Clinical Medicine VI. (Poster discussion will take place on the terrace of the room during the Coffee Break)
Dr. Liliana, Szabo
Semmelweis University Heart and Vascular Center
+36304843367
sz.liliana.e@gmail.com
Pericardiac adipose tissue radiomics reveal an adverse fat pattern among heart failure patients in the UK Biobank imaging study
Liliana Szabo 1,2,3, Ahmed Salih 1,2, Esmeralda Ruiz Pujadas 4, Andrew Bard 1,2, Celeste McCracken 5, Hajnalka Vago 3, Bela Merkely 3, Stefan Neubauer5, Charalambos Antoniades 6, Karim Lekadir4, Steffen E. Petersen 1,2, Zahra Raisi-Estabragh 1,2
1. William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK
2. Barts Heart Centre, St Bartholomew’s Hospital, Barts Health NHS Trust, West Smithfield, London, EC1A 7BE, UK
3. Semmelweis University, Heart and Vascular Center, Budapest, Hungary
4. Departament de Matematiques i Informatica, Universitat de Barcelona, Artificial Intelligence in Medicine Lab (BCN-AIM), Barcelona, Spain
5. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, National Institute for Health Research Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 9DU, UK
6. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, John Radcliffe Hospital, Headley Way, Oxford OX39DU, Oxford UK
Poszter
Clinical Medicine VI. (Poster discussion will take place on the terrace of the room during the Coffee Break)
English
Clinical Medicine
Background: Obesity is a rising public health crisis. It is increasingly recognized that different fat compartments have different risk relationships. Fat accumulation, specifically disproportionate deposition of metabolically active visceral and pericardial adipose tissue (PAT), is linked to an increased hazard of obesity-related cardiovascular outcomes. Furthermore, current data suggest a distinct mechanistic role for PAT in driving adverse cardiovascular outcomes. Existing work is limited to describing PAT quantity. However, the character of PAT also has likely mechanistic importance.
Aims: In this study, we use radiomics measures of PAT geometry and tissue character derived from pixel-level magnetic resonance imaging to define imaging signatures of PAT which discriminate heart failure (HF).
Methods and results: We studied 43,226 UK Biobank participants with cardiovascular magnetic resonance (CMR), of these 297 had prevalent HF at the time of imaging. We obtained PAT contours using an automated pipeline. The PyRadiomics platform was adopted to extract shape, first-order and texture features (n=105). To create a balanced cohort, we randomly matched equal number of individuals without HF as comparator group (n=297). The data were split into training and test sets. (20%). We applied 6 classification models with 10-folds cross-validation and hyperparameter tuning. All sex and age-adjusted classification models achieved good discrimination between HF patients and controls. The best discriminative power was reached using the voting classifier method (Accuracy: 0.79, F1 score: 0.79). We applied SHAP to describe the feature importance of PAT radiomics parameters. We found that texture (e.g. High Gray level emphasis) and shape features were the most important metrics distinguishing prevalent HF.
Conclusion: We demonstrated that HF patients have distinct radiomics PAT phenotypes with important information from both shape and texture features. Our findings provide new insights into mechanisms of PAT-HF associations and propose novel imaging biomarkers for their investigation.
Funding: LS was supported by the EFOP-3.6.3-VEKOP-16-2017-00009.
Semmelweis University, Doctoral School of Theoretical and Translational Medicine
William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK
Hajnalka Vago and Zahra Raisi-Estabragh
I do not give consent to the publication of my abstract on the website of the congress.
Szabad
elfogadva
poszter
nem rendelkezett róla
4153
11:10
11:15
Liliana Szabo 1,2,3, Ahmed Salih 1,2, Esmeralda Ruiz Pujadas 4, Andrew Bard 1,2, Celeste McCracken 5, Hajnalka Vago 3, Bela Merkely 3, Stefan Neubauer5, Charalambos Antoniades 6, Karim Lekadir4, Steffen E. Petersen 1,2, Zahra Raisi-Estabragh 1,2
1. William Harvey Research Institute, NIHR Barts Biomedical Research Centre, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK
2. Barts Heart Centre, St Bartholomew’s Hospital, Barts Health NHS Trust, West Smithfield, London, EC1A 7BE, UK
3. Semmelweis University, Heart and Vascular Center, Budapest, Hungary
4. Departament de Matematiques i Informatica, Universitat de Barcelona, Artificial Intelligence in Medicine Lab (BCN-AIM), Barcelona, Spain
5. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, National Institute for Health Research Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 9DU, UK
6. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, John Radcliffe Hospital, Headley Way, Oxford OX39DU, Oxford UK