Copyright
©The Author(s) 2019.
World J Gastroenterol. Aug 14, 2019; 25(30): 4043-4050
Published online Aug 14, 2019. doi: 10.3748/wjg.v25.i30.4043
Published online Aug 14, 2019. doi: 10.3748/wjg.v25.i30.4043
Compounds and molecules | Metabolic disturbances |
Nitrogen derivatives | |
Ammonia[14] | Altered urea cycle |
Trimethylamine[29] | Reduced hepatic catabolism of trimethylamine and/or increased degradation and absorption of dietary phosphatidylcholine and choline mediated by altered intestinal microbiome |
Ketones[16] | Increased insulin resistance, hepatic glycogen exhaustion, hepatic gluconeogenesis impairment |
Sulfur derivatives[8] | Incomplete metabolism of sulfur-containing amino acids in the transamination pathway |
Dimethylsulfide[12] | Main responsible for fetor hepaticus |
Alkanes, alkenes, terpenes and aliphatic acids[29] | Lipid peroxidation mediated by oxygen radical produced by hepatic CYP activity |
Ethane and pentane[30] | More typical of alcohol induced liver injury |
Limonene[13] | Impaired biotransformation by CYP2C (partially dependent on dietary intake of citrus fruits and vegetable) |
Acetic and propionic acid[9] | Reduced hepatic metabolism of short chain fatty acids produced by gut microbiome |
Alcohols | |
Methanol[22] | Pectin degradation; its levels are partially dependent on dietary intake of fruits and on a variable role of intestinal microbiome |
Ethanol[31] | More typical of NAFLD, even in complete absence of alcohol consumption; possible role of intestinal microbiome in the production of ethanol in obese patients |
- Citation: De Vincentis A, Vespasiani-Gentilucci U, Sabatini A, Antonelli-Incalzi R, Picardi A. Exhaled breath analysis in hepatology: State-of-the-art and perspectives. World J Gastroenterol 2019; 25(30): 4043-4050
- URL: https://www.wjgnet.com/1007-9327/full/v25/i30/4043.htm
- DOI: https://dx.doi.org/10.3748/wjg.v25.i30.4043