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. 2017 Jan 8;9(1):1–17. doi: 10.4254/wjh.v9.i1.1

Table 2.

Significantly altered metabolites in cirrhosis patients vs healthy volunteers

Ref. Platform Tissue (organism) Significantly altered metabolites in cirrhosis patients vs healthy volunteers Main pathways distinguishing cirrhosis from healthy volunteers
Gao et al[33] 1H NMR Serum (human) Isoleucine ↓ Amino acid metabolism
Leucine ↓
Valine ↓
Glutamine ↑
Tyrosine ↑
Phenylalanine ↑
1-methylhistidine ↑
N-acetylglycoproteins ↑
Acetate ↑ N-acetylglycoprotein
Acetoacetate ↓ Ketonogenesis
Pyruvate ↑
α-ketoglutarate ↑ Glycolysis
Choline ↓ TCA cycle
Taurine ↑
Glycerol ↑ Bile acid metabolism
Li et al[42] UPLC/QTOF-MS Serum (mouse) Leucine ↓ Amino acid metabolism
Phenylpyruvic acid ↓
Phenylalanine ↓
Tryptophan ↓
LPE (16:0) ↓ LPE metabolism
LPE (18:0) ↓
LPC (16:0) ↓ LPC metabolism
LPC (20:1) ↓
LPC (22:6) ↑
PC (16:0/18:3) ↑ Phosphatidylcholine metabolism
PC (12:1/24:3) ↑
PC (16:0/20:4) ↑
PC (16:0/22:6) ↑
PC (18:0/20:4) ↑ Sphingomyelin metabolism
SM (d18:0/16:1) ↓
Soga et al[35] Capillary elecrtophore-sis/TOF-MS Serum (human) γ-glutamylalanine ↑ Glutathione metabolism
γ-glutamylvaline ↑
γ-glutamylglutamine ↑
γ-glutamylphenyl-
γ-glutamylcitrulline ↑
Alanine ↑ Amino acid metabolism
Methionine sulfoxide ↑
Wang et al[38] UPLC/MS-MS; LC/QTOF-MS Serum (human) LPC-16:0 ↓ LPC metabolism
LPC-18:0 ↓
16:0/18:1-PC ↓
16:0/18:2-PC ↓
16:0/20:4-PC ↓
16:0/22:6-PC ↓
18:0/18:2-PC ↓
Oleamide ↑ Fatty acid metabolism
Phenylalanine ↑
GCDCA ↑ Bile acid metabolism
Canavaninosuccinate ↓ Arginosuccinate synthetase pathway
Zhou et al[39] UPLC/QTOF-MS Serum (human) Phenylalanine ↑ Amino acid metabolism
GCA ↑ Bile acid metabolism
GDCA ↑
Bilirubin ↑ Hemoglobin metabolism
LPE (18:2) ↓ Lysolipid metabolism
LPC (22:6) ↓
LPC (18:2) ↓
LPC (20:4) ↓
LPC (16:0) ↓
LPC (18:0) ↓
C18:1-CN ↑ CPT shuttle system
Chen et al[30] UPLC/QTOF-MS Serum (human); Inositol ↓ TCA cycle
Urine (human) 2,2-bipyridine ↓
Methionine ↓ Amino acid metabolism
Tyrosine ↓
Arginine ↓ Fatty acid metabolism
Stearic acid ↓
Palmitic acid ↓
Citric acid ↓
2-piperidine carboxylic acid ↓
5-Hydroxy-tryptophan ↓
Cao et al[32] UPLC/MS Fecal (human) Chenodeoxycholic Bile acid metabolism
Acid dimeride ↓
Urobilin ↓ Hemoglobin metabolism
Urobilinogen ↓
7-ketolithocholic acid ↓ Microbiome metabolism
LPC C18:0 ↑ LPC metabolism
LPC C16:0 ↑
Yin et al[41] RPLC/MS Serum (human) Hypoxanthine ↓ Purine synthesis
Inosine ↓
Bilirubin ↑ Hemoglobin metabolism
GCA ↑ Bile acid metabolism
GCDCA ↑
Taurine ↓
LPC C18:2 ↓ LPC metabolism
LPC C18:3 ↓
LPC C16:1 ↓
LPC C18:0 ↓
LPC C16:1 ↓
L-acetylcarnitine ↑ CPT shuttle system
6-Methylnicotinic acid ↓ Nicotine metabolism
Fitian et al[45] Integrated UPLC/MS-MS and GC/MS Serum (human) Glycocholate (GCA) ↑ Bile acid metabolism
Tauroursodeoxycholate ↑
Glychochemodeoxycholate ↑
Azelate (nonanedioate) ↑ Dicarboxylic acid metabolism
Undecanedioate ↑
Sebacate (decanedioate) ↑
Hexadecanedioate↑
Tetradecanedioate↑
DSGEGDFXAEGGGVR ↑ Fibrinogen cleavage peptide
ADSGEGDFXAEGGGVR ↑
Bilirubin (Z,Z) ↑ Hemoglobin catabolism metabolite
Biliverdin ↑
1,2-propanediol ↑ Ketogenesis
Succinylcarnitine ↑ CPT shuttle system
Acetylcarnitine ↑
Glutarylcarnitine ↑
Gao et al[46] GC-TOF/MS Serum (human) Palmitic acid ↑ Fatty acid metabolism
Stearic acid ↑
Oleic acid ↑
Arachidic acid ↑ Arachidonic acid metabolism
Aminomalonic acid ↑ Dicarboxylic acid metabolism
Phenylalanine ↑ Amino acid metabolism
Cysteine ↑
Leucine ↑
Citric acid ↑
Oxoproline ↑

EtOH: Alcohol; TOCSY: Total correlation spectroscopy; HH: Hereditary hemochromatosis; TCA: Tricarboxylic acid; UPLC: Ultrahigh-performance liquid chromatography; QTOF: Quadrupole time of flight; SELDI: Surface-enhanced laser desorption/ionization; HRMAS: High-resolution magic angle spinning; LPE: Lysophosphatidyethanolamine; LPC: Lysophosphatidylcholine; MS: Mass spectrometry; TOF: Time-of-flight; NMR: Nuclear magnetic resonance; LC: Liquid chromatography; GC: Gas chromatography; CPT: Carnitine palmitoyltransferase; TCA: Tricarboxylic acid.