Christophersen Ingrid E, Magnani Jared W, Yin Xiaoyan, Barnard John, Weng Lu-Chen, Arking Dan E, Niemeijer Maartje N, Lubitz Steven A, Avery Christy L, Duan Qing, Felix Stephan B, Bis Joshua C, Kerr Kathleen F, Isaacs Aaron, Müller-Nurasyid Martina, Müller Christian, North Kari E, Reiner Alex P, Tinker Lesley F, Kors Jan A, Teumer Alexander, Petersmann Astrid, Sinner Moritz F, Buzkova Petra, Smith Jonathan D, Van Wagoner David R, Völker Uwe, Waldenberger Melanie, Peters Annette, Meitinger Thomas, Limacher Marian C, Wilhelmsen Kirk C, Psaty Bruce M, Hofman Albert, Uitterlinden Andre, Krijthe Bouwe P, Zhang Zhu-Ming, Schnabel Renate B, Kääb Stefan, van Duijn Cornelia, Rotter Jerome I, Sotoodehnia Nona, Dörr Marcus, Li Yun, Chung Mina K, Soliman Elsayed Z, Alonso Alvaro, Whitsel Eric A, Stricker Bruno H, Benjamin Emelia J, Heckbert Susan R, Ellinor Patrick T
Circ Cardiovasc Genet. 2017 Aug;10(4). doi: 10.1161/CIRCGENETICS.116.001667.
The P wave on an ECG is a measure of atrial electric function, and its characteristics may serve as predictors for atrial arrhythmias. Increased mean P-wave duration and P-wave terminal force traditionally have been used as markers for left atrial enlargement, and both have been associated with increased risk of atrial fibrillation. Here, we explore the genetic basis of P-wave morphology through meta-analysis of genome-wide association study results for P-wave duration and P-wave terminal force from 12 cohort studies.
We included 44 456 individuals, of which 6778 (16%) were of African ancestry. Genotyping, imputation, and genome-wide association study were performed at each study site. Summary-level results were meta-analyzed centrally using inverse-variance weighting. In meta-analyses of P-wave duration, we identified 6 significant (<5×10) novel loci and replicated a prior association with S We identified 3 loci at , , and that were jointly associated with the PR interval, PR segment, and P-wave duration. We identified 6 novel loci in meta-analysis of P-wave terminal force. Four of the identified genetic loci were significantly associated with gene expression in 329 left atrial samples. Finally, we observed that some of the loci associated with the P wave were linked to overall atrial conduction, whereas others identified distinct phases of atrial conduction.
We have identified 6 novel genetic loci associated with P-wave duration and 6 novel loci associated with P-wave terminal force. Future studies of these loci may aid in identifying new targets for drugs that may modify atrial conduction or treat atrial arrhythmias.
心电图上的P波是心房电功能的一种测量指标,其特征可作为房性心律失常的预测指标。传统上,平均P波时限延长和P波终末电势增加一直被用作左心房扩大的标志物,且二者均与房颤风险增加相关。在此,我们通过对12项队列研究中P波时限和P波终末电势的全基因组关联研究结果进行荟萃分析,探索P波形态的遗传基础。
我们纳入了44456名个体,其中6778名(16%)为非洲裔。在每个研究地点进行基因分型、插补和全基因组关联研究。汇总水平的结果使用逆方差加权法进行集中荟萃分析。在P波时限的荟萃分析中,我们确定了6个显著(<5×10)的新位点,并复制了先前与S的关联。我们在、和处确定了3个位点,它们与PR间期、PR段和P波时限共同相关。在P波终末电势的荟萃分析中,我们确定了6个新位点。所确定的4个基因位点与329份左心房样本中的基因表达显著相关。最后,我们观察到一些与P波相关的位点与整体心房传导有关,而其他位点则确定了心房传导的不同阶段。
我们确定了6个与P波时限相关的新基因位点和6个与P波终末电势相关的新位点。对这些位点的进一步研究可能有助于确定可改变心房传导或治疗房性心律失常的药物新靶点。