精神分裂症患者外周血单个核细胞NLRP3炎性体表达增加:一项病例对照研究

Gulin Ozdamar Unal, Kuyas Hekimler Ozturk, Huseyin Emre Inci
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引用次数: 2

摘要

目的:研究P2X嘌呤受体7 (P2X7R)-节点样受体pyrin结构域蛋白3 (NLRP3)信号通路在精神分裂症(SCZ)患者和健康对照(HC)外周血单个核细胞(PBMCs)中的基因表达,揭示其与临床变量的关系。方法:选取32例SCZ患者和41例健康对照。采用阳性症状评估量表(SAPS)和阴性症状评估量表(SANS)、整体功能评估量表(GAF)和功能评估短测试量表(FAST)。实时聚合酶链反应检测pmcs中P2X7R、NLRP3、IL-1β和IL-18基因的表达水平。结果:SCZ患者外周血NLRP3、P2RX7、IL-1β和IL-18的表达水平明显高于HC组。NLRP3基因表达水平与GAF和FAST评分呈负相关。IL-18表达水平与GAF、FAST评分呈负相关,与SAPS评分呈正相关。结论:根据我们的研究结果,全身性炎症参与了SCZ的发病机制,这表明NLRP3通路可能参与其中。NLRP3炎性小体可能作为SCZ的生物标志物,其药理调控可能是一种有前景的治疗方法。我们假设NLRP3通路可能参与精神分裂症的发病机制。精神分裂症患者NLRP3、IL-1β和IL-18 mRNA水平高于健康对照组。NLRP3基因表达水平与GAF和FAST评分呈负相关。IL-18表达水平与GAF、FAST评分呈负相关。SAPS评分与IL-18表达水平呈正相关。综上所述,NLRP3炎性体可能在精神分裂症的发病机制和症状中发挥作用。
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Increased NLRP3 inflammasome expression in peripheral blood mononuclear cells of patients with schizophrenia: a case-control study.

Objective: This study aimed to evaluate the gene expression of the P2X purinoceptor 7 (P2X7R)- nod-like receptor pyrin domain-containing protein 3 (NLRP3) signal pathway in peripheral blood mononuclear cells (PBMCs) between schizophrenia (SCZ) patients and healthy controls (HC) to reveal its relationship with clinical variables.

Methods: Thirty-two SCZ patients and 41 healthy controls were included in this study. The Scale for the Assessment of Positive Symptoms (SAPS) and the Scale for the Assessment of Negative Symptoms (SANS), The Global Assessment of Functioning (GAF) scale and the Functioning Assessment Short Test (FAST) scales were applied. P2X7R, NLRP3, IL-1β and IL-18 gene expression levels were evaluated by real-time polymerase chain reaction in PBMCs.

Results: NLRP3, P2RX7, IL-1β and IL-18 expression levels were significantly higher in PBMCs of SCZ patients than in HC subjects. Negative correlations were found between NLRP3 gene expression levels and GAF and FAST scales scores. There was a negative correlation between IL-18 expression levels and the GAF and FAST scales scores and a positive correlation with the SAPS scale scores.

Conclusions: Systemic inflammation is implicated in SCZ pathogenesis, according to our findings, which suggest that the NLRP3 pathway may be involved. The NLRP3 inflammasome may serve as a biomarker for SCZ, and its pharmacological regulation may be a promising treatment approach.Key pointsWe hypothesised that the NLRP3 pathway may contribute to the etiopathogenesis of schizophrenia.NLRP3, IL-1β and IL-18 mRNA levels were higher in patients with schizophrenia compared to healthy controls.Negative correlations were found between NLRP3 gene expression levels and GAF and FAST scales scores.There was a negative correlation between IL-18 expression levels and the GAF and FAST scales scores.The SAPS scale scores and IL-18 expression levels had a positive correlation.Given all these findings, it can be stated that NLRP3 inflammasome may play a role in the pathogenesis and symptoms of schizophrenia.

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来源期刊
CiteScore
6.00
自引率
3.30%
发文量
42
审稿时长
>12 weeks
期刊介绍: International Journal of Psychiatry in Clinical Practice provides an international forum for communication among health professionals with clinical, academic and research interests in psychiatry. The journal gives particular emphasis to papers that integrate the findings of academic research into realities of clinical practice. Focus on the practical aspects of managing and treating patients. Essential reading for the busy psychiatrist, trainee and interested physician. Includes original research papers, comprehensive review articles and short communications. Key words: Psychiatry, Neuropsychopharmacology, Mental health, Neuropsychiatry, Clinical Neurophysiology, Psychophysiology, Psychotherapy, Addiction, Schizophrenia, Depression, Bipolar Disorders and Anxiety.
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