Oral and Gut Dysbiosis in Migraine: Oral Microbial Signatures as Biomarkers of Migraine.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Soomi Cho, Yeonjae Jung, Hyun-Seok Oh, Jungyon Yum, Seungwon Song, JaeWook Jeong, Woo-Seok Ha, Kyung Min Kim, Won-Joo Kim, Min Kyung Chu
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引用次数: 0

Abstract

Background and objectives: Emerging evidence suggests that oral health conditions may exacerbate migraine, and saliva is a potential source of biomarkers for migraine. The 3-way interaction of the oral-gut-brain axis has been implicated in several neurologic disorders, but has rarely been studied in migraine. This study examined the oral and gut microbiomes simultaneously and identified several key oral microbes that may influence migraine.

Methods: In this cross-sectional case-control study, participants were divided into 3 groups: episodic migraine (n = 55), chronic migraine (n = 55), and healthy control (HC) (n = 55). Demographic and clinical characteristics; lifestyle factors; and biological samples including saliva, stool, and blood were collected. Composition, function, and community type of the oral and gut microbiomes were compared among the 3 groups.

Results: Oral dysbiosis was more pronounced than gut dysbiosis in the migraine groups, with 13 oral genera significantly enriched or depleted compared with HCs. The migraine groups showed increased abundance of Gemella, Streptococcus, Granulicatella, and Rothia and decreased abundance of Alloprevotella, Veillonella, Haemophilus, Selenomonas, Campylobacter, Cardiobacterium, Megasphaera, and Kingella after adjustment for demographic and lifestyle factors including diet. The enriched oral genera within the migraine groups were associated with carbohydrate metabolic pathways, whereas the depleted oral genera were associated with pathways related to nitrogen. A significant proportion of the oral microbial signatures of migraine included genera capable of reducing nitrate and/or nitrite. Some of these oral microbial signatures of migraine had a relative abundance that was positively or negatively associated with the number of headache days per 30 days and formed distinct microbial clusters in both the oral cavity and gut. Machine learning classifiers using the oral microbiome effectively classified migraine status, with an area under the receiver-operating characteristic curve of 0.83-0.88.

Discussion: Our findings suggest that oral dysbiosis may be involved in the development of migraine and highlight specific oral microbes as potential diagnostic biomarkers and therapeutic targets for migraine.

偏头痛的口腔和肠道生态失调:口腔微生物特征作为偏头痛的生物标志物。
背景和目的:越来越多的证据表明口腔健康状况可能加剧偏头痛,唾液是偏头痛生物标志物的潜在来源。口腔-肠-脑轴的三向相互作用与几种神经系统疾病有关,但很少在偏头痛中进行研究。这项研究同时检查了口腔和肠道微生物组,并确定了几种可能影响偏头痛的关键口腔微生物。方法:在这项横断面病例对照研究中,参与者被分为3组:发作性偏头痛(n = 55),慢性偏头痛(n = 55)和健康对照组(n = 55)。人口统计学和临床特征;生活方式因素;并收集了唾液、粪便和血液等生物样本。比较三组患者口腔和肠道微生物组的组成、功能和群落类型。结果:在偏头痛组中,口腔生态失调比肠道生态失调更为明显,与hc相比,有13个口腔属显着富集或减少。偏头痛组在调整人口统计学和生活方式因素(包括饮食)后,Gemella、Streptococcus、Granulicatella和Rothia的丰度增加,Alloprevotella、Veillonella、Haemophilus、Selenomonas、Campylobacter、Cardiobacterium、Megasphaera和Kingella的丰度减少。偏头痛组中富含的口腔属与碳水化合物代谢途径有关,而缺乏的口腔属与氮代谢途径有关。偏头痛的口腔微生物特征的显著比例包括能够减少硝酸盐和/或亚硝酸盐的属。偏头痛的一些口腔微生物特征相对丰富,与每30天头痛天数呈正相关或负相关,并在口腔和肠道中形成不同的微生物群。使用口腔微生物组的机器学习分类器有效地分类了偏头痛状态,接受者-操作特征曲线下的面积为0.83-0.88。讨论:我们的研究结果表明,口腔生态失调可能与偏头痛的发展有关,并强调了特定的口腔微生物作为偏头痛的潜在诊断生物标志物和治疗靶点。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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