# The Metabolic Signature of Cardiorespiratory Fitness

**Authors:** Julia Bork, Marcello R. P. Markus, Ralf Ewert, Matthias Nauck, Christian Templin, Henry Völzke, Gabi Kastenmüller, Anna Artati, Jerzy Adamski, Marcus Dörr, Nele Friedrich, Martin Bahls

PMC · DOI: 10.1111/sms.70034 · 2025-03-12

## TL;DR

This study identifies a sex-specific metabolic signature linked to cardiorespiratory fitness, highlighting differences in lipid and energy metabolites between men and women.

## Contribution

The study reveals a sex-specific metabolic profile associated with cardiorespiratory fitness using targeted and untargeted metabolomics.

## Key findings

- Lipids, especially sphingomyelins, showed bidirectional relationships with CRF, varying by sex.
- Energy-related metabolites like citrate and succinylcarnitine were linked to CRF only in men.
- Xenobiotics such as hippurate and stachydrine were associated with CRF in women.

## Abstract

High cardiorespiratory fitness (CRF) is associated with better overall health. This study aimed to find a metabolic signature associated with CRF to identify health‐promoting effects. CRF based on cardiopulmonary exercise testing, targeted and untargeted metabolomics approaches based on mass spectrometry, and clinical data from two independent cohorts of the Study of Health in Pomerania (SHIP) were used. Sex‐stratified linear regression models were adjusted for age, smoking, and height to relate CRF with individual metabolites. A total of 132 (SHIP‐START‐2: 483 men with a median age of 58 years and 450 women with a median age of 56 years) and 118 (SHIP‐TREND‐0: 341 men and 371 women both with a median age of 51 years) metabolites were associated with CRF. Lipids showed bidirectional relations to CRF independent of sex. Specific subsets of sphingomyelins were positively related to CRF in men (SM (OH) C14:1, SM(OH)C22:2 SM C16:0, SM C20:2 SM(OH)C24:1) and inversely in women (SM C16:1, SM C18:0, SM C18:1). Metabolites involved in energy production (citrate and succinylcarnitine) were only associated with CRF in men. In women, xenobiotics (hippurate, stachydrine) were related to CRF. The sex‐specific metabolic signature of CRF is influenced by sphingomyelins, energy substrates, and xenobiotics. The greater effect estimates seen in women may emphasize the important role of CRF in maintaining metabolic health. Future research should explore how this profile changes with different types of exercise interventions or diseases in diverse populations and how these metabolites could be implemented in primary prevention settings.

## Linked entities

- **Chemicals:** citrate (PubChem CID 31348), succinylcarnitine (PubChem CID 131802075), hippurate (PubChem CID 464), stachydrine (PubChem CID 115244), SM C16:1 (PubChem CID 124202091)

## Full-text entities

- **Chemicals:** stachydrine (MESH:C003342), Lipids (MESH:D008055), sphingomyelins (MESH:D013109), hippurate (MESH:C030514), citrate (MESH:D019343), SM C16:1 (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11899505/full.md

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Source: https://tomesphere.com/paper/PMC11899505