# Time Exposure and Fat Mass Reduction Drive Trimethylamine N-Oxide Modulation During a Very-Low-Energy Ketogenic Therapy (VLEKT) in Women with Obesity

**Authors:** Giuseppe Annunziata, Ludovica Verde, Maria Maisto, Martina Galasso, Giulia De Alteriis, Vincenzo Piccolo, Gian Carlo Tenore, Silvia Savastano, Annamaria Colao, Giovanna Muscogiuri, Luigi Barrea

PMC · DOI: 10.3390/metabo16030150 · Metabolites · 2026-02-24

## TL;DR

A very-low-energy ketogenic therapy reduces TMAO levels in obese women, with the effect linked to treatment duration and fat loss.

## Contribution

The study identifies treatment duration and fat mass reduction as key drivers of TMAO modulation during VLEKT in women with obesity.

## Key findings

- VLEKT significantly reduced body weight, BMI, waist girth, fat mass, and TMAO levels.
- Greater TMAO reduction was associated with longer treatment duration and greater fat mass loss.
- A fat mass reduction of ≥14.25% was identified as a clinically relevant threshold for TMAO lowering.

## Abstract

Background/Objectives: Trimethylamine N-oxide (TMAO) is a gut microbiota-derived metabolite increasingly recognized as a pro-atherogenic factor and a biomarker of cardiometabolic risk. Dietary patterns and adiposity are key modulators of circulating TMAO levels; however, evidence on the impact of very-low-energy ketogenic therapy (VLEKT) on TMAO metabolism, particularly in women with obesity, remains limited. This study aimed to investigate the effects of VLEKT on circulating TMAO concentrations, with specific focus on treatment duration and body composition (BC) changes. Methods: This study included 43 adult women with obesity eligible for VLEKT based on meal replacements. Anthropometric measurements and BC were assessed using standardized protocols and bioelectrical impedance analysis at baseline and post-intervention. Serum TMAO concentrations were quantified by validated HPLC–ESI–MS/MS. Results: After VLEKT, participants exhibited significant reductions in body weight, BMI, waist girth, fat mass (FM), and circulating TMAO levels. Greater reductions in TMAO were observed in women with longer ketogenic exposure and more pronounced FM loss. Changes in TMAO levels correlated negatively with VLEKT duration and positively with FM variations. In multivariate models, treatment duration and FM reduction emerged as independent predictors of TMAO decrease. A Receiver Operating Characteristic (ROC) analysis identified a FM reduction ≥14.25% as the optimal threshold associated with clinically relevant TMAO lowering. Conclusions: VLEKT reduces circulating TMAO levels in women with obesity. This effect appears to be primarily driven by the duration of ketogenic exposure and the magnitude of FM loss, rather than total weight reduction alone, highlighting the relevance of BC-targeted interventions in modulating gut microbiota-derived cardiometabolic risk markers.

## Linked entities

- **Chemicals:** Trimethylamine N-oxide (PubChem CID 1145), TMAO (PubChem CID 1145)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** FMO3 (flavin containing dimethylaniline monoxygenase 3) [NCBI Gene 2328] {aka FMOII, TMAU, dJ127D3.1}, FMO1 (flavin containing dimethylaniline monoxygenase 1) [NCBI Gene 2326], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, Fmo3 (flavin containing monooxygenase 3) [NCBI Gene 14262]
- **Diseases:** hyperandrogenism (MESH:D017588), inflammation (MESH:D007249), endothelial dysfunction (MESH:D014652), skin diseases (MESH:D012871), adiposity (MESH:D018205), metabolic syndrome (MESH:D024821), polycystic ovary syndrome (MESH:D011085), hepatic or renal disorders (MESH:D008107), heart failure (MESH:D006333), weight loss (MESH:D015431), malignant diseases (MESH:D009369), VLEKT (MESH:D009800), overweight (MESH:D050177), Ketosis (MESH:D007662), diabetic ketoacidosis (MESH:D016883), metabolic disorders (MESH:D008659), myocardial infarction (MESH:D009203), FM (MESH:C536030), TMAO (MESH:C536108), atherogenesis (MESH:D050197), gastrointestinal disorders (MESH:D005767), micronutrient deficiencies (MESH:D007153), endothelial (MESH:D005642), oligo-amenorrhea (MESH:D000568), CVD (MESH:D002318), muscle (MESH:D019042), III obesity (MESH:D009765), BC (MESH:C564221), insulin resistance (MESH:D007333), injury to (MESH:D014947), stroke (MESH:D020521)
- **Chemicals:** formic acid (MESH:C030544), short-chain fatty acid (MESH:D005232), sugar (MESH:D000073893), ammonium acetate (MESH:C018824), TMA (MESH:C023336), water (MESH:D014867), carbohydrate (MESH:D002241), betaine (MESH:D001622), NO (MESH:D009614), choline (MESH:D002794), olive oil (MESH:D000069463), omega-3 fatty acid (MESH:D015525), TMAO (MESH:C005855), methanol (MESH:D000432), phosphatidylcholine (MESH:D010713), ROS (MESH:D017382), sodium (MESH:D012964), magnesium (MESH:D008274), Fat (MESH:D005223), potassium (MESH:D011188), ketone (MESH:D007659), alcohol (MESH:D000438), ketone body (MESH:D007657), L-carnitine (MESH:D002331), B-complex vitamins (-), calcium (MESH:D002118)
- **Species:** Lactobacillus (genus) [taxon 1578], Bifidobacterium (genus) [taxon 1678], Bacillota (clostridial firmicutes, phylum) [taxon 1239], Bacteroidia (class) [taxon 200643], Powellomyces sp. EA (species) [taxon 252690], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

77 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028172/full.md

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Source: https://tomesphere.com/paper/PMC13028172