IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation

KCNQ1 Mutations in Early-Onset Lone AF IntroductionAtrial fibrillation (AF) is the most frequent cardiac arrhythmia. The potassium current I-Ks is essential for cardiac repolarization. Gain-of-function mutation in KCNQ1, the gene encoding the pore-forming -subunit of the I-Ks channel (K(V)7.1), was the first ion channel dysfunction to be associated with familial AF. We hypothesized that early-onset lone AF is associated with a high prevalence of mutations in KCNQ1. Methods and ResultsWe bidirectionally sequenced the entire coding sequence of KCNQ1 in 209 unrelated patients with early-onset lone AF (<40 years) and investigated the identified mutations functionally in a heterologous expression system. We found 4 nonsynonymous KCNQ1 mutations (A46T, R195W, A302V, and R670K) in 4 unrelated patients (38, 31, 39, and 36 years, respectively). None of the mutations were present in the control group (n = 416 alleles). No other mutations were found in genes previously associated with AF. The mutations A46T, R195W, and A302V have previously been associated with long-QT syndrome. In line with previous reports, we found A302V to display a pronounced loss-of-function of the I-Ks current, while the other mutants exhibited a gain-of-function phenotype. ConclusionsMutations in the I-Ks channel leading to gain-of-function have previously been described in familial AF, yet this is the first time a loss-of-function mutation in KCNQ1 is associated with early-onset lone AF. These findings suggest that both gain-of-function and loss-of-function of cardiac potassium currents enhance the susceptibility to AF.