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. 2016 May 26;11(5):e0156166. doi: 10.1371/journal.pone.0156166

Table 2. Detailed information of hub areas in differentially covaried network of CHB.

Involved pathway/function Metabolites/Covariations Change in CHB* Significance**
Glycine metabolism Glycine synthesis Glycine(S) 0.68 (76.6%) P = 0.00026
Glycine(U)—Glycerate(S) Decreased (0.55→-0.085) Z = -3.33
Phenolic compound metabolism Glycine(U)—4-Hydroxyhippurate(U) Increased (-0.11→0.49) Z = 3.57
Tyrosine(S) 1.43 (66.2%) P = 0.01
Bile acid synthesis Glycine(S)—Cholesterol(S) Increased (-0.27→0.34) Z = 3.71
Bile acid (Clinical indicator) 2.30 (54.6%) P = 1.29E-05
Entering into TCA cycle Glycine(S)—Malic acid(S) Increased (-0.58→0.19) Z = -4.16
TCA cycle Fatty acids~ TCA cycle Succinate(S)—Oleic acid(S) Decreased (0.70→0.007) Z = -3.30
Citrate(U)—Glycerol 1-octadecanoate(S) Decreased (0.59→-0.026) Z = -2.99
Fatty acids Hexadecanoic acid(S) 1.65 (75.9%) P = 0.0019
Oleic acid 1.61 (75.2%) P = 0.0031
Stearic acid(S) 1.43 (68.3%) P = 0.0075

* For metabolites, the data is presented as the fold change (CHB/health) followed by proportion of CHB patients showing higher/lower level than the average value of healthy controls. For covariations, the data is presented as increased/decreased (CorhealthCorCHB).

** For metabolites, the significance was measured by P-value from two tailed student’s t test; and for covariations, Z-score was used instead. A significant difference between CHB group and healthy control exists if p-value < 0.05 or |Z| > 3.