Characterization of Intestinal Microbiota in Ulcerative Colitis Patients with and without Primary Sclerosing Cholangitis

被引:64
作者
Kevans, D. [1 ,2 ]
Tyler, A. D. [1 ]
Holm, K. [3 ]
Jorgensen, K. K. [3 ,4 ]
Vatn, M. H. [5 ,6 ]
Karlsen, T. H. [3 ,7 ]
Kaplan, G. G. [8 ]
Eksteen, B. [8 ]
Gevers, D. [9 ]
Hov, J. R. [3 ,7 ]
Silverberg, M. S. [1 ,2 ]
机构
[1] Mt Sinai Hosp, Zane Cohen Ctr Digest Dis, IBD Grp, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Med, Div Gastroenterol, Toronto, ON, Canada
[3] Oslo Univ Hosp, Norwegian PSC Res Ctr, Oslo, Norway
[4] Akershus Univ Hosp, Dept Gastroenterol, Lorenskog, Norway
[5] Univ Oslo, Inst Clin Epidemiol & Mol Biol EpiGen, Oslo, Norway
[6] Univ Oslo, KG Jebsen Inflammat Res Ctr, Oslo, Norway
[7] Oslo Univ Hosp, Dept Transplantat Med, Oslo, Norway
[8] Univ Calgary, Dept Med, Calgary, AB, Canada
[9] Broad Inst MIT & Harvard, Cambridge, MA USA
基金
加拿大健康研究院;
关键词
PSC; intestinal microbiota; next generation sequencing; INFLAMMATORY-BOWEL-DISEASE; GUT MICROBIOTA;
D O I
10.1093/ecco-jcc/jjv204
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aims: There is an unexplained association between ulcerative colitis [UC] and primary sclerosing cholangitis [PSC], with the intestinal microbiota implicated as an important factor. The study aim was to compare the structure of the intestinal microbiota of patients with UC with and without PSC. Methods: UC patients with PSC [PSC-UC] and without PSC [UC] were identified from biobanks at Oslo University Hospital, Foothills Hospital Calgary and Mount Sinai Hospital Toronto. Microbial DNA was extracted from colonic tissue and sequencing performed of the V4 region of the 16S rRNA gene on Illumina MiSeq. Sequences were assigned to operational taxonomic units [OTUs] using Quantitative Insights Into Microbial Ecology [QIIME]. Microbial alpha diversity, beta diversity, and relative abundance were compared between PSC-UC and UC phenotypes. Results: In all, 31 PSC-UC patients and 56 UC patients were included. Principal coordinate analysis [PCoA] demonstrated that city of sample collection was the strongest determinant of taxonomic profile. In the Oslo cohort, Chao 1 index was modestly decreased in PSC-UC compared with UC [p = 0.04] but did not differ significantly in the Calgary cohort. No clustering by PSC phenotype was observed using beta diversity measures. For multiple microbial genera there were nominally significant differences between UC and PSC-UC, but results were not robust to false-discovery rate correction. Conclusions: No strong PSC-specific microbial associations in UC patients consistent across different cohorts were identified. Recruitment centre had a strong effect on microbial composition. Future studies should include larger cohorts to increase power and the ability to control for confounding factors.
引用
收藏
页码:330 / 337
页数:8
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