4.5 Article

Metabolic pathways associated with right ventricular adaptation to pulmonary hypertension: 3D analysis of cardiac magnetic resonance imaging

期刊

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ehjci/jey175

关键词

pulmonary hypertension; metabolomics; wall stress; cardiac magnetic resonance imaging; image segmentation; machine learning

资金

  1. British Heart Foundation [NH/17/1/32725, RE/13/4/30184, FS/15/59/31839]
  2. Academy of Medical Sciences [SGL015/1006]
  3. Wellcome Trust [100211/Z/12/Z]
  4. Medical Research Council
  5. National Institute for Health Research (NIHR) Clinical Research Facility
  6. National Institute for Health Research (NIHR) Biomedical Research Centre at Imperial College London Healthcare NHS Trust and Imperial College London
  7. MRC [MC_UP_1102/19] Funding Source: UKRI
  8. Wellcome Trust [100211/Z/12/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

Aims We sought to identify metabolic pathways associated with right ventricular (RV) adaptation to pulmonary hypertension (PH). We evaluated candidate metabolites, previously associated with survival in pulmonary arterial hypertension, and used automated image segmentation and parametric mapping to model their relationship to adverse patterns of remodelling and wall stress. Methods and results In 312 PH subjects (47.1% female, mean age 60.8 +/- 15.9 years), of which 182 (50.5% female, mean age 58.6 +/- 16.8 years) had metabolomics, we modelled the relationship between the RV phenotype, haemodynamic state, and metabolite levels. Atlas-based segmentation and co-registration of cardiac magnetic resonance imaging was used to create a quantitative 3D model of RV geometry and function-including maps of regional wall stress. Increasing mean pulmonary artery pressure was associated with hypertrophy of the basal free wall (beta = 0.29) and reduced relative wall thickness (beta = -0.38), indicative of eccentric remodelling. Wall stress was an independent predictor of all-cause mortality (hazard ratio = 1.27, P = 0.04). Six metabolites were significantly associated with elevated wall stress (beta = 0.28-0.34) including increased levels of tRNA-specific modified nucleosides and fatty acid acylcarnitines, and decreased levels (beta = -0.40) of sulfated androgen. Conclusion Using computational image phenotyping, we identify metabolic profiles, reporting on energy metabolism and cellular stress-response, which are associated with adaptive RV mechanisms to PH.

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