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Virtual hearts get to the crux of sudden cardiac death

Watching hundreds of genetically different hearts beating in a supercomputer is helping doctors identify who is at risk from unexpectedly dropping down dead

Virtual human hearts beating on supercomputers are helping get to the bottom of the most mysterious of heart diseases 鈥 sudden arrhythmic death syndrome.

When someone dies suddenly and unexpectedly, there is often an underlying cardiac problem. If a post-mortem doesn鈥檛 find one, is recorded as the cause. SADS can result from a that affect the way electrical signals pass through the cardiac muscle making the heart beat. One day 鈥 often during physical exertion 鈥 the person鈥檚 heart may begin to beat in a fast, uncontrolled way. This can kill them if their heart doesn鈥檛 right itself quickly enough. Around , and the same genetic problems may also play a role in sudden infant deaths.

If someone has the genetic mutations, they can be treated with drugs or have a defibrillator implanted in their chest. But how do you work out who is at risk? Genetic tests can help but not everyone with the altered genes seems to have the syndrome. Electrocardiograms or ECGs can measure the heart鈥檚 electrical activity, but exactly how features on the ECG relate to risk is not fully understood.

All in the t-wave

Enter the virtual heart. By running hundreds of genetically customised hearts on a supercomputer, each for many thousands of beats, and his colleagues from the Victor Change Cardiac Research Institute in Sydney, Australia, have cracked some of the secrets of SADS.

One sign that someone has the genetic condition that most commonly leads to SADS, known as , is a distinctive bump or notched t-wave in their ECG readout. 鈥淔or the past 30 years, that notched t-wave has been in the diagnostic criteria but nobody鈥檚 known what鈥檚 caused it,鈥 says Hill. 鈥淲e show what causes it.鈥

With the wealth of virtual data created by running the simulations, they were able to establish that the more extreme the bump in the ECG is, the higher a person鈥檚 risk of dying. What鈥檚 more, they found the main genes thought to cause the problem can be either amplified or compensated for by complex combinations of other genes.

Better diagnosis

鈥淲e show that the degree of t-wave notching is correlated with how much risk they are at,鈥 says team member Arash Sadrieh. 鈥淪o person A can have the mutation [but his ECG shows] he鈥檚 absolutely normal, so you don鈥檛 need to do the complex surgery to prevent sudden cardiac death. And if his sister has a more notched t-wave, then she is at more risk.鈥

It would have been impractical to use real hearts for this research as you鈥檇 need huge numbers of people with specific genetic combinations, all with their full genome sequenced, hooked up to an ECG for days.

Hill says the team has taken the virtual trial data, applied it to patient records of ECGs and found the finer grained analysis of the ECG led to more accurate diagnoses. They鈥檙e also making progress using the simulations to distinguish between different types of long QT syndrome.

鈥淭he work is quite a milestone in terms of how thoroughly they鈥檝e investigated this issue of the notched t-wave鈥nd how you interpret it,鈥 says Peter Hunter from the University of Auckland in New Zealand, one of the world鈥檚 leading cardiac modelling experts. 鈥淭his has pushed it to a new level.鈥

Journal Reference: Nature Communications, DOI:

Topics: Genetics