Aydin Atakan, Bähring Sylvia, Dahm Stefan, Guenther Ulf P, Uhlmann Regina, Busjahn Andreas, Luft Friedrich C
HELIOS Klinikum, Max Delbrück Center for Molecular Medicine, Medical Faculty of the Charité, Berlin, Germany.
J Mol Med (Berl). 2005 Feb;83(2):159-65. doi: 10.1007/s00109-004-0595-3. Epub 2004 Dec 15.
We screened a white population for single nucleotide polymorphisms (SNPs) in five long QT syndrome genes, namely, KCNQ1 (LQT1), HERG (LQT2), SCN5A (LQT3), KCNE1 (LQT5), and KCNE2 (LQT6). We found 35 SNPs, 10 of which have not been previously described. Ten SNPs were in KCNE1, six in HERG, eight in KCNQ1, four in KCNE2, and seven in SCN5A. Four SNPs were associated with QTc interval in our 141 subjects, one in KCNE1, one in KCNE2, and two in SCN5A. Two of these SNPs have not been described. We conclude that these five long QT syndrome genes contain common variants, some of which are associated with QTc interval in normal persons. We suggest that analysis of these SNPs in a much larger cohort would enable establishment of common haplotypes that are associated with QTc. These haplotypes could facilitate prediction of arrhythmia risk in the general population.
