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Analysis of Gut Microbiota in Rheumatoid Arthritis Patients: Disease-Related Dysbiosis and Modifications Induced by Etanercept.类风湿关节炎患者肠道微生物组分析:疾病相关的菌群失调和依那西普诱导的改变。
Int J Mol Sci. 2018 Sep 27;19(10):2938. doi: 10.3390/ijms19102938.
2
Molecular profiling of mucosal tissue associated microbiota in patients manifesting acute exacerbations and remission stage of ulcerative colitis.溃疡性结肠炎急性发作和缓解期患者黏膜组织相关微生物群的分子特征分析。
World J Microbiol Biotechnol. 2018 May 23;34(6):76. doi: 10.1007/s11274-018-2449-0.
3
Comparison of the microbial community structure between inflamed and non-inflamed sites in patients with ulcerative colitis.溃疡性结肠炎患者炎症部位与非炎症部位微生物群落结构的比较。
J Gastroenterol Hepatol. 2018 Feb 20. doi: 10.1111/jgh.14129.
4
Age and fecal microbial strain-specific differences in patients with spondyloarthritis.年龄和粪便微生物菌株特异性差异在脊柱关节炎患者中。
Arthritis Res Ther. 2018 Jan 30;20(1):14. doi: 10.1186/s13075-018-1510-6.
5
Proteobacteria: A Common Factor in Human Diseases.变形菌门:人类疾病的共同因素。
Biomed Res Int. 2017;2017:9351507. doi: 10.1155/2017/9351507. Epub 2017 Nov 2.
6
Meta-analysis of gut microbiome studies identifies disease-specific and shared responses.基于宏基因组关联研究的肠道微生物组分析鉴定出疾病特异性和共享反应。
Nat Commun. 2017 Dec 5;8(1):1784. doi: 10.1038/s41467-017-01973-8.
7
A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients.富含炎症性肠病患者的新型格尔曼梭菌分支。
Genome Med. 2017 Nov 28;9(1):103. doi: 10.1186/s13073-017-0490-5.
8
Gut Microbiota Perturbations in Reactive Arthritis and Postinfectious Spondyloarthritis.肠菌失调与反应性关节炎和感染后脊柱关节炎。
Arthritis Rheumatol. 2018 Feb;70(2):242-254. doi: 10.1002/art.40359. Epub 2018 Jan 3.
9
Experimental colitis delays and reduces the severity of collagen-induced arthritis in mice.实验性结肠炎会延迟并减轻小鼠胶原诱导性关节炎的严重程度。
PLoS One. 2017 Sep 19;12(9):e0184624. doi: 10.1371/journal.pone.0184624. eCollection 2017.
10
Quantitative metagenomics reveals unique gut microbiome biomarkers in ankylosing spondylitis.定量宏基因组学揭示强直性脊柱炎中独特的肠道微生物组生物标志物。
Genome Biol. 2017 Jul 27;18(1):142. doi: 10.1186/s13059-017-1271-6.

慢性风湿性和炎症性肠病的肠道微生物组:相似性和差异性。

Gut microbiome in chronic rheumatic and inflammatory bowel diseases: Similarities and differences.

机构信息

IMoPA, UMR7365 CNRS-Université de Lorraine, Vandœuvre Les Nancy, France.

Division of Integrative Systems Medicine and Digestive Disease, Imperial College London, UK.

出版信息

United European Gastroenterol J. 2019 Oct;7(8):1008-1032. doi: 10.1177/2050640619867555. Epub 2019 Aug 1.

DOI:10.1177/2050640619867555
PMID:31662859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6794689/
Abstract

INTRODUCTION

Inflammatory bowel diseases (IBDs) and chronic rheumatic diseases (CRDs) are systemic chronic disorders sharing common genetic, immune and environmental factors. About half of patients with IBD develop rheumatic ailments and microscopic intestinal inflammation is present in up to half of CRD patients. IBD and CRD patients also share a common therapeutic armamentarium. Disequilibrium in the complex realm of microbes (known as dysbiosis) that closely interact with the gut mucosal immune system has been associated with both IBD and CRD (spondyloarthritis and rheumatoid arthritis). Whether dysbiosis represents an epiphenomenon or a prodromal feature remains to be determined.

METHODS

In an attempt to further investigate whether specific gut dysbiosis may be the missing link between IBD and CRD in patients developing both diseases, we performed here a systematic literature review focusing on studies looking at bacterial microbiota in CRD and/or IBD patients.

RESULTS

We included 80 studies, with a total of 3799 IBD patients without arthritis, 1084 CRD patients without IBD, 132 IBD patients with arthropathy manifestations and 12 spondyloarthritis patients with IBD history. Overall, this systematic review indicates that an increase in s, and genera, as well as a decrease in genera and species belonging to Verrucomicrobia and Fusobacteria phyla are common features in IBD and CRD patients, whereas dozens of bacterial species are specific features of CRD and IBD.

CONCLUSION

Further work is needed to understand the functions of bacteria and of their metabolites but also to characterize fungi and viruses that are commonly found in these patients.

摘要

简介

炎症性肠病(IBD)和慢性风湿性疾病(CRD)是系统性慢性疾病,具有共同的遗传、免疫和环境因素。约有一半的 IBD 患者会出现风湿性疾病,而多达一半的 CRD 患者存在微观肠道炎症。IBD 和 CRD 患者也有共同的治疗方法。与肠道黏膜免疫系统密切相互作用的微生物(称为菌群失调)的失衡与 IBD 和 CRD(脊柱关节炎和类风湿关节炎)都有关。菌群失调是否代表一种伴随现象或前驱特征仍有待确定。

方法

为了进一步研究特定的肠道菌群失调是否可能是同时患有这两种疾病的患者的 IBD 和 CRD 之间缺失的环节,我们在此进行了一项系统的文献综述,重点研究了观察 CRD 和/或 IBD 患者细菌微生物群的研究。

结果

我们纳入了 80 项研究,共有 3799 名无关节炎的 IBD 患者、1084 名无 IBD 的 CRD 患者、132 名有关节病表现的 IBD 患者和 12 名有 IBD 病史的脊柱关节炎患者。总的来说,这项系统综述表明,s、和 属的增加,以及属于 Verrucomicrobia 和 Fusobacteria 门的 属和物种的减少是 IBD 和 CRD 患者的常见特征,而数十种细菌物种是 CRD 和 IBD 的特有特征。

结论

需要进一步研究以了解细菌及其代谢物的功能,但也要对这些患者中常见的真菌和病毒进行特征描述。