Limited predictive value of the gut microbiome and metabolome for response to biological therapy in inflammatory bowel disease

被引:4
|
作者
Prins, Femke M. [1 ,2 ]
Hidding, Iwan J. [1 ]
Klaassen, Marjolein A. Y. [1 ]
Collij, Valerie [1 ]
Schultheiss, Johannes P. D. [3 ]
Venema, Werna T. C. Uniken [1 ]
Bangma, Amber [1 ]
Aardema, Jurne B. [1 ]
Jansen, Bernadien H. [1 ]
Mares, Wout G. N. [4 ]
Witteman, Ben J. M. [4 ]
Festen, Eleonora A. M. [1 ]
Dijkstra, Gerard [1 ]
Visschedijk, Marijn C. [1 ]
Fidder, Herma H. [3 ]
Vila, Arnau Vich [5 ,6 ]
Oldenburg, Bas [3 ]
Gacesa, Ranko [1 ,7 ]
Weersma, Rinse K. [1 ,7 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, POB 30 001, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Groningen, Netherlands
[3] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[4] Gelderse Vallei Hosp, Bennekom, Netherlands
[5] Rega Inst Med Res, Dept Microbiol & Immunol, Leuven, Belgium
[6] VIB, Ctr Microbiol, Leuven, Belgium
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
关键词
Inflammatory bowel disease; biologics; microbiome; vedolizumab; ustekinumab; prediction; metabolomics; MULTI-OMICS;
D O I
10.1080/19490976.2024.2391505
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Emerging evidence suggests the gut microbiome's potential in predicting response to biologic treatments in patients with inflammatory bowel disease (IBD). In this prospective study, we aimed to predict treatment response to vedolizumab and ustekinumab, integrating clinical data, gut microbiome profiles based on metagenomic sequencing, and untargeted fecal metabolomics. We aimed to identify predictive biomarkers and attempted to replicate microbiome-based signals from previous studies. We found that the predictive utility of the gut microbiome and fecal metabolites for treatment response was marginal compared to clinical features alone. Testing our identified microbial ratios in an external cohort reinforced the lack of predictive power of the microbiome. Additionally, we could not confirm previously published predictive signals observed in similar sized cohorts. Overall, these findings highlight the importance of external validation and larger sample sizes, to better understand the microbiome's impact on therapy outcomes in the setting of biologicals in IBD before potential clinical implementation.
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页数:18
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