Plasma Trimethylamine N-Oxide and Its Precursors: Population Epidemiology, Parent–Child Concordance, and Associations with Reported Dietary Intake in 11- to 12-Year-Old Children and Their Parents

Author:

Andraos Stephanie1ORCID,Lange Katherine23,Clifford Susan A23,Jones Beatrix4,Thorstensen Eric B1,Kerr Jessica A23,Wake Melissa23ORCID,Saffery Richard23ORCID,Burgner David P235,O'Sullivan Justin M1ORCID

Affiliation:

1. Liggins Institute, The University of Auckland, Auckland, New Zealand

2. The Murdoch Children's Research Institute, Parkville, Victoria, Australia

3. Department of Paediatrics, University of Melbourne, Parkville, Victoria, Australia

4. Department of Statistics, Faculty of Science, The University of Auckland, Auckland, New Zealand

5. Department of Paediatrics, Monash University, Clayton, Victoria, Australia

Abstract

Abstract Background Trimethylamine N-oxide (TMAO) is a microbiome- and diet-derived metabolite implicated in adverse cardiovascular outcomes. To date, studies of plasma TMAO concentrations have largely focused on individuals with metabolic disease. As such, data on TMAO concentrations in population settings and parent–child dyads are lacking. Objectives This study aimed to investigate parent–child concordance, age, and sex effects on plasma concentrations of TMAO and its precursors [l-carnitine, choline, betaine, and dimethylglycine (DMG)]. Associations between concentrations of TMAO and its precursors and self-reported dietary intakes of animal protein (i.e., red meat, meat products, chicken, fish, milk products, and cheese) and fast-food meals were also investigated. Methods A total of 1166 children (mean ± SD age: 11 ± 0.5 y, 51% female) and 1324 parents (mean ± SD age: 44 ± 5.1 y, 87% female) had a biomedical assessment as part of Growing Up in Australia's Child Health Checkpoint. Plasma TMAO and precursor concentrations were quantified using ultra-high-pressure LC coupled with tandem MS. Results Familial dyads significantly contributed to plasma TMAO and precursor concentrations (P < 0.0001), explaining 37% of variance for TMAO concentrations. Least-square mean ± SE plasma TMAO was lower in children (0.79 ± 0.02 µM on the log-scale) than in adults (1.22 ± 0.02 µM). By contrast, children's betaine (40.30 ± 0.34 µM) and DMG concentrations (1.02 ± 0.01 µM on the log-scale) were higher than adults’ betaine (37.50 ± 0.32 µM) and DMG concentrations (0.80 ± 0.01 µM) (P < 0.0001). Mean values of all metabolites, except adult TMAO, were higher in males than in females (P < 0.001). Greater reported intake of red meat and fish was associated with higher TMAO concentrations in both children [estimates (95% CIs) for red meat: 0.06 (0.01, 0.10); fish: 0.11 (0.06, 0.17)] and adults [red meat: 0.13 (0.08, 0.17); meat products: 0.07 (0.03, 0.12); and fish: 0.09 (0.04, 0.14)]. Conclusions Age, sex, and shared family factors, including diet, contribute to variation in plasma concentrations of TMAO and its precursors.

Funder

Ministry of Business, Innovation and Employment

The New Zealand-Australia Life Course Collaboration on Genes, Environment, Nutrition and Obesity

National Health and Medical Research Council

Children's Hospital Foundation

Financial Markets Foundation for Children

Victorian Deaf Education Institute

Murdoch Children's Research Institute

Victorian Government's Operational Infrastructure Support Program

New Zealand International Doctoral Research Scholarship 2017

National Heart Foundation of Australia

Honorary Future Leader Fellowship

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Food Science,Medicine (miscellaneous)

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