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The nasal and gut microbiome in Parkinson's disease and idiopathic rapid eye movement sleep behavior disorder

快速眼动睡眠 微生物群 快速眼动睡眠行为障碍 疾病 某种肠道细菌 扩增子测序 眼球运动 肠道菌群 生物 医学 帕金森病 内科学 免疫学 生物信息学 神经科学 遗传学 16S核糖体RNA 细菌
作者
Anna Heintz‐Buschart,Urvashi Pandey,Tamara Wicke,Friederike Sixel‐Döring,Annette Janzen,Elisabeth Sittig‐Wiegand,Claudia Trenkwalder,Wolfgang H. Oertel,Brit Mollenhauer,Paul Wilmes
出处
期刊:Movement Disorders [Wiley]
卷期号:33 (1): 88-98 被引量:547
标识
DOI:10.1002/mds.27105
摘要

ABSTRACT Background Increasing evidence connects the gut microbiota and the onset and/or phenotype of Parkinson's disease (PD). Differences in the abundances of specific bacterial taxa have been reported in PD patients. It is, however, unknown whether these differences can be observed in individuals at high risk, for example, with idiopathic rapid eye movement sleep behavior disorder, a prodromal condition of α‐synuclein aggregation disorders including PD. Objectives To compare microbiota in carefully preserved nasal wash and stool samples of subjects with idiopathic rapid eye movement sleep behavior disorder, manifest PD, and healthy individuals. Methods Microbiota of flash‐frozen stool and nasal wash samples from 76 PD patients, 21 idiopathic rapid eye movement sleep behavior disorder patients, and 78 healthy controls were assessed by 16S and 18S ribosomal RNA amplicon sequencing. Seventy variables, related to demographics, clinical parameters including nonmotor symptoms, and sample processing, were analyzed in relation to microbiome variability and controlled differential analyses were performed. Results Differentially abundant gut microbes, such as Akkermansia , were observed in PD, but no strong differences in nasal microbiota. Eighty percent of the differential gut microbes in PD versus healthy controls showed similar trends in idiopathic rapid eye movement sleep behavior disorder, for example, Anaerotruncus and several Bacteroides spp., and correlated with nonmotor symptoms. Metagenomic sequencing of select samples enabled the reconstruction of genomes of so far uncharacterized differentially abundant organisms. Conclusion Our study reveals differential abundances of gut microbial taxa in PD and its prodrome idiopathic rapid eye movement sleep behavior disorder in comparison to the healthy controls, and highlights the potential of metagenomics to identify and characterize microbial taxa, which are enriched or depleted in PD and/or idiopathic rapid eye movement sleep behavior disorder. © 2017 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

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