精神分裂症患者的白细胞介素-5、嗜酸性粒细胞和免疫球蛋白A水平

IF 3.5 Q3 PSYCHIATRY
Alpha psychiatry Pub Date : 2025-08-26 eCollection Date: 2025-08-01 DOI:10.31083/AP46059
Xi Li, Xiaoyu Wang, Qianqian Zhou, Qiushan Zhang, Shujuan Pan
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引用次数: 0

摘要

目的:分析白细胞介素-5 (IL-5)、嗜酸性粒细胞(EOS)、免疫球蛋白A (IgA)水平与精神分裂症的相关性,探讨其作为精神分裂症辅助诊断指标的潜力。方法:选取2023年3月至2024年8月在北京回龙观医院住院的57例首发精神分裂症患者和340例复发性或慢性精神分裂症患者,并招募72名健康志愿者作为对照组。入院后第2天采集所有受试者的空腹静脉血。对于首发精神分裂症患者,治疗两个月后进行第二次抽血。同时采用阳性和阴性症状量表(PANSS)对受试者进行评估。流式细胞术检测IL-5、EOS水平;免疫比浊法测定IgA水平。采用SPSS v.29.0进行t检验、单因素方差分析、相关分析和受试者工作特征(ROC)曲线分析。结果:首发精神分裂症组和复发/慢性精神分裂症组IL-5水平高于健康对照组;然而,EOS水平的增加在复发/慢性精神分裂症组中被特别观察到。治疗后,首发组IL-5水平明显降低。相关分析显示,在精神分裂症患者中,IL-5水平与EOS呈正相关(r = 0.338, p < 0.001), EOS水平与病程呈正相关(r = 0.171, p < 0.05), ROC曲线分析显示,IL-5预测精神分裂症的敏感性为52.9%,特异性为69.4%,临界值为2.445 pg/mL。结论:在精神分裂症患者中,IL-5和EOS水平升高似乎与疾病相关,而非药物诱导,提示它们可能参与精神分裂症的炎症发病机制。此外,与EOS相比,IL-5对精神分裂症的预测准确性更高,这表明IL-5可能作为精神分裂症辅助诊断和分层分析的有价值的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interleukin-5, Eosinophil, and Immunoglobulin A Levels in Schizophrenia Patients.

Interleukin-5, Eosinophil, and Immunoglobulin A Levels in Schizophrenia Patients.

Objective: To analyze the correlation between interleukin-5 (IL-5), eosinophils (EOS), and immunoglobulin A (IgA) levels with schizophrenia, and assess their potential as auxiliary diagnostic markers for schizophrenia.

Methods: This study comprised 57 patients with first-episode schizophrenia and 340 patients with recurrent or chronic schizophrenia who were hospitalized at Beijing Huilongguan Hospital from March 2023 to August 2024, and 72 healthy volunteers were recruited as the control group. Fasting venous blood samples were collected from all participants on the second day after admission. For patients with first-episode schizophrenia, a second blood draw was performed after two months of treatment. Simultaneously, the Positive and Negative Symptom Scale (PANSS) was administered to assess the subjects. IL-5 and EOS levels were measured using flow cytometry; IgA levels were measured using immunoturbidimetry. SPSS v.29.0 was used to conduct t-tests, one-way ANOVA, correlation analysis and receiver operating characteristic (ROC) curve analysis.

Results: The first-episode schizophrenia group and the recurrent/chronic schizophrenia group had elevated IL-5 levels relative to healthy controls; however, the increase in EOS levels was specifically observed in the recurrent/chronic schizophrenia group. After treatment, the IL-5 level in the first-episode group was markedly reduced. Correlation analysis revealed that in patients with schizophrenia, IL-5 levels were positively correlated with EOS (r = 0.338, p < 0.001), and EOS levels were positively associated with disease duration (r = 0.171, p < 0.05), the ROC curve analysis revealed that IL-5 had a sensitivity of 52.9%, specificity of 69.4%, and a cut-off value of 2.445 pg/mL for predicting schizophrenia.

Conclusion: In patients with schizophrenia, the elevated levels of IL-5 and EOS appear to be disease-related rather than medication-induced, suggesting their potential involvement in the inflammatory pathogenesis of schizophrenia. Furthermore, IL-5 exhibits greater predictive accuracy for schizophrenia compared to EOS, suggesting that IL-5 may serve as a valuable biomarker for auxiliary diagnosis and stratification analysis in schizophrenia.

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