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


Journal

Clinical chemistry and laboratory medicine
ISSN: 1437-4331
Titre abrégé: Clin Chem Lab Med
Pays: Germany
ID NLM: 9806306

Informations de publication

Date de publication:
28 04 2020
Historique:
received: 06 11 2019
accepted: 26 01 2020
pubmed: 23 2 2020
medline: 21 5 2021
entrez: 22 2 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32084001
doi: 10.1515/cclm-2019-1146
pii: /j/cclm.ahead-of-print/cclm-2019-1146/cclm-2019-1146.xml
doi:
pii:

Substances chimiques

Biomarkers 0
Methylamines 0
trimethyloxamine FLD0K1SJ1A

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

733-740

Auteurs

Arne Gessner (A)

Institute of Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

Romina di Giuseppe (R)

Institute of Epidemiology, University Hospital of Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Manja Koch (M)

Institute of Epidemiology, University Hospital of Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Martin F Fromm (MF)

Institute of Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

Wolfgang Lieb (W)

Institute of Epidemiology, University Hospital of Schleswig-Holstein, Campus Kiel, Kiel, Germany.

Renke Maas (R)

Institute of Experimental and Clinical Pharmacology and Toxicology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.

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Classifications MeSH