|
1.
|
Fuster V, Rydén LE, Cannom DS, Crijns HJ,
Curtis AB, Ellenbogen KA, Halperin JL, Kay GN, Le Huezey JY, Lowe
JE, Olsson SB, Prystowsky EN, Tamargo JL, Wann LS, Smith SC Jr,
Priori SG, Estes NA III, Ezekowitz MD, Jackman WM, January CT, Lowe
JE, Page RL, Slotwiner DJ, Stevenson WG, Tracy CM, Jacobs AK,
Anderson JL, Albert N, Buller CE, Creager MA, Ettinger SM, Guyton
RA, Halperin JL, Hochman JS, Kushner FG, Ohman EM, Stevenson WG,
Tarkington LG and Yancy CW; American College of Cardiology
Foundation/American Heart Association Task Force: 2011 ACCF/AHA/HRS
focused updates incorporated into the ACC/AHA/ESC 2006 guidelines
for the management of patients with atrial fibrillation: a report
of the American College of Cardiology Foundation/American Heart
Association Task Force on practice guidelines. Circulation.
123:e269–e367. 2011.
|
|
2.
|
Go AS, Hylek EM, Phillips KA, Chang Y,
Henault LE, Selby JV and Singer DE: Prevalence of diagnosed atrial
fibrillation in adults: national implications for rhythm management
and stroke prevention: the AnTicoagulation and Risk Factors in
Atrial Fibrillation (ATRIA) Study. JAMA. 285:2370–2375. 2001.
View Article : Google Scholar : PubMed/NCBI
|
|
3.
|
Lloyd-Jones DM, Wang TJ, Leip EP, Larson
MG, Levy D, Vasan RS, D’Agostino RB, Massaro JM, Beiser A, Wolf PA
and Benjamin EJ: Lifetime risk for development of atrial
fibrillation: the Framingham Heart Study. Circulation.
110:1042–1046. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
4.
|
Wolf PA, Abbott RD and Kannel WB: Atrial
fibrillation as an independent risk factor for stroke: the
Framingham Study. Stroke. 22:983–988. 1991. View Article : Google Scholar : PubMed/NCBI
|
|
5.
|
Benjamin EJ, Wolf PA, D’Agostino RB,
Silbershatz H, Kannel WB and Levy D: Impact of atrial fibrillation
on the risk of death: the Framingham Heart Study. Circulation.
98:946–952. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
6.
|
Magnani JW, Rienstra M, Lin H, Sinner MF,
Lubitz SA, McManus DD, Dupuis J, Ellinor PT and Benjamin EJ: Atrial
fibrillation: current knowledge and future directions in
epidemiology and genomics. Circulation. 124:1982–1993. 2011.
View Article : Google Scholar : PubMed/NCBI
|
|
7.
|
Darbar D, Herron KJ, Ballew JD, Jahangir
A, Gersh BJ, Shen WK, Hammill SC, Packer DL and Olson TM: Familial
atrial fibrillation is a genetically heterogeneous disorder. J Am
Coll Cardiol. 41:2185–2192. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
8.
|
Ellinor PT, Yoerger DM, Ruskin JN and
MacRae CA: Familial aggregation in lone atrial fibrillation. Hum
Genet. 118:179–184. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
9.
|
Arnar DO, Thorvaldsson S, Manolio TA,
Thorgeirsson G, Kristjansson K, Hakonarson H and Stefansson K:
Familial aggregation of atrial fibrillation in Iceland. Eur Heart
J. 27:708–712. 2006. View Article : Google Scholar : PubMed/NCBI
|
|
10.
|
Junttila MJ, Raatikainen MJ, Perkiömäki
JS, Hong K, Brugada R and Huikuri HV: Familial clustering of lone
atrial fibrillation in patients with saddleback-type ST-segment
elevation in right precordial leads. Eur Heart J. 28:463–468. 2007.
View Article : Google Scholar : PubMed/NCBI
|
|
11.
|
Christophersen IE, Ravn LS,
Budtz-Joergensen E, Skytthe A, Haunsoe S, Svendsen JH and
Christensen K: Familial aggregation of atrial fibrillation: a study
in Danish twins. Circ Arrhythm Electrophysiol. 2:378–383. 2009.
View Article : Google Scholar : PubMed/NCBI
|
|
12.
|
Yang YQ, Zhang XL, Wang XH, Tan HW, Shi
HF, Fang WY and Liu X: Familial aggregation of lone atrial
fibrillation in the Chinese population. Intern Med. 49:2385–2391.
2010. View Article : Google Scholar : PubMed/NCBI
|
|
13.
|
Lubitz SA, Yin X, Fontes JD, Magnani JW,
Rienstra M, Pai M, Villalon ML, Vasan RS, Pencina MJ, Levy D,
Larson MG, Ellinor PT and Benjamin EJ: Association between familial
atrial fibrillation and risk of new-onset atrial fibrillation.
JAMA. 304:2263–2269. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
14.
|
Fox CS, Parise H, D’Agostino RB Sr,
Lloyd-Jones DM, Vasan RS, Wang TJ, Levy D, Wolf PA and Benjamin EJ:
Parental atrial fibrillation as a risk factor for atrial
fibrillation in offspring. JAMA. 291:2851–2855. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
15.
|
Brugada R, Tapscott T, Czernuszewicz GZ,
Marian AJ, Iglesias A, Mont L, Brugada J, Girona J, Domingo A,
Bachinski LL and Roberts R: Identification of a genetic locus for
familial atrial fibrillation. N Engl J Med. 336:905–911. 1997.
View Article : Google Scholar : PubMed/NCBI
|
|
16.
|
Ellinor PT, Shin JT, Moore RK, Yoerger DM
and MacRae CA: Locus for atrial fibrillation maps to chromosome
6q14–16. Circulation. 107:2880–2883. 2003.PubMed/NCBI
|
|
17.
|
Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang
Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN, Yang YQ, Li YB, Liu Y,
Xu HJ, Li XF, Ma N, Mou CP, Chen Z, Barhanin J and Huang W: KCNQ1
gain-of-function mutation in familial atrial fibrillation. Science.
299:251–254. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
18.
|
Oberti C, Wang L, Li L, Dong J, Rao S, Du
W and Wang Q: Genome-wide linkage scan identifies a novel genetic
locus on chromosome 5p13 for neonatal atrial fibrillation
associated with sudden death and variable cardiomyopathy.
Circulation. 110:3753–3759. 2004. View Article : Google Scholar
|
|
19.
|
Darbar D, Hardy A, Haines JL and Roden DM:
Prolonged signal-averaged P-wave duration as an intermediate
phenotype for familial atrial fibrillation. J Am Coll Cardiol.
51:1083–1089. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
20.
|
Zhang X, Chen S, Yoo S, Chakrabarti S,
Zhang T, Ke T, Oberti C, Yong SL, Fang F, Li L, de la Fuente R,
Wang L, Chen Q and Wang QK: Mutation in nuclear pore component
NUP155 leads to atrial fibrillation and early sudden cardiac death.
Cell. 135:1017–1027. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
21.
|
Yang Y, Xia M, Jin Q, Bendahhou S, Shi J
and Chen Y, Liang B, Lin J, Liu Y, Liu B, Zhou Q, Zhang D, Wang R,
Ma N, Su X, Niu K, Pei Y, Xu W, Chen Z, Wan H, Cui J, Barhanin J
and Chen Y: Identification of a KCNE2 gain-of-function mutation in
patients with familial atrial fibrillation. Am J Hum Genet.
75:899–905. 2004. View
Article : Google Scholar : PubMed/NCBI
|
|
22.
|
Lundby A, Ravn LS, Svendsen JH, Hauns S,
Olesen SP and Schmitt N: KCNE3 mutation V17M identified in a
patient with lone atrial fibrillation. Cell Physiol Biochem.
21:47–54. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
23.
|
Ravn LS, Aizawa Y, Pollevick GD,
Hofman-Bang J, Cordeiro JM, Dixen U, Jensen G, Wu Y, Burashnikov E,
Haunso S, Guerchicoff A, Hu D, Svendsen JH, Christiansen M and
Antzelevitch C: Gain of function in IKs secondary to a mutation in
KCNE5 associated with atrial fibrillation. Heart Rhythm. 5:427–435.
2008. View Article : Google Scholar : PubMed/NCBI
|
|
24.
|
Hong K, Bjerregaard P, Gussak I and
Brugada R: Short QT syndrome and atrial fibrillation caused by
mutation in KCNH2. J Cardiovasc Electrophysiol. 16:394–396. 2005.
View Article : Google Scholar : PubMed/NCBI
|
|
25.
|
Xia M, Jin Q, Bendahhou S, He Y, Larroque
MM and Chen Y, Zhou Q, Yang Y, Liu Y, Liu B, Zhu Q, Zhou Y, Lin J,
Liang B, Li L, Dong X, Pan Z, Wang R, Wan H, Qiu W, Xu W, Eurlings
P, Barhanin J and Chen Y: A Kir2.1 gain-of-function mutation
underlies familial atrial fibrillation. Biochem Biophys Res Commun.
332:1012–1019. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
26.
|
Olson TM, Alekseev AE, Liu XK, Park S,
Zingman LV, Bienengraeber M, Sattiraju S, Ballew JD, Jahangir A and
Terzic A: Kv1.5 channelopathy due to KCNA5 loss-of-function
mutation causes human atrial fibrillation. Hum Mol Genet.
15:2185–2191. 2006. View Article : Google Scholar : PubMed/NCBI
|
|
27.
|
Yang Y, Li J, Lin X, Yang Y, Hong K, Wang
L, Liu J, Li L, Yan D, Liang D, Xiao J, Jin H, Wu J, Zhang Y and
Chen YH: Novel KCNA5 loss-of-function mutations responsible for
atrial fibrillation. J Hum Genet. 54:277–283. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
28.
|
Olson TM, Michels VV, Ballew JD, Reyna SP,
Karst ML, Herron KJ, Horton SC, Rodeheffer RJ and Anderson JL:
Sodium channel mutations and susceptibility to heart failure and
atrial fibrillation. JAMA. 293:447–454. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
29.
|
Darbar D, Kannankeril PJ, Donahue BS,
Kucera G, Stubblefield T, Haines JL, George AL Jr and Roden DM:
Cardiac sodium channel (SCN5A) variants associated with atrial
fibrillation. Circulation. 117:1927–1935. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
30.
|
Watanabe H, Darbar D, Kaiser DW,
Jiramongkolchai K, Chopra S, Donahue BS, Kannankeril PJ and Roden
DM: Mutations in sodium channel beta1- and beta2-subunits
associated with atrial fibrillation. Circ Arrhythm Electrophysiol.
2:268–275. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
31.
|
Olesen MS, Holst AG, Svendsen JH, Haunsø S
and Tfelt-Hansen J: SCN1Bb R214Q found in 3 patients: 1 with
Brugada syndrome and 2 with lone atrial fibrillation. Heart Rhythm.
9:770–773. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
32.
|
Wang P, Yang Q, Wu X, Yang Y, Shi L, Wang
C, Wu G, Xia Y, Yang B, Zhang R, Xu C, Cheng X, Li S, Zhao Y, Fu F,
Liao Y, Fang F, Chen Q, Tu X and Wang QK: Functional
dominant-negative mutation of sodium channel subunit gene SCN3B
associated with atrial fibrillation in a Chinese GeneID population.
Biochem Biophys Res Commun. 398:98–104. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
33.
|
Olesen MS, Jespersen T, Nielsen JB, Liang
B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø
S, Schmitt N and Svendsen JH: Mutations in sodium channel β-subunit
SCN3B are associated with early-onset lone atrial fibrillation.
Cardiovasc Res. 89:786–793. 2011.
|
|
34.
|
Hodgson-Zingman DM, Karst ML, Zingman LV,
Heublein DM, Darbar D, Herron KJ, Ballew JD, de Andrade M, Burnett
JC Jr and Olson TM: Atrial natriuretic peptide frameshift mutation
in familial atrial fibrillation. N Engl J Med. 359:158–165. 2008.
View Article : Google Scholar : PubMed/NCBI
|
|
35.
|
Thibodeau IL, Xu J, Li Q, Liu G, Lam K,
Veinot JP, Birnie DH, Jones DL, Krahn AD, Lemery R, Nicholson BJ
and Gollob MH: Paradigm of genetic mosaicism and lone atrial
fibrillation: physiological characterization of a connexin
43-deletion mutant identified from atrial tissue. Circulation.
122:236–244. 2010. View Article : Google Scholar
|
|
36.
|
Gollob MH, Jones DL, Krahn AD, Danis L,
Gong XQ, Shao Q, Liu X, Veinot JP, Tang AS, Stewart AF, Tesson F,
Klein GJ, Yee R, Skanes AC, Guiraudon GM, Ebihara L and Bai D:
Somatic mutations in the connexin 40 gene (GJA5) in atrial
fibrillation. N Engl J Med. 354:2677–2688. 2006. View Article : Google Scholar : PubMed/NCBI
|
|
37.
|
Yang YQ, Zhang XL, Wang XH, Tan HW, Shi
HF, Jiang WF, Fang WY and Liu X: Connexin40 nonsense mutation in
familial atrial fibrillation. Int J Mol Med. 26:605–610.
2010.PubMed/NCBI
|
|
38.
|
Jiang JQ, Shen FF, Fang WY, Liu X and Yang
YQ: Novel GATA4 mutations in lone atrial fibrillation. Int J Mol
Med. 28:1025–1032. 2011.PubMed/NCBI
|
|
39.
|
Yang YQ, Wang MY, Zhang XL, Tan HW, Shi
HF, Jiang WF, Wang XH, Fang WY and Liu X: GATA4 loss-of-function
mutations in familial atrial fibrillation. Clin Chim Acta.
412:1825–1830. 2011. View Article : Google Scholar : PubMed/NCBI
|
|
40.
|
Wang J, Sun YM and Yang YQ: Mutation
spectrum of the GATA4 gene in patients with idiopathic atrial
fibrillation. Mol Biol Rep. 39:8127–8135. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
41.
|
Yang YQ, Wang J, Wang XH, Wang Q, Tan HW,
Zhang M, Shen FF, Jiang JQ, Fang WY and Liu X: Mutational spectrum
of the GATA5 gene associated with familial atrial fibrillation. Int
J Cardiol. 157:305–307. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
42.
|
Yang YQ, Wang XH, Tan HW, Jiang WF, Fang
WY and Liu X: Prevalence and spectrum of GATA6 mutations associated
with familial atrial fibrillation. Int J Cardiol. 155:494–496.
2012. View Article : Google Scholar : PubMed/NCBI
|
|
43.
|
Yang YQ, Li L, Wang J, Zhang XL, Li RG, Xu
YJ, Tan HW, Wang XH, Jiang JQ, Fang WY and Liu X: GATA6
loss-of-function mutation in atrial fibrillation. Eur J Med Genet.
55:520–526. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
44.
|
Li J, Liu WD, Yang ZL and Yang YQ: Novel
GATA6 loss-of-function mutation responsible for familial atrial
fibrillation. Int J Mol Med. 30:783–790. 2012.PubMed/NCBI
|
|
45.
|
Meadows LS and Isom LL: Sodium channels as
macromolecular complexes: implications for inherited arrhythmia
syndromes. Cardiovasc Res. 67:448–458. 2005. View Article : Google Scholar : PubMed/NCBI
|
|
46.
|
Schwartz PJ, Moss AJ, Vincent GM and
Crampton RS: Diagnostic criteria for the long QT syndrome: an
update. Circulation. 88:782–784. 1993. View Article : Google Scholar : PubMed/NCBI
|
|
47.
|
Yu FH, Westenbroek RE, Silos-Santiago I,
McCormick KA, Lawson D, Ge P, Ferriera H, Lilly J, DiStefano PS,
Catterall WA, Scheuer T and Curtis R: Sodium channel beta4, a new
disulfide-linked auxiliary subunit with similarity to beta2. J
Neurosci. 23:7577–7585. 2003.PubMed/NCBI
|
|
48.
|
Maier SK, Westenbroek RE, McCormick KA,
Curtis R, Scheuer T and Catterall WA: Distinct subcellular
localization of different sodium channel alpha and beta subunits in
single ventricular myocytes from mouse heart. Circulation.
109:1421–1427. 2004. View Article : Google Scholar
|
|
49.
|
Terrenoire C, Simhaee D and Kass RS: Role
of sodium channels in propagation in heart muscle: how subtle
genetic alterations result in major arrhythmic disorders. J
Cardiovasc Electrophysiol. 18:900–905. 2007. View Article : Google Scholar : PubMed/NCBI
|
|
50.
|
Nattel S: New ideas about atrial
fibrillation 50 years on. Nature. 415:219–226. 2002.PubMed/NCBI
|
|
51.
|
Makiyama T, Akao M, Shizuta S, Doi T,
Nishiyama K, Oka Y, Ohno S, Nishio Y, Tsuji K, Itoh H, Kimura T,
Kita T and Horie M: A novel SCN5A gain-of-function mutation M1875T
associated with familial atrial fibrillation. J Am Coll Cardiol.
52:1326–1334. 2008. View Article : Google Scholar : PubMed/NCBI
|
|
52.
|
Li Q, Huang H, Liu G, Lam K, Rutberg J,
Green MS, Birnie DH, Lemery R, Chahine M and Gollob MH:
Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances
cellular excitability and lowers the threshold for action potential
firing. Biochem Biophys Res Commun. 380:132–137. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
53.
|
Blana A, Kaese S, Fortmüller L, Laakmann
S, Damke D, van Bragt K, Eckstein J, Piccini I, Kirchhefer U,
Nattel S, Breithardt G, Carmeliet P, Carmeliet E, Schotten U,
Verheule S, Kirchhof P and Fabritz L: Knock-in gain-of-function
sodium channel mutation prolongs atrial action potentials and
alters atrial vulnerability. Heart Rhythm. 7:1862–1869. 2010.
View Article : Google Scholar : PubMed/NCBI
|
|
54.
|
Moric-Janiszewska E, Markiewicz-Łoskot G,
Loskot M, Weglarz L, Hollek A and Szydlowski L: Challenges of
diagnosis of long-QT syndrome in children. Pacing Clin
Electrophysiol. 30:1168–1170. 2007. View Article : Google Scholar : PubMed/NCBI
|
|
55.
|
Medeiros-Domingo A, Kaku T, Tester DJ,
Iturralde-Torres P, Itty A, Ye B, Valdivia C, Ueda K,
Canizales-Quinteros S, Tusié-Luna MT, Makielski JC and Ackerman MJ:
SCN4B-encoded sodium channel beta4 subunit in congenital long-QT
syndrome. Circulation. 116:134–142. 2007. View Article : Google Scholar : PubMed/NCBI
|
|
56.
|
Tan BH, Pundi KN, Van Norstrand DW,
Valdivia CR, Tester DJ, Medeiros-Domingo A, Makielski JC and
Ackerman MJ: Sudden infant death syndrome-associated mutations in
the sodium channel beta subunits. Heart Rhythm. 7:771–778. 2010.
View Article : Google Scholar : PubMed/NCBI
|
