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. 2023 Jan 1;13(1):66. doi: 10.3390/metabo13010066

Table 2.

Pathway topological analysis showing the human metabolic pathways most significantly affected by acute sore throat disease pathology; the number of metabolites featured in each pathway, and the number of metabolite ‘hits’ are shown, as are the corresponding FDR-corrected p values for these contributions. The Homo sapiens pathway library was selected, which contained a total of 80 pathways. The chosen pathway library code was hsa (KEGG organisms abbreviation). The selected pathway enrichment analysis method and node importance measure for this toplogical analysis were globaltest and relative betweenness centrality, respectively. The ‘betweenness centrality’ determines the shortest path number passing through the node, and this is also employed as an importance measure for metabolites, since in this case the metabolic network is directed. The impact is the pathway impact value, which represents the matched metabolite node cumulative percentage values from all such nodes featured (computed from this pathway topological analysis). As many as 13 other metabolic pathways had FDR-corrected p values lying between 7.18 × 10−11 and 0.045, and these also may be implicated in the pathogenesis of pharyngitis, although less significantly so than those displayed in this Table.

Metabolic Pathway Total Metabolites No. of Hits FDR Impact
Arginine and proline metabolism 38 2 7.94 × 10−39 0.09
Alanine, aspartate and glutamate
metabolism
28 4 3.38 × 10−34 0.31
Cysteine and methionine metabolism 33 1 6.94 × 10−13 0.00
Glyoxylate and dicarboxylate
metabolism
32 4 6.94 × 10−13 0.11
Histidine metabolism 16 1 2.50 × 10−12 0.00
Nitrogen metabolism 6 2 1.99 × 10−11 0.00
Pyruvate metabolism 22 2 1.99 × 10−11 0.21
Glycolysis/Gluconeogenesis 26 2 1.99 × 10−11 0.10
Butanoate metabolism 15 2 2.27 × 10−11 0.00
Glutathione metabolism 28 2 7.18 × 10−11 0.10