Compositional and Temporal Changes in the Gut Microbiome of Pediatric Ulcerative Colitis Patients Are Linked to Disease Course.
Compositional and Temporal Changes in the Gut Microbiome of Pediatric Ulcerative Colitis Patients Are Linked to Disease Course.
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DOI:
10.1016/j.chom.2018.09.009
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发表时间:
2018-10-10
影响因子:
30.3
通讯作者:
Xavier RJ
中科院分区:
文献类型:
--
作者:
Schirmer M;Denson L;Vlamakis H;Franzosa EA;Thomas S;Gotman NM;Rufo P;Baker SS;Sauer C;Markowitz J;Pfefferkorn M;Oliva-Hemker M;Rosh J;Otley A;Boyle B;Mack D;Baldassano R;Keljo D;LeLeiko N;Heyman M;Griffiths A;Patel AS;Noe J;Kugathasan S;Walters T;Huttenhower C;Hyams J;Xavier RJ
Evaluating progression risk and determining optimal therapy for ulcerative colitis (UC) is challenging as many patients exhibit incomplete responses to treatment. As part of the PROTECT (Predicting Response to Standardized Colitis Therapy) Study, we evaluated the role of the gut microbiome in disease course for 405 pediatric, new-onset, treatment-naive UC patients. Patients were monitored for one year upon treatment initiation, and microbial taxonomic composition was analyzed from fecal samples and rectal biopsies. Depletion of core gut microbes and expansion of bacteria typical of the oral cavity were associated with baseline disease severity. Remission and refractory disease were linked to species-specific temporal changes that may be implicative of therapy efficacy, and a pronounced increase in microbiome variability was observed prior to colectomy. Finally, microbial associations with disease-associated serological markers suggest host-microbial interactions in UC. These insights will help improve existing treatments and develop therapeutic approaches guiding optimal medical care. Many patients exhibit incomplete responses to ulcerative colitis (UC) therapy. Schirmer et al. investigate the gut microbiome's role in pediatric UC treated with two conventional therapies. Baseline and longitudinal microbial trends are implicated in disease severity and progression, including remission and colectomy requirement. These insights may motivate new therapeutic approaches.
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影响因子:
16.6
作者:
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通讯作者:
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DOI:
10.1126/science.aan4526
发表时间:
2017-10-20
期刊:
Science (New York, N.Y.)
影响因子:
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10.1016/j.cgh.2008.04.032
发表时间:
2008-10
期刊:
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
影响因子:
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作者:
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发表时间:
2012-08
期刊:
The ISME journal
影响因子:
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作者:
通讯作者:
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影响因子:
64.5
作者:
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通讯作者:
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