Aug 2026· JACC. Heart failure· Vol 14, pp.
103283
· 1 citation· 34 references
Medicine
TL;DR
The 5-year cumulative diagnostic yield of screening childhood relatives is twofold higher in G+ families, but a childhood diagnosis was still made in 8% of G- families, supporting the need for universal screening of first-degree childhood relatives with HCM irrespective of genotype status.
Abstract
Background
Serial clinical screening of first-degree relatives of individuals with hypertrophic cardiomyopathy (HCM) is recommended. A lower yield of screening in adult relatives with genotype-negative disease might mean a one-off assessment is appropriate, but it is unknown if these findings can be extrapolated to pediatric relatives.
Objectives
This study aims to determine the yield of clinical screening in pediatric relatives of genotype-negative families.
Methods
Clinical and outcome data were collected from 404 children (≤18 years) from 227 genotype-positive (G+) families and 292 children from 170 genotype-negative (G-) families referred for family screening.
Results
Individuals from G- families were less likely to have a family history of childhood disease or sudden cardiac death. Over a follow-up of 68.9 ± 49.7 months, a diagnosis was made in 66 (9.5%) individuals with a higher 5-year cumulative incidence in individuals from G+ families than in those from G- families (11.1 [95% CI: 8.3-15.0] vs 4.0 [95% CI: 1.7-9.1]; P = 0.010). A diagnosis was made in 41 (18.1%) G+ families screened compared with 14 (8.2%) G- families (P < 0.001). The age and clinical features at diagnosis did not differ. Over a follow-up of 8.6 ± 4.1 years, there was no difference in the incidence of death or arrhythmic events, but symptoms (19 [36.5%] vs 2 [14.3%]; P = 0.034) and implantable cardioverter-defibrillator implantation (22 [42.3%] vs 1 [7.1%]; P = 0.014) were more common in the G+ group.
Conclusions
The 5-year cumulative diagnostic yield of screening childhood relatives is twofold higher in G+ families, but a childhood diagnosis was still made in 8% of G- families. These results support the need for universal screening of first-degree childhood relatives with HCM irrespective of genotype status. Further work to determine whether the frequency or timing of screening can be modified is required.
One in five relatives of ECG‑positive phenotype-negative adolescents received a cardiomyopathy diagnosis or had early cardiomyopathy traits, indicating that extending screening to relatives of ECG-positive, phenotype-negative adolescents is justified.
M. Abela, J. Debattista, J. Scerri et al.· European Journal of Pediatri...· 0 citations
BACKGROUND
Cardiomyopathy guidelines recommend routine screening of at-risk relatives with dilated cardiomyopathy (DCM). Titin-truncating variants are the most prevalent cause. However, the diagnostic yield of screening is low. Risk-based stratification could optimize screening intervals and resource allocation. This s...
S. Muller, N. Beelen, A. Paldino et al.· Circulation: Heart Failure· 0 citations
In this population of children with primary HCM, severe LVH was associated with a younger age at enrollment and a higher likelihood of harboring a pathogenic variant in MYBPC3.
E. Pahl, Stephanie M. Ware, Ling Shi et al.· JACC. Heart failure· 1 citation
The frequency of cascade family screening in the current era with either cardiovascular imaging (cascade cardiac screening) and/or genetic testing (cascade genetic screening) and the impact of such testing on adverse outcomes in first degree family members was evaluated.
Bradley J. Schwartz, L. Starr, Drew M. Cratsenberg et al.· Pediatric Cardiology· 0 citations
Patients with LMNA variants showed no improvement in the left heart function, with right ventricular enlargement and worsening tricuspid regurgitation, suggesting progression to right-sided heart failure.
Masayoshi Yamamoto, N. Murakoshi, K. Minami et al.· Internal medicine· 0 citations
The interdisciplinary CPS consultation model contributes to identifying hereditary cancer predisposition in pediatric patients and families and provides a scalable foundation for systematic CPS assessment and development of standardized, evidence-based surveillance protocols in pediatric oncology.
N. Dikow, Anna-Katharina Nitschke, S. Hirsch et al.· European Journal of Human Ge...· 0 citations
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