Calendar An icon of a desk calendar. Cancel An icon of a circle with a diagonal line across. Caret An icon of a block arrow pointing to the right. Email An icon of a paper envelope. Facebook An icon of the Facebook "f" mark. Google An icon of the Google "G" mark. Linked In An icon of the Linked In "in" mark. Logout An icon representing logout. Profile An icon that resembles human head and shoulders. Telephone An icon of a traditional telephone receiver. Tick An icon of a tick mark. Is Public An icon of a human eye and eyelashes. Is Not Public An icon of a human eye and eyelashes with a diagonal line through it. Pause Icon A two-lined pause icon for stopping interactions. Quote Mark A opening quote mark. Quote Mark A closing quote mark. Arrow An icon of an arrow. Folder An icon of a paper folder. Breaking An icon of an exclamation mark on a circular background. Camera An icon of a digital camera. Caret An icon of a caret arrow. Clock An icon of a clock face. Close An icon of the an X shape. Close Icon An icon used to represent where to interact to collapse or dismiss a component Comment An icon of a speech bubble. Comments An icon of a speech bubble, denoting user comments. Comments An icon of a speech bubble, denoting user comments. Ellipsis An icon of 3 horizontal dots. Envelope An icon of a paper envelope. Facebook An icon of a facebook f logo. Camera An icon of a digital camera. Home An icon of a house. Instagram An icon of the Instagram logo. LinkedIn An icon of the LinkedIn logo. Magnifying Glass An icon of a magnifying glass. Search Icon A magnifying glass icon that is used to represent the function of searching. Menu An icon of 3 horizontal lines. Hamburger Menu Icon An icon used to represent a collapsed menu. Next An icon of an arrow pointing to the right. Notice An explanation mark centred inside a circle. Previous An icon of an arrow pointing to the left. Rating An icon of a star. Tag An icon of a tag. Twitter An icon of the Twitter logo. Video Camera An icon of a video camera shape. Speech Bubble Icon A icon displaying a speech bubble WhatsApp An icon of the WhatsApp logo. Information An icon of an information logo. Plus A mathematical 'plus' symbol. Duration An icon indicating Time. Success Tick An icon of a green tick. Success Tick Timeout An icon of a greyed out success tick. Loading Spinner An icon of a loading spinner. Facebook Messenger An icon of the facebook messenger app logo. Facebook An icon of a facebook f logo. Facebook Messenger An icon of the Twitter app logo. LinkedIn An icon of the LinkedIn logo. WhatsApp Messenger An icon of the Whatsapp messenger app logo. Email An icon of an mail envelope. Copy link A decentered black square over a white square.

Discovery could prevent stents failing in heart disease patients

A new molecule to tackle the inflammation which causes heart stent failure has been discovered by scientists (Royal Marsden Cancer Charity/PA)
A new molecule to tackle the inflammation which causes heart stent failure has been discovered by scientists (Royal Marsden Cancer Charity/PA)

Heart stent failures could be prevented thanks to a discovery by scientists at Heriot-Watt University.

Thousands of people across the UK have stents permanently inserted to expand their arteries and to keep blood flowing, treating the underlying cause of coronary heart disease (CHD).

However, approximately 5% of patients suffer damage and inflammation to the artery walls, leading to failure of the stent and annual readmittance to hospital.

Dr Stephen Yarwood, a biochemist from Heriot-Watt’s Institute of Biological Chemistry, Biophysics and Bioengineering, has identified a molecule to tackle the inflammation.

The research, funded by the British Heart Foundation (BHF) and the Scottish University Life Science Association (SULSA), should help towards reducing the number of stents rejected by patients’ bodies and the associated costs to the NHS.

Dr Yarwood said: “Our mission is to find new formulations for stents that make inflammation, and failure of the stent, much less likely.

“We knew that an enzyme called EPAC1, which sits in the cells of blood vessels, turns off inflammatory signals, like a molecular switch.

“We tested thousands of chemicals that had potential as good starting points for drug discovery projects but with no currently-known use. We found that a molecule called I942 can regulate EPAC1’s activity.

“Now we know that this molecule can prevent or reduce inflammation, our next task is to make it more effective by modifying its structure.

“It’s like a key – we know it fits in the lock, now we have to change its shape so that we can unlock the door.”

Dr Yarwood used the facilities at the European Screening Centre, Newhouse, to test thousands of chemicals to find out whether any of them could target EPAC1.

Head of biology at the European Screening Centre Dr Stuart McElroy said: “This collaboration combined Dr Yarwood’s knowledge of EPAC1’s  biology with our experience of using drug discovery to develop new tools for drug research.

“We used BioAscent’s Compound Cloud chemical library and its unique robotic capabilities to perform a smart screen of a subset of only 5,000 chemicals. We then analysed the chemical structures of promising candidates to cherry pick similar molecules from the full library to identify I942. This is a great example of the power of BioAscent’s technology.”

James Cant, BHF Scotland director, added: “Since the BHF was established, the number of people dying from coronary heart disease in Scotland has more than halved.

“However CHD is still Scotland’s single biggest killer. It claims the lives of over 6,700 people every year and there are an estimated 240,000 people in Scotland living with CHD.

“Our pioneering research into stents and new treatments for CHD has achieved a great deal but we want to do more. That’s why we are funding important projects like this by Dr Stephen Yarwood and his team at Heriot-Watt University to help improve techniques and develop new procedures for the future.”