Characteristic alterations of gut microbiota and serum metabolites in patients with chronic tinnitus: a multi-omics analysis.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Jiang Wang, Jia-Hui Xiang, Xu-Yuan Peng, Min Liu, Le-Jia Sun, Min Zhang, Li-Yuan Zhang, Zhi-Bin Chen, Zheng-Quan Tang, Lei Cheng
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引用次数: 0

Abstract

Chronic tinnitus is a central nervous system disorder. Currently, the effects of gut microbiota on tinnitus remain unexplored. To explore the connection between gut microbiota and tinnitus, we conducted 16S rRNA sequencing of fecal microbiota and serum metabolomic analysis in a cohort of 70 patients with tinnitus and 30 healthy volunteers. We used the weighted gene co-expression network method to analyze the relationship between the gut microbiota and the serum metabolites. The random forest technique was utilized to select metabolites and gut taxa to construct predictive models. A pronounced gut dysbiosis in the tinnitus group, characterized by reduced bacterial diversity, an increased Firmicutes/Bacteroidetes ratio, and some opportunistic bacteria including Aeromonas and Acinetobacter were enriched. In contrast, some beneficial gut probiotics decreased, including Lactobacillales and Lactobacillaceae. In serum metabolomic analysis, serum metabolic disturbances in tinnitus patients and these differential metabolites were enriched in pathways of neuroinflammation, neurotransmitter activity, and synaptic function. The predictive models exhibited great diagnostic performance, achieving 0.94 (95% CI: 0.85-0.98) and 0.96 (95% CI: 0.86-0.99) in the test set. Our study suggests that changes in gut microbiota could potentially influence the occurrence and chronicity of tinnitus, and exert regulatory effects through changes in serum metabolites. Overall, this research provides new perceptions into the potential role of gut microbiota and serum metabolite in the pathogenesis of tinnitus, and proposes the "gut-brain-ear" concept as a pathomechanism underlying tinnitus, with significant clinical diagnostic implications and therapeutic potential.IMPORTANCETinnitus affects millions of people worldwide. Severe cases may lead to sleep disorders, anxiety, and depression, subsequently impacting patients' lives and increasing societal healthcare expenditures. However, tinnitus mechanisms are poorly understood, and effective therapeutic interventions are currently lacking. We discovered the gut microbiota and serum metabolomics changes in patients with tinnitus, and provided the potential pathological mechanisms of dysregulated gut flora in chronic tinnitus. We proposed the innovative concept of the "gut-brain-ear axis," which underscores the exploration of gut microbiota impact on susceptibility to chronic tinnitus through serum metabolic profile modulation. We also reveal novel biomarkers associated with chronic tinnitus, offering a new conceptual framework for further investigations into the susceptibility of patients, potential treatment targets for tinnitus, and assessing patient prognosis. Subsequently, gut microbiota and serum metabolites can be used as molecular markers to assess the susceptibility and prognosis of tinnitus.Furthermore, fecal transplantation may be used to treat tinnitus.

慢性耳鸣患者肠道微生物群和血清代谢物的特征性变化:多组学分析。
慢性耳鸣是一种中枢神经系统疾病。目前,肠道微生物群对耳鸣的影响仍未得到研究。为了探索肠道微生物群与耳鸣之间的联系,我们对 70 名耳鸣患者和 30 名健康志愿者进行了粪便微生物群 16S rRNA 测序和血清代谢组学分析。我们使用加权基因共表达网络方法分析了肠道微生物群与血清代谢物之间的关系。我们利用随机森林技术选择代谢物和肠道类群来构建预测模型。耳鸣组的肠道菌群失调明显,其特点是细菌多样性减少,固着菌/类杆菌比例增加,包括气单胞菌和醋杆菌在内的一些机会性细菌富集。相反,一些有益的肠道益生菌却减少了,包括乳杆菌科和乳酸杆菌科。在血清代谢组学分析中,耳鸣患者的血清代谢紊乱和这些差异代谢物富集在神经炎症、神经递质活性和突触功能的通路中。预测模型表现出很高的诊断性能,在测试集中分别达到了 0.94(95% CI:0.85-0.98)和 0.96(95% CI:0.86-0.99)。我们的研究表明,肠道微生物群的变化有可能影响耳鸣的发生和慢性化,并通过血清代谢物的变化发挥调节作用。总之,这项研究对肠道微生物群和血清代谢物在耳鸣发病机制中的潜在作用提供了新的认识,并提出了 "肠-脑-耳 "概念作为耳鸣的病理机制,具有重要的临床诊断意义和治疗潜力。严重的耳鸣可能导致睡眠障碍、焦虑和抑郁,进而影响患者的生活并增加社会医疗支出。然而,人们对耳鸣的机制知之甚少,目前也缺乏有效的治疗干预措施。我们发现了耳鸣患者的肠道微生物群和血清代谢组学变化,并提供了慢性耳鸣肠道菌群失调的潜在病理机制。我们提出了 "肠-脑-耳轴 "这一创新概念,强调通过调节血清代谢谱来探索肠道微生物群对慢性耳鸣易感性的影响。我们还揭示了与慢性耳鸣相关的新型生物标志物,为进一步研究患者的易感性、耳鸣的潜在治疗目标以及评估患者预后提供了新的概念框架。随后,肠道微生物群和血清代谢物可作为分子标记物来评估耳鸣的易感性和预后。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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