Systemic proteomic dynamics of acute exercise reveal genetic links to health and disease
Nature Metabolism, 2026
Kurgan N., Kjærgaard J., Jespersen N., Díez-Obrero V., Svenstrup V., Moreno-Justicia R., Heywood S., Lindqvist C., Ottander L., Samodova-Sommer D., Malita A., Kubrak O., Ahrentløv N., Nielsen N., Durrer C., Texada M., Ried-Larsen M., Rasmussen S., Rewitz K., Loos R., Smit R., Pedersen B., Deshmukh A.
| Disease area | Application area | Sample type | Products |
|---|---|---|---|
Wider Proteomics Studies | Wellness Studies | Plasma | Olink Explore HT |
Abstract
Physical activity improves metabolic health, but the molecular responses that mediate its benefits are not fully characterized. Here we present a high-resolution, time-resolved proteomics atlas across plasma, saliva and urine from 25 healthy men in response to acute exercise. We find that exercise regulates more than 3,000 proteins through distinct, fluid-specific temporal dynamics. Network analysis uncovers coordinated remodelling of protein secretion, extracellular matrix and immune activation across body fluids. Replication in an independent cohort shows that many exercise-responsive plasma proteins exhibit consistent responses across age, sex and exercise modalities. Integration with human genome-wide association study data links secreted, exercise-responsive proteins to cardiometabolic diseases. Functional validation of genetically prioritized muscle-specific secreted proteins in Drosophila confirms their role in endurance, behaviour and metabolism. Overall, this open-access atlas (https://cbmr.ku.dk/research/research-groups/deshmukh-group/shiny-apps/) provides a multifluid resource that complements existing exercise-omics efforts for defining molecular adaptations to exercise and for prioritizing candidate exerkines.