Insulin resistance modifies longitudinal multi-omics responses to habitual diet
How habitual diet influences the gut microbiome and plasma metabolome across insulin resistance states remains unclear. We conducted year-long multi-omics profiling of 71 deeply phenotyped adults, integrating repeated assessments of diet, metabolome, gut microbiome, clinical laboratory measures, and inflammatory markers. Using gold-standard insulin suppression tests and machine learning-derived dietary patterns, we examined how dietary patterns relate to metabolic and microbial landscapes by insulin resistance status. Insulin-sensitive individuals exhibited stronger and more numerous diet-omics associations than insulin-resistant individuals, identifying metabolic flexibility as a central determinant of dietary responsiveness. Parabacteroides emerged as a candidate microbial mediator between refined carbohydrate-rich dietary patterns and host metabolic signatures. Integrated into a cardiovascular risk prediction model, diet, metabolites, microbial taxa, and immune markers each contributed to 10-year atherosclerotic cardiovascular disease risk. These findings show that inter-individual variation in cardiometabolic risk partly reflects differences in molecular responsiveness to habitual diet, informing precision nutrition and cardiovascular prevention.
Authors
- Alessandra Celli (ORCID: https://orcid.org/0009-0000-2186-0892)
- Rachel Battersby
- Yingzhou Lu (ORCID: https://orcid.org/0009-0008-7774-6018)
- Heyjun Park (ORCID: https://orcid.org/0000-0003-3724-9590)
- Caroline Bejikian
- PRANAV BERRY
- Xiaotao Shen
- Sophia Miryam Schussler Fiorenza
- Dalia Perelma
- Michael Snyder
Institutions
- Johns Hopkins University (US)
- Nanyang Technological University (SG)
- VA Palo Alto Health Care System (US)
- Stanford University (US)
Publication Details
- Journal
- bioRxiv (Cold Spring Harbor Laboratory)
- Published
- 2026-02-18
- DOI
- https://doi.org/10.64898/2026.02.17.706440
- Primary Topic
- Gut microbiota and health
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Institutes of Health