The PhD student will work in a strong interdisciplinary setting that builds on the cross-college collaboration between Cardiovascular Sciences and Informatics. Our research aim is to improve treatment of heart rhythm disturbances (arrhythmias) using novel biomedical signal processing and intelligent algorithms.
Atrial fibrillation (AF) is the commonest sustained arrhythmia in the clinical practice affecting 1-2% general population1, but incidence increases sharply with age occurring in >10% people over 70 years old. AF is associated with a five-fold increase in stroke and increased mortality2. The mechanistic origin of AF is still poorly understood. Catheter ablation is an effective treatment for early stage of the disease (paroxysmal AF) by inserting catheters in the heart to ‘burn’ (ablate) and eliminate the triggers causing AF3.
However, results are poor in more advanced form of the disease (persistent AF) as there is interplay between trigger and substrate whereby simply eliminating the triggers would not produce an effective outcome4. Also, accurate identification of relevant substrate targets cannot be achieved currently as the electrical signals (electrograms) during AF exhibit complex and chaotic behaviour which require more advanced methods of analysis. Identification of atrial sites which are effective ablation targets remains challenging. A variety of signal processing techniques (i.e. complex fractionated electrogram, dominant frequency, local activation time mapping and rotational focal activity by phase mapping) have been developed and applied in clinical studies but failed to generate consistent outcome. Usually, a certain set of ‘rules’ were pre-defined for such single-hypothesis-driven techniques. However, multiple mechanisms may co-exist during AF.
This project aims to develop novel machine learning algorithms (i.e. deep learning, convolutional neural network, pattern recognition) based on advanced signal processing techniques5-12, which may provide better performance than traditional methods, in unveiling the underlying mechanisms of persistent AF and provide new insight in the strategy of catheter ablation.
The student will gain skills in a wide range of areas including: cardiac electrophysiology, digital signal processing, statistics, bioinformatics and machine learning to analyse high throughput biological data previously collected. The large database13 of digitised data from several patient cohorts include standard ECG, intracardiac high density non-contact multi-site (2048) electrograms as well as body surface potential mapping signals (128 leads) during AF and in normal sinus rhythm during and following interventions including cardioversion and catheter ablation.
This project will suit an enthusiastic and dynamic student with a background in computer science, biomedical engineering or medical sciences with a keen interest in multidisciplinary research. This work will provide unique mechanistic insight, which will generate high impact interdisciplinary publications as well as new machine learning tools identifying the source of AF as suitable targets for catheter ablation. These tools have great potential to facilitate industrial collaboration and further translation into clinical tools for effective interventional treatment and improved patient outcome.
Applicants are required to hold/or expect to obtain a data science related UK Bachelor Degree 2:1 or better (e.g. Computer Science, Bioinformatics, Biostatistics), and preferably also a similar MSc qualification. The University of Leicester English language requirements apply where applicable: https://le.ac.uk/study/research-degrees/entry-reqs/eng-lang-reqs
How to apply:
You should submit your application using our online application system: https://www2.le.ac.uk/research-degrees/phd/applyphd
Apply for a PhD in Cardiovascular Sciences Research
In the funding section of the application please indicate you wish to be considered for a CLS HDRUK Studentship
In the proposal section please provide the name of the supervisor and project you want to be considered for – please list both your first and second choices.
1. Wyndham, C.R.C. Texas Heart Institute Journal 27, 257-267 (2000). 2. Oral, H. Atrial Fibrillation: Vol. Vol. 2000 (eds. Zipes, D.P. & Jalife, J.) 3. Haissaguerre, M., et al. New Engl J Med 339, 659-666 (1998). 4. Verma, A., et al. New Engl J Med 372, 1812-1822 (2015). 5. Salinet, J.L., et al. J Cardiovasc Electrophysiol 25, 371-379 (2014). 6. Almeida, T.P., et al. Medical & Biological Engineering & Computing (2015). 7. Salinet, J., et al. Heart Rhythm 14, 1269-1278 (2017). 8. Li, X., et al. EP Europace 19, i3-i3 (2017). 9. Li, X., et al. EP Europace 19, i14-i14 (2017). 10. Almeida, T.P. et al. Med Biol Eng Comput 56, 71-83 (2018). 11. Almeida, T.P. et al. Frontiers in Physiology 8(2017). 12. Almeida, T.P. et al. Chaos 28, 085710 (2018). 13. Chu, G.S., et al. Europace 17, v1-v2 (2016).