A specific microbiota signature is associated to various degrees of ulcerative colitis as assessed by a machine learning approach

被引:61
作者
Barberio, Brigida [1 ]
Facchin, Sonia [1 ]
Patuzzi, Ilaria [2 ]
Ford, Alexander C. [3 ,4 ]
Massimi, Davide [1 ]
Valle, Giorgio [5 ,6 ]
Sattin, Eleonora [7 ]
Simionati, Barbara [2 ]
Bertazzo, Elena [1 ]
Zingone, Fabiana [1 ]
Savarino, Edoardo Vincenzo [1 ]
机构
[1] Univ Padua, Dept Surg Oncol & Gastroenterol Sci, Div Gastroenterol, Padua, Italy
[2] Univ Padua, Res & Dev Div, Padua, Italy
[3] St James Univ Hosp, Leeds Gastroenterol Inst, Leeds, W Yorkshire, England
[4] Univ Leeds, Leeds Inst Biomed & Clin Sci, Leeds, W Yorkshire, England
[5] Univ Padua, Dept Biol, Padua, Italy
[6] Univ Padua, Cribi Biotechnol Ctr, Padua, Italy
[7] BMR Genom, Via Redipuglia 22, Padua, Italy
关键词
Inflammatory bowel disease; microbiota; ulcerative colitis; machine learning; INFLAMMATORY-BOWEL-DISEASE; CROHNS-DISEASE; FAECALIBACTERIUM-PRAUSNITZII; GUT MICROBIOTA; PATHOGENESIS;
D O I
10.1080/19490976.2022.2028366
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Ulcerative colitis (UC) is a complex immune-mediated disease in which the gut microbiota plays a central role, and may determine prognosis and disease progression. We aimed to assess whether a specific microbiota profile, as measured by a machine learning approach, can be associated with disease severity in patients with UC. In this prospective pilot study, consecutive patients with active or inactive UC and healthy controls (HCs) were enrolled. Stool samples were collected for fecal microbiota assessment analysis by 16S rRNA gene sequencing approach. A machine learning approach was used to predict the groups' separation. Thirty-six HCs and forty-six patients with UC (20 active and 26 inactive) were enrolled. Alpha diversity was significantly different between the three groups (Shannon index: p-values: active UC vs HCs = 0.0005; active UC vs inactive UC = 0.0273; HCs vs inactive UC = 0.0260). In particular, patients with active UC showed the lowest values, followed by patients with inactive UC, and HCs. At species level, we found high levels of Bifidobacterium adolescentis and Haemophilus parainfluenzae in inactive UC and active UC, respectively. A specific microbiota profile was found for each group and was confirmed with sparse partial least squares discriminant analysis, a machine learning-supervised approach. The latter allowed us to observe a perfect class prediction and group separation using the complete information (full Operational Taxonomic Unit table), with a minimal loss in performance when using only 5% of features. A machine learning approach to 16S rRNA data identifies a bacterial signature characterizing different degrees of disease activity in UC. Follow-up studies will clarify whether such microbiota profiling are useful for diagnosis and management.
引用
收藏
页数:12
相关论文
共 34 条
[21]   phyloseq: An R Package for Reproducible Interactive Analysis and Graphics of Microbiome Census Data [J].
McMurdie, Paul J. ;
Holmes, Susan .
PLOS ONE, 2013, 8 (04)
[22]   Highlighting New Phylogenetic Specificities of Crohn's Disease Microbiota [J].
Mondot, S. ;
Kang, S. ;
Furet, J. P. ;
de Carcer, D. Aguirre ;
McSweeney, C. ;
Morrison, M. ;
Marteau, P. ;
Dore, J. ;
Leclerc, M. .
INFLAMMATORY BOWEL DISEASES, 2011, 17 (01) :185-192
[23]   From bench to bedside: fecal calprotectin in inflammatory bowel diseases clinical setting [J].
Mumolo, Maria Gloria ;
Bertani, Lorenzo ;
Ceccarelli, Linda ;
Laino, Gabriella ;
Di Fluri, Giorgia ;
Albano, Eleonora ;
Tapete, Gherardo ;
Costa, Francesco .
WORLD JOURNAL OF GASTROENTEROLOGY, 2018, 24 (33) :3681-3694
[24]   Role of the microbiota in inflammatory bowel diseases [J].
Nagalingam, Nabeetha A. ;
Lynch, Susan V. .
INFLAMMATORY BOWEL DISEASES, 2012, 18 (05) :968-980
[25]   mixOmics: An R package for 'omics feature selection and multiple data integration [J].
Rohart, Florian ;
Gautier, Benoit ;
Singh, Amrit ;
Le Cao, Kim-Anh .
PLOS COMPUTATIONAL BIOLOGY, 2017, 13 (11)
[26]   Inflammatory bowel disease pathogenesis: what is new? [J].
Scharl, Michael ;
Rogler, Gerhard .
CURRENT OPINION IN GASTROENTEROLOGY, 2012, 28 (04) :301-309
[27]   The application of omics techniques to understand the role of the gut microbiota in inflammatory bowel disease [J].
Segal, Jonathan P. ;
Mullish, Benjamin H. ;
Quraishi, Mohammed Nabil ;
Acharjee, Animesh ;
Williams, Horace R. T. ;
Igbal, Tariq ;
Hart, Ailsa L. ;
Marchesi, Julian R. .
THERAPEUTIC ADVANCES IN GASTROENTEROLOGY, 2019, 12
[28]   Low Counts of Faecalibacterium prausnitzii in Colitis Microbiota [J].
Sokol, H. ;
Seksik, P. ;
Furet, J. P. ;
Firmesse, O. ;
Nion-Larmurier, L. ;
Beaugerie, L. ;
Cosnes, J. ;
Corthier, G. ;
Marteau, P. ;
Dore, J. .
INFLAMMATORY BOWEL DISEASES, 2009, 15 (08) :1183-1189
[29]   Active Crohn's disease and ulcerative colitis can be specifically diagnosed and monitored based on the biostructure of the fecal flora [J].
Swidsinski, Alexander ;
Loening-Baucke, Vera ;
Vaneechoutte, Mario ;
Doerffel, Yvonne .
INFLAMMATORY BOWEL DISEASES, 2008, 14 (02) :147-161
[30]   Big data in IBD: big progress for clinical practice [J].
Tabib, Nasim Sadat Seyed ;
Madgwick, Matthew ;
Sudhakar, Padhmanand ;
Verstockt, Bram ;
Korcsmaros, Tamas ;
Vermeire, Severine .
GUT, 2020, 69 (08) :1520-1532