Literature DB >> 18785031

Common variation in NOS1AP and KCNH2 genes and QT interval duration in young adults. The Cardiovascular Risk in Young Finns Study.

Olli T Raitakari1, Jaana Blom-Nyholm, Tuomas A Koskinen, Mika Kähönen, Jorma S A Viikari, Terho Lehtimäki.   

Abstract

BACKGROUND: Common genetic variants in the nitric oxide synthase 1 adaptor protein gene (NOS1AP) and in the HERG potassium channel gene (KCNH2) have been associated with cardiac repolarization in middle-aged and elderly subjects. AIM: We examined the relation between these variants and QT interval duration in a population of healthy young adults.
METHODS: We measured QT interval duration and genotyped rs10494366 T>G (NOS1AP gene, n=1,842) and rs1805123 A>C (KCNH2 gene, n=1,894) in subjects aged 24-39 years.
RESULTS: The NOS1AP variant was significantly related with heart rate-corrected QT interval duration (QTc). Additive regression model adjusting for age, sex, systolic blood pressure, body mass index, alcohol use, and smoking indicated that the G allele was associated with a 3.2 ms (95% confidence interval (CI) 1.7-4.6 ms, P<0.0001) increase in QTc interval duration for each additional copy. The KCNH2 variant was not significantly related with QTc interval duration in the study sample.
CONCLUSION: These findings provide evidence from a population of healthy young adults that a common variation in the NOS1AP gene influences cardiac repolarization within the normal physiological range. Further studies are warranted to investigate the effects of this variant on sudden cardiac death and ventricular arrhythmias.

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Year:  2009        PMID: 18785031     DOI: 10.1080/07853890802392529

Source DB:  PubMed          Journal:  Ann Med        ISSN: 0785-3890            Impact factor:   4.709


  19 in total

1.  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

2.  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

3.  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

4.  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

5.  The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.

Authors:  Iliana Tzimas; Jana-Christin Zingraf; Thomas Bajanowski; Micaela Poetsch
Journal:  Int J Legal Med       Date:  2016-07-26       Impact factor: 2.686

6.  NOS1AP Functionally Associates with YAP To Regulate Hippo Signaling.

Authors:  Leanne Clattenburg; Michael Wigerius; Jiansong Qi; Jan K Rainey; Jillian L Rourke; Shanmugam Muruganandan; Christopher J Sinal; James P Fawcett
Journal:  Mol Cell Biol       Date:  2015-04-27       Impact factor: 4.272

Review 7.  Common genetic variants in sudden cardiac death.

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

8.  Associations between NOS1AP single nucleotide polymorphisms (SNPs) and QT interval duration in four racial/ethnic groups in the Multi-Ethnic Study of Atherosclerosis (MESA).

Authors:  Sidharth A Shah; David M Herrington; Timothy D Howard; Jasmin Divers; Donna K Arnett; Greg L Burke; Weng Hong Kao; Xiuqing Guo; David S Siscovick; Aravinda Chakravarti; Joao A Lima; Bruce M Psaty; Gordon F Tomaselli; Stephen S Rich; Donald W Bowden; Wendy Post
Journal:  Ann Noninvasive Electrocardiol       Date:  2013-01       Impact factor: 1.468

9.  Pharmacogenetic effects of 'candidate gene complexes' on stroke in the GenHAT study.

Authors:  Izel F Sørensen; Ana I Vazquez; Marguerite R Irvin; Peter Sørensen; Barry R Davis; Charles E Ford; Eric Boerwinkle; John H Eckfeldt; Donna K Arnett
Journal:  Pharmacogenet Genomics       Date:  2014-11       Impact factor: 2.089

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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