Cytokine profile among a sample of bipolar and schizophrenic patients: a comparative study

Shaimaa Arafa, Shaimaa Abdelhafeez
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引用次数: 2

Abstract

Background Bipolar disorder (BD) and schizophrenia are serious forms of mental illness which are considered to be complex and multisystemic conditions. Several lines of evidence point to the key role of immune dysfunction in both disorders, with recent reports citing abnormal blood levels of cytokines where the most obvious mechanism is a dysregulation of the balance of proinflammatory and anti-inflammatory cytokines. Objective The aim was to explore the presence of immune dysfunction in BD in comparison with schizophrenia and to compare them to apparently healthy control persons. Participants and methods This study was a cross-sectional study on 90 individuals (30 diagnosed as BD, 30 as schizophrenic, and 30 apparently healthy controls). Age matched and sex matched. They were assessed by general medical and neurological examination. Semistructured clinical interview for DSM-IV (SCIDI), positive and negative schizophrenia scale (PANSS) for the schizophrenia group, Yearsania rating scale (YMRS) for the bipolar group, and laboratory investigations include: serum interleukin (IL)1B level and serum IL6 level for the three groups. Result The mean serum IL1B level was found to be higher in the bipolar group than that of the control group and schizophrenia group .The mean serum IL1B level in the schizophrenia group was higher than that of the control group. The mean serum IL6 level was higher in the bipolar and schizophrenia groups than that of the control group. It was also found that serum IL1B showed a highly significant correlation with the duration of illness in the bipolar group, while serum IL6 showed a significance with the duration of illness in the bipolar and schizophrenia groups. In the bipolar group, significant correlation was found between IL6 and number of episodes, while in the schizophrenia group, a significant correlation was found between IL6 and age at onset of illness and number of episodes. Conclusion There is mounting evidence of increased immune markers, particularly proinflammatory cytokines in BD and schizophrenia patients. So, identifying the biomarkers could represent new tools which could help to improve diagnosis and find prognostic markers which offers great promises toward a better understanding of the etio-pathological mechanisms involved in BD and schizophrenia, and for the development of prevention and personalized treatments.
双相情感障碍和精神分裂症患者样本中的细胞因子谱:一项比较研究
双相情感障碍(BD)和精神分裂症是严重的精神疾病,被认为是复杂的多系统疾病。一些证据表明,免疫功能障碍在这两种疾病中都起着关键作用,最近的报道援引了血液中细胞因子水平的异常,其中最明显的机制是促炎和抗炎细胞因子平衡的失调。目的探讨双相障碍患者与精神分裂症患者是否存在免疫功能障碍,并将其与表面健康对照者进行比较。本研究是一项对90名个体(30名诊断为双相障碍,30名诊断为精神分裂症,30名表面健康对照)的横断面研究。年龄匹配,性别匹配。他们通过一般医学和神经学检查进行评估。DSM-IV (SCIDI)半结构化临床访谈,精神分裂症组阳性和阴性精神分裂症量表(PANSS),双相情感障碍组Yearsania评定量表(YMRS),实验室调查包括:三组血清白细胞介素(IL)1B水平和血清IL6水平。结果躁郁症患者血清IL1B水平高于对照组和精神分裂症患者,精神分裂症患者血清IL1B水平高于对照组。双相情感障碍组和精神分裂症组的平均血清IL6水平高于对照组。同时发现血清IL1B与双相情感障碍组病程高度显著相关,血清IL6与双相情感障碍组和精神分裂症组病程显著相关。在双相情感障碍组中,il - 6与发作次数显著相关,而在精神分裂症组中,il - 6与发病年龄和发作次数显著相关。结论越来越多的证据表明,双相障碍和精神分裂症患者的免疫标志物,特别是促炎细胞因子增加。因此,识别这些生物标志物可以作为一种新的工具,有助于提高诊断和发现预后标志物,从而更好地了解双相障碍和精神分裂症的病因病理机制,并为预防和个性化治疗的发展提供了巨大的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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