Literature DB >> 29050564

A Missense Variant in PLEC Increases Risk of Atrial Fibrillation.

Rosa B Thorolfsdottir1, Gardar Sveinbjornsson2, Patrick Sulem2, Anna Helgadottir2, Solveig Gretarsdottir2, Stefania Benonisdottir2, Audur Magnusdottir2, Olafur B Davidsson2, Sridharan Rajamani2, Dan M Roden3, Dawood Darbar4, Terje R Pedersen5, Marc S Sabatine6, Ingileif Jonsdottir7, David O Arnar8, Unnur Thorsteinsdottir9, Daniel F Gudbjartsson10, Hilma Holm2, Kari Stefansson11.   

Abstract

BACKGROUND: Genome-wide association studies (GWAS) have yielded variants at >30 loci that associate with atrial fibrillation (AF), including rare coding mutations in the sarcomere genes MYH6 and MYL4.
OBJECTIVES: The aim of this study was to search for novel AF associations and in doing so gain insights into the mechanisms whereby variants affect AF risk, using electrocardiogram (ECG) measurements.
METHODS: The authors performed a GWAS of 14,255 AF cases and 374,939 controls, using whole-genome sequence data from the Icelandic population, and tested novel signals in 2,002 non-Icelandic cases and 12,324 controls. They then tested the AF variants for effect on cardiac electrical function by using measurements in 289,297 ECGs from 62,974 individuals.
RESULTS: The authors discovered 2 novel AF variants, the intergenic variant rs72700114, between the genes LINC01142 and METTL11B (risk allele frequency = 8.1%; odds ratio [OR]: 1.26; p = 3.1 × 10-18), and the missense variant p.Gly4098Ser in PLEC (frequency = 1.2%; OR: 1.55; p = 8.0 × 10-10), encoding plectin, a cytoskeletal cross-linking protein that contributes to integrity of cardiac tissue. The authors also confirmed 29 reported variants. p.Gly4098Ser in PLEC significantly affects various ECG measurements in the absence of AF. Other AF variants have diverse effects on the conduction system, ranging from none to extensive.
CONCLUSIONS: The discovery of a missense variant in PLEC affecting AF combined with recent discoveries of variants in the sarcomere genes MYH6 and MYL4 points to an important role of myocardial structure in the pathogenesis of the disease. The diverse associations between AF variants and ECG measurements suggest fundamentally different categories of mechanisms contributing to the development of AF.
Copyright © 2017 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  arrhythmia; atrial fibrillation; electrocardiogram; plectin

Mesh:

Substances:

Year:  2017        PMID: 29050564      PMCID: PMC5704994          DOI: 10.1016/j.jacc.2017.09.005

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN: 0735-1097            Impact factor:   24.094


  52 in total

1.  Weighting sequence variants based on their annotation increases power of whole-genome association studies.

Authors:  Gardar Sveinbjornsson; Anders Albrechtsen; Florian Zink; Sigurjón A Gudjonsson; Asmundur Oddson; Gísli Másson; Hilma Holm; Augustine Kong; Unnur Thorsteinsdottir; Patrick Sulem; Daniel F Gudbjartsson; Kari Stefansson
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

2.  LD Score regression distinguishes confounding from polygenicity in genome-wide association studies.

Authors:  Brendan K Bulik-Sullivan; Po-Ru Loh; Hilary K Finucane; Stephan Ripke; Jian Yang; Nick Patterson; Mark J Daly; Alkes L Price; Benjamin M Neale
Journal:  Nat Genet       Date:  2015-02-02       Impact factor: 38.330

3.  PLEC1 mutations underlie adult-onset dilated cardiomyopathy in epidermolysis bullosa simplex with muscular dystrophy.

Authors:  Maria C Bolling; Hendri H Pas; Marianne de Visser; Eleonora Aronica; Ellen G Pfendner; Maarten P van den Berg; Gilles F H Diercks; Albert J H Suurmeijer; Marcel F Jonkman
Journal:  J Invest Dermatol       Date:  2009-12-17       Impact factor: 8.551

Review 4.  Patterns of expression in the developing myocardium: towards a morphologically integrated transcriptional model.

Authors:  D Franco; W H Lamers; A F Moorman
Journal:  Cardiovasc Res       Date:  1998-04       Impact factor: 10.787

5.  Large-scale whole-genome sequencing of the Icelandic population.

Authors:  Daniel F Gudbjartsson; Hannes Helgason; Sigurjon A Gudjonsson; Florian Zink; Asmundur Oddson; Arnaldur Gylfason; Soren Besenbacher; Gisli Magnusson; Bjarni V Halldorsson; Eirikur Hjartarson; Gunnar Th Sigurdsson; Simon N Stacey; Michael L Frigge; Hilma Holm; Jona Saemundsdottir; Hafdis Th Helgadottir; Hrefna Johannsdottir; Gunnlaugur Sigfusson; Gudmundur Thorgeirsson; Jon Th Sverrisson; Solveig Gretarsdottir; G Bragi Walters; Thorunn Rafnar; Bjarni Thjodleifsson; Einar S Bjornsson; Sigurdur Olafsson; Hildur Thorarinsdottir; Thora Steingrimsdottir; Thora S Gudmundsdottir; Asgeir Theodors; Jon G Jonasson; Asgeir Sigurdsson; Gyda Bjornsdottir; Jon J Jonsson; Olafur Thorarensen; Petur Ludvigsson; Hakon Gudbjartsson; Gudmundur I Eyjolfsson; Olof Sigurdardottir; Isleifur Olafsson; David O Arnar; Olafur Th Magnusson; Augustine Kong; Gisli Masson; Unnur Thorsteinsdottir; Agnar Helgason; Patrick Sulem; Kari Stefansson
Journal:  Nat Genet       Date:  2015-03-25       Impact factor: 38.330

6.  Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Authors:  Ingrid E Christophersen; Michiel Rienstra; Carolina Roselli; Xiaoyan Yin; Bastiaan Geelhoed; John Barnard; Honghuang Lin; Dan E Arking; Albert V Smith; Christine M Albert; Mark Chaffin; Nathan R Tucker; Molong Li; Derek Klarin; Nathan A Bihlmeyer; Siew-Kee Low; Peter E Weeke; Martina Müller-Nurasyid; J Gustav Smith; Jennifer A Brody; Maartje N Niemeijer; Marcus Dörr; Stella Trompet; Jennifer Huffman; Stefan Gustafsson; Claudia Schurmann; Marcus E Kleber; Leo-Pekka Lyytikäinen; Ilkka Seppälä; Rainer Malik; Andrea R V R Horimoto; Marco Perez; Juha Sinisalo; Stefanie Aeschbacher; Sébastien Thériault; Jie Yao; Farid Radmanesh; Stefan Weiss; Alexander Teumer; Seung Hoan Choi; Lu-Chen Weng; Sebastian Clauss; Rajat Deo; Daniel J Rader; Svati H Shah; Albert Sun; Jemma C Hopewell; Stephanie Debette; Ganesh Chauhan; Qiong Yang; Bradford B Worrall; Guillaume Paré; Yoichiro Kamatani; Yanick P Hagemeijer; Niek Verweij; Joylene E Siland; Michiaki Kubo; Jonathan D Smith; David R Van Wagoner; Joshua C Bis; Siegfried Perz; Bruce M Psaty; Paul M Ridker; Jared W Magnani; Tamara B Harris; Lenore J Launer; M Benjamin Shoemaker; Sandosh Padmanabhan; Jeffrey Haessler; Traci M Bartz; Melanie Waldenberger; Peter Lichtner; Marina Arendt; Jose E Krieger; Mika Kähönen; Lorenz Risch; Alfredo J Mansur; Annette Peters; Blair H Smith; Lars Lind; Stuart A Scott; Yingchang Lu; Erwin B Bottinger; Jussi Hernesniemi; Cecilia M Lindgren; Jorge A Wong; Jie Huang; Markku Eskola; Andrew P Morris; Ian Ford; Alex P Reiner; Graciela Delgado; Lin Y Chen; Yii-Der Ida Chen; Roopinder K Sandhu; Man Li; Eric Boerwinkle; Lewin Eisele; Lars Lannfelt; Natalia Rost; Christopher D Anderson; Kent D Taylor; Archie Campbell; Patrik K Magnusson; David Porteous; Lynne J Hocking; Efthymia Vlachopoulou; Nancy L Pedersen; Kjell Nikus; Marju Orho-Melander; Anders Hamsten; Jan Heeringa; Joshua C Denny; Jennifer Kriebel; Dawood Darbar; Christopher Newton-Cheh; Christian Shaffer; Peter W Macfarlane; Stefanie Heilmann-Heimbach; Peter Almgren; Paul L Huang; Nona Sotoodehnia; Elsayed Z Soliman; Andre G Uitterlinden; Albert Hofman; Oscar H Franco; Uwe Völker; Karl-Heinz Jöckel; Moritz F Sinner; Henry J Lin; Xiuqing Guo; Martin Dichgans; Erik Ingelsson; Charles Kooperberg; Olle Melander; Ruth J F Loos; Jari Laurikka; David Conen; Jonathan Rosand; Pim van der Harst; Marja-Liisa Lokki; Sekar Kathiresan; Alexandre Pereira; J Wouter Jukema; Caroline Hayward; Jerome I Rotter; Winfried März; Terho Lehtimäki; Bruno H Stricker; Mina K Chung; Stephan B Felix; Vilmundur Gudnason; Alvaro Alonso; Dan M Roden; Stefan Kääb; Daniel I Chasman; Susan R Heckbert; Emelia J Benjamin; Toshihiro Tanaka; Kathryn L Lunetta; Steven A Lubitz; Patrick T Ellinor
Journal:  Nat Genet       Date:  2017-07-27       Impact factor: 38.330

7.  A rare variant in MYH6 is associated with high risk of sick sinus syndrome.

Authors:  Hilma Holm; Daniel F Gudbjartsson; Patrick Sulem; Gisli Masson; Hafdis Th Helgadottir; Carlo Zanon; Olafur Th Magnusson; Agnar Helgason; Jona Saemundsdottir; Arnaldur Gylfason; Hrafnhildur Stefansdottir; Solveig Gretarsdottir; Stefan E Matthiasson; Gu Mundur Thorgeirsson; Aslaug Jonasdottir; Asgeir Sigurdsson; Hreinn Stefansson; Thomas Werge; Thorunn Rafnar; Lambertus A Kiemeney; Babar Parvez; Raafia Muhammad; Dan M Roden; Dawood Darbar; Gudmar Thorleifsson; G Bragi Walters; Augustine Kong; Unnur Thorsteinsdottir; David O Arnar; Kari Stefansson
Journal:  Nat Genet       Date:  2011-03-06       Impact factor: 38.330

8.  Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese.

Authors:  Steven A Lubitz; Kathryn L Lunetta; Honghuang Lin; Dan E Arking; Stella Trompet; Guo Li; Bouwe P Krijthe; Daniel I Chasman; John Barnard; Marcus E Kleber; Marcus Dörr; Kouichi Ozaki; Albert V Smith; Martina Müller-Nurasyid; Stefan Walter; Joanne M Murabito; Moritz F Sinner; Vilmundur Gudnason; Stephan B Felix; Winfried März; Mina Chung; Christine M Albert; Bruno H Stricker; Toshihiro Tanaka; Susan R Heckbert; J Wouter Jukema; Alvaro Alonso; Emelia J Benjamin; Patrick T Ellinor; Sunil K Agarwal; Joshua C Bis; Jennifer A Brody; Lin Y Chen; Brendan M Everett; Ian Ford; Oscar H Franco; Tamara B Harris; Albert Hofman; Stefan Kääb; Saagar Mahida; Sekar Kathiresan; Michiaki Kubo; Lenore J Launer; Peter W MacFarlane; Jared W Magnani; Barbara McKnight; David D McManus; Annette Peters; Bruce M Psaty; Lynda M Rose; Jerome I Rotter; Guenther Silbernagel; Jonathan D Smith; Nona Sotoodehnia; David J Stott; Kent D Taylor; Andreas Tomaschitz; Tatsuhiko Tsunoda; Andre G Uitterlinden; David R Van Wagoner; Uwe Völker; Henry Völzke
Journal:  J Am Coll Cardiol       Date:  2014-01-30       Impact factor: 24.094

9.  Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture.

Authors:  K Andrä; H Lassmann; R Bittner; S Shorny; R Fässler; F Propst; G Wiche
Journal:  Genes Dev       Date:  1997-12-01       Impact factor: 11.361

10.  Common variants in KCNN3 are associated with lone atrial fibrillation.

Authors:  Patrick T Ellinor; Kathryn L Lunetta; Nicole L Glazer; Arne Pfeufer; Alvaro Alonso; Mina K Chung; Moritz F Sinner; Paul I W de Bakker; Martina Mueller; Steven A Lubitz; Ervin Fox; Dawood Darbar; Nicholas L Smith; Jonathan D Smith; Renate B Schnabel; Elsayed Z Soliman; Kenneth M Rice; David R Van Wagoner; Britt-M Beckmann; Charlotte van Noord; Ke Wang; Georg B Ehret; Jerome I Rotter; Stanley L Hazen; Gerhard Steinbeck; Albert V Smith; Lenore J Launer; Tamara B Harris; Seiko Makino; Mari Nelis; David J Milan; Siegfried Perz; Tõnu Esko; Anna Köttgen; Susanne Moebus; Christopher Newton-Cheh; Man Li; Stefan Möhlenkamp; Thomas J Wang; W H Linda Kao; Ramachandran S Vasan; Markus M Nöthen; Calum A MacRae; Bruno H Ch Stricker; Albert Hofman; André G Uitterlinden; Daniel Levy; Eric Boerwinkle; Andres Metspalu; Eric J Topol; Aravinda Chakravarti; Vilmundur Gudnason; Bruce M Psaty; Dan M Roden; Thomas Meitinger; H-Erich Wichmann; Jacqueline C M Witteman; John Barnard; Dan E Arking; Emelia J Benjamin; Susan R Heckbert; Stefan Kääb
Journal:  Nat Genet       Date:  2010-02-21       Impact factor: 38.330

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  23 in total

Review 1.  Genetics of Atrial Fibrillation in 2020: GWAS, Genome Sequencing, Polygenic Risk, and Beyond.

Authors:  Carolina Roselli; Michiel Rienstra; Patrick T Ellinor
Journal:  Circ Res       Date:  2020-06-18       Impact factor: 17.367

Review 2.  [Syndromes with skin fragility].

Authors:  A Reimer; C Has
Journal:  Hautarzt       Date:  2019-07       Impact factor: 0.751

3.  Genetically Determined Birthweight Associates With Atrial Fibrillation: A Mendelian Randomization Study.

Authors:  Rachel L Kember; Michael G Levin; Diana L Cousminer; Noah Tsao; Renae Judy; Gayatri M Schur; Steven A Lubitz; Patrick T Ellinor; Shana E McCormack; Struan F A Grant; Daniel J Rader; Benjamin F Voight; Scott M Damrauer
Journal:  Circ Genom Precis Med       Date:  2020-04-27

4.  Association of Sinoatrial Node Radiation Dose With Atrial Fibrillation and Mortality in Patients With Lung Cancer.

Authors:  Kyung Hwan Kim; Jaewon Oh; Gowoon Yang; Joongyo Lee; Jihun Kim; Seo-Yeon Gwak; Iksung Cho; Seung Hyun Lee; Hwa Kyung Byun; Hyo-Kyoung Choi; Jinsung Kim; Jee Suk Chang; Seok-Min Kang; Hong In Yoon
Journal:  JAMA Oncol       Date:  2022-09-22       Impact factor: 33.006

Review 5.  Big Data and Atrial Fibrillation: Current Understanding and New Opportunities.

Authors:  Qian-Chen Wang; Zhen-Yu Wang
Journal:  J Cardiovasc Transl Res       Date:  2020-05-06       Impact factor: 4.132

6.  Genetic insight into sick sinus syndrome.

Authors:  Rosa B Thorolfsdottir; Gardar Sveinbjornsson; Hildur M Aegisdottir; Stefania Benonisdottir; Lilja Stefansdottir; Erna V Ivarsdottir; Gisli H Halldorsson; Jon K Sigurdsson; Christian Torp-Pedersen; Peter E Weeke; Søren Brunak; David Westergaard; Ole B Pedersen; Erik Sorensen; Kaspar R Nielsen; Kristoffer S Burgdorf; Karina Banasik; Ben Brumpton; Wei Zhou; Asmundur Oddsson; Vinicius Tragante; Kristjan E Hjorleifsson; Olafur B Davidsson; Sridharan Rajamani; Stefan Jonsson; Bjarni Torfason; Atli S Valgardsson; Gudmundur Thorgeirsson; Michael L Frigge; Gudmar Thorleifsson; Gudmundur L Norddahl; Anna Helgadottir; Solveig Gretarsdottir; Patrick Sulem; Ingileif Jonsdottir; Cristen J Willer; Kristian Hveem; Henning Bundgaard; Henrik Ullum; David O Arnar; Unnur Thorsteinsdottir; Daniel F Gudbjartsson; Hilma Holm; Kari Stefansson
Journal:  Eur Heart J       Date:  2021-05-21       Impact factor: 29.983

Review 7.  Genetics of atrial fibrillation-practical applications for clinical management: if not now, when and how?

Authors:  Shinwan Kany; Bruno Reissmann; Andreas Metzner; Paulus Kirchhof; Dawood Darbar; Renate B Schnabel
Journal:  Cardiovasc Res       Date:  2021-06-16       Impact factor: 10.787

8.  Genome-wide analysis yields new loci associating with aortic valve stenosis.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Solveig Gretarsdottir; Olafur A Stefansson; Vinicius Tragante; Rosa B Thorolfsdottir; Ingileif Jonsdottir; Thorsteinn Bjornsson; Valgerdur Steinthorsdottir; Niek Verweij; Jonas B Nielsen; Wei Zhou; Lasse Folkersen; Andreas Martinsson; Mahyar Heydarpour; Siddharth Prakash; Gylfi Oskarsson; Tomas Gudbjartsson; Arnar Geirsson; Isleifur Olafsson; Emil L Sigurdsson; Peter Almgren; Olle Melander; Anders Franco-Cereceda; Anders Hamsten; Lars Fritsche; Maoxuan Lin; Bo Yang; Whitney Hornsby; Dongchuan Guo; Chad M Brummett; Gonçalo Abecasis; Michael Mathis; Dianna Milewicz; Simon C Body; Per Eriksson; Cristen J Willer; Kristian Hveem; Christopher Newton-Cheh; J Gustav Smith; Ragnar Danielsen; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Daniel F Gudbjartsson; Hilma Holm; Kari Stefansson
Journal:  Nat Commun       Date:  2018-03-07       Impact factor: 14.919

Review 9.  Atrial fibrillation-a complex polygenetic disease.

Authors:  Julie H Andersen; Laura Andreasen; Morten S Olesen
Journal:  Eur J Hum Genet       Date:  2020-12-05       Impact factor: 4.246

10.  A SHOX2 loss-of-function mutation underlying familial atrial fibrillation.

Authors:  Ning Li; Zhang-Sheng Wang; Xin-Hua Wang; Ying-Jia Xu; Qi Qiao; Xiu-Mei Li; Ruo-Min Di; Xiao-Juan Guo; Ruo-Gu Li; Min Zhang; Xing-Biao Qiu; Yi-Qing Yang
Journal:  Int J Med Sci       Date:  2018-10-20       Impact factor: 3.738

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