帕金森病亚型伴快速眼动睡眠行为障碍的肠道代谢物富集

IF 8.2 1区 医学 Q1 NEUROSCIENCES
Sunjae Lee, Jihyun Kim, Jae Woo Baek, Ki-Young Jung, Yunjong Lee, Ara Koh, Han-Joon Kim
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引用次数: 0

摘要

最近的报道表明,肠道微生物特征的帕金森病(PD)样变化发生在特发性快速眼动睡眠行为障碍(iRBD)中,这是α-突触核蛋白病的前驱症状。然而,50%的PD病例在发病时表现为RBD,强调了PD的异质性。使用非靶向代谢组学,分析了伴有和不伴有RBD的PD患者、iRBD受试者和健康对照者的血浆样本,以表征伴有和不伴有RBD的PD患者的代谢差异。代谢组学分析显示,患有RBD的PD患者肠道微生物源代谢物(如次级胆汁酸和对甲酚硫酸盐)富集,而与神经精神疾病相关的代谢物在没有RBD的PD患者中升高。此外,我们预测富含肠道微生物来源的RBD组的对甲酚硫酸盐会穿过血脑屏障,这表明肠道微生物生态失调、iRBD和PD与RBD之间存在潜在的机制联系。我们的研究阐明了PD亚型的异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enrichment of gut-derived metabolites in a Parkinson’s disease subtype with REM sleep behavior disorder

Enrichment of gut-derived metabolites in a Parkinson’s disease subtype with REM sleep behavior disorder

Recent reports indicate that Parkinson’s disease (PD)-like changes in gut microbial signatures develop in idiopathic REM sleep behavior disorder (iRBD), a prodrome of α-synucleinopathies. However, <50% of PD cases exhibit RBD at onset, underscoring PD’s heterogeneity. Using untargeted metabolomics, plasma samples from PD patients with and without RBD, iRBD subjects, and healthy controls were analyzed to characterize the metabolic differences in PD patients with and without RBD. Metabolomic analysis revealed the enrichment of gut microbial-origin metabolites, such as secondary bile acids and p-cresol sulfate, in PD patients with RBD, while metabolites linked to neuropsychiatric diseases were elevated in PD patients without RBD. Additionally, our prediction that p-cresol sulfate, enriched in the RBD groups with a gut microbial origin, crosses the blood-brain barrier, suggests a potential mechanistic link between gut microbial dysbiosis, iRBD, and PD with RBD. Our study elucidates the heterogeneous nature of PD subtypes.

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来源期刊
NPJ Parkinson's Disease
NPJ Parkinson's Disease Medicine-Neurology (clinical)
CiteScore
9.80
自引率
5.70%
发文量
156
审稿时长
11 weeks
期刊介绍: npj Parkinson's Disease is a comprehensive open access journal that covers a wide range of research areas related to Parkinson's disease. It publishes original studies in basic science, translational research, and clinical investigations. The journal is dedicated to advancing our understanding of Parkinson's disease by exploring various aspects such as anatomy, etiology, genetics, cellular and molecular physiology, neurophysiology, epidemiology, and therapeutic development. By providing free and immediate access to the scientific and Parkinson's disease community, npj Parkinson's Disease promotes collaboration and knowledge sharing among researchers and healthcare professionals.
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