Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing

David J. Tester, Laura J. Kopplin, Melissa L. Will, Michael J. Ackerman

Research output: Contribution to journalArticle

111 Scopus citations

Abstract

Background: Mutations in the RyR2-encoded cardiac ryanodine receptor/ calcium release channel cause type 1 catecholaminergic polymorphic ventricular tachycardia (CPVT1). Objectives: Because CPVT and concealed long QT syndrome (LQTS) phenotypically mimic one other, we sought to determine the spectrum and prevalence of RyR2 mutations in a cohort of unrelated patients who were referred specifically for LQTS genetic testing. Methods: Using denaturing high-performance liquid chromatography and direct DNA sequencing, targeted mutational analysis of 23 RyR2 exons previously implicated in CPVT1 was performed on genomic DNA from 269 unrelated patients (180 females, average age at diagnosis 24 ± 17 years) who were referred to Mayo Clinic's Sudden Death Genomics Laboratory for LQTS genetic testing. Previously, comprehensive mutational analysis of the five LQTS-associated cardiac channel genes proved negative for this entire subset of patients now designated as "genotype-negative" LQTS referrals. Results: Fifteen distinct RyR2 mutations (14 missense, 1 duplication/ insertion, 12 novel) were found in 17 (6.3%) of 269 patients. None of these mutations were present in 400 reference alleles. Two mutations localized to the calstabin-2 (FKBP12.6) binding domain. Upon review of the clinical records, the referral diagnosis for all 17 patients was "atypical" or "borderline" LQTS. Conclusion: Putative pathogenic CPVT1-causing mutations in RyR2 were detected in 6% of unrelated, genotype-negative LQTS referrals. These findings suggest that CPVT may be underrecognized among physicians referring patients because of a suspected channelopathy. A diagnosis of "atypical LQTS" may warrant consideration of CPVT and analysis of RyR2 if the standard cardiac channel gene screen for LQTS is negative.

Original languageEnglish (US)
Pages (from-to)1099-1105
Number of pages7
JournalHeart rhythm
Volume2
Issue number10
DOIs
StatePublished - Oct 1 2005

Keywords

  • CPVT
  • Catecholaminergic polymorphic ventricular tachycardia
  • Genetic testing
  • Ion channel
  • LQTS
  • Long QT syndrome
  • Ryanodine receptor

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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