Evaluation of age at symptom onset, proband status, and sex as predictors of disease severity in pediatric catecholaminergic polymorphic ventricular tachycardia
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, multicentrická studie, práce podpořená grantem
PubMed
34333088
DOI
10.1016/j.hrthm.2021.07.061
PII: S1547-5271(21)01991-3
Knihovny.cz E-zdroje
- Klíčová slova
- Catecholaminergic polymorphic ventricular tachycardia, Inherited arrhythmia, Pediatrics, Risk predictors, Ryanodine receptor,
- MeSH
- dítě MeSH
- katecholaminergní polymorfní komorová tachykardie MeSH
- komorová tachykardie epidemiologie terapie MeSH
- lidé MeSH
- mladiství MeSH
- rizikové faktory MeSH
- sexuální faktory MeSH
- stupeň závažnosti nemoci MeSH
- věk při počátku nemoci MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Kanada epidemiologie MeSH
- Spojené státy americké epidemiologie MeSH
BACKGROUND: Children with catecholaminergic polymorphic ventricular tachycardia (CPVT) are at risk for sudden death, and a risk stratification tool does not exist. OBJECTIVE: The purpose of this study was to determine whether proband status, age at symptom onset, and/or sex are independent predictors of cardiac events. METHODS: A multicenter, ambispective, cohort of pediatric CPVT patients was categorized by sex, proband status, and age at symptom onset (D1: first decade of life [symptom onset <10 years] or D2: second decade of life [symptom onset 10-18 years, inclusive]). Demographics, therapy, genetics, and outcomes were compared between groups. RESULTS: A total of 133 patients were included and stratified into 58 D1 and 75 D2 patients (68 female and 65 male; 106 probands and 27 relatives). Localization of RYR2 variants to hotspots differed based on proband status and age at symptom onset. The cardiac event rate was 33% (n = 44/133), inclusive of a 3% (n = 4/133) mortality rate, over a median of 6 years (interquartile range 3-11) after time of symptom onset. Proband status, rather than age at of symptom onset or sex, was an independent predictor of time to first cardiac event (P = .008; hazard ratio = 4.4). The 5-, 10- and 15-year event-free survival rates for probands were 77%, 56%, and 46%, respectively, and for relatives were 96%, 91%, and 86%, respectively. Event risk after diagnosis was 48% (32/67) in patients on β-blocker or flecainide alone vs 10% (5/48) in patients on β-blocker plus flecainide and/or left cardiac sympathetic denervation (P <.001). CONCLUSION: Proband status, but not age at symptom onset or male sex, independently predicted an earlier onset of cardiac events. A larger sample size would enable a comprehensive investigation of other risk factors.
BC Children's Hospital Vancouver Canada
Children's Hospital Los Angeles Los Angeles California
Children's Hospital of Wisconsin Milwaukee Wisconsin
Cleveland Clinic Cleveland Ohio
Division of Cardiology University of British Columbia Vancouver Canada
Hong Kong Children's Hospital Hong Kong SAR China
Indiana University School of Medicine Indianapolis Indiana
Motol University Hospital Prague Czech Republic
Nationwide Children's Hospital Columbus Ohio
Nemours Children's Clinic Orlando Florida
Oregon Health Science University Portland Oregon
Rady Children's Hospital San Diego California
Sibley Heart Center Children's Healthcare of Atlanta Atlanta Georgia
University Alabama Birmingham Birmingham Alabama
University of Alberta Edmonton Canada
University of Gottingen Gottingen Germany
University of Iowa Stead Family Children's Hospital Iowa City Iowa
University of Louisville Louisville Kentucky
University of Michigan Ann Arbor Michigan
University of Utah Salt Lake City Utah
Citace poskytuje Crossref.org