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. 2024 May 8;16(1):2347715. doi: 10.1080/19490976.2024.2347715

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© 2024 Société des Produits Nestlé SA. Published with license by Taylor & Francis Group, LLC.

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

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Figure 1. — Fecal BL NCC3001 relative abundance and associations with clinical outcomes.

A) BL NCC3001 abundance in feces at baseline (V1) and at the end of intervention (V2) per group. B) Fecal BL NCC3001 abundance in responders [≥2 points improvement in HADD score (1)] and not responders [<2 points improvement in HADD score (0)]; p-value of Wilcoxon test. C) Correlation between the difference of HADD score (V2-V1) and BL NCC3001 abundance at V2; Spearman test. D) Correlation between amygdala activation (fMRi) and BL NCC3001 abundance at V2; Spearman test. E) Fecal BL NCC3001 abundance in responders [≥2 points improvement in HADA score (1)] and non-responders [<2 points improvement in HADA score (0)]; p-value of Wilcoxon test. F) Correlation between the difference in HADA score (V2-V1) and BL NCC3001 abundance at V2; Spearman test. BL NCC3001 (BL, open circle); Placebo (P, closed circle).