Clinical Diagnosis of Calcium Release Deficiency Syndrome in a Family With Sudden Cardiac Death

Importance: Calcium release deficiency syndrome (CRDS) is a recently described inherited arrhythmia caused by loss-of-function variants in the cardiac ryanodine receptor (RYR2). Diagnosis currently requires in vitro functional testing and availability limits diagnosis; a recently proposed burst pacing provocation test offers a potential clinical diagnostic tool, but its performance remains to be validated. Objective: To demonstrate how the novel CRDS provocation test can clinically establish the diagnosis in a family with unexplained sudden cardiac arrest and death. Design, Setting, and Participants: This case series examines a 5-generation pedigree with clinical, genetic, and functional data conducted among a large French Canadian family with an extensive history of unexplained sudden cardiac arrest and death. The study was conducted at a multidisciplinary cardiac genetics clinic at a tertiary referral center in Canada. Data were gathered and analyzed from June 2024 through March 2025. Exposures: Clinical provocation with burst pacing and/or spontaneous atrial or ventricular arrhythmia detected on ambulatory monitoring. Main Outcomes and Measures: The primary outcome was diagnostic T-wave augmentation following burst pacing or spontaneous atrial or ventricular arrhythmia. Results: In this case series, 5 RYR2 variant carriers (2 female [40%]; age range at first evaluation, 17-59 years) demonstrated diagnostic T-wave augmentation after pacing or spontaneous arrhythmia consistent with CRDS. Pause dependence was essential for diagnostic sensitivity. Functional studies of the novel RYR2-p.Glu336Gly variant confirmed that it results in loss of function. This appears to be the first such variant reported within a hot spot previously restricted to gain-of-function variants. Conclusions and Relevance: This case series provides the first clinical application of the CRDS provocation test in a family with a history of unexplained sudden cardiac death. Findings underscore the diagnostic importance of pause dependence and highlight the need for improved risk stratification in CRDS.

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Publication Details

Journal
JAMA Cardiology
Published
2026-05-27
DOI
https://doi.org/10.1001/jamacardio.2026.1067
Primary Topic
Cardiac electrophysiology and arrhythmias
Type
article
Field-Weighted Citation Impact
0.00
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article

Clinical Diagnosis of Calcium Release Deficiency Syndrome in a Family With Sudden Cardiac Death

Jason D. Roberts, Benjamin Neveu, John Paul Estillore, Léna Rivard et al.
JAMA Cardiology
Cardiac electrophysiology and arrhythmias
article

Clinical Diagnosis of Calcium Release Deficiency Syndrome in a Family With Sudden Cardiac Death

Jason D. Roberts, Benjamin Neveu, John Paul Estillore, Léna Rivard, Julia C. Isbister, S.R.W. Chen, Johannie Gagnon, Ruiwu Wang, Shanshan Tian, Julia Cadrin-Tourigny, Laura Robb, Rafik Tadros
article en

Abstract

Importance: Calcium release deficiency syndrome (CRDS) is a recently described inherited arrhythmia caused by loss-of-function variants in the cardiac ryanodine receptor (RYR2). Diagnosis currently requires in vitro functional testing and availability limits diagnosis; a recently proposed burst pacing provocation test offers a potential clinical diagnostic tool, but its performance remains to be validated. Objective: To demonstrate how the novel CRDS provocation test can clinically establish the diagnosis in a family with unexplained sudden cardiac arrest and death. Design, Setting, and Participants: This case series examines a 5-generation pedigree with clinical, genetic, and functional data conducted among a large French Canadian family with an extensive history of unexplained sudden cardiac arrest and death. The study was conducted at a multidisciplinary cardiac genetics clinic at a tertiary referral center in Canada. Data were gathered and analyzed from June 2024 through March 2025. Exposures: Clinical provocation with burst pacing and/or spontaneous atrial or ventricular arrhythmia detected on ambulatory monitoring. Main Outcomes and Measures: The primary outcome was diagnostic T-wave augmentation following burst pacing or spontaneous atrial or ventricular arrhythmia. Results: In this case series, 5 RYR2 variant carriers (2 female [40%]; age range at first evaluation, 17-59 years) demonstrated diagnostic T-wave augmentation after pacing or spontaneous arrhythmia consistent with CRDS. Pause dependence was essential for diagnostic sensitivity. Functional studies of the novel RYR2-p.Glu336Gly variant confirmed that it results in loss of function. This appears to be the first such variant reported within a hot spot previously restricted to gain-of-function variants. Conclusions and Relevance: This case series provides the first clinical application of the CRDS provocation test in a family with a history of unexplained sudden cardiac death. Findings underscore the diagnostic importance of pause dependence and highlight the need for improved risk stratification in CRDS.

JAMA Cardiology
University of Calgary (CA), Montreal Heart Institute (CA), Population Health Research Institute (CA), Libin Cardiovascular Institute of Alberta (CA), Université de Montréal (CA), Hamilton Health Sciences (CA), McMaster University (CA)
Good health and well-being
Openalex Percentile: Top 7%
Cardiac electrophysiology and arrhythmias
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