Otomo Mayuko, Tashiro Ryosuke, Tokuno Hidetaka, Kanoke Atsushi, Tominaga Keita, Nagai Arata, Aikawa Takashi, Ando Daisuke, Sakata Hiroyuki, Sato Takeya, Abe Takaaki, Endo Hidenori, Niizuma Kuniyasu, Tominaga Teiji
Department of Neurosurgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Neurosurgery, Kohnan Hospital, Sendai, Japan.
Cerebrovasc Dis. 2025 Mar 26:1-9. doi: 10.1159/000545478.
Moyamoya disease (MMD) is a cerebrovascular disease characterized by progressive steno-occlusive lesions in the terminal portion of the internal carotid artery. Despite its unknown etiology, immune dysregulation is regarded as a critical trigger for delineating the pathophysiology of MMD. The gut microbiota produces short-chain fatty (SCFA) and organic acids, influencing immune regulation and vascular remodeling. We aimed to characterize the gut microbiota in patients with MMD.
Sixteen patients with MMD and sixteen healthy controls (CON) were included in this study. We performed 16S rRNA sequencing of fecal samples, analyzed microbiome diversity and composition, and quantified SCFA and organic acid levels using liquid chromatography.
There were no significant differences in α- and β-diversities among feces from the MMD patients and CON. However, 16S rRNA sequencing identified defective Lactococcus lactis (0 ± 0 in the MMD patients vs. 0.026 ± 0.084 in healthy CON, p = 0.0181) and abundant Gordinobacter pamelaeae (0.030 ± 0.039 in the patients vs. 0.001 ± 0.005 in healthy CON, p = 0.003) are strongly linked to MMD. Propionic acid levels were significantly lower in feces of the MMD patients compared to healthy CON (0.83 ± 0.34 mg/g in the MMD patients vs. 1.20 ± 0.55 mg/g in healthy CON, p = 0.028).
Decreased L. lactis can result in reduced lactic acid and propionic acid levels in the feces of the patients. This imbalance in the gut microbiome and SCFA/organic acid levels could contribute to immune dysregulation underlying the vascular remodeling seen in MMD.
烟雾病(MMD)是一种脑血管疾病,其特征是颈内动脉末端进行性狭窄闭塞性病变。尽管其病因不明,但免疫失调被认为是阐明烟雾病病理生理学的关键触发因素。肠道微生物群产生短链脂肪酸(SCFA)和有机酸,影响免疫调节和血管重塑。我们旨在对烟雾病患者的肠道微生物群进行特征分析。
本研究纳入了16例烟雾病患者和16例健康对照(CON)。我们对粪便样本进行了16S rRNA测序,分析了微生物群的多样性和组成,并使用液相色谱法对SCFA和有机酸水平进行了定量分析。
烟雾病患者和健康对照的粪便中,α-多样性和β-多样性没有显著差异。然而,16S rRNA测序发现,乳酸乳球菌缺陷(烟雾病患者为0±0,健康对照为0.026±0.084,p = 0.0181)和大量的帕氏戈登菌(患者为0.030±0.039,健康对照为0.001±0.005,p = 0.003)与烟雾病密切相关。与健康对照相比,烟雾病患者粪便中的丙酸水平显著降低(烟雾病患者为0.83±0.34 mg/g,健康对照为1.20±0.55 mg/g,p = 0.028)。
乳酸乳球菌减少可导致患者粪便中乳酸和丙酸水平降低。肠道微生物群以及SCFA/有机酸水平的这种失衡可能导致烟雾病中所见血管重塑背后的免疫失调。