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未经治疗和用药的精神分裂症患者中长链非编码 RNA 的表达模式。

Expression pattern of long non-coding RNAs in treatment-naïve and medicated schizophrenia patients.

机构信息

Student Research Committee, School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Sci Rep. 2024 Nov 12;14(1):27654. doi: 10.1038/s41598-024-78220-w.

DOI:10.1038/s41598-024-78220-w
PMID:39532914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11557838/
Abstract

Schizophrenia is a disabling mental disorder that affects 1% of people over their lifetime. The etiology and mechanism of schizophrenia are very complex, and many genes are involved in many different signaling pathways in the etiology of this disease. According to recent studies, one of the important mechanisms altered in this disorder is the regulation of immune system and the inflammation mechanism. In the present study, we evaluated the peripheral blood expression pattern of four lncRNAs and three protein-coding genes in the treatment- naïve patients, and medicated patients compared with sex and age-matched controls. In the medicated-patients, expression levels of IFNG, IL18RAP, AC007278.2 were significantly up-regulated (P < 0.05); and the expression level of IFNG-AS1-001 was significantly down-regulated compared to healthy controls (P < 0.05). However, levels of IL18R1, AC007278.3 and IFNG-AS1-003 were not different between these groups. In the treatment-naïve patients, IFNG, IL18R1, IL18RAP, IFNG-AS1-001, AC007278.2, and AC007278.3 were significantly up-regulated compared to controls. On the other hand, IFNG-AS1-003 was significantly down-regulated in the treatment-naïve patients compared to controls. Based on the Spearman correlation matrix, there was a significant correlation between genes in the treatment-naïve patients. We also showed the high sensitivity and specificity of IFNG-AS1-003, IFNG, IL18R1, and AC007278.3 in the identification of treatment-naïve patients from controls. The current study contributes further evidence to the understanding of the role of lncRNAs in the pathogenesis of schizophrenia. Future research is necessary to establish the validity of lncRNAs as peripheral markers for this condition.

摘要

精神分裂症是一种使人丧失能力的精神障碍,影响人们一生的 1%。精神分裂症的病因和发病机制非常复杂,许多基因参与了这种疾病发病的许多不同信号通路。根据最近的研究,这种疾病改变的一个重要机制是免疫系统的调节和炎症机制。在本研究中,我们评估了未经治疗和经药物治疗的患者与性别和年龄匹配的对照组之间的外周血中四个 lncRNA 和三个蛋白质编码基因的表达模式。在用药患者中,IFNG、IL18RAP 和 AC007278.2 的表达水平显著上调(P<0.05);与健康对照组相比,IFNG-AS1-001 的表达水平显著下调(P<0.05)。然而,IL18R1、AC007278.3 和 IFNG-AS1-003 的水平在这些组之间没有差异。在未经治疗的患者中,IFNG、IL18R1、IL18RAP、IFNG-AS1-001、AC007278.2 和 AC007278.3 的表达水平与对照组相比显著上调。另一方面,IFNG-AS1-003 在未经治疗的患者中与对照组相比显著下调。基于 Spearman 相关矩阵,在未经治疗的患者中基因之间存在显著相关性。我们还显示了 IFNG-AS1-003、IFNG、IL18R1 和 AC007278.3 在识别未经治疗的患者与对照组方面具有高灵敏度和特异性。本研究进一步证明了 lncRNA 在精神分裂症发病机制中的作用。未来的研究有必要建立 lncRNA 作为该疾病外周标志物的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/1dd012a0650a/41598_2024_78220_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/b0e823d07a5d/41598_2024_78220_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/b48f12191e33/41598_2024_78220_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/1dd012a0650a/41598_2024_78220_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/6a6f980bfa6f/41598_2024_78220_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/4438fd582ef3/41598_2024_78220_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/dad50d6acc3d/41598_2024_78220_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/0af11524a338/41598_2024_78220_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/b0e823d07a5d/41598_2024_78220_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/b48f12191e33/41598_2024_78220_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3632/11557838/1dd012a0650a/41598_2024_78220_Fig7_HTML.jpg

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