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. 2023 Nov 16;11:1220976. doi: 10.3389/fped.2023.1220976

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© 2023 Monleón-Getino, Pujol-Muncunill, Méndez Viera, Álvarez Carnero, Sanseverino, Paytuví-Gallart and Martín de Carpí.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Principal component analysis (PCA) biplot (variables and cases) of the clinical, biodiversity (richness, abundance, biodiversity indices) and other variables (DNA concentration, DNA purity) of all the samples and experimental groups of the study (CD, Crohn's disease; UC, ulcerative colitis; OR, oral samples; FE, faecal samples; HC, healthy control; DE, sampling points at disease onset/baseline; 3M, 3 months; 6M, 6 months). A point has been plotted for each of the 143 samples using sample type (FE, OR) and sample number (e.g., 102-DE, patient 102 at disease onset).