Article Text

Original research
Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes
  1. Ella Field1,2,
  2. Gabrielle Norrish1,2,
  3. Vanessa Acquaah2,
  4. Kathleen Dady1,2,
  5. Marcos Nicolas Cicerchia3,
  6. Juan Pablo Ochoa3,
  7. Petros Syrris2,
  8. Karen McLeod4,
  9. Ruth McGowan5,
  10. Hannah Fell1,
  11. Luis R Lopes2,6,
  12. Elena Cervi1,2,
  13. Juan Pablo Pablo Kaski1,2
  1. 1 Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK
  2. 2 Institute of Cardiovascular Science, University College London, London, UK
  3. 3 Health in Code, A Coruna, Galicia, Spain
  4. 4 Department of Paediatric Cardiology, Royal Hospital for Children, Glasgow, UK
  5. 5 West of Scotland Centre for Genomic Medicine, Glasgow, UK
  6. 6 Inherited Cardiovascular Disease Unit, Saint Bartholomew's Hospital Barts Heart Centre, London, UK
  1. Correspondence to Dr Juan Pablo Pablo Kaski, Centre for Inherited Cardiovascular Diseases, Great Ormond Street Hospital For Children NHS Trust, London, UK; j.kaski{at}ucl.ac.uk

Abstract

Background Variants in the cardiac myosin-binding protein C gene (MYBPC3) are a common cause of hypertrophic cardiomyopathy (HCM) in adults and have been associated with late-onset disease, but there are limited data on their role in paediatric-onset HCM. The objective of this study was to describe natural history and clinical outcomes in a large cohort of children with HCM and pathogenic/likely pathogenic (P/LP) MYBPC3 variants.

Methods and results Longitudinal data from 62 consecutive patients diagnosed with HCM under 18 years of age and carrying at least one P/LP MYBPC3 variant were collected from a single specialist referral centre. The primary patient outcome was a major adverse cardiac event (MACE). Median age at diagnosis was 10 (IQR: 2–14) years, with 12 patients (19.4%) diagnosed in infancy. Forty-seven (75%) were boy and 31 (50%) were probands. Median length of follow-up was 3.1 (IQR: 1.6–6.9) years. Nine patients (14.5%) experienced an MACE during follow-up and five (8%) died. Twenty patients (32.3%) had evidence of ventricular arrhythmia, including 6 patients (9.7%) presenting with out-of-hospital cardiac arrest. Five-year freedom from MACE for those with a single or two MYBPC3 variants was 95.2% (95% CI: 78.6% to 98.5%) and 68.4% (95% CI: 40.6% to 88.9%), respectively (HR 4.65, 95% CI: 1.16 to 18.66, p=0.03).

Conclusions MYBPC3 variants can cause childhood-onset disease, which is frequently associated with life-threatening ventricular arrhythmia. Clinical outcomes in this cohort vary substantially from aetiologically and genetically mixed paediatric HCM cohorts described previously, highlighting the importance of identifying specific genetic subtypes for clinical management of childhood HCM.

  • cardiomyopathies
  • pediatrics

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

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Introduction

Hypertrophic cardiomyopathy (HCM) is the most common genetic heart disease in adults, with a prevalence of 1 in 500.1 In contrast, childhood-onset disease is rare, with estimated prevalence rates from population-based studies of ~3 per 100 000.2 3 HCM is most commonly inherited as an autosomal dominant trait, caused by mutations in genes encoding components of the cardiac sarcomere in up to 60% of cases, even in young children.4–6 Around 70% of HCM-causing variants occur in one of the two genes: β-myosin heavy chain (MYH7) or myosin-binding protein C (MYBPC3).7 While substantial phenotypic heterogeneity and age-related penetrance are recognised in most sarcomeric HCM-causing gene variants, MYBPC3 variants in particular have been reported to cause relatively late-onset disease with a milder phenotype.8 9

Previous paediatric HCM cohort studies have described aetiologically mixed patient groups, with little focus on specific genotypes.10–12 Although individual case reports describe childhood-onset disease and sudden cardiac death (SCD) caused by compound heterozygous or homozygous MYBPC3 variants,13–19 there have been no previous studies systematically characterising MYBPC3 variants as a cause of HCM in children, particularly in heterozygosity. The aim of this study was to describe the natural history and clinical outcomes in a large cohort of consecutive children diagnosed with HCM and carrying variants in MYBPC3.

Methods

Patients

All consecutive children diagnosed with HCM under the age of 18 years with at least one variant in MYBPC3 classified as pathogenic or likely pathogenic (P/LP) at the time of testing evaluated at the Great Ormond Street Hospital Centre for Inherited Cardiovascular Diseases between 1998 and 2018 were included in this study. Diagnosis of HCM was made where left ventricular wall thickness was more than 2 SD greater than the body surface area-corrected predicted mean, not solely explained by abnormal loading conditions.20 Individuals carrying a variant in MYBPC3 who did not meet diagnostic criteria for HCM (phenotype-negative mutation carriers) were excluded, since the study aim was to describe paediatric-onset disease phenotypes and outcomes, rather than paediatric carriers of MYBPC3 variants.

Clinical evaluation

All patients underwent systematic clinical evaluation at baseline and throughout follow-up, until transition to adult services at 18 years. Anonymised clinical data were collected at baseline, during 6–12 monthly follow-up and at the most recent clinical review, including demographics; family history; symptoms; medical therapy; genetic test results; resting 12-lead ECG; 2D and Doppler echocardiogram; and, where available, cardiopulmonary exercise testing (CPET); cardiac MRI (cMRI); and ambulatory ECG monitoring.

Echocardiographic measurements were made according to current guidelines.21 Maximal left ventricular wall thickness (MLVWT) was defined as the greatest thickness in any single segment, measured on 2D echocardiography at end diastole in the parasternal short-axis view in four places at basal and mid-ventricular level (anterior and posterior septum, lateral and posterior wall) and two places at apical level (anterior and posterior septum), as previously described.22 Left atrial diameter was measured in the parasternal long-axis view using 2D or M-Mode. Left ventricular outflow tract obstruction (LVOTO) was defined as a Doppler-derived pressure gradient >30 mm Hg on echocardiography.20 Non-sustained ventricular tachycardia (NSVT) was defined as three or more consecutive beats with a rate faster than 120 bpm, self-resolving within 30 s20 and recorded by either ambulatory ECG or by indwelling monitoring device.

Clinical outcomes

The primary patient outcome was a major adverse cardiac event (MACE), defined as death (SCD or heart failure-related death), cardiac transplantation, haemodynamically compromising sustained ventricular arrhythmia or appropriate therapy from an implanted cardioverter defibrillator (ICD). ICD therapy was considered appropriate where a defibrillation shock was triggered by documented ventricular tachycardia or fibrillation, according to information stored by the device. Information relating to the clinical outcomes of patients transitioned to adult services was sourced from adult cardiology centres.

Genetic evaluation

Genetic sequencing methods varied according to era, type of test requested (diagnostic or predictive) and individual laboratory conducting testing. Targeted testing of HCM genes was performed using direct Sanger sequencing (3–11 genes) prior to 2011. After 2011, next-generation sequencing was more widely available (21–104 gene panels). Pathogenicity of all variants was reclassified using current American College of Medical Genetics (ACMG) guidelines.23 Additional variants occurring in other genes previously associated with inherited heart muscle disease were also recorded, where reported. Patients carrying more than one variant with a potential impact on cardiac phenotype were considered to have ‘complex’ genotypes for the purpose of analysis. Genetic variants are described following the Human Genome Variation Society (HGVS) recommendations.24

Statistical analysis

R Studio software V.1.2.1335 was used for statistical analysis of clinical data.25 Z-scores were used to describe echocardiogram and cMRI measurements relative to corresponding mean values in children of the same body size.26 Mean values (±SD) were calculated for continuous variables and median values with IQRs were calculated for skewed data. Normal distribution was determined using the Shapiro-Wilk normality test. The Welch two-sample t-test was used to compare the means of normally distributed numerical data and the Wilcoxon rank-sum test with continuity correction for non-normally distributed numerical data, with one-way analysis of variance used to compare three groups. Pearson’s χ2 test with Yates’ continuity correction and Fisher’s exact test were used for comparing independent categorical variables. Survival analysis was undertaken using Kaplan-Meier curves with log rank analysis and univariate Cox proportional hazard regression analysis. A p value of <0.05 was considered statistically significant.

Results

Clinical characteristics

Sixty-two patients from 59 families with disease-causing MYBPC3 variants were identified. Median age at diagnosis was 10 years (IQR: 2–14) (online supplemental figure 1). Twelve patients (19.4%) were diagnosed in infancy (below 1 year of age). Forty-seven patients (75%) were boy, 31 (50%) were the proband in the family and 15 (24%) had a family history of SCD. Twenty-six patients (41.9%) were diagnosed through clinical screening due to family history, 18 (29%) incidentally (following detection of a murmur, during investigation of another health condition or during cardiac screening programmes in the community), 11 (17.7%) due to symptoms and 6 (9.7%) following presentation with an out-of-hospital cardiac arrest (OOHCA). Fifteen patients (24.2%) were diagnosed prior to 2000, 13 (21%) between 2000 and 2009 and 34 (54.8%) from 2010 onwards. Where sufficient data relating to family history were available, family history of childhood-onset HCM was identified in six families (11.5% of those with information available). In four cases, these paediatric relatives presented with SCD. The baseline clinical and echocardiographic characteristics are summarised in table 1.

Supplemental material

Table 1

Baseline cohort characteristics

Baseline cMRI and CPET data are summarised in online supplemental table 1. Briefly, 14 patients (22.6%) underwent baseline and follow-up cMRI. At the start of follow-up, median indexed left ventricular mass was 83 g/m2 (IQR: 66–119) and mean ejection fraction was 72.4%±6.5%. Late gadolinium enhancement (LGE) was observed in 6 of 11 patients (54.5%) who received contrast at baseline. One additional patient without LGE at baseline developed this during follow-up. Thirty-two patients (51.6%) underwent CPET. No patients developed arrhythmia during exercise; 10 children developed ST segment depression or T-wave changes, of which 9 were patients carrying more than one variant in MYBPC3. Mean peak VO2 was 33.4±10.4 mL/kg/min.

Genetic testing strategy and results

All patients had undergone genetic testing, which identified at least one variant in MYBPC3 (see online supplemental table 2 for full list of variants). Forty-one patients (66.1%) underwent diagnostic genetic panel testing, 1 underwent whole exome sequencing and 20 patients (32.3%) underwent predictive testing for a familial variant. Fifty patients (80.6%) carried a single MYBPC3 variant and 12 patients (19.4%) carried two distinct genetic changes in MYBPC3. Nine patients (18%) with a single MYBPC3 variant were found to carry an additional genetic variant in another gene of interest: MYH7 (n=2), TNNT2 (n=2), FLNC, GLA, JUP, MYH6, ANKRD1, BRAF and MAP2K1. One patient carried two additional variants in MYH7 and ANKRD1 and one patient carried two additional variants in TNNT2 and JUP. A total of 21 patients (33.9%) therefore had a ‘complex’ genetic status, carrying more than one variant with a potential impact on cardiac phenotype.

After reclassification against current ACMG criteria, 40 (64.5%) patients carried a primary MYBPC3 variant classified as pathogenic, 19 (30.6%) as likely pathogenic and 3 (4.8%) as variants of uncertain significance (VUS). Among the 12 patients carrying two variants in MYBPC3, the second variant was classified as pathogenic in 3, likely pathogenic in 6, and VUS in 3.

Among patients with a single MYBPC3 variant, 20 (48.8%) were missense substitution variants, 2 (4.9%) were nonsense substitution variants, 11 (26.8%) were insertions or deletions of nucleotides within the gene and the remaining 8 (19.5%) were intronic/splice-site variants. Among the 21 patients with complex genetic status, the breakdown of primary MYBPC3 variants was: 10 missense, 1 nonsense, 5 insertions/deletions and 5 intronic/splice-site. In the 12 patients with a second genetic variant in MYBPC3, 11 of these were missense variants and 1 was a frameshift variant. A total of 62 exonic MYBPC3 variants were identified across the cohort, with 19 (30.6%) of these in exons 16 and 17 (see figure 1), corresponding to the C3 functional domain of the cMyBP-C protein (residues 449–539), thought to be required for flexibility of the N-terminal region and consequently important for interaction with myosin S2 or actin.27

Figure 1

Distribution of MYBPC3 exonic variants—a histogram illustrating the location of MYBPC3 exonic variants identified within the cohort. Nineteen (30.6%) variants were located in exons 16 and 17, corresponding to the C3 functional domain of the cMyBP-C protein and thought to be important for interaction with myosin S2 or actin.26

Three patients carried a single MYBPC3 variant classified as a VUS under ACMG criteria, but felt by the clinical team to be likely pathogenic, based on a combination of the clinical and laboratory information available at the time. These patients were all genetic probands, diagnosed at a mean age of 4.72±6.4 years and with mean MLVWT Z-score at baseline of 13.4±8.5. In all three cases, the MYBPC3 variant segregated with affected first-degree relatives and was not identified in undiagnosed family members. None of these patients experienced adverse clinical outcomes during follow-up.

Clinical outcomes

Median length of follow-up was 3.1 years (IQR: 1.6–6.9). Fifty-one patients (82%) were alive at last clinic review. Six patients (9.7%) were lost to follow-up after transition to adult services. Clinical outcomes are summarised in table 2. Nine patients (14.5%) experienced MACE during follow-up and five (8%) died: three of these were SCDs, one was a pulseless electrical activity cardiac arrest during a catheter procedure following transplantation and one death occurred in a patient on the cardiac transplant waiting list. Whole cohort survival free from MACE is illustrated in figure 2A. Twenty patients (32.3%) had evidence of ventricular arrhythmia (OOHCA (n=6); SCD (n=3); appropriate ICD therapy (n=5); or NSVT (n=10)). None of the patients diagnosed during infancy experienced MACE during follow-up (figure 2B).

Figure 2

(A) Whole cohort survival free from MACE (major adverse cardiac event): Kaplan-Meier curve to show whole cohort survival free from composite MACE endpoint over the course of diagnosed follow-up. (B) Kaplan-Meier curve to show survival free from composite MACE endpoint over the course of diagnosed follow-up for patients diagnosed in infancy vs those diagnosed in later childhood. (C) Kaplan-Meier curve to show survival free from composite MACE endpoint over the course of diagnosed follow-up for patients with a single MYBPC3 variant vs those with additional MYBPC3 variant. (D) Kaplan-Meier curve to show survival free from death or equivalent event over course of diagnosed follow-up for probands vs non-probands.

Table 2

Clinical outcomes

Baseline echocardiographic data for patients with and without sustained ventricular arrhythmia are compared in table 3, where sustained ventricular arrhythmia includes patients experiencing SCD, appropriate ICD therapy and OOHCA, but excludes those with only NSVT. Patients with sustained ventricular arrhythmia had significantly higher mean end-systolic diameter (27.1±5.5 mm vs 18.8±5.8 mm; p=0.00086), higher mean end-diastolic LV diameter (40.9±5.1 mm vs 34.9±8.1 mm; p=0.0072) and lower mean fractional shortening (34.2%±10.8% vs 45.1±8.3%; p=0.012). These differences were also statistically significant at the end of follow-up: 34.1±6.4 mm vs 23.1±5.3 mm (p=0.007), 45.7±6.0 mm vs 39.3±6.8 mm (p=0.04) and 26.7±6.8% vs 41.3±6.8% (p=0.002), respectively. None of the patients with resting LVOT at baseline or at the end of follow-up experienced sustained ventricular arrhythmia. Resting LVOTO developed between baseline and follow-up in two individuals.

Table 3

Comparison of baseline variables in patients with and without sustained ventricular arrhythmia

Among patients with a single MYBPC3 variant, one patient with a missense variant had MACE (5%) compared with 3 (14.3%) with other variant types (p=0.63). No baseline echocardiographic parameters were significantly different in patients with missense variants when compared patients with other variant types (data not shown).

Single vs complex genotypes

Eight patients (66.7%) with two MYBPC3 variants experienced ventricular arrhythmia compared with 12 patients (24%) with a single MYBPC3 variant (p=0.013). Excluding NSVT, 6 patients (50%) with two variants experienced ventricular arrhythmia compared with 5 patients (10%) with a single variant (p=0.005).

Nine patients (75%) with two MYBPC3 variants underwent ICD implantation compared with 14 patients (28%) with a single variant (p=0.007). Five-year freedom from MACE for those with a single or two MYBPC3 variants was 95.2% (95% CI: 78.6% to 98.5%) and 68.4% (95% CI: 40.6% to 88.9%), respectively (HR 4.65, 95% CI: 1.16 to 18.66, p=0.03) (see figure 2C). There was no statistically significant difference in MACE between patients carrying a single MYBPC3 variant (n=4; 9.8%) and those with an additional variant of interest in a different gene (n=1; 11.1%) (p>0.999). Exclusion of those individuals with a second MYBPC3 variant classified as a VUS from the two MYBPC3 variants group did not affect the findings; there was no statistically significant relationship between the pathogenicity of secondary MYBPC3 variants and likelihood of a patient experiencing an MACE during follow-up (p=0.48). Of note, among the three patients with a secondary MYBPC3 variant classified as a VUS, one presented with an OOHCA. Data regarding MYBPC3 variant phase was available for five of the patients with two MYBPC3 variants and this confirmed that the variants were carried in trans in these individuals. Familial genetic testing in the other families was either incomplete or results were unavailable.

Probands versus non-probands

Online supplemental table 3 shows the differences between probands and non-probands. There was no significant difference between probands and non-probands in relation to survival (see figure 2D). Five-year freedom from MACE for probands and non-probands was 84.7% (95% CI: 62.2% to 93.5%) and 94.9% (95% CI: 68.8% to 99.3%), respectively (HR 1.03, 95% CI: 0.24 to 4.31, p=0.97). Eight probands (25.8%) experienced ventricular arrhythmia excluding NSVT compared with three non-probands (9.7%) (p=0.18).

Discussion

To our knowledge, this study describes the largest paediatric cohort with MYBPC3-associated HCM reported to date. The principal finding is that MYBPC3 variants, even in heterozygosity, can cause HCM in young children, often with a severe and highly arrhythmogenic phenotype, in contrast to the notion that such variants are associated with late-onset disease.

MYBPC3 as a cause of childhood HCM

While early studies of HCM suggested that MYBPC3 variants were primarily associated with late-onset disease,8 9 more recent data have demonstrated significant phenotypic heterogeneity, even among members of the same family.28–38 Our results provide further evidence for this and extend the spectrum of MYBPC3 disease, showing that HCM caused by MYBPC3 variants can present during childhood. This phenotypic heterogeneity suggests that additional genetic and epigenetic modifiers may play an important role in disease progression.

Probands were diagnosed earlier than non-probands and exhibited more severe disease phenotypes at baseline. Non-probands were primarily diagnosed through family screening while probands were more likely to be diagnosed due to symptoms. Despite this, there was no significant difference in survival or outcomes between probands and non-probands.

Our data suggest that early-onset disease is not limited to probands or to individuals with a family history of early-onset disease. Current European HCM guidelines20 recommend that routine HCM screening should commence at the age of 10 years. In the present cohort, 10 patients attending for family screening reached diagnostic criteria for HCM before the age of 10 years. Together with previously published data,22 39 our data suggest that HCM screening should commence at an earlier age. This is reflected in the updated American HCM guidelines,40 which now advocate clinical screening in children from the time that HCM is diagnosed in a family member, regardless of the child’s age.

Clinical features of paediatric MYBPC3 variant carriers

Across the cohort, significant and progressive left ventricular hypertrophy was observed, with phenotypes characterised by non-obstructive, arrhythmic disease. In contrast, left atrial dilatation was rare and haemodynamically significant resting LVOTO was less widespread than has been described in previous adult and paediatric HCM studies.12 41 42

A major finding in this study is the high proportion of patients experiencing ICD therapy, SCD, OOHCA or non-sustained VT. This is in keeping with findings in adults31 and suggests that arrhythmia is a common phenotype in both adult and paediatric MYBPC3-related HCM, with implications for SCD prevention strategies.

Importantly, there was no significant correlation between variant type or location and clinical phenotypic severity or outcomes. This is in keeping with recent findings in 1316 individuals with HCM caused by MYBPC3 variants (including 163 diagnosed below the age of 18 years) from the SHaRe Registry.43 Together, these data suggest that genotype–phenotype correlations in HCM are dependent on additional as yet unidentified genetic and epigenetic factors.

In keeping with previous studies of adult HCM,31 44 a distinct gender imbalance was observed in this paediatric MYBPC3 cohort. Four of the five deaths occurred in male patients, all three SCDs occurred in boys and all patients presenting with OOHCA were boy. The only female death occurred in a patient carrying two MYBPC3 variants.

In adults with HCM, disease penetrance appears consistently higher and diagnosis generally occurs at an earlier age in male patients, but female patients, once diagnosed, are more likely to develop heart failure symptoms with increased mortality.44–47 Findings in the present cohort are consistent with this, suggesting that male MYBPC3 variant carriers are more likely to present during childhood. While clinical outcomes in male paediatric patients were significantly worse than in girls, this may simply represent the same disease process with earlier onset in boys. Further long-term studies are required to fully explore sex differences in MYPBC3 HCM. The underlying reasons for the male–female disparity in HCM remain unclear, but recent evidence implicates modifier genes on the sex chromosomes or sex hormones, which may prevent or delay development of hypertrophy.44 45 Oestrogen, progesterone and androgen receptors which are present in the heart tissue may mediate sex-specific effects in the cardiovascular system, and there is evidence that oestrogen receptors play a role in the development of hypertrophy in animal models.48 49 Microvascular density has also been shown to vary between boys and girls and may be associated with likelihood of cardiac fibrosis and with markers of diastolic function.50

Previous studies have indicated poor outcomes, including increased risk of death or transplantation, in children diagnosed with HCM during infancy.10 12 In contrast, none of the 12 patients diagnosed during infancy in the present study experienced MACE during follow-up, and only 3 of these patients presented due to symptoms. This difference may be explained by the fact that previous studies have included patients presenting with underlying metabolic disease or malformation syndromes, highlighting the importance of the underlying aetiology in determining outcomes in infantile HCM.

Effect of complex genetic status

MYBPC3 variants in homozygosity or compound heterozygosity have previously been associated with very early onset and severe disease with poor clinical prognosis,13 14 16 18 19 and the effect of gene dosage on disease severity in MYBPC3 HCM has been described in adult cohorts and family studies.15 17 51–54 The findings in the present study that patients carrying a second variant in MYBPC3 were significantly more likely to experience ventricular arrhythmia than those patients carrying a single MYBPC3 variant and had significantly worse clinical outcomes are consistent with this.

Our data contrast with previous findings of severe, infant-onset disease in patients with compound heterozygous MYBPC3 variants, since all but one of the patients with a second MYBPC3 variant were diagnosed after the first year of life. This suggests that additional MYBPC3 variants can play a role in clinical disease expression and penetrance beyond infancy, most likely in addition to other genetic and epigenetic factors.

Genome-wide association studies have recently demonstrated the existence of numerous novel susceptibility loci for HCM, which may play an important role in disease expression and outcomes. The presence of common genetic variation at one or more of these loci may explain the variable disease expression observed in carriers of pathogenic sarcomeric variants.55 Epigenetic factors may also influence HCM phenotype development by acting on signalling cascades, membrane receptors and transcription factors, or through proteomic upstream regulators of disease pathomechanisms, post-translational gene expression regulators and histone modification.56–58

Confirmed variant pathogenicity was not always necessary for the apparent gene dosage effect to be observed, since increased risk of poor clinical outcomes was observed in patients carrying two recognised pathogenic MYBPC3 variants, as well as in those with a second MYBPC3 variant of uncertain pathogenicity. Indeed, some of the most severe phenotypes were observed in children carrying two MYBPC3 variants, with one variant having been inherited from each parent. The normal or very mild cardiac phenotypes detected in the parents of these individuals demonstrate that undetected secondary MYBPC3 variants (including VUS) may be of clinical importance as disease modifiers in some families affected by MYBPC3 HCM.

Limitations

Missing and inconsistent clinical data is a limitation of the retrospective study design. In particular, different genetic testing techniques and protocols across the different eras in this study mean that additional variants in other genes of interest may have not been detected in those patients who had only undergone Sanger sequencing. Furthermore, 20 patients underwent predictive testing for a single familial variant, which may have failed to identify additional variants of potential relevance. Data relating to variant phase in the patients carrying a second MYBPC3 variant was not available for all patients, limiting our ability to interpret the true relevance of secondary MYBPC3 variants.

Recruitment of the cohort from a single specialist referral centre may result in recruitment bias and may have skewed the cohort towards individuals with more severe and difficult-to-manage disease; however, the fact that over 50% of the cohort were referred through family screening or following an incidental finding suggests that the cohort is likely to be representative of the wider MYBPC3-related paediatric HCM population.

Conclusions

This study demonstrates that children with MYBPC3 variants can develop early-onset HCM, which can be associated with life-threatening ventricular arrhythmias, in contrast to previous reports of MYBPC3 as a late-onset HCM gene. Outcomes in the present cohort varied significantly from the aetiologically and genetically mixed paediatric HCM cohorts described previously. These observations indicate the importance of distinguishing genetic subtypes of paediatric disease for clinical management and in future research.

Data availability statement

All data relevant to the study are included in the article or uploaded as supplementary information.

Ethics statements

Patient consent for publication

Ethics approval

The study was approved by the Great Ormond Street Hospital/University College London Institute of Child Health Joint Research and Development Office before data collection commenced (local reference: 18HL01/19HL04). The study was conducted using anonymised, retrospective data, and patient consent was therefore waived in line with local approval.

Acknowledgments

We wish to thank the Inherited Cardiovascular Diseases Team, Great Ormond Street Hospital, London, UK, for their role in the clinical management of these patients. EF wishes to acknowledge the academic support of Dr Sarah Fitzpatrick, Plymouth University, UK.

References

Supplementary materials

  • Supplementary Data

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Footnotes

  • Twitter @MarcosCicerchia, @jpocardio

  • Contributors EF, GN and JPPK designed the study. EF, GN, VA, KD, MCC, JPO, PS, KM, RM, HF, LRL, EC and JPPK were involved in data acquisition, analysis and interpretation. EF, GN, VA, KD, MCC, JPO, PS, KM, RM, HF, LRL, EC and JPPK were involved in drafting, reviewing and revising of the manuscript and have approved the final version. All authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

  • Funding This work was partly funded by a British Heart Foundation Alliance Learning and Development Grant and by Great Ormond Street Hospital NHS Foundation Trust. EF is funded by Max’s Foundation and the Great Ormond Street Hospital Children’s Charity. GN is supported by the British Heart Foundation. JPPK is supported by the British Heart Foundation, Medical Research Council Clinical Academic Partnership (CARP) award, Max’s Foundation and the Great Ormond Street Hospital Children’s Charity. LRL is funded by a Medical Research Council (MRC) Clinical Academic Research Partnership (CARP) award. This work is supported by the NIHR GOSH Biomedical Research Centre.

  • Disclaimer The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.