Literature DB >> 32822252

Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.

Lu-Chen Weng1,2, Amelia Weber Hall1,2, Seung Hoan Choi2, Sean J Jurgens2, Jeffrey Haessler3, Nathan A Bihlmeyer4, Niels Grarup5, Honghuang Lin6,7, Alexander Teumer8,9, Ruifang Li-Gao10, Jie Yao11, Xiuqing Guo11,12, Jennifer A Brody13, Martina Müller-Nurasyid14,15,16, Katharina Schramm14,15,16, Niek Verweij17,18, Marten E van den Berg19, Jessica van Setten20, Aaron Isaacs21,22, Julia Ramírez23,24, Helen R Warren23,24, Sandosh Padmanabhan25, Jan A Kors26, Rudolf A de Boer18, Peter van der Meer18, Moritz F Sinner15,27, Melanie Waldenberger27,28,29, Bruce M Psaty30,31, Kent D Taylor11,12, Uwe Völker8,32, Jørgen K Kanters33, Man Li34, Alvaro Alonso35, Marco V Perez36, Ilonca Vaartjes37, Michiel L Bots37, Paul L Huang1, Susan R Heckbert38, Henry J Lin11,12, Jelena Kornej6, Patricia B Munroe23,24, Cornelia M van Duijn39,40, Folkert W Asselbergs20,41,42, Bruno H Stricker43,44,45, Pim van der Harst18,46,47, Stefan Kääb15,27, Annette Peters27,28,48, Nona Sotoodehnia13, Jerome I Rotter11,49, Dennis O Mook-Kanamori10,50, Marcus Dörr8,51, Stephan B Felix8,51, Allan Linneberg52,53, Torben Hansen5, Dan E Arking4, Charles Kooperberg3, Emelia J Benjamin6,54,55, Kathryn L Lunetta6,56, Patrick T Ellinor1,57,2, Steven A Lubitz57,2.   

Abstract

BACKGROUND: The P-wave duration (PWD) is an electrocardiographic measurement that represents cardiac conduction in the atria. Shortened or prolonged PWD is associated with atrial fibrillation (AF). We used exome-chip data to examine the associations between common and rare variants with PWD.
METHODS: Fifteen studies comprising 64 440 individuals (56 943 European, 5681 African, 1186 Hispanic, 630 Asian) and ≈230 000 variants were used to examine associations with maximum PWD across the 12-lead ECG. Meta-analyses summarized association results for common variants; gene-based burden and sequence kernel association tests examined low-frequency variant-PWD associations. Additionally, we examined the associations between PWD loci and AF using previous AF genome-wide association studies.
RESULTS: We identified 21 common and low-frequency genetic loci (14 novel) associated with maximum PWD, including several AF loci (TTN, CAND2, SCN10A, PITX2, CAV1, SYNPO2L, SOX5, TBX5, MYH6, RPL3L). The top variants at known sarcomere genes (TTN, MYH6) were associated with longer PWD and increased AF risk. However, top variants at other loci (eg, PITX2 and SCN10A) were associated with longer PWD but lower AF risk.
CONCLUSIONS: Our results highlight multiple novel genetic loci associated with PWD, and underscore the shared mechanisms of atrial conduction and AF. Prolonged PWD may be an endophenotype for several different genetic mechanisms of AF.

Entities:  

Keywords:  atrial fibrillation; electrophysiology; exome; genetic; genome-wide association studies; population

Mesh:

Substances:

Year:  2020        PMID: 32822252      PMCID: PMC7578098          DOI: 10.1161/CIRCGEN.119.002874

Source DB:  PubMed          Journal:  Circ Genom Precis Med        ISSN: 2574-8300


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