Serum Trimethylamine N-Oxide as a Diagnostic and Prognostic Biomarker in Dogs with Chronic Kidney Disease: A Pilot Study

Trimethylamine N-oxide (TMAO) is known to increase in human cardiovascular, metabolic, and renal diseases. In human medicine, TMAO has recently been utilized as a diagnostic and prognostic biomarker for renal dysfunction, and research is ongoing regarding its potential as a therapeutic target. This...

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Main Authors: Seung-Ju Kang, Wan-Gyu Kim, Keon Kim, Chang-Hyeon Choi, Jong-Hwan Park, Seog-Jin Kang, Chang-Min Lee, Yoon Jung Do, Woong-Bin Ro
Format: Article
Language:English
Published: MDPI AG 2025-07-01
Series:Animals
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Online Access:https://www.mdpi.com/2076-2615/15/15/2170
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Summary:Trimethylamine N-oxide (TMAO) is known to increase in human cardiovascular, metabolic, and renal diseases. In human medicine, TMAO has recently been utilized as a diagnostic and prognostic biomarker for renal dysfunction, and research is ongoing regarding its potential as a therapeutic target. This study aimed to evaluate the diagnostic and prognostic potential of TMAO as a supportive biomarker in dogs with chronic kidney disease (CKD). To assess its diagnostic utility, TMAO concentrations were compared between a CKD group (<i>n</i> = 32) and a healthy control group (<i>n</i> = 32). In addition, patients with CKD were subdivided into stages 2 (<i>n</i> = 12), 3 (<i>n</i> = 11), and 4 (<i>n</i> = 9) and compared individually with the healthy controls. For prognostic evaluation, the CKD group was monitored over six months, and the TMAO levels were compared between survivors (<i>n</i> = 18) and non-survivors (<i>n</i> = 14). The TMAO concentrations showed a highly significant difference between patients with CKD and healthy controls (<i>p</i> < 0.0001). Patients with each different CKD stage exhibited statistically significant differences compared with the healthy controls (<i>p</i> < 0.05). Furthermore, the median TMAO levels tended to increase with advancing CKD stage; however, the differences among stages were not statistically significant. In addition, within the CKD group, TMAO concentrations were significantly higher in non-survivors than in survivors at the six-month follow-up (<i>p</i> = 0.0142). This pilot study highlights the potential of TMAO as a supportive renal biomarker for diagnostic and prognostic evaluation in canine CKD.
ISSN:2076-2615