with the Positive and Negative Syndrome Scale (PANSS). The results showed that the plasma IL-33 levels were elevated in SCZ-Ag compared with NSCZ-Ag and HCs, with no significant difference between NSCZ-Ag and HCs. In the patient group, partial correlation analysis indicated a positive correlation between IL-33 levels and PANSS total scores, positive symptom subscores, and MOAS total scores. Regression analysis showed that a higher likelihood of aggression in SCZ was associated with elevated plasma IL-33 levels (OR = 1.075, 95 % CI: 1.023–1.129). ROC curve analysis showed that IL-33 (AUC = 0.713, 95 % CI: 0.582–0.844) demonstrated moderate performance in distinguishing SCZ-Ag from NSCZ-Ag. These findings suggest that elevated plasma IL-33 levels are a potential risk factor for aggression in patients with SCZ and are implicated in the clinical symptoms of patients. Increased plasma IL-33 levels may serve as a potential marker for aggression in SCZ. These findings require further validation in future studies.
期刊介绍:
The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication.