# Integrating TMAO into the pathogenesis of obesity and type 2 diabetes: a mini review

**Authors:** Dana Stoian, Denisa Pescari, Andreea Bena, Corina Paul, Simina Mihuta

PMC · DOI: 10.3389/fcdhc.2026.1765794 · Frontiers in Clinical Diabetes and Healthcare · 2026-01-28

## TL;DR

This mini review explores how TMAO, a gut-derived metabolite, may contribute to obesity and type 2 diabetes, and highlights differences in findings between children and adults.

## Contribution

The paper introduces a novel comparison of TMAO's role in pediatric and adult populations with obesity and diabetes.

## Key findings

- Higher TMAO levels are linked to obesity, type 2 diabetes, and cardiovascular complications.
- TMAO may reflect hepatic insulin resistance, connecting it to diabetes and cardiovascular risk.
- Findings vary across studies due to differences in controlling for confounders and population characteristics.

## Abstract

Increasing circulating levels of trimethylamine N-oxide (TMAO), a metabolite originating from both dietary sources and microbial metabolism in the gut, have drawn significant attention for their possible contribution to cardiometabolic disorders, such as type 2 diabetes and carotid intima–media thickening in individuals with excess weight. Yet, evidence from longitudinal and retrospective investigations remains inconsistent, with studies often reaching divergent conclusions. Higher circulating TMAO levels have been observed in people with overweight, obesity, and type 2 diabetes who subsequently develop cardiovascular complications, as well as in diabetic individuals who experience renal impairment. Still, the strength and consistency of these links vary considerably between cohorts and are shaped by how thoroughly studies control for underlying confounders. Given that insulin modulates FMO3 activity within hepatocytes, circulating TMAO concentrations might reflect underlying hepatic insulin resistance, offering a possible mechanistic link to its reported associations with diabetes and cardiovascular risk. This mini review summarizes current evidence on TMAO in obesity and type 2 diabetes, highlighting the novel comparison between pediatric and adult findings. This approach may help clarify how TMAO-related mechanisms evolve across the lifespan and inform future risk assessment and prevention strategies.

## Linked entities

- **Chemicals:** trimethylamine N-oxide (PubChem CID 1145), TMAO (PubChem CID 1145)
- **Diseases:** type 2 diabetes (MONDO:0005148), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, FMO3 (flavin containing dimethylaniline monoxygenase 3) [NCBI Gene 2328] {aka FMOII, TMAU, dJ127D3.1}
- **Diseases:** renal impairment (MESH:D007674), overweight (MESH:D050177), cardiovascular complications (MESH:D002318), insulin resistance (MESH:D007333), cardiometabolic disorders (MESH:D024821), diabetes (MESH:D003920), type 2 diabetes (MESH:D003924), obesity (MESH:D009765)
- **Chemicals:** TMAO (MESH:C005855)

## Full text

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## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12890643/full.md

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Source: https://tomesphere.com/paper/PMC12890643