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. 2018 Apr 18;8:6153. doi: 10.1038/s41598-018-23844-y

Table 1.

Detected differential metabolites between NDS and NDAPS1 groups by LC-MS.

Metabolites Ion(m/z) Mean intensity Fold change p-value Physiological function Metabolic pathway
NDS NDAPS1 (NDAPS1/NDS)
Carnitine 162.112 267596.07 441492.50 1.65 0.009 Fatty acid degradation Lipid metabolism
Hexadecanoyl-L-carnitine 422.324 134.10 1892.88 14.12 0.017 Fatty acid degradation Lipid metabolism
L-Gulono-1,4-lactone 177.040 199.88 1880.93 9.41 0.017 Ascorbate biosynthesis Ascorbate and aldarate metabolism
L-Acetylcarnitine 204.123 845970.59 1018787.57 1.20 0.026 Insulin resistance Lipid metabolism
D-Glucurono-6,3-lactone 175.024 12205.64 2117.76 0.17 0.026 Ascorbic acid synthesis Ascorbate and aldarate metabolism
Hydroxykynurenine 225.086 1663.02 283.58 0.17 0.026 Amino acid biosynthesis Tryptophan metabolism
Pyruvic acid 87.008 4556.93 332.37 0.07 0.026 Energy source Citrate cycle
Taurocholate 514.284 1666.34 89307.51 53.60 0.041 Conjugated bile acid biosynthesis Taurine and hypotaurine metabolism
D-Glutamine 169.058 6640.24 8602.06 1.30 0.041 Insulin and glucose modulation D-Glutamine and D-glutamate metabolism
β-Aminoisobutyric acid 104.070 1459.53 3631.36 2.49 0.044 Branched-chain amino acid degradation Amino acid metabolism
Glycerol 3-phosphate 171.006 1163.82 420.82 0.36 0.044 Triacylglycerol biosynthesis Lipid metabolism

1 n = 6 per group.

2 Fold change was calculated by dividing the mean of the peak intensity of each metabolite from NDS and NDAPS1 groups.

3 Statistical analysis was conducted by using unpaired two-tailed student’s t-test.