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Table 1.

Baseline demographic and clinical characteristics.

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Fig 1.

Measures of alpha-diversity (Shannon Index and number (#) of observed operationalized taxonomic units (ESVs)) by ≤ vs. > median weight adjusted TAC dose (1A and 1B) and by ≤ vs. > median Level/Dose (L/D) ratio (1C and 1D).

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Fig 2.

Principle coordinates, derived from the Bray-Curtis dissimilarity index, plotted according tovs. > median weight adjusted TAC dose (left) andvs. > median Level/Dose (L/D) ratio (right). Ellipses represent a 95% confidence interval for the data, assuming a normal distribution.

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Fig 2 Expand

Fig 3.

Top: Relative abundance of phyla per sample in ≤ vs > median weight adjusted TAC dose. Bottom: phyla composition by sample. No statistically significant difference was observed in phyla relative abundance by TAC dose group.

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Fig 3 Expand

Fig 4.

Firmicutes to Bacteroidetes ratio (using rarefied data) by TAC group.

There is no statistical significance (p-value = 0.76) and the mean values are similar (165 and 188, respectively).

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Fig 4 Expand

Fig 5.

Stacked bar chart showing relative abundance of ESVs observed to be statistically significantly different between patients with ≤ vs. > median weight adjusted TAC dose.

Taxa shown signififcantly differed in both adjusted and unadjusted analyses. Segments within a stack correspond to a single ESV and are colored according to genera. ESVs that did not significantly differ between TAC dose group are not displayed.

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Fig 5 Expand

Table 2.

Biomarkers of endotoxemia (LPS), inflammation(TNF-alpha) and oxidative stress (isoprostane) by tacrolimus dosing requirements.

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Table 2 Expand

Table 3.

Correlation between Shannon index and number of observed ESVs (alpha diversity metrics) and biomarkers of inflammation, endotoxemia and oxidative stress.

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Table 3 Expand