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. Author manuscript; available in PMC: 2017 Nov 15.
Published in final edited form as: Am J Cardiol. 2016 Aug 24;118(10):1493–1496. doi: 10.1016/j.amjcard.2016.08.010

Table 3.

Metabolites previously studied

First author, Year Metabolite source Main findings
Metabolomics studies
Alonso, 201514 Human serum Higher incident AF risk associated with higher concentrations of glycolithocholate sulfate and glycocholenate sulfate
De Souza, 20102 Canine atrial tissue After 2 weeks of ventricular-tachypacing, ADP+ATP, alanine, betaine, glucose, glutamate, NAD+NADH, and taurine levels were increased and α-ketoisovalerate level was decreased
Mayer, 20081 Human atrial tissue Higher concentrations of β-hydroxybuterate and glycine in the AF group compared to the sinus rhythm group
Non-metabolomics studies
Tamariz, 20115 Human serum Higher risk of AF associated with higher uric acid concentration
Neuman, 20079 Human plasma Increased oxidation of glutathione and derivatives of reactive oxygen metabolites in the AF group compared to control
Ramlawai, 200710 Human atrial tissue, serum Tissue: Higher peroxide level in the AF group compared to control
Serum: Higher peroxide level in the AF group at 6 hours after surgery but not at post-operative day 4
Mihm, 20018 Human atrial tissue MM-CK activity was reduced and 3-nitrotyrosine concentration was increased in the AF group compared to control
Ausma, 20003 Goat atrial tissue Phosphocreatine level dropped during the first 8 weeks of AF induction and then returned to normal at 16 weeks; levels of creatine, ATP, ADP, AMP, GDP, GTP, and NAD did not change significantly.
Uno, 19864 Canine plasma cGMP concentration increased significantly with AF induction; cAMP concentration did not change

ADP, adenosine diphosphate; AF, atrial fibrillation; ATP, adenosine triphosphate; cAMP, cyclic (c) adenosine monophosphate (AMP); cGMP, cyclic (c) guanosine monophosphate (GMP); GDP, guanosine diphosphate; GTP, guanosine triphosphate; NADH, nicotinamide adenine dinucleotide (NAD) + hydrogen (H); MM-CK, myofibrillar creatine kinase