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

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
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
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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. 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引用次数: 0

摘要

背景:越来越多的证据表明,炎性细胞因子白细胞介素-6(IL-6)是精神障碍的病理生理学因素之一。目的:研究血清 IL-6 浓度与早发型精神分裂症(EOS)临床特征之间的关系:我们测量了74名慢性精神分裂症患者的血清IL-6水平,其中包括33名发病年龄小于21岁的患者(EOS组)和41名发病年龄大于21岁的患者(成人型精神分裂症(AOS)组),以及41名健康对照者。用阳性和阴性综合征量表(PANSS)评估症状的严重程度: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),但在控制了年龄、体重指数和其他协变量后,EOS组和AOS组之间没有显著差异(P > 0.05)。EOS 组的负面症状评分高于 AOS 组(F = 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)和逃避/社会性子分数(r = -0.387,P = 0.026)呈负相关:结论:在慢性期,EOS 患者的阴性症状可能比成年型精神分裂症患者更严重。IL-6信号传导可能会调节早发型慢性精神分裂症患者的阴性症状及其逃避/社会性亚症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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CiteScore
7.20
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