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An estimated 35,000 Canadians experience cardiac arrest each year when their hearts stop beating suddenly. Fewer than 10 per cent of these people survive.

Sudden cardiac arrest can occur in people with previous heart conditions, such as heart attacks or heart failure, but sometimes, seemingly healthy people — even, rarely, children — can experience sudden cardiac death.

About 20 years ago, with the escalation of genetic research, scientists began discovering the root cause of these deaths.

They started off by studying mutations of the ryanodine receptor 2 (RyR2), a large ion channel protein found in heart cells that controls the heartbeat. Scientists linked these genetic mutations to a deadly cardiac arrhythmia called catecholaminergic polymorphic ventricular tachycardia (CPVT).

Because of the high risk of sudden cardiac arrest, individuals with mutations of the RyR2 are routinely tested for CPVT, which is relatively easy to diagnose through standard exercise stress testing and can be effectively treated with medication in most instances.

Unfortunately, some individuals with RyR2 mutations who test negative for CPVT may also be at risk of sudden cardiac arrest. The cause of this paradox has remained a mystery until now.

Critical step to prevent cardiac arrhythmias and sudden death

After a decade of work, an international team led by Dr. Wayne Chen, PhD, a professor at the (CSM), has discovered the reason behind these unexplained sudden deaths and come up with potential treatments for individuals at risk.

“Sometimes people die suddenly, and doctors can’t explain the cause,” says Chen. “That’s because they have loss-of-function RyR2 mutations, which cause a new cardiac arrythmia syndrome.”

The team has also identified a diagnostic test and two drugs, which are already in use, with potential to manage individuals with this lethal cardiac disease.

The Chen lab at the worked with numerous arrhythmia centres around the world on this new disorder, termed RyR2 calcium release deficiency syndrome (CRDS). To date, Chen’s team has identified at least 20 loss-of-function RyR2 mutations associated with CRDS. The work, conducted in mice, is published in . Drs. Bo Sun, PhD, Jinjing Yao, PhD, and Mingke Ni, PhD, students of Chen, are the first authors on the study.

Dr. Henry Duff, MD, PhD, a cardiologist and researcher at the CSM, is impressed with the study, noting the experiment could be repeated in human trials, a critical step on the journey to developing therapies to prevent cardiac arrhythmias and sudden death.  

“This study provides a stimulation protocol that might be useable in humans to uncover the propensity to arrhythmias and likely sudden death,” he says.

Unusual electrical patterns in the heart

Dr. Robert Rose, PhD, a researcher at the CSM and a member of the Libin Cardiovascular Institute, assisted in the study. Using specialized optical equipment, the lab mapped the unusual electrical patterns in the heart associated with the newly identified syndrome.

He said the study offers hope for individuals with the mutations who may be at risk of sudden cardiac death.

“This is a highly novel and highly important study,” says Rose. “The attention on ryanodine receptor mediated arrhythmia has been mostly on conditions in which the receptor is overactive. This study identifies mutations that work in a very different way, providing new insight into causes of sudden cardiac death.”

Dr. Satish Raj, MD, the medical director of the section of cardiology that specializes in problems in the electrical system of the heart, says although life-threatening arrhythmias are relatively uncommon, when they occur, they are devastating.

"We know that people do die suddenly, and that there may be genetic risks. Not knowing why can be very scary. These are early days, but this study points to more causes that we can look for, and hopefully treat in a targeted way," he says. 

“We are very proud of this,” says Chen. “We have identified a new mechanism, a new diagnosis and a potential treatment for a deadly syndrome. These discoveries will fundamentally change the diagnosis and management of these patients and their families, potentially saving lives.”