Literature DB >> 18511491

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations.

Martin D Tobin1, Mika Kähönen, Peter Braund, Tuomo Nieminen, Cother Hajat, Maciej Tomaszewski, Jari Viik, Rami Lehtinen, G Andre Ng, Peter W Macfarlane, Paul R Burton, Terho Lehtimäki, Nilesh J Samani.   

Abstract

BACKGROUND: A longer heart-rate corrected QT interval (QTc) is associated with increased risk of ventricular arrhythmias. Women have longer resting QTc and are more likely than men to develop drug-induced QT prolongation. Recent studies have shown association between resting QTc and a common variant (rs10494366) of the NOS1 regulator, NOS1AP. We investigated the association between rs10494366 in NOS1AP and QTc, and assessed gender-specific NOS1AP associations with QTc during rest and after exercise.
METHODS: We investigated the SNP associations with resting QTc in 919 women and 918 men from 504 representative families in the UK GRAPHIC study, and with QTc at rest and at 3 min recovery after exercise in 699 women and 1225 men referred for exercise testing in the Finnish FINCAVAS study.
RESULTS: In the GRAPHIC study the minor allele (G) of the NOS1AP SNP rs10494366 prolonged QTc by 4.59 ms (95% CI 2.77-6.40; P = 7.63/10(7)) in women, but only by 1.62 ms (95% CI -0.15 to 3.38; P = 0.073) in men (gender-SNP interaction term P = 0.025). In the FINCAVAS study the G allele significantly prolonged QTc in both women (P = 0.0063) and men (P = 0.0043) at 3 min recovery after exercise, but at rest an association was only seen in women (P = 0.020 excluding outliers).
CONCLUSIONS: A common NOS1AP variant prolongs QTc with a difference between genders. Further studies should aim to confirm this finding and to assess whether NOS1AP genotype influences the risk of drug-induced QT prolongation and risk of consequent arrhythmias.

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Year:  2008        PMID: 18511491     DOI: 10.1093/ije/dyn091

Source DB:  PubMed          Journal:  Int J Epidemiol        ISSN: 0300-5771            Impact factor:   7.196


  27 in total

1.  Common genetic variants, QT interval, and sudden cardiac death in a Finnish population-based study.

Authors:  Peter A Noseworthy; Aki S Havulinna; Kimmo Porthan; Annukka M Lahtinen; Antti Jula; Pekka J Karhunen; Markus Perola; Lasse Oikarinen; Kimmo K Kontula; Veikko Salomaa; Christopher Newton-Cheh
Journal:  Circ Cardiovasc Genet       Date:  2011-04-21

2.  A common variant of NOS1AP is associated with QT interval duration in a Chinese population with Type 2 diabetes.

Authors:  J Lu; C Hu; W Hu; R Zhang; C Wang; W Qin; W Yu; K Xiang; W Jia
Journal:  Diabet Med       Date:  2010-09       Impact factor: 4.359

3.  Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.

Authors:  W H Linda Kao; Dan E Arking; Wendy Post; Thomas D Rea; Nona Sotoodehnia; Ronald J Prineas; Bryan Bishe; Betty Q Doan; Eric Boerwinkle; Bruce M Psaty; Gordon F Tomaselli; Josef Coresh; David S Siscovick; Eduardo Marbán; Peter M Spooner; Gregory L Burke; Aravinda Chakravarti
Journal:  Circulation       Date:  2009-02-09       Impact factor: 29.690

4.  Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.

Authors:  Mark Eijgelsheim; Christopher Newton-Cheh; Adrianus L H J Aarnoudse; Charlotte van Noord; Jacqueline C M Witteman; Albert Hofman; André G Uitterlinden; Bruno H C Stricker
Journal:  Hum Mol Genet       Date:  2009-07-30       Impact factor: 6.150

Review 5.  Molecular mechanisms of neuronal nitric oxide synthase in cardiac function and pathophysiology.

Authors:  Yin Hua Zhang; Chun Zi Jin; Ji Hyun Jang; Yue Wang
Journal:  J Physiol       Date:  2014-04-22       Impact factor: 5.182

6.  Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.

Authors:  Annukka M Lahtinen; Aki S Havulinna; Peter A Noseworthy; Antti Jula; Pekka J Karhunen; Markus Perola; Christopher Newton-Cheh; Veikko Salomaa; Kimmo Kontula
Journal:  Ann Med       Date:  2013-05-08       Impact factor: 4.709

7.  Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population.

Authors:  Lei Huang; Yangeng Yu; Yili Chen; David J Tester; Shuangbo Tang; Michael J Ackerman; Zichuang Yuan; Jianding Cheng
Journal:  Int J Legal Med       Date:  2014-02-07       Impact factor: 2.686

Review 8.  Common genetic variants in sudden cardiac death.

Authors:  Alfred L George
Journal:  Heart Rhythm       Date:  2009-09-01       Impact factor: 6.343

9.  Common variants at ten loci influence QT interval duration in the QTGEN Study.

Authors:  Christopher Newton-Cheh; Mark Eijgelsheim; Kenneth M Rice; Paul I W de Bakker; Xiaoyan Yin; Karol Estrada; Joshua C Bis; Kristin Marciante; Fernando Rivadeneira; Peter A Noseworthy; Nona Sotoodehnia; Nicholas L Smith; Jerome I Rotter; Jan A Kors; Jacqueline C M Witteman; Albert Hofman; Susan R Heckbert; Christopher J O'Donnell; André G Uitterlinden; Bruce M Psaty; Thomas Lumley; Martin G Larson; Bruno H Ch Stricker
Journal:  Nat Genet       Date:  2009-03-22       Impact factor: 38.330

10.  Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.

Authors:  Ilja M Nolte; Chris Wallace; Stephen J Newhouse; Daryl Waggott; Jingyuan Fu; Nicole Soranzo; Rhian Gwilliam; Panos Deloukas; Irina Savelieva; Dongling Zheng; Chrysoula Dalageorgou; Martin Farrall; Nilesh J Samani; John Connell; Morris Brown; Anna Dominiczak; Mark Lathrop; Eleftheria Zeggini; Louise V Wain; Christopher Newton-Cheh; Mark Eijgelsheim; Kenneth Rice; Paul I W de Bakker; Arne Pfeufer; Serena Sanna; Dan E Arking; Folkert W Asselbergs; Tim D Spector; Nicholas D Carter; Steve Jeffery; Martin Tobin; Mark Caulfield; Harold Snieder; Andrew D Paterson; Patricia B Munroe; Yalda Jamshidi
Journal:  PLoS One       Date:  2009-07-09       Impact factor: 3.240

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