Trimethylamine <i>N</i> ‐oxide is elevated in postmenopausal women relative to age‐matched men and premenopausal women among individuals with obesity

Trimethylamine N-oxide (TMAO) is linked to arterial stiffness and atherosclerosis. Cardiovascular disease (CVD) risk increases following menopause in women. Whether menopause influences plasma TMAO metabolism to mediate CVD risk is unknown. Women with obesity were classified as premenopausal (n = 13; 40.3 ± 2.7 years; 39.4 ± 2.0 kg/m<sup>2</sup>) or postmenopausal (n = 22; 56.5 ± 1.1 years; 35.6 ± 0.9 kg/m<sup>2</sup>) via self-reported presence/absence of menses (last 12 months). Men were age- and body mass index-matched to postmenopausal women (n = 16; 55.9 ± 2.1 years; 34.3 ± 1.2 kg/m<sup>2</sup>) as controls to discern potential menopause-driven TMAO differences. Carotid-femoral pulse wave velocity (cfPWV) and pulse wave analysis (applanation tonometry) were analysed to assess arterial stiffness, aortic waveforms and blood pressure. Fasting plasma TMAO and precursors (carnitine, choline, betaine and trimethylamine (TMA)) were assessed (mass spectroscopy). A 180 min 75 g oral glucose tolerance test was performed to approximate insulin sensitivity and quantify vascular cell (vascular cell adhesion molecule 1 (VCAM-1)) and intercellular adhesion molecules (intercellular adhesion molecule 1 (ICAM-1)). Body composition (DXA/BodPod) and fitness ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>V</mml:mi> <mml:mo>̇</mml:mo></mml:mover> <mml:mrow><mml:msub><mml:mi>O</mml:mi> <mml:mn>2</mml:mn></mml:msub> <mml:mi>peak</mml:mi></mml:mrow> </mml:msub> <mml:annotation>${\dot V_{{{\mathrm{O}}_2}{\mathrm{peak}}}}$</mml:annotation></mml:semantics> </mml:math> ) were measured. Premenopausal women were younger than men and postmenopausal women (P < 0.0001, η<sup>2</sup> = 2.29). Men had lower body fat (P = 0.001, η<sup>2</sup> = 0.80) and higher fat-free mass (P = 0.004, η<sup>2</sup> = 0.42) compared to both pre- and postmenopausal women. There were no differences among groups in fitness, insulin sensitivity, ICAM-1 or blood pressure (P > 0.05), but men had higher cfPWV (P = 0.040, η<sup>2</sup> = 0.27) and VCAM-1 (P = 0.041, η<sup>2</sup> = 0.32). Postmenopausal women had elevated TMAO (P = 0.040, η<sup>2</sup> = 0.29), compared with men and premenopausal women, yet men had elevated TMA (P = 0.041, η<sup>2</sup> = 0.17), carnitine (P = 0.003, η<sup>2</sup> = 0.27), choline (P = 0.022, η<sup>2</sup> = 0.35) and betaine (P < 0.0001, η<sup>2</sup> = 0.59). Thus when taken together, menopause may raise TMAO in women, while older men appear to have unique TMAO precursor metabolism linked to CVD risk.

Authors

Institutions

Publication Details

Journal
Experimental Physiology
Published
2025-07-20
DOI
https://doi.org/10.1113/ep092550
Citations
1
Primary Topic
Cardiovascular Health and Disease Prevention
Type
article
Field-Weighted Citation Impact
1.39

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Trimethylamine N ‐oxide is elevated in postmenopausal women relative to age‐matched men and premenopausal women among individuals with obesity

Daniel J. Battillo, Steven K. Malin
1 citations
Experimental Physiology
Cardiovascular Health and Disease Prevention
1.39
article

Trimethylamine N ‐oxide is elevated in postmenopausal women relative to age‐matched men and premenopausal women among individuals with obesity

Daniel J. Battillo, Steven K. Malin
article en
1 citations

Abstract

Trimethylamine N-oxide (TMAO) is linked to arterial stiffness and atherosclerosis. Cardiovascular disease (CVD) risk increases following menopause in women. Whether menopause influences plasma TMAO metabolism to mediate CVD risk is unknown. Women with obesity were classified as premenopausal (n = 13; 40.3 ± 2.7 years; 39.4 ± 2.0 kg/m<sup>2</sup>) or postmenopausal (n = 22; 56.5 ± 1.1 years; 35.6 ± 0.9 kg/m<sup>2</sup>) via self-reported presence/absence of menses (last 12 months). Men were age- and body mass index-matched to postmenopausal women (n = 16; 55.9 ± 2.1 years; 34.3 ± 1.2 kg/m<sup>2</sup>) as controls to discern potential menopause-driven TMAO differences. Carotid-femoral pulse wave velocity (cfPWV) and pulse wave analysis (applanation tonometry) were analysed to assess arterial stiffness, aortic waveforms and blood pressure. Fasting plasma TMAO and precursors (carnitine, choline, betaine and trimethylamine (TMA)) were assessed (mass spectroscopy). A 180 min 75 g oral glucose tolerance test was performed to approximate insulin sensitivity and quantify vascular cell (vascular cell adhesion molecule 1 (VCAM-1)) and intercellular adhesion molecules (intercellular adhesion molecule 1 (ICAM-1)). Body composition (DXA/BodPod) and fitness ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"> <mml:semantics> <mml:msub><mml:mover><mml:mi>V</mml:mi> <mml:mo>̇</mml:mo></mml:mover> <mml:mrow><mml:msub><mml:mi>O</mml:mi> <mml:mn>2</mml:mn></mml:msub> <mml:mi>peak</mml:mi></mml:mrow> </mml:msub> <mml:annotation>${\dot V_{{{\mathrm{O}}_2}{\mathrm{peak}}}}$</mml:annotation></mml:semantics> </mml:math> ) were measured. Premenopausal women were younger than men and postmenopausal women (P < 0.0001, η<sup>2</sup> = 2.29). Men had lower body fat (P = 0.001, η<sup>2</sup> = 0.80) and higher fat-free mass (P = 0.004, η<sup>2</sup> = 0.42) compared to both pre- and postmenopausal women. There were no differences among groups in fitness, insulin sensitivity, ICAM-1 or blood pressure (P > 0.05), but men had higher cfPWV (P = 0.040, η<sup>2</sup> = 0.27) and VCAM-1 (P = 0.041, η<sup>2</sup> = 0.32). Postmenopausal women had elevated TMAO (P = 0.040, η<sup>2</sup> = 0.29), compared with men and premenopausal women, yet men had elevated TMA (P = 0.041, η<sup>2</sup> = 0.17), carnitine (P = 0.003, η<sup>2</sup> = 0.27), choline (P = 0.022, η<sup>2</sup> = 0.35) and betaine (P < 0.0001, η<sup>2</sup> = 0.59). Thus when taken together, menopause may raise TMAO in women, while older men appear to have unique TMAO precursor metabolism linked to CVD risk.

Experimental PhysiologyVol. 111(3)
Rutgers, The State University of New Jersey (US)
National Institutes of Health
Good health and well-being
Openalex Percentile: Top 17%
Cardiovascular Health and Disease Prevention
1.39
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.