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We read with interest the work by Pascal et al published recently in Gut.1 Here, they report the volatile microbial signatures of patients with Crohn’s disease (CD), a quality that greatly hinders our ability to classify healthy from affected subjects using 16S rRNA profiles from stool. Nonetheless, their work overcame these and other complications,2 producing a decision tree that classifies subjects with CD, UC, irritable bowel syndrome and anorexia. Although the authors note that both subtypes of IBD, particularly CD, have increased microbial community instability, this information is not used as a feature to improve classifier accuracy. Could microbiome instability become actionable by creating a new classifier that benefits from repeated measurements? If so, how many samples per individual are needed to assess instability?
We collected daily stool samples for up to 6 weeks from 19 CD subjects and 12 controls (see the analysis notebook for cohort description, methods and data, https://github.com/knightlab-analyses/longitudinal-ibd) over two separate periods of 2 or 4 weeks spread over 2 and 5 months, for a total of 960 samples. We believe that this is the most densely sampled longitudinal study of CD; previous studies collected samples every 1–3 months.1 3 Our cohort shows decreased alpha diversity and increased stability, as previously reported in CD and other subtypes of IBD.1 3–5 We also noted that subjects who underwent resection have lower alpha diversity than other CD-affected subjects (see analysis notebooks, https://github.com/knightlab-analyses/longitudinal-ibd).
A critical experimental design question for clinical studies is whether a finite budget should best be spent collecting samples from more patients or collecting more serial samples from each patient? Therefore, we created a Random Forests6 model based on per subject aggregation of longitudinal data for alpha diversity,7 beta diversity8 and abundances of two phylogenetic factors found to be associated with CD in ileal biopsies5 9 (figure 1). With one sample per subject, our model performs worse than a classifier that uses microbial relative abundances at a single time point, but when more samples per subject are added, the classifier outperforms that approach and results previously only attained with biopsy samples.5 Furthermore, we replicate this observation with a different cohort (table 1).
Novel analyses aggregating features over time and combining both alpha and beta diversity over time using our intensive daily sampling demonstrate that the main benefits are already obtained by collecting between three and five faecal specimens, and no additional benefits are obtained beyond seven serial samples. Similar results are found for monthly sampling. These results highlight the importance of treating CD as a volatile, time-varying condition, even during clinical remission, but provide hope to clinicians in that a relatively small number of samples yield large additional benefits, facilitating patient compliance. This information can be used to design collection of faecal samples for a large prospective cohort of patients with CD for longitudinal studies of host–microbial interactions over time.
The methods demonstrated here have not previously been used for microbiome analyses but have been used for other engineering applications, for example, in production lines to predict product specification outcomes in a steel manufacturer’s facility.10 We expect the results to generalise in other systems, including other GI and hepatic disorders, where dynamic features of the microbiome, host gene expression or other accessible descriptors can act as indicators of underlying dysbiotic states.
We thank the research coordinators of the UNC Multidisciplinary IBD Center at UNC for patient recruitment. Additionally, we thank Gail Ackermann, Jamie Morton and Justin Silverman for their invaluable feedback and discussion provided in the preparation of this manuscript.
HHH, RBS and RK contributed equally.
Contributors YVB wrote the manuscript, managed the data depositions and interpreted and analysed the data. AG contributed to the manuscript and interpreted and analysed the data. ZZX interpreted and analysed the data. AW contributed to the manuscript and interpreted and analysed the data. HHH contributed to the manuscript, designed the experiment and interpreted and analysed the data. RBS wrote the manuscript, designed the experiment and interpreted and analysed the data. RK wrote the manuscript and interpreted, sequenced and analysed the data. All authors finalised and approved the current version of the manuscript.
Funding We acknowledge grant support by NIH (P01-DK094779) and the Crohn’s and Colitis Foundation.
Competing interests None declared.
Ethics approval University of North Carolina.
Provenance and peer review Not commissioned; internally peer reviewed.
Data sharing statement The sequences will be deposited in EBI. In addition, the processed sequences and sample information can be found in the Qiita (https://qiita.ucsd.edu/study/description/2538) database under the study identifier 2538.Jupyter notebooks, and source code describing all the analyses in this paper can be found online (https://github.com/knightlab-analyses/longitudinal-ibd).
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