Several common variants modulate heart rate, PR interval and QRS duration

To access publisher full text version of this article. Please click on the hyperlink in Additional Links field Electrocardiographic measures are indicative of the function of the cardiac conduction system. To search for sequence variants that modulate heart rate, PR interval and QRS duration in indi...

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Published in:Nature Genetics
Main Authors: Holm, Hilma, Gudbjartsson, Daniel F, Arnar, David O, Thorleifsson, Gudmar, Thorgeirsson, Gudmundur, Stefansdottir, Hrafnhildur, Gudjonsson, Sigurjon A, Jonasdottir, Aslaug, Mathiesen, Ellisiv B, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin M, Hveem, Kristian, Stoltenberg, Camilla, Løchen, Maja-Lisa, Kong, Augustine, Thorsteinsdottir, Unnur, Stefansson, Kari
Other Authors: deCODE genetics, Reykjavik, Iceland. hilma.holm@decode.is
Format: Article in Journal/Newspaper
Language:English
Published: Nature Pub. Co. 2010
Subjects:
Online Access:http://hdl.handle.net/2336/96605
https://doi.org/10.1038/ng.511
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spelling ftlandspitaliuni:oai:www.hirsla.lsh.is:2336/96605 2023-05-15T16:50:41+02:00 Several common variants modulate heart rate, PR interval and QRS duration Holm, Hilma Gudbjartsson, Daniel F Arnar, David O Thorleifsson, Gudmar Thorgeirsson, Gudmundur Stefansdottir, Hrafnhildur Gudjonsson, Sigurjon A Jonasdottir, Aslaug Mathiesen, Ellisiv B Njølstad, Inger Nyrnes, Audhild Wilsgaard, Tom Hald, Erin M Hveem, Kristian Stoltenberg, Camilla Løchen, Maja-Lisa Kong, Augustine Thorsteinsdottir, Unnur Stefansson, Kari deCODE genetics, Reykjavik, Iceland. hilma.holm@decode.is 2010-04-15 http://hdl.handle.net/2336/96605 https://doi.org/10.1038/ng.511 en eng Nature Pub. Co. http://dx.doi.org/10.1038/ng.511 Nat. Genet. 2010, 42(2):117-22 1546-1718 20062063 doi:10.1038/ng.511 http://hdl.handle.net/2336/96605 Nature genetics Aged Arrhythmias Cardiac Atrial Fibrillation Atrioventricular Block Cardiac Myosins Electrocardiography Female Genetic Loci Genetic Variation Genome-Wide Association Study Heart Conduction System Heart Rate Iceland Inheritance Patterns Male Middle Aged Myosin Heavy Chains Pacemaker Artificial Reproducibility of Results Sick Sinus Syndrome Article 2010 ftlandspitaliuni https://doi.org/10.1038/ng.511 2022-05-29T08:21:31Z To access publisher full text version of this article. Please click on the hyperlink in Additional Links field Electrocardiographic measures are indicative of the function of the cardiac conduction system. To search for sequence variants that modulate heart rate, PR interval and QRS duration in individuals of European descent, we performed a genome-wide association study in approximately 10,000 individuals and followed up the top signals in an additional approximately 10,000 individuals. We identified several genome-wide significant associations (with P < 1.6 x 10(-7)). We identified one locus for heart rate (MYH6), four for PR interval (TBX5, SCN10A, CAV1 and ARHGAP24) and four for QRS duration (TBX5, SCN10A, 6p21 and 10q21). We tested for association between these loci and subjects with selected arrhythmias in Icelandic and Norwegian case-control sample sets. We observed correlations between TBX5 and CAV1 and atrial fibrillation (P = 4.0 x 10(-5) and P = 0.00032, respectively), between TBX5 and advanced atrioventricular block (P = 0.0067), and between SCN10A and pacemaker implantation (P = 0.0029). We also replicated previously described associations with the QT interval. Article in Journal/Newspaper Iceland Hirsla - Landspítali University Hospital research archive Nature Genetics 42 2 117 122
institution Open Polar
collection Hirsla - Landspítali University Hospital research archive
op_collection_id ftlandspitaliuni
language English
topic Aged
Arrhythmias
Cardiac
Atrial Fibrillation
Atrioventricular Block
Cardiac Myosins
Electrocardiography
Female
Genetic Loci
Genetic Variation
Genome-Wide Association Study
Heart Conduction System
Heart Rate
Iceland
Inheritance Patterns
Male
Middle Aged
Myosin Heavy Chains
Pacemaker
Artificial
Reproducibility of Results
Sick Sinus Syndrome
spellingShingle Aged
Arrhythmias
Cardiac
Atrial Fibrillation
Atrioventricular Block
Cardiac Myosins
Electrocardiography
Female
Genetic Loci
Genetic Variation
Genome-Wide Association Study
Heart Conduction System
Heart Rate
Iceland
Inheritance Patterns
Male
Middle Aged
Myosin Heavy Chains
Pacemaker
Artificial
Reproducibility of Results
Sick Sinus Syndrome
Holm, Hilma
Gudbjartsson, Daniel F
Arnar, David O
Thorleifsson, Gudmar
Thorgeirsson, Gudmundur
Stefansdottir, Hrafnhildur
Gudjonsson, Sigurjon A
Jonasdottir, Aslaug
Mathiesen, Ellisiv B
Njølstad, Inger
Nyrnes, Audhild
Wilsgaard, Tom
Hald, Erin M
Hveem, Kristian
Stoltenberg, Camilla
Løchen, Maja-Lisa
Kong, Augustine
Thorsteinsdottir, Unnur
Stefansson, Kari
Several common variants modulate heart rate, PR interval and QRS duration
topic_facet Aged
Arrhythmias
Cardiac
Atrial Fibrillation
Atrioventricular Block
Cardiac Myosins
Electrocardiography
Female
Genetic Loci
Genetic Variation
Genome-Wide Association Study
Heart Conduction System
Heart Rate
Iceland
Inheritance Patterns
Male
Middle Aged
Myosin Heavy Chains
Pacemaker
Artificial
Reproducibility of Results
Sick Sinus Syndrome
description To access publisher full text version of this article. Please click on the hyperlink in Additional Links field Electrocardiographic measures are indicative of the function of the cardiac conduction system. To search for sequence variants that modulate heart rate, PR interval and QRS duration in individuals of European descent, we performed a genome-wide association study in approximately 10,000 individuals and followed up the top signals in an additional approximately 10,000 individuals. We identified several genome-wide significant associations (with P < 1.6 x 10(-7)). We identified one locus for heart rate (MYH6), four for PR interval (TBX5, SCN10A, CAV1 and ARHGAP24) and four for QRS duration (TBX5, SCN10A, 6p21 and 10q21). We tested for association between these loci and subjects with selected arrhythmias in Icelandic and Norwegian case-control sample sets. We observed correlations between TBX5 and CAV1 and atrial fibrillation (P = 4.0 x 10(-5) and P = 0.00032, respectively), between TBX5 and advanced atrioventricular block (P = 0.0067), and between SCN10A and pacemaker implantation (P = 0.0029). We also replicated previously described associations with the QT interval.
author2 deCODE genetics, Reykjavik, Iceland. hilma.holm@decode.is
format Article in Journal/Newspaper
author Holm, Hilma
Gudbjartsson, Daniel F
Arnar, David O
Thorleifsson, Gudmar
Thorgeirsson, Gudmundur
Stefansdottir, Hrafnhildur
Gudjonsson, Sigurjon A
Jonasdottir, Aslaug
Mathiesen, Ellisiv B
Njølstad, Inger
Nyrnes, Audhild
Wilsgaard, Tom
Hald, Erin M
Hveem, Kristian
Stoltenberg, Camilla
Løchen, Maja-Lisa
Kong, Augustine
Thorsteinsdottir, Unnur
Stefansson, Kari
author_facet Holm, Hilma
Gudbjartsson, Daniel F
Arnar, David O
Thorleifsson, Gudmar
Thorgeirsson, Gudmundur
Stefansdottir, Hrafnhildur
Gudjonsson, Sigurjon A
Jonasdottir, Aslaug
Mathiesen, Ellisiv B
Njølstad, Inger
Nyrnes, Audhild
Wilsgaard, Tom
Hald, Erin M
Hveem, Kristian
Stoltenberg, Camilla
Løchen, Maja-Lisa
Kong, Augustine
Thorsteinsdottir, Unnur
Stefansson, Kari
author_sort Holm, Hilma
title Several common variants modulate heart rate, PR interval and QRS duration
title_short Several common variants modulate heart rate, PR interval and QRS duration
title_full Several common variants modulate heart rate, PR interval and QRS duration
title_fullStr Several common variants modulate heart rate, PR interval and QRS duration
title_full_unstemmed Several common variants modulate heart rate, PR interval and QRS duration
title_sort several common variants modulate heart rate, pr interval and qrs duration
publisher Nature Pub. Co.
publishDate 2010
url http://hdl.handle.net/2336/96605
https://doi.org/10.1038/ng.511
genre Iceland
genre_facet Iceland
op_relation http://dx.doi.org/10.1038/ng.511
Nat. Genet. 2010, 42(2):117-22
1546-1718
20062063
doi:10.1038/ng.511
http://hdl.handle.net/2336/96605
Nature genetics
op_doi https://doi.org/10.1038/ng.511
container_title Nature Genetics
container_volume 42
container_issue 2
container_start_page 117
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