Genetic research led by Queen Mary University of London could open the way to earlier identification of people at risk of heart failure and to the development of new treatments.
The Queen Mary University of London team applied an artificial intelligence (AI) technique to analyse the heart MRI images of 17,000 healthy UK Biobank volunteers. They found that genetic factors accounted for 22-39 per cent of variation in the size and function of the heart’s left ventricle, the organ’s main pumping chamber. Enlargement and reduced pumping function of the left ventricle can lead to heart failure.
The research, which was part-funded by the Wellcome Trust and the British Heart Foundation and published today in the journal
Circulation
, suggests that genetic factors significantly influence the variation in heart structure and function. The team identified or confirmed 14 regions in the human genome associated with the size and function of the left ventricle – each containing genes that regulate the early development of heart chambers and the contraction of heart muscle.
Lead researcher Dr Nay Aung from Queen Mary University of London, said: “It is exciting that the state-of-the-art AI techniques now allow rapid and accurate measurement of the tens of thousands of heart MRI images required for genetic studies. The findings open up the possibility of earlier identification of those at risk of heart failure and of new targeted treatments. The genetic risk scores established from this study could be tested in future studies to create an integrated and personalised risk assessment tool for heart failure.
“The AI tool allowed us to analyse images in a fraction of the time it would otherwise have taken. Our academic and commercial partners are further developing these AI algorithms to analyse other aspects of cardiac structure and function. This should translate to time and cost savings for the NHS and could potentially improve the efficiency of patient care.”
Steffen Petersen, Professor of Cardiovascular Medicine at Queen Mary University of London, who also worked on the project, said: “Previous studies have shown that differences in the size and function of the heart are partly influenced by genes but we have not really understood the extent of that genetic influence. This study has shown that several genes known to be important in heart failure also appear to regulate the heart size and function in healthy people. That understanding of the genetic basis of heart structure and function in the general population improves our knowledge of how heart failure evolves.
“The study provides a blueprint for future genetic research involving the heart MRI images in the UK Biobank and beyond.”
Patricia Munroe, Professor of Molecular Medicine at Queen Mary University of London, who also worked on the project, said “High fidelity MRI measures combined with genetics is reassuringly validating many known heart structural proteins, but our work also finds new genes from more heritable functional measures that are associated with ventricular remodelling and fibrosis. Further genetic studies including analyses of additional heart MRI chambers are expected to provide deeper insights into heart biology.”
It is expected that many more genetic markers for cardiac conditions will be identified as the UK Biobank database grows. Earlier this month UK Biobank announced it will begin sequencing the whole human genome of 450,000 participants, following the success of the pilot sequencing programme in 50,000 participants.
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For more information, please contact: Chris Mahony Communications Executive (School of Medicine and Dentistry)
Queen Mary University of London
[E-mail]
c.mahony@qmul.ac.uk
Tel: +44 0207 8825315 / +44 (0)781 2692722
Notes to the editor
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Research paper: Genome-wide association study of LV phenotype. Authors
Circulation
DOI 10.1161/CIRCULATIONAHA.119.041161 -
The article is available here after the embargo lifts:
https://
www.
ahajournals.
org/
doi/
10.
1161/
CIRCULATIONAHA.
119.
041161
About Queen Mary University of London
Queen Mary University of London (QMUL) is one of the UK’s leading universities, and one of the largest institutions in the University of London, with 20,260 students from more than 150 countries.
A member of the Russell Group, we work across the humanities and social sciences, medicine and dentistry, and science and engineering, with inspirational teaching directly informed by our research – in the most recent national assessment of the quality of research, we were placed ninth in the UK (REF 2014).
We also offer something no other university can: a stunning self-contained residential campus in London’s East End. As well as our home at Mile End, we have campuses at Whitechapel, Charterhouse Square and West Smithfield dedicated to the study of medicine, and a base for legal studies at Lincoln’s Inn Fields.
We have a rich history in London with roots in Europe’s first public hospital, St Barts; England’s first medical school, The London; one of the first colleges to provide higher education to women, Westfield College; and the Victorian philanthropic project, the People’s Palace based at Mile End.
QMUL has an annual turnover of £350m, a research income worth £100m, and generates employment and output worth £700m to the UK economy each year.
This part of information is sourced from https://www.eurekalert.org/pub_releases/2019-09/qmuo-aig092319.php
Rupert Marquand
44-020-788-23004
r.marquand@qmul.ac.uk
http://www.qmul.ac.uk