Cited by 122Dialysis and Renal Disease ManagementParathyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Mechanism of Prominent Trimethylamine Oxide (TMAO) Accumulation in Hemodialysis Patients

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Hai, Xin, Landeras, Veeda, Dobre, Mirela A., DeOreo, Peter, Meyer, Timothy W., Hostetter, Thomas H.·2015·PLOS ONE

Abstract

Large size, protein binding and intracellular sequestration are well known to limit dialytic removal of compounds. In studying the normal renal and dialytic handling of trimethylamine oxide (TMAO), a molecule associated with cardiovascular disease in the general population, we discovered two largely unrecognized additional limitations to sustained reduction of a solute by chronic hemodialysis. We measured solute levels and handling in subjects on chronic hemodialysis (ESRD, n = 7) and compared these with levels and clearance in normal controls (NLS, n = 6). The ESRD patients had much higher peak predialysis plasma levels of TMAO than NLS (77 ± 26 vs 2±1 μM, mean ± SD, p<0.05). For comparison, predialysis BUN levels in ESRD subjects were 45±11 mg/dl and 15±3 mg/dl in NLS. Thus TMAO levels in ESRD average about 40 fold those in NLS while BUN is 3 fold NLS. However, the fractional reduction of TMAO concentration during dialysis, was in fact greater than that of urea (86±3 vs 74±6%, TMAO vs urea, p < 0.05) and its dialytic clearance while somewhat lower than that of urea was comparable to creatinine's. Also production rates were similar (533±272 vs 606 ± 220 μ moles/day, ESRD vs NLS, p>0.05). However, TMAO has a volume of distribution about one half that of urea. Also in NLS the urinary clearance of TMAO was high (219±78 ml/min) compared to the urinary urea and creatinine clearances (55±14 and 119±21 ml/min, respectively). Thus, TMAO levels achieve multiples of normal much greater than those of urea due mainly to 1) TMAO's high clearance by the normal kidney relative to urea and 2) its smaller volume of distribution. Modelling suggests that only much more frequent dialysis would be required to lower levels Thus, additional strategies such as reducing production should be explored. Furthermore, using urea as the sole marker of dialysis adequacy may be misleading since a molecule, TMAO, that is dialyzed readily accumulates to much higher multiples of normal with urea based dialysis prescriptions.

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  • TMAO is cleared more efficiently than urea by normal kidney function but not by dialysis.

    “TMAO is cleared more efficiently than urea by the normal kidney function but not by dialysis (45).”
  • Accumulation of TMAO in ESRD patients on chronic hemodialysis is mainly due to a previously unrecognized limitation of chronic dialysis.

    “It was suggested that the accumulation of TMAO in end-stage renal disease patients who receive chronic hemodialysis is mainly due to the previously unrecognized limitation of chronic dialysis (45).”
  • The high renal clearance rate of TMAO indicates that in addition to glomerular filtration, at least 50% of its renal excretion possibly occurs through tubular secretion.

    “The high renal clearance rate of TMAO indicates that in addition to glomerular filtration, at least 50% of its renal excretion possibly occurs through tubular secretion.”

    From Trimethylamine N-oxide: the good, the bad and the unknown. (2016) · cites this paper as [26]

  • TMAO has a small volume of distribution-about one half that of urea-but a higher renal clearance compared to urea and creatinine.

    “Studies on pharmacokinetics [25] and renal clearance of TMAO [26] in healthy human subjects suggest that TMAO has a small volume of distribution—about one half that of urea—but a higher renal clearance compared to urea and creatinine.”

    From Trimethylamine N-oxide: the good, the bad and the unknown. (2016) · cites this paper as [26]

  • In normal subjects, urinary clearance of TMAO was 219 ± 78 mL/min compared to urinary urea and creatinine clearances 55 ± 14 and 119 ± 21 mL/min, respectively.

    “In normal subjects, the urinary clearance of TMAO was 219 ± 78 mL/min compared to the urinary urea and creatinine clearances 55 ± 14 and 119 ± 21 mL/min, respectively.”

    From Trimethylamine N-oxide: the good, the bad and the unknown. (2016) · cites this paper as [26]

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References 17 · Cited by 122

Authors
Hai, X., Landeras, V., Dobre, M. A., DeOreo, P., Meyer, T. W., & Hostetter, T. H.
Affiliations
  • Case Western Reserve University (US)
  • Stanford Medicine (US)
Corresponding author
Hostetter, Thomas H.
Venue
PLOS ONE
Published
2015-12-09
Volume
10
Issue
12
Pages
e0143731
ISSN
1932-6203 (ISSN-L)
OpenAlex
W2190510948
Cited by
122
References
17
Citations by year
2026: 8 · 2025: 16 · 2024: 12 · 2023: 13 · 2022: 13 · 2021: 12 · 2020: 12 · 2019: 7 · 2018: 14 · 2017: 7 · 2016: 7
FWCI
8.09
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, public-domain)
  • Europe PMC (PubMed Central) (publishedVersion, public-domain)
  • PubMed Central (publishedVersion, public-domain)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • American Heart Association
  • Rosenberg Foundation
  • National Institutes of Health
  • National Institute of Diabetes and Digestive and Kidney Diseases (R01DK080123)
Topics
  • Health Sciences › Medicine › Nephrology › Dialysis and Renal Disease Management
  • Health Sciences › Medicine › Nephrology › Parathyroid Disorders and Treatments
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
Keywords
trimethylamine N-oxide, maintenance hemodialysis, end-stage renal disease, dialytic clearance, urea clearance, volume of distribution, urinary clearance, dialysis adequacy, cardiovascular biomarkers, urea reduction ratio
MeSH terms
Adult, Creatinine, Female, Renal Dialysis, Humans, Kidney Failure, Chronic, Male, Methylamines, Urea, Biomarkers, Case-Control Studies

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