Trimethylamine N-oxide (TMAO) Is not Associated with Cardiometabolic Phenotypes and Inflammatory Markers in Children and Adults.

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dc.contributor.author Andraos, Stephanie
dc.contributor.author Jones, Beatrix
dc.contributor.author Lange, Katherine
dc.contributor.author Clifford, Susan A
dc.contributor.author Thorstensen, Eric B
dc.contributor.author Kerr, Jessica A
dc.contributor.author Wake, Melissa
dc.contributor.author Saffery, Richard
dc.contributor.author Burgner, David P
dc.contributor.author O'Sullivan, Justin M
dc.coverage.spatial United States
dc.date.accessioned 2023-07-25T03:22:33Z
dc.date.available 2023-07-25T03:22:33Z
dc.date.issued 2021-01
dc.identifier.citation (2021). Current Developments in Nutrition, 5(1), nzaa179-.
dc.identifier.issn 2475-2991
dc.identifier.uri https://hdl.handle.net/2292/65053
dc.description.abstract <h4>Background</h4>Trimethylamine N-oxide (TMAO) is a diet- and microbiome-derived metabolite and a proposed biomarker of adverse cardiometabolic outcomes. TMAO studies have mainly been conducted in individuals with cardiometabolic disease, and studies in population-derived samples are limited.<h4>Objective</h4>We aimed to investigate the associations between plasma TMAO concentrations and its precursors [carnitine, choline, betaine, and dimethylglycine (DMG)] with metabolic syndrome (MetS) scores, preclinical cardiovascular phenotypes, and inflammatory biomarkers (i.e. high-sensitivity C-reactive protein and serum glycoprotein acetyls) in a population-derived cohort of children and their parents.<h4>Methods</h4>The concentrations of TMAO and its precursors were quantified using UHPLC coupled with tandem MS (UHPLC/MS-MS) in 1166 children (mean age 11 y ± 0.5 y, 51% female) and 1324 adults (44 y ± 5.1 y, 87% female) participating in The Growing Up in Australia's Child Health CheckPoint Study. We developed multivariable fractional polynomial models to analyze associations between TMAO, its precursors, MetS (adjusted for sex and age), and cardiovascular phenotypes (adjusted for sex, age, BMI, household income, and the urinary albumin to creatinine ratio). Pearson's correlations were computed to identify associations between TMAO, its precursors, and inflammatory biomarkers.<h4>Results</h4>The concentrations of TMAO precursors, but not TMAO itself, were associated with MetS, cardiovascular phenotypes, and inflammatory biomarkers in children and adults.<h4>Conclusions</h4>TMAO precursors, but not TMAO itself, were associated with adverse cardiometabolic and inflammatory phenotypes in children and adults. TMAO precursor concentrations may better reflect cardiovascular health and inflammatory status within the wider population. Replication in other population settings and mechanistic studies are warranted.
dc.format.medium Electronic-eCollection
dc.language eng
dc.publisher Elsevier
dc.relation.ispartofseries Current developments in nutrition
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.rights.uri http://creativecommons.org/licenses/by-nc/4.0/
dc.subject Growing Up in Australia
dc.subject TMAO
dc.subject adults
dc.subject cardiovascular preclinical phenotypes
dc.subject children
dc.subject epidemiology
dc.subject Nutrition
dc.subject Pediatric
dc.subject Clinical Research
dc.subject Heart Disease
dc.subject Cardiovascular
dc.subject 3 Good Health and Well Being
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Nutrition & Dietetics
dc.subject AGED 11-12 YEARS
dc.subject POPULATION EPIDEMIOLOGY
dc.subject METABOLIC SYNDROME
dc.subject PLASMA DIMETHYLGLYCINE
dc.subject L-CARNITINE
dc.subject RISK
dc.subject CONCORDANCE
dc.subject CHOLINE
dc.subject BETAINE
dc.subject PHOSPHATIDYLCHOLINE
dc.title Trimethylamine N-oxide (TMAO) Is not Associated with Cardiometabolic Phenotypes and Inflammatory Markers in Children and Adults.
dc.type Journal Article
dc.identifier.doi 10.1093/cdn/nzaa179
pubs.issue 1
pubs.begin-page nzaa179
pubs.volume 5
dc.date.updated 2023-06-28T03:13:08Z
dc.rights.holder Copyright: The authors en
dc.identifier.pmid 33501405 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/33501405
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/OpenAccess en
pubs.subtype research-article
pubs.subtype Journal Article
pubs.elements-id 831973
pubs.org-id Liggins Institute
pubs.org-id Science
pubs.org-id Statistics
dc.identifier.eissn 2475-2991
dc.identifier.pii nzaa179
pubs.number nzaa179
pubs.record-created-at-source-date 2023-06-28
pubs.online-publication-date 2020-12-11


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