Gut bacteria associated with an atherogenic TMAO-dietary pattern and choline-rich foods among aging women

Nutr Metab Cardiovasc Dis. 2026 Jul;36(7):104635. doi: 10.1016/j.numecd.2026.104635. Epub 2026 Feb 18.

Abstract

Background and aims: Choline can be metabolized by gut bacteria with a choline utilization gene, CutC, as identified through genome sequencing studies. This metabolism produces trimethylamine, the precursor to the atherosclerotic metabolite trimethylamine N-oxide (TMAO). Bacterial species involved in trimethylamine production in free-living humans have been under-investigated. We previously developed the TMAO dietary pattern (TMAO-DP), which is predictive of plasma TMAO and choline. We evaluated associations between the TMAO-DP, dietary choline, and choline-rich foods (fish, red meat, eggs) with the abundance of species with CutC. We also explored associations between the TMAO-DP and microbiome diversity.

Methods and results: This cross-sectional analysis included 287 women (mean age = 79.6 years) from the Women's Health Initiative. Diet was assessed using a food frequency questionnaire. Stool samples were collected and the V3-V4 regions of the 16S ribosomal RNA were sequenced. Adjusted linear regression models evaluated associations between the TMAO-DP with the CLR-transformed abundance of species with CutC and with alpha-diversity indices. For beta-diversity, PERMANOVA examined measures of Aitchison distance within and between quartiles of the TMAO-DP. Associations between dietary choline and choline-rich foods with the abundance of species were evaluated using linear regression. The TMAO-DP was associated with Acidaminococcus intestini [Beta (SE): 0.23 (0.09), p-value = 0.035] and Desulfovibrio desulfuricans [Beta (SE): 0.16 (0.6), p = 0.035]. The TMAO-DP was not associated with alpha- or beta-diversity.

Conclusion: This study provides evidence that Desulfovibrio desulfuricans and Acidaminococcus intestini, two species identified as having CutC by gene sequencing, may produce trimethylamine from diet in free-living women.

Keywords: Choline; Diet patterns; Metabolism; Microbiome; Older women; Postmenopausal; Trimethylamine n-oxide.

MeSH terms

  • Age Factors
  • Aged
  • Aged, 80 and over
  • Atherosclerosis* / diagnosis
  • Atherosclerosis* / epidemiology
  • Atherosclerosis* / microbiology
  • Atherosclerosis* / prevention & control
  • Bacteria* / classification
  • Bacteria* / genetics
  • Bacteria* / metabolism
  • Choline* / administration & dosage
  • Choline* / metabolism
  • Cross-Sectional Studies
  • Diet* / adverse effects
  • Feces / microbiology
  • Female
  • Gastrointestinal Microbiome*
  • Humans
  • Methylamines* / blood
  • Methylamines* / metabolism
  • Ribotyping
  • Risk Factors

Substances

  • Methylamines
  • Choline
  • trimethyloxamine