Alteration of the fecal microbiota in Chinese patients with Parkinson's disease

被引:308
作者
Qian, Yiwei [1 ,2 ]
Yang, Xiaodong [1 ,2 ]
Xu, Shaoqing [1 ,2 ]
Wu, Chunyan [3 ]
Song, Yanyan [4 ]
Qin, Nan [3 ]
Chen, Sheng-Di [1 ,2 ]
Xiao, Qin [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Dept Neurol, Shanghai 200025, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Collaborat Innovat Ctr Brain Sci, Shanghai 200025, Peoples R China
[3] Realbio Genom Inst, Shanghai 200050, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Inst Med Sci, Dept Biostat, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金; 国家重点研发计划;
关键词
Neurodegenerative disorder; Gut microbiota; 16S rRNA gene; GUT MICROBIOTA; CONSTIPATION; PREVALENCE; DIFFERS; BRAIN; AGE;
D O I
10.1016/j.bbi.2018.02.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Emerging evidences suggest that gut microbiota dysbiosis plays a role in Parkinson's disease (PD). However, the alterations in fecal microbiome in Chinese PD patients remains unknown. This case control study was conducted to explore fecal microbiota compositions in Chinese PD patients. Microbiota communities in the feces of 45 patients and their healthy spouses were investigated using high-throughput Illumina Miseq sequencing targeting the V3-V4 region of 16S ribosomal RNA (rRNA) gene. The relationships between fecal microbiota and PD clinical characteristics were analyzed. The structure and richness of the fecal microbiota differed between PD patients and healthy controls. Genera Clostridium IV, Aquabacterium, Holdemania, Sphingomonas, Clostridium XVIII, Butyricicoccus and Anaerotruncus were enriched in the feces of PD patients after adjusting for age, gender, body mass index (BMI), and constipation. Furthermore, genera Escherichia/Shigella were negatively associated with disease duration. Genera Dorea and Phascolarctobacterium were negatively associated with levodopa equivalent doses (LED). Among the non-motor symptoms (NMSs), genera Butyricicoccus and Clostridium XIVb were associated with cognitive impairment. Overall, we confirmed that gut microbiota dysbiosis occurs in Chinese patients with PD. A well-controlled population involved was beneficial for the identification of microbiota associated with diseases. Additionally, the fecal microbiota was closely related to PD clinical characteristics. Elucidating these differences in the fecal microbiome will provide a foundation to improve our understanding the pathogenesis of PD and to support the potentially therapeutic options modifying the gut microbiota. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:194 / 202
页数:9
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