The gut microbial profile in patients with primary sclerosing cholangitis is distinct from patients with ulcerative colitis without biliary disease and healthy controls

被引:345
作者
Kummen, Martin [1 ,2 ,3 ]
Holm, Kristian [3 ]
Anmarkrud, Jarl Andreas [3 ]
Nygard, Stale [4 ,5 ,6 ,7 ,8 ]
Vesterhus, Mette [9 ]
Hoivik, Marte L. [10 ]
Troseid, Marius [1 ,11 ]
Marschall, Hanns-Ulrich [12 ]
Schrumpf, Erik [2 ]
Moum, Bjorn [2 ,10 ]
Rosjo, Helge [7 ,8 ,13 ]
Aukrust, Pal [1 ,2 ,3 ,11 ]
Karlsen, Tom H. [1 ,2 ,3 ,14 ,15 ]
Hov, Johannes R. [1 ,2 ,3 ,15 ]
机构
[1] Univ Oslo, KG Jebsen Inflammat Res Ctr, Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Oslo, Norway
[3] Natl Hosp Norway, Oslo Univ Hosp, Res Inst Internal Med, Oslo, Norway
[4] Oslo Univ Hosp, Inst Med Informat, Bioinformat Core Facil, Oslo, Norway
[5] Oslo Univ Hosp, Inst Expt Med Res, Oslo, Norway
[6] Univ Oslo, Oslo, Norway
[7] Univ Oslo, KG Jebsen Cardiac Res Ctr, Oslo, Norway
[8] Univ Oslo, Ctr Heart Failure Res, Oslo, Norway
[9] Haukeland Hosp, Dept Med, Natl Ctr Ultrasound Gastroenterol, Bergen, Norway
[10] Oslo Univ Hosp Ulleval, Dept Gastroenterol, Oslo, Norway
[11] Natl Hosp Norway, Oslo Univ Hosp, Sect Clin Immunol & Infect Dis, Oslo, Norway
[12] Univ Gothenburg, Sahlgrenska Acad, Inst Med, Dept Mol & Clin Med, Gothenburg, Sweden
[13] Akershus Univ Hosp, Div Med, Lorenskog, Norway
[14] Univ Bergen, Dept Clin Med, Bergen, Norway
[15] Natl Hosp Norway, Oslo Univ Hosp, Dept Transplantat Med, Sect Gastroenterol, Oslo, Norway
关键词
INFLAMMATORY-BOWEL-DISEASE; MUCOSA-ASSOCIATED MICROBIOTA; INTESTINAL MICROBIOME; EPITHELIAL-CELLS; DYSBIOSIS; DIVERSITY; ASSOCIATION; METAGENOME; CIRRHOSIS; BACTERIA;
D O I
10.1136/gutjnl-2015-310500
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Gut microbiota could influence gut, as well as hepatic and biliary immune responses. We therefore thoroughly characterised the gut microbiota in primary sclerosing cholangitis (PSC) compared with healthy controls (HC) and patients with ulcerative colitis without liver disease. Design We prospectively collected 543 stool samples. After a stringent exclusion process, bacterial DNA was submitted for 16S rRNA gene sequencing. PSC and HC were randomised to an exploration panel or a validation panel, and only significant results (p<0.05, Q(FDR)<0.20) in both panels were reported, followed by a combined comparison of all samples against UC. Results Patients with PSC (N=85) had markedly reduced bacterial diversity compared with HC (N=263, p<0.0001), and a different global microbial composition compared with both HC (p<0.001) and UC (N=36, p<0.01). The microbiota of patients with PSC with and without IBD was similar. Twelve genera separated PSC and HC, out of which 11 were reduced in PSC. However, the Veillonella genus showed a marked increase in PSC compared with both HC (p<0.0001) and UC (p<0.02). Using receiver operating characteristic analysis, Veillonella abundance yielded an area under the curve (AUC) of 0.64 to discriminate PSC from HC, while a combination of PSC-associated genera yielded an AUC of 0.78. Conclusions Patients with PSC exhibited a gut microbial signature distinct from both HC and UC without liver disease, but similar in PSC with and without IBD. The Veillonella genus, which is also associated with other chronic inflammatory and fibrotic conditions, was enriched in PSC.
引用
收藏
页码:611 / 619
页数:9
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