The KCNE1 D85N minor allele was associated with a 10.5 ms prolongation of the adjusted QT interval (P=3.6 x 10(-11)), with additional associations confirmed for KCNH2 and NOSA1P variants.
Observational (n=5,043)
Are common LQTS and NOS1AP gene variants associated with QT interval duration in the general population?
Common genetic variants in KCNE1, KCNH2, and NOS1AP are significantly associated with QT interval duration in the general population, potentially modulating arrhythmia susceptibility.
Effect estimate: 10.5 ms prolongation
p-value: p=3.6 x 10(-11)
OBJECTIVES: QT interval prolongation is associated with increased risk of sudden cardiac death at the population level. As 30-40% of the QT-interval variability is heritable, we tested the association of common LQTS and NOS1AP gene variants with QT interval in a Finnish population-based sample. METHODS: We genotyped 12 common LQTS and NOS1AP genetic variants in Health 2000, an epidemiological sample of 5043 Finnish individuals, using Sequenom MALDI-TOF mass spectrometry. ECG parameters were measured from digital 12-lead ECGs and QT intervals were adjusted for age, gender and heart rate with a nomogram (Nc) method derived from the present study population. RESULTS: The KCNE1 D85N minor allele (frequency 1.4%) was associated with a 10.5 ms (SE 1.6) or 0.57 SD prolongation of the adjusted QT(Nc) interval (P=3.6 x 10(-11)) in gender-pooled analysis. In agreement with previous studies, we replicated the association with QT(Nc) interval with minor alleles of KCNH2 intronic SNP rs3807375 1.6 ms (SE 0.4) or 0.08 SD, P=4.7 x 10(-5), KCNH2 K897T -2.6 ms (SE 0.5) or -0.14 SD, P=2.1 x 10(-7) and NOSA1P variants including rs2880058 4.0 ms (SE 0.4) or 0.22 SD, P=3.2 x 10(-24) under additive models. CONCLUSIONS: We demonstrate that each additional copy of the KCNE1 D85N minor allele is associated with a considerable 10.5 ms prolongation of the age-, gender- and heart rate-adjusted QT interval and could thus modulate repolarization-related arrhythmia susceptibility at the population level. In addition, we robustly confirm the previous findings that three independent KCNH2 and NOSA1P variants are associated with adjusted QT interval.
Marjamaa et al. (Tue,) conducted a observational in QT interval prolongation (n=5,043). LQTS and NOS1AP gene variants was evaluated on QT interval adjusted for age, gender and heart rate (10.5 ms prolongation, p=3.6 x 10(-11)). The KCNE1 D85N minor allele was associated with a 10.5 ms prolongation of the adjusted QT interval (P=3.6 x 10(-11)), with additional associations confirmed for KCNH2 and NOSA1P variants.