జర్నల్ ఆఫ్ మెటబాలిక్ సిండ్రోమ్

The utility of genetic testing in cardiac arrhythmias

Abstract

Bijal Vyas Bhatia

Introduction: The common life-threatening cardiac arrhythmias, Long QT (LQTS type 1-13) and Brugada (BrS type 1-12) present with syncope/palpitations/ seizures/aborted cardiac arrest. They have incomplete penetrance and variable expressivity. The three common genes (KCNQ1, KCNH2, and SCN5A) account for 75% of all LQTS cases and the SCN5A gene in BrS accounts for 25% of all cases.

Aim: To identify the causative variation in the associated genes responsible for causing cardiac channelopathies in Indian patients.

Materials & Methods: Hundred patients who fulfilled the inclusion criteria of the study were enrolled. Mutation analysis was performed in the most probable candidate gene by direct sequencing using primers flanking exon-intron boundaries. If a mutation was not identified, NGS was performed to identify mutations in other cardiac genes in patients. Parents and siblings were screened if a mutation was identified in the proband. Novel mutations were evaluated for pathogenicity using ACMG guidelines, bioinformatics, and molecular modeling software.

Results: Mutations were identified in 23 of 100 (23%) patients by Sanger sequencing, 20 had LQTS, and 3 had BrS. Among the LQT syndromes, mutations were identified in 17 in KCNQ1 (LQTS1), one in KCNH2 (LQTS2), and two in SCN5A (LQTS3). Among the LQTS1 patients, ten were identified with biallelic mutations. The three BrS patients had mutations in SCN5A (BrS1). Ten of 23 mutations were novel. NGS identified mutation in 22 (49%) of 45 patients negative for mutations by Sanger and with significant family history and/or strong clinical indication. Of which, 20 had LQTS and two had BrS. Out of these 46 mutations, 18 were novel. Cascade screening identified mutations in two symptomatic and forty asymptomatic family members. Genetic counseling was provided to the proband and family members.

Conclusion: Genotyping is important for confirming the type of LQTS/BrS, which has implications for management, cascade screening, and risk assessment.