A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

被引:393
|
作者
Arking, Dan E.
Pfeufer, Arne
Post, Wendy
Kao, W. H. Linda
Newton-Cheh, Christopher
Ikeda, Morna
West, Kristen
Kashuk, Carl
Akyol, Mahmut
Perz, Siegfried
Jalilzadeh, Shapour
Illig, Thomas
Gieger, Christian
Guo, Chao-Yu
Larson, Martin G.
Wichmann, H. Erich
Marban, Eduardo
O'Donnell, Christopher J.
Hirschhorn, Joel N.
Kaeaeb, Stefan
Spooner, Peter M.
Meitinger, Thomas
Chakravarti, Aravinda [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[3] Tech Univ Munich, Inst Human Genet, D-81675 Munich, Germany
[4] GSF, Natl Res Ctr Environm & Hlth, Inst Human Genet, D-85764 Neuherberg, Germany
[5] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[6] NHLBI, Framingham Heart Study, Framingham, MA 01702 USA
[7] Harvard Univ, Broad Inst, Cambridge, MA 02139 USA
[8] MIT, Cambridge, MA 02139 USA
[9] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[10] GSF, Natl Res Ctr Environm & Hlth, Inst Epidemiol, D-85764 Neuherberg, Germany
[11] Boston Univ, Dept Math & Stat, Boston, MA 02215 USA
[12] Univ Munich, Inst Informat Management Biometry & Epidemiol, D-81377 Munich, Germany
[13] Childrens Hosp, Div Genet, Boston, MA 02115 USA
[14] Childrens Hosp, Div Endocrinol, Boston, MA 02115 USA
[15] Childrens Hosp, Program Genom, Boston, MA 02115 USA
[16] Univ Munich, Dept Med 1, D-81377 Munich, Germany
[17] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
D O I
10.1038/ng1790
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Extremes of the electrocardiographic QT interval, a measure of cardiac repolarization, are associated with increased cardiovascular mortality. We identified a common genetic variant influencing this quantitative trait through a genome-wide association study on 200 subjects at the extremes of a population-based QT interval distribution of 3,966 subjects from the KORA cohort in Germany, with follow-up screening of selected markers in the remainder of the cohort. We validated statistically significant findings in two independent samples of 2,646 subjects from Germany and 1,805 subjects from the US Framingham Heart Study. This genome-wide study identified NOS1AP ( CAPON), a regulator of neuronal nitric oxide synthase, as a new target that modulates cardiac repolarization. Approximately 60% of subjects of European ancestry carry at least one minor allele of the NOS1AP genetic variant, which explains up to 1.5% of QT interval variation.
引用
收藏
页码:644 / 651
页数:8
相关论文
共 50 条
  • [31] NOS1AP Modulates Intracellular Ca2+ in Cardiac Myocytes and is Up-Regulated in Dystrophic Cardiomyopathy
    Treuer, Adriana V.
    Gonzalez, Daniel R.
    BIOPHYSICAL JOURNAL, 2014, 106 (02) : 116A - 116A
  • [32] Research progress in NOS1AP in neurological and psychiatric diseases
    Wang, Jie
    Jin, Lei
    Zhu, Yufu
    Zhou, Xiuping
    Yu, Rutong
    Gao, Shangfeng
    BRAIN RESEARCH BULLETIN, 2016, 125 : 99 - 105
  • [33] Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population
    Hu, C.
    Wang, C.
    Zhang, R.
    Ng, M. C.
    Bao, Y.
    Wang, C.
    So, W. Y.
    Ma, R. C.
    Ma, X.
    Chan, J. C.
    Xiang, K.
    Jia, W.
    DIABETOLOGIA, 2010, 53 (02) : 290 - 298
  • [34] The interaction between NOS-I and NOS1AP in dendrite development: implications for schizophrenia
    Freudenberg, F.
    Kollert, L.
    Candemir, E.
    Toepner, T.
    Geis, M.
    Mueller, A.
    Weissflog, L.
    Reif, A.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2014, 24 : S487 - S488
  • [35] Association of NOS1AP variants and depression phenotypes in schizophrenia
    Cheah, Sern-Yih
    Lawford, Bruce R.
    Young, Ross McD
    Morris, C. Phillip
    Voisey, Joanne
    JOURNAL OF AFFECTIVE DISORDERS, 2015, 188 : 263 - 269
  • [36] GENETIC DELETION OF NOS1AP INDUCES VENTRICULAR TACHYCARDIA AND SUDDEN CARDIAC DEATH IN PRESSURE OVERLOADED CONDITION
    Sasano, T.
    Matsubara, S.
    Furukawa, T.
    Hirao, K.
    Isobe, M.
    JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2011, 22 : S125 - S126
  • [37] Association of Cardiovascular Drugs and NOS1AP with QTc Prolongation
    van Noord, C.
    Aarnoudse, A.
    Sturkenboom, M.
    Straus, S.
    Witteman, J.
    Stricker, B.
    DRUG SAFETY, 2008, 31 (10) : 901 - 901
  • [38] Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population
    C. Hu
    C. Wang
    R. Zhang
    M. C. Ng
    Y. Bao
    C. Wang
    W. Y. So
    R. C. Ma
    X. Ma
    J. C. Chan
    K. Xiang
    W. Jia
    Diabetologia, 2010, 53 : 290 - 298
  • [39] Evaluating Common NOS1AP Variants in Patients with Implantable Cardioverter Defibrillators for Secondary Prevention
    Zang, Xiaobiao
    Zhang, Shulong
    Li, Sisi
    Wang, Xianqing
    Song, Weifeng
    Chen, Ke
    Ma, Jifang
    Tu, Xin
    Xia, Yunlong
    Zhao, Yonghui
    Gao, Chuanyu
    JOURNAL OF INTERVENTIONAL CARDIAC ELECTROPHYSIOLOGY, 2022, 64 (03) : 793 - 800
  • [40] Is NOS1 a genetic link between RLS and ADHD?
    Reif, Andreas
    JOURNAL OF PSYCHIATRIC RESEARCH, 2010, 44 (01) : 60 - 61