Key result
MYH7-related cardiomyopathy exhibited high phenotypic variability by age, with infants showing a severe DCM phenotype and patients under 12 having a similar symptom burden to older patients.
Why the study?
MYH7 is commonly mutated in cardiomyopathy patients with severe health outcomes, but clinical presentation and natural history across age groups required characterization.
Cohort (n=48)
No
MYH7-related cardiomyopathy presents with high age-dependent phenotypic variability, including severe dilated cardiomyopathy in infants.
Answers are grounded in this paper and cite their sources.
Supports age-specific surveillance in MYH7 carriers; hypothesis-generating for genotype-guided pediatric trials.
Cardiomyopathies (CMPs) are a heterogeneous group of diseases, frequently genetic, affecting the heart muscle. The symptoms range from asymptomatic to dyspnea, arrhythmias, syncope, and sudden cardiac death. This study is focused on MYH7 (beta-myosin heavy chain), as this gene is commonly mutated in cardiomyopathy patients. Due to the high combined prevalence of MYH7 variants and severe health outcomes, it is one of the most frequently tested genes in clinical settings. We analyzed the clinical presentation and natural history of 48 patients with MYH7-related cardiomyopathy belonging to a cohort from a tertiary center at Helsinki University Hospital, Finland. We made special reference to three age subgroups (0–1, 1–12, and >12 years). Our results characterize a clinically significant MYH7 cohort, emphasizing the high variability of the CMP phenotype depending on age. We observed a subgroup of infants (0–1 years) with MYH7 associated severe DCM phenotype. We further demonstrate that patients under the age of 12 years have a similar symptom burden compared to older patients.
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Vepsäläinen et al. (2022) conducted a cohort in MYH7-related cardiomyopathy (n=48). MYH7 mutation was evaluated on Clinical presentation and natural history. MYH7-related cardiomyopathy exhibited high phenotypic variability by age, with infants showing a severe DCM phenotype and patients under 12 having a similar symptom burden to older patients.
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