Gut microbiome-associated predictors as biomarkers of response to advanced therapies in inflammatory bowel disease: a systematic review

被引:11
|
作者
Meade, Susanna [1 ,2 ]
Kiow, Jeremy Liu Chen [1 ,2 ]
Massaro, Cristian [3 ,4 ]
Kaur, Gurpreet [2 ,3 ]
Squirell, Elizabeth [1 ,2 ]
Bressler, Brian [1 ,2 ]
Lunken, Genelle [2 ,3 ,4 ]
机构
[1] Univ British Columbia, Dept Med, Vancouver, BC, Canada
[2] IBD Ctr BC, Vancouver, BC, Canada
[3] Univ British Columbia, Univeris British Columbia, Vancouver, BC, Canada
[4] BC Childrens Hosp, Res Inst, 950 W 28th Ave, Vancouver, BC, Canada
关键词
Inflammatory bowel disease; Crohn's disease; ulcerative colitis; microbiome; metabolome; immunosuppressive therapy; treatment response; SIDED ULCERATIVE-COLITIS; FECAL MICROBIOTA; CROHNS-DISEASE; DOUBLE-BLIND; MULTI-OMICS; BUTYRATE; DIET; PROFILES; CANDIDA; VIROME;
D O I
10.1080/19490976.2023.2287073
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Loss of response to therapy in inflammatory bowel disease (IBD) has led to a surge in research focusing on precision medicine. Three systematic reviews have been published investigating the associations between gut microbiota and disease activity or IBD therapy. We performed a systematic review to investigate the microbiome predictors of response to advanced therapy in IBD. Unlike previous studies, our review focused on predictors of response to therapy; so the included studies assessed microbiome predictors before the proposed time of response or remission. We also provide an update of the available data on mycobiomes and viromes. We highlight key themes in the literature that may serve as future biomarkers of treatment response: the abundance of fecal SCFA-producing bacteria and opportunistic bacteria, metabolic pathways related to butyrate synthesis, and non-butyrate metabolomic predictors, including bile acids (BAs), amino acids, and lipids, as well as mycobiome predictors of response.
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页数:29
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