Chen Peng, Yang Hai-Dong, Wang Jun-Jie, Zhu Zhen-Hua, Zhao Hui-Min, Yin Xu-Yuan, Cai Yuan, Zhu Hong-Liang, Fu Jia-Lin, Zhang Xin-Zhu, Sun Wen-Xi, Hui Li, Zhang Xiao-Bin
Suzhou Medical College of Soochow University, Suzhou 215123, Jiangsu Province, China.
Department of Psychiatry, Suzhou Psychiatric Hospital, Institute of Mental Health, The Affiliated Guangji Hospital of Soochow University, Suzhou 215137, Jiangsu Province, China.
World J Psychiatry. 2024 Jun 19;14(6):794-803. doi: 10.5498/wjp.v14.i6.794.
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).
To investigate the relationship between serum IL-6 concentration and the clinical features of EOS.
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).
Serum IL-6 concentrations were higher in both EOS and AOS groups than healthy controls ( = 22.32, < 0.01), but did not differ significantly between EOS and AOS groups ( > 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 ( = 6.199, = 0.015). Serum IL-6 concentrations in the EOS group were negatively correlated with both total PANSS-negative symptom score ( = -0.389, = 0.032) and avolition/asociality subscore ( = -0.387, = 0.026).
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.
越来越多的证据表明,炎性细胞因子白细胞介素-6(IL-6)参与了精神疾病的病理生理过程。然而,尚无关于早发性精神分裂症(EOS)慢性期IL-6浓度与临床特征之间关系的研究。
探讨血清IL-6浓度与EOS临床特征之间的关系。
我们测定了74例慢性精神分裂症患者的血清IL-6水平,其中包括33例发病年龄<21岁的患者(EOS组)和41例发病年龄≥21岁的患者[成人发病型精神分裂症(AOS)组],以及41名健康对照者。使用阳性和阴性症状量表(PANSS)评估症状严重程度。
EOS组和AOS组的血清IL-6浓度均高于健康对照组(F = 22.32,P < 0.01),但在控制年龄、体重指数和其他协变量后,EOS组和AOS组之间无显著差异(P > 0.05)。EOS组的阴性症状评分高于AOS组(t = 6.199,P = 0.015)。EOS组的血清IL-6浓度与PANSS阴性症状总分(r = -0.389,P = 0.032)和意志缺乏/社交退缩子评分(r = -0.387,P = 0.026)均呈负相关。
在疾病的慢性期,EOS患者可能比成人发病型精神分裂症患者有更严重的阴性症状。IL-6信号通路可能调节早发性慢性精神分裂症患者的阴性症状及其意志缺乏/社交退缩子症状。