Validation and Functional Exploration of Exosome-Derived ITGA9-AS1 and WNT5A-AS1 as Candidate Diagnostic Biomarkers for Schizophrenia.

IF 3.2 3区 医学 Q2 Medicine
Neuropsychiatric Disease and Treatment Pub Date : 2026-06-15 eCollection Date: 2026-01-01 DOI:10.2147/NDT.S600571
Yangyang Xu, Yan Wang, Fuyi Qin, Ling Yu, Weihao Li, Xu You, Li Guo, Yilin Liu, Yong Zeng
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引用次数: 0

Abstract

Objective: Schizophrenia lacks objective biomarkers, and its complex aetiology demands epigenetic insight. Given the regulatory roles of long non-coding RNAs (lncRNAs) in the nervous system and brain-relevant signals in peripheral exosomes, we evaluated lncRNA expression in patient blood cells and plasma exosomes, assessed their diagnostic value, and explored potential functions and mechanisms.

Methods: Differentially expressed lncRNAs in schizophrenia-related exosomes were identified from GEO (GSE228881), and 15 candidates were selected for validation. In a clinical cohort, RT-qPCR assessed their expression in peripheral blood cells and plasma exosomes. Diagnostic accuracy was evaluated by ROC analysis. Top dysregulated lncRNAs underwent bioinformatic analyses: subcellular localization, evolutionary conservation, ceRNA network construction, and GO/KEGG enrichment.

Results: ITGA9-AS1 and WNT5A-AS1 were significantly upregulated in both peripheral blood cells and plasma exosomes from patients. Both showed favorable diagnostic potential, with AUC values of 0.8422 and 0.8073, respectively, in peripheral blood; their combination yielded an AUC of 0.9180. Bioinformatics analysis revealed that ITGA9-AS1 primarily localizes to the cytoplasm, whereas WNT5A-AS1 is enriched in exosomes, with both exhibiting high evolutionary conservation. Functional predictions suggest ITGA9-AS1 may regulate neuroplasticity-related pathways such as "long-term potentiation" and "cAMP signaling pathway" via a ceRNA mechanism. WNT5A-AS1 may mediate intercellular communication through exosomes, influencing developmental and metabolic pathways, including the "Notch signaling pathway" and "cysteine and methionine metabolism".

Conclusion: Our findings suggest that ITGA9-AS1 and WNT5A-AS1 are highly promising biomarker candidates for schizophrenia. They may be involved in the disease process through distinct mechanisms (intracellular regulation and intercellular communication), thus providing a new theoretical framework and suggesting potential therapeutic targets.

外泌体衍生的ITGA9-AS1和WNT5A-AS1作为精神分裂症候选诊断生物标志物的验证和功能探索
目的:精神分裂症缺乏客观的生物标志物,其复杂的病因需要表观遗传学的洞察力。鉴于长链非编码rna (lncRNA)在神经系统和外周外泌体中脑相关信号中的调节作用,我们评估了lncRNA在患者外周血和血浆外泌体中的表达,评估了其诊断价值,并探讨了其潜在的功能和机制。方法:从GEO (GSE228881)中鉴定出精神分裂症相关外泌体中差异表达的lncrna,并选择15个候选基因进行验证。在一个临床队列中,RT-qPCR评估了它们在外周血和血浆外泌体中的表达。采用ROC分析评估诊断准确性。对顶级失调lncrna进行生物信息学分析:亚细胞定位、进化保护、ceRNA网络构建和GO/KEGG富集。结果:ITGA9-AS1和WNT5A-AS1在患者外周血和血浆外泌体中均显著上调。两者在外周血中的AUC值分别为0.8422和0.8073,具有良好的诊断潜力;其组合产生的AUC为0.9180。生物信息学分析显示,ITGA9-AS1主要定位于细胞质,而WNT5A-AS1富集于外泌体,两者均表现出高度的进化保守性。功能预测提示ITGA9-AS1可能通过ceRNA机制调节神经可塑性相关通路,如“长期增强”和“cAMP信号通路”。WNT5A-AS1可能通过外泌体介导细胞间通讯,影响发育和代谢途径,包括“Notch信号通路”和“半胱氨酸和蛋氨酸代谢”。结论:我们的研究结果表明,ITGA9-AS1和WNT5A-AS1是极有希望的精神分裂症生物标志物候选者。它们可能通过不同的机制(细胞内调节和细胞间通讯)参与疾病过程,从而提供了新的理论框架并提示潜在的治疗靶点。
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来源期刊
Neuropsychiatric Disease and Treatment
Neuropsychiatric Disease and Treatment CLINICAL NEUROLOGY-PSYCHIATRY
CiteScore
5.10
自引率
3.10%
发文量
328
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of clinical therapeutics and pharmacology focusing on concise rapid reporting of clinical or pre-clinical studies on a range of neuropsychiatric and neurological disorders.
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