Study reveals underlying genetic risks for a type of heart attack largely affecting younger women

(Press-News.org) Research led by the National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC) and Universite Paris Cite, and supported by worldwide partners in Canada, the USA and Australia, has identified new genes that are associated with an increased risk of a type of heart attack primarily affecting young to middle-aged women. The results are published in Nature Genetics today, 29 May 2023.

SCAD – or Spontaneous Coronary Artery Dissection – is when a bruise or bleed occurs in the wall of a coronary artery, cutting off the blood to part of the heart. This leads to a heart attack. Unlike other types of heart attack, SCAD is most common in women under the age of 60 and is a leading cause of heart attacks around the time of pregnancy. Furthermore, people who have had a SCAD tend to be generally healthy and SCAD can sometimes happen more than once.

To date, little is known about why a SCAD happens, often striking out of the blue, meaning that it is currently impossible to prevent.

The researchers present a genome-wide association meta-analysis involving a total of 1,917 cases of SCAD and 9,292 controls from European ancestry. They found 16 genes that increased the risk of a SCAD. The identified genes are involved in processes that determine how the cells and connective tissue hold together, and also how the blood clots when bleeding occurs in tissues.

Interestingly, the researchers found that, while many genes linked to a higher risk of SCAD are shared with risk genes for conventional coronary artery disease (CAD), they have an opposite effect. This means patients with a SCAD have some genetic protection from the risk of CAD, and is further evidence that these diseases are very different. The only shared risk factor appeared to be genetically elevated blood pressure.

Dr David Adlam, Associate Professor of Acute and Interventional Cardiology at the University of Leicester, and lead author of the study, said: “This research confirms that there are multiple genes involved in determining the risk of a person having a SCAD. These genes give us the first key insight into the underlying causes of this disease and provide new lines of enquiry, which we hope will guide future new treatment approaches.

“We are grateful to Beat SCAD, the NIHR and the British Heart Foundation for funding our work, to our international partners for their collaboration and for all the patients with SCAD and healthy volunteers who gave their time to advance this research.”

The paper “Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation” is published in Nature Genetics today.

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Notes for editors

For more information, contact:

Rachael Dowling, Head of Research Communications, University Hospitals of Leicester NHS Trust, rachael.dowling@uhl-tr.nhs.uk or 07950891193.

University of Leicester press office, press@leicester.ac.uk / 0116 252 2160.

This is independent research funded in the UK by the British Heart Foundation and BeatSCAD, and carried out at the National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC). The views expressed are those of the author(s) and not necessarily those of the British Heart Foundation, BeatSCAD, the NIHR or the Department of Health and Social Care.

 

The NIHR Leicester Biomedical Research Centre

 

The National Institute for Health and Care Research (NIHR) Leicester Biomedical Research Centre (BRC) is part of the NIHR and hosted by the University Hospitals of Leicester NHS Trust in partnership with the University of Leicester, Loughborough University and the University Hospitals of Northamptonshire NHS Group.

 

The NIHR Leicester BRC undertakes translational clinical research in priority areas of high disease burden and clinical need. These are:

Respiratory and infectious diseases Personalised cancer prevention and treatment Lifestyle (including diabetes) Environment and health Data innovation for multiple long term health conditions and ethnic health Cardiovascular disease  

The BRC harnesses the power of experimental science to explore and develop ways to help prevent and treat chronic disease. It brings together 120 highly skilled researchers, 45 academic ‘rising stars’, more than 90 support staff and students and over 450 public contributors. By having scientists working closely with clinicians and the public, the BRC can deliver research that is relevant to both patients and the professionals who treat them. www.leicesterbrc.nihr.ac.uk

 

The mission of the National Institute for Health and Care Research (NIHR) is to improve the health and wealth of the nation through research. We do this by:

Funding high quality, timely research that benefits the NHS, public health and social care; Investing in world-class expertise, facilities and a skilled delivery workforce to translate discoveries into improved treatments and services; Partnering with patients, service users, carers and communities, improving the relevance, quality and impact of our research; Attracting, training and supporting the best researchers to tackle complex health and social care challenges; Collaborating with other public funders, charities and industry to help shape a cohesive and globally competitive research system; Funding applied global health research and training to meet the needs of the poorest people in low and middle income countries. NIHR is funded by the Department of Health and Social Care. Its work in low and middle income countries is principally funded through UK Aid from the UK government.

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