Key result
Genetic testing of 11,945 Chinese individuals identified 1,018 variants in KCNQ1, KCNH2, and SCN5A, with 84% having uncertain clinical significance and prevalence highest in inherited arrhythmia (35%).
Why the study?
Genetic variant frequencies of KCNQ1, KCNH2, and SCN5A in different Chinese disease cohorts were largely unknown.
Observational (n=11,945)
Yes
This large-scale genetic analysis of Chinese cohorts reveals a high proportion of variants of uncertain significance in major arrhythmia genes and highlights significant inconsistencies in pathogenicity interpretations between commercial testing companies.
High VUS rate in Chinese cohorts warrants interpretive caution; leaves open need for ancestry-specific databases and harmonized classifications.
KCNQ1, KCNH2, and SCN5A are the most common genes responsible for long QT syndrome and Brugada syndrome. However, the genetic variant frequencies of the three genes in different Chinese disease cohorts are largely unknown. In this study, we analyzed the genetic variants of KCNQ1, KCNH2, and SCN5A in patients from seven cohorts (total N = 11945, including patients clinically suspected to have inherited arrhythmia [n = 122], other cardiovascular diseases [n = 1045], epilepsy [n = 4797], or other diseases [n = 5841], and healthy controls [n = 140]) who had undergone genetic testing. All of these variants were identified via genetic testing by two Chinese companies using the Hi-Seq 2000 platform. A total of 1018 variants (minor allele frequency <0.01) were identified, with 186 (18%), 374 (37%), and 458 (46%) variants in the coding exons of KCNQ1, KCNH2, and SCN5A, respectively. Of these variants, 84% had unknown or uncertain clinical significance. The frequency of identified ClinVar pathological/likely pathological variants was higher for KCNQ1 (13/186, 7.0%) than for KCNH2 (6/374, 1.6%) or SCN5A (10/458, 2.2%), and KCNH2 held the highest number and proportion of radical mutations (30/374, 8%). The prevalence of variants was highest in the inherited arrhythmia cohort (35%) and lowest in the healthy controls (<4%), as expected. Noticeably, the variant prevalence was relatively high in the epilepsy cohort (27%). Finally, only 22 of the 82 variants (26%) identified by both companies had consistent interpretations of pathogenicity between the two companies. Our study demonstrated a comprehensive spectrum of variants in KCNQ1, KCNH2, and SCN5A in a large number of Chinese individuals, including inherited arrhythmia, cardiovascular diseases, and epilepsy. The detailed variant frequency data of each cohort could serve as a valuable reference to facilitate further variant classification by others. We also found that the interpretations of pathogenicity differed greatly among the companies.
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Li et al. (2019) conducted an observational in Inherited arrhythmia, cardiovascular diseases, and epilepsy (n=11,945). Genetic variants in KCNQ1, KCNH2, and SCN5A was evaluated on Prevalence and classification of genetic variants in KCNQ1, KCNH2, and SCN5A. Genetic testing of 11,945 Chinese individuals identified 1,018 variants in KCNQ1, KCNH2, and SCN5A, with 84% having uncertain clinical significance and prevalence highest in inherited arrhythmia (35%).
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