Key result
Targeted next-generation sequencing identifies genomic variants in ~48% of HCM and fewer DCM patients.
Why the study?
HCM and DCM are the most common referrals in inherited cardiovascular condition services, requiring discussion of genetic testing and surveillance options for patients and families.
Observational (n=62)
No
Next-generation sequencing and cascade testing in a Thai clinical genetics service successfully identified pathogenic variants in up to 32% of HCM and 16% of DCM patients, as well as new cases among asymptomatic relatives.
NGS may aid variant detection in HCM/DCM; extends prevalence data to this cohort but leaves broader adoption and outcomes open.
Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are the most common referrals in the Inherited Cardiovascular Condition (ICC) Genetics Service. Several issues must be discussed with patients and their families during the genetic consultation session, including the options for genetic testing and cardiovascular surveillance in family members. We developed an ICC registry and performed next-generation-based DNA sequencing for all patients affected by non-syndromic HCM and idiopathic DCM in our joint specialist genetics service. The target gene sequencing panel relied on the Human Phenotype Ontology with 237 genes for HCM (HP:0001639) and 142 genes for DCM (HP:0001644). All subjects were asked to contact their asymptomatic first-degree relatives for genetic counseling regarding their risks and to initiate cardiovascular surveillance and cascade genetic testing. The study was performed from January 1, 2014, to December 31, 2020, and a total of 62 subjects (31-HCM and 31-DCM) were enrolled. The molecular detection frequency was 48.39% (32.26% pathogenic/likely pathogenic, 16.13% variant of uncertain significance or VUS for HCM, and 25.81% (16.13% pathogenic/likely pathogenic, 9.68% VUS) for DCM. The most prevalent gene associated with HCM was MYBPC3. The others identified in this study included ACTN2, MYL2, MYH7, TNNI3, TPM1, and VCL. Among the DCM subjects, variants were detected in two cases with the TTN nonsense variants, while the others were missense and identified in MYH7, DRSP3, MYBPC3, and SCN5A. Following the echocardiogram surveillance and cascade genetic testing in the asymptomatic first-degree relatives, the detection rate of new cases was 8.82% and 6.25% in relatives of HCM and DCM subjects, respectively. Additionally, a new pre-symptomatic relative belonging to an HCM family was identified, although the genomic finding in the affected case was absent. Thus, ICC service is promising for the national healthcare system, aiming to prevent morbidity and mortality in asymptomatic family members.
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Trachoo et al. (2022) conducted an observational in Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) (n=62). Next-generation-based DNA sequencing was evaluated on Molecular detection frequency of genomic variants. Targeted next-generation sequencing identified genomic variants in 48.39% of patients with hypertrophic cardiomyopathy and 25.81% of patients with dilated cardiomyopathy.
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