The yield on re-interpretation of genetic variants in pediatric cardiomyopathy

BackgroundVariant interpretation can change over time as new knowledge emerges. Our aim was to determine the frequency and causes of variant reinterpretation on systematic re-evaluation in pediatric patients with cardiomyopathy. MethodsOverall, 227 unrelated pediatric patients with cardiomyopathy enrolled in the Heart Centre Biobank harbored a pathogenic/likely pathogenic (P/LP) variant and/or a variant of uncertain significance (VUS) on clinical genetic testing (2005-2022). Variant pathogenicity was re-evaluated using the American College of Medical Genetics and Genomics (ACMG) guidelines. Additional extension cohorts (n=4547, cases) were analyzed to assess variant burden in cases versus controls (gnomAD 4.1.0). Results382 variants (110 P/LP, 272 VUS) in 227 patients were re-evaluated. Forty-nine variants in 49 patients (21.6%) changed classification. Twelve (10.9%) P/LP variants were downgraded to VUS in 14 patients. Leading criteria were high population allele frequency and variant not located in mutational hotspot or critical functional gene domain. Thirty-seven (13.6%) VUS were upgraded to P/LP in 35 patients. Leading criteria were variant location in mutational hotspot for gene, and deleteriousness on in silico prediction. Only 8 reclassified variants had been reported back by the clinical genetic testing laboratory at the time of the study. Ten of the 37 VUS upgraded to P/LP were significantly enriched in cardiomyopathy cases (n=4796) versus controls. ConclusionsOne in five patients with cardiomyopathy had a clinically relevant change in variant pathogenicity on systematic re-evaluation that would require modifying family clinical screening and cascade genetic testing. These findings underscore the clinical importance of regular variant re-interpretation on follow-up.