The rs3807989 G/A Polymorphism in CAV1 is associated with the risk of atrial fibrillation in Chinese Han populations

PACE - Pacing and Clinical Electrophysiology

Volumn 38, Issue 2, 2015, Pages 164-170

  Liu, Yaowu ^a   Ni, Bixian ^b   Lin, Yuan ^b   Chen, Xin Guang ^a   Chen, Minglong ^a   Hu, Zhibin ^b   Zhang, Fengxiang ^a  

^a THE FIRST AFFILIATED HOSPITAL OF NANJING MEDICAL UNIVERSITY   (China)

^b NANJING MEDICAL UNIVERSITY   (China)

Author keywords

7q31; atrial fibrillation (AF); CAV1; rs3807989; single nucleotide polymorphism (SNP)

Indexed keywords

GENOMIC DNA; CAV1 PROTEIN, HUMAN; CAVEOLIN 1; GENETIC MARKER;

ADULT; ARTICLE; BLOOD SAMPLING; CASE CONTROL STUDY; CONTROLLED STUDY; ETHNIC GROUP; FEMALE; GENETIC ASSOCIATION; GENOTYPE; HAN CHINESE; HEART ARRHYTHMIA; HEART ATRIUM FIBRILLATION; HUMAN; MAJOR CLINICAL STUDY; MALE; META ANALYSIS (TOPIC); POPULATION GENETICS; RISK; SINGLE NUCLEOTIDE POLYMORPHISM; ATRIAL FIBRILLATION; CHINA; GENETIC MARKER; GENETIC PREDISPOSITION; GENETICS; INCIDENCE; MIDDLE AGED; POINT MUTATION; REPRODUCIBILITY; RISK FACTOR; SENSITIVITY AND SPECIFICITY;

ATRIAL FIBRILLATION; CAVEOLIN 1; CHINA; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INCIDENCE; MALE; MIDDLE AGED; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; RISK FACTORS; SENSITIVITY AND SPECIFICITY;

EID: 84922652953     PISSN: 01478389     EISSN: 15408159     Source Type: Journal    
DOI: 10.1111/pace.12494     Document Type: Article

References (31)

1. Fuster V, Ryden LE, Cannom DS, Crijns HJ, Curtis AB, Ellenbogen KA, Halperin JL, et al. 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 developed in partnership with the European Society of Cardiology and in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society. J Am Coll Cardiol 2011; 57: e101-e198.
2. Camm AJ, Lip GYH, De, Caterina R, Savelieva I, Atar D, Hohnloser SH, Hindricks G, et al. 2012 focused update of the ESC guidelines for the management of atrial fibrillation. An update of the 2010 ESC guidelines for the management of atrial fibrillation developed with the special contribution of the European Heart Rhythm Association. Europace 2012; 14: 1385-1413.
3. Benjamin EJ, Wolf PA, D'Agostino RB, Silbershatz H, Kannel WB, Levy D,. Impact of atrial fibrillation on the risk of death: The Framingham Heart Study. Circulation 1998; 98: 946-952.
4. Kannel WB, Abbott RD, Savage DD, McNamara PM,. Epidemiologic features of chronic atrial fibrillation: The Framingham study. N Engl J Med 1982; 306: 1018-1022.
5. Benjamin EJ, Levy D, Vaziri SM, D'Agostino RB, Belanger AJ, Wolf PA,. Independent risk factors for atrial fibrillation in a population-based cohort. The Framingham Heart Study. J Am Med Assoc 1994; 271: 840-844.
6. Psaty BM, Manolio TA, Kuller LH, Kronmal RA, Cushman M, Fried LP, White R, et al. Incidence of and risk factors for atrial fibrillation in older adults. Circulation 1997; 96: 2455-2461.
7. Kopecky SL, Gersh BJ, McGoon MD, Whisnant JP, Holmes DR Jr., Ilstrup DM, Frye RL,. The natural history of lone atrial fibrillation. A population-based study over three decades. N Engl J Med 1987; 317: 669-674.
8. Arnar DO, Thorvaldsson S, Manolio TA, Thorgeirsson G, Kristjansson K, Hakonarson H, Stefansson K,. Familial aggregation of atrial fibrillation in Iceland. Eur Heart J 2006; 27: 708-712.
9. Fox CS, Parise H, D'Agostino RB Sr., Lloyd-Jones DM, Vasan RS, Wang TJ, Levy D, et al. Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring. J Am Med Assoc 2004; 291: 2851-2855.
10. Tsai CT, Lai LP, Hwang JJ, Lin JL, Chiang FT,. Molecular genetics of atrial fibrillation. J Am Coll Cardiol 2008; 52: 241-250.
11. Brugada R, Tapscott T, Czernuszewicz GZ, Marian AJ, Iglesias A, Mont L, Brugada J, et al. Identification of a genetic locus for familial atrial fibrillation. N Engl J Med 1997; 336: 905-911.
12. Christophersen IE, Ravn LS, Budtz-Joergensen E, Skytthe A, Haunsoe S, Svendsen JH, Christensen K,. Familial aggregation of atrial fibrillation: A study in Danish twins. Circ Arrhythm Electrophysiol 2009; 2: 378-383.
13. Gudbjartsson DF, Arnar DO, Helgadottir A, Gretarsdottir S, Holm H, Sigurdsson A, Jonasdottir A, et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature 2007; 448: U353-U359.
14. Benjamin EJ, Rice KM, Arking DE, Pfeufer A, van Noord C, Smith AV, Schnabel RB, et al. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat Genet 2009; 41: 879-881.
15. Gudbjartsson DF, Holm H, Gretarsdottir S, Thorleifsson G, Walters GB, Thorgeirsson G, Gulcher J, et al. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Nat Genet 2009; 41: 876-878.
16. Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, et al. Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet 2010; 42: 240-244.
17. Shi L, Li C, Wang C, Xia Y, Wu G, Wang F, Xu C, et al. Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population. Hum Genet 2009; 126: 843-849.
18. Li C, Wang F, Yang Y, Fu F, Xu C, Shi L, Li S, et al. Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population. Hum Genet 2011; 129: 239-246.
19. Olesen MS, Holst AG, Jabbari J, Nielsen JB, Christophersen IE, Sajadieh A, Haunso S, et al. Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years. Can J Cardiol 2012; 28: 191-195.
20. Ellinor PT, Lunetta KL, Albert CM, Glazer NL, Ritchie MD, Smith AV, Arking DE, et al. Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat Genet 2012; 44: 670-675.
21. Albarino CG, Romanowski V,. Phenol extraction revisited: A rapid method for the isolation and preservation of human genomic DNA from whole blood. Mol Cell Probes 1994; 8: 423-427.
22. Lubitz SA, Yi BA, Ellinor PT,. Genetics of atrial fibrillation. Heart Fail Clin 2010; 6: 239-247.
23. Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, et al. Genome-wide association study of PR interval. Nat Genet 2010; 42: 153-159.
24. Hamoudane M, Maffioli S, Cordera R, Maggi D, Salani B,. Caveolin-1 and polymerase I and transcript release factor: New players in insulin-like growth factor-I receptor signaling. J Endocrinol Invest 2013; 36: 204-208.
25. Zhao YY, Liu Y, Stan RV, Fan L, Gu Y, Dalton N, Chu PH, et al. Defects in caveolin-1 cause dilated cardiomyopathy and pulmonary hypertension in knockout mice. Proc Natl Acad Sci U S A 2002; 99: 11375-11380.
26. Lin J, Lin S, Choy PC, Shen X, Deng C, Kuang S, Wu J, et al. The regulation of the cardiac potassium channel (HERG) by caveolin-1. Biochem Cell Biol 2008; 86: 405-415.
27. Sinner MF, Pfeufer A, Akyol M, Beckmann BM, Hinterseer M, Wacker A, Perz S, et al. The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: Results from a systematic candidate gene-based analysis of KCNH2 (HERG). Eur Heart J 2008; 29: 907-914.
28. Pojoga LH, Underwood PC, Goodarzi MO, Williams JS, Adler GK, Jeunemaitre X, Hopkins PN, et al. Variants of the caveolin-1 gene: A translational investigation linking insulin resistance and hypertension. J Clin Endocrinol Metab 2011; 96: E1288-E1292.
29. Yi SL, Liu XJ, Zhong JQ, Zhang Y,. Role of caveolin-1 in atrial fibrillation as an anti-fibrotic signaling molecule in human atrial fibroblasts. PLoS One 2014; 9: e85144.
30. Greenwood TA, Kelsoe JR,. Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene. Genomics 2003; 82: 511-520.
31. Wang Q, Lan Y, Cho ES, Maltby KM, Jiang R,. Odd-skipped related 1 (Odd 1) is an essential regulator of heart and urogenital development. Dev Biol 2005; 288: 582-594.