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Licensed Unlicensed Requires Authentication Published by De Gruyter February 21, 2020

Trimethylamine-N-oxide (TMAO) determined by LC-MS/MS: distribution and correlates in the population-based PopGen cohort

  • Arne Gessner EMAIL logo , Romina di Giuseppe , Manja Koch , Martin F. Fromm , Wolfgang Lieb and Renke Maas

Abstract

Background

Accumulating evidence indicates that trimethylamine-N-oxide (TMAO) may play a causal role in cardiovascular disease (CVD), chronic kidney disease (CKD) and type 2 diabetes (T2D). TMAO plasma concentrations show considerable intra- and inter-individual variation, underscoring the need for a reference interval in the general population to identify elevated TMAO concentrations.

Methods

TMAO concentrations were determined using an LC-MS/MS assay in a community-based sample of the PopGen control cohort consisting of 694 participants (54% men; aged 25–82 years) free of clinical CVD, CKD and T2D. We defined reference intervals for TMAO concentrations in human plasma using the 2.5th and 97.5th percentiles. Using multivariable regression analysis we analyzed the association of estimated glomerular filtration rate (eGFR), sex, and dietary intake and TMAO plasma concentrations.

Results

TMAO plasma concentrations were positively skewed and differed by sex. The median TMAO plasma concentration in men was 3.91 (Q1–Q3: 2.87–6.10) μmol/L and the reference interval 1.28–19.67 μmol/L (2.5th–97.5th percentile). In women median TMAO plasma concentration was 3.56 (Q1–Q3: 2.41–5.15) μmol/L and the reference interval 1.08–17.12 μmol/L. In multivariable regression analysis plasma TMAO was associated with sex, renal function and diet. The association of TMAO and diet was significant for intake of fish and shellfish in men only.

Conclusions

In a community-based sample free of apparent CVD and renal disease, we report the distribution of TMAO plasma concentrations with sex, renal function and diet as factors associated with plasma TMAO, and suggest reference intervals. These data may facilitate standardized comparisons of TMAO across populations.


Corresponding author: Dr. Arne Gessner, Institute of Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Fahrstr. 17, 91054 Erlangen, Germany, Phone: +49 9131 85 22869, Fax: +49 9131 85 22773

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplementary Material

The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2019-1146).


Received: 2019-11-06
Accepted: 2020-01-26
Published Online: 2020-02-21
Published in Print: 2020-04-28

©2020 Walter de Gruyter GmbH, Berlin/Boston

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