# Characteristics of pulmonary artery strain assessed by cardiovascular magnetic resonance imaging and associations with metabolomic pathways in human ageing

**Authors:** Hongzhou Zhang, Shuang Leng, Fei Gao, Jean-Paul Kovalik, Hai Ning Wee, Kee Voon Chua, Jianhong Ching, John C. Allen, Xiaodan Zhao, Ru-San Tan, Qinghua Wu, Tim Leiner, Angela S. Koh, Liang Zhong

PMC · DOI: 10.3389/fcvm.2024.1346443 · Frontiers in Cardiovascular Medicine · 2024-02-29

## TL;DR

This study explores how pulmonary artery strain relates to aging and metabolism in older adults without heart disease.

## Contribution

The study identifies novel associations between pulmonary artery strain and specific metabolomic pathways in aging.

## Key findings

- PA GLS was significantly linked to age, heart rate, and cardiovascular risk factors.
- Alanine and proline showed significant associations with PA GLS after adjusting for risk factors.
- Several acylcarnitines were significantly associated with PA GLS, suggesting metabolic involvement in vascular stiffness.

## Abstract

Pulmonary artery (PA) strain is associated with structural and functional alterations of the vessel and is an independent predictor of cardiovascular events. The relationship of PA strain to metabolomics in participants without cardiovascular disease is unknown.

In the current study, community-based older adults, without known cardiovascular disease, underwent simultaneous cine cardiovascular magnetic resonance (CMR) imaging, clinical examination, and serum sampling. PA global longitudinal strain (GLS) analysis was performed by tracking the change in distance from the PA bifurcation to the pulmonary annular centroid, using standard cine CMR images. Circulating metabolites were measured by cross-sectional targeted metabolomics analysis.

Among n = 170 adults (mean age 71 ± 6.3 years old; 79 women), mean values of PA GLS were 16.2 ± 4.4%. PA GLS was significantly associated with age (β = −0.13, P = 0.017), heart rate (β = −0.08, P = 0.001), dyslipidemia (β = −2.37, P = 0.005), and cardiovascular risk factors (β = −2.49, P = 0.001). Alanine (β = −0.007, P = 0.01) and proline (β = −0.0009, P = 0.042) were significantly associated with PA GLS after adjustment for clinical risk factors. Medium and long-chain acylcarnitines were significantly associated with PA GLS (C12, P = 0.027; C12-OH/C10-DC, P = 0.018; C14:2, P = 0.036; C14:1, P = 0.006; C14, P = 0.006; C14-OH/C12-DC, P = 0.027; C16:3, P = 0.019; C16:2, P = 0.006; C16:1, P = 0.001; C16:2-OH, P = 0.016; C16:1-OH/C14:1-DC, P = 0.028; C18:1-OH/C16:1-DC, P = 0.032).

By conventional CMR, PA GLS was associated with aging and vascular risk factors among a contemporary cohort of older adults. Metabolic pathways involved in PA stiffness may include gluconeogenesis, collagen synthesis, and fatty acid oxidation.

## Linked entities

- **Chemicals:** alanine (PubChem CID 239), proline (PubChem CID 614)
- **Diseases:** dyslipidemia (MONDO:0002525)

## Full-text entities

- **Diseases:** cardiovascular disease (MESH:D002318), dyslipidemia (MESH:D050171), Pulmonary artery (PA) strain (MESH:D013180)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10937542/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC10937542/full.md

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Source: https://tomesphere.com/paper/PMC10937542