과제정보
연구 과제 주관 기관 : Korean Society of Cardiology, Ministry of Health and Welfare
참고문헌
- Sohara H, Amitani S, Kurose M, Miyahara K. Atrial fibrillation activates platelets and coagulation in a time-dependent manner: a study in patients with paroxysmal atrial fibrillation. J Am Coll Cardiol 1997;29:106-12. https://doi.org/10.1016/S0735-1097(96)00427-5
- Li-Saw-Hee FL, Blann AD, Lip GY. Effect of degree of blood pressure on the hypercoagulable state in chronic atrial fibrillation. Am J Cardiol 2000;86:795-7, A9. https://doi.org/10.1016/S0002-9149(00)01086-9
- Freestone B, Lip GY. The endothelium and atrial fibrillation. The prothrombotic state revisited. Hamostaseologie 2008;28:207-12.
- Cai H, Li Z, Goette A, et al. Downregulation of endocardial nitric oxide synthase expression and nitric oxide production in atrial fibrillation: potential mechanisms for atrial thrombosis and stroke. Circulation 2002;106:2854-8. https://doi.org/10.1161/01.CIR.0000039327.11661.16
- Dudley SC Jr, Hoch NE, McCann LA, et al. Atrial fibrillation increases production of superoxide by the left atrium and left atrial appendage: role of the NADPH and xanthine oxidases. Circulation 2005;112:1266-73. https://doi.org/10.1161/CIRCULATIONAHA.105.538108
- Sung ML, Wu CC, Chang HI, et al. Shear stress inhibits homocysteineinduced stromal cell-derived factor-1 expression in endothelial cells. Circ Res 2009;105:755-63. https://doi.org/10.1161/CIRCRESAHA.109.206524
- Malmstrom RE, Settergren M, Pernow J. Endothelin attenuates endothelium-dependent platelet inhibition in man. Acta Physiol (Oxf) 2010;198:441-8. https://doi.org/10.1111/j.1748-1716.2009.02062.x
- Abi-Younes S, Sauty A, Mach F, Sukhova GK, Libby P, Luster AD. The stromal cell-derived factor-1 chemokine is a potent platelet agonist highly expressed in atherosclerotic plaques. Circ Res 2000;86:131-8. https://doi.org/10.1161/01.RES.86.2.131
- Chen CN, Chang SF, Lee PL, et al. Neutrophils, lymphocytes, and monocytes exhibit diverse behaviors in transendothelial and subendothelial migrations under coculture with smooth muscle cells in disturbed flow. Blood 2006;107:1933-42. https://doi.org/10.1182/blood-2005-08-3137
- Urbich C, Dimmeler S. Endothelial progenitor cells: characterization and role in vascular biology. Circ Res 2004;95:343-53. https://doi.org/10.1161/01.RES.0000137877.89448.78
- Frenette PS, Moyna C, Hartwell DW, Lowe JB, Hynes RO, Wagner DD. Platelet-endothelial interactions in inflamed mesenteric venules. Blood 1998;91:1318-24.
- Rosenblum WI, Murata S, Nelson GH, Werner PK, Ranken R, Harmon RC. Anti-CD31 delays platelet adhesion/aggregation at sites of endothelial injury in mouse cerebral arterioles. Am J Pathol 1994;145:33-6.
- Liao CH, Akazawa H, Tamagawa M, et al. Cardiac mast cells cause atrial fibrillation through PDGF-A-mediated fibrosis in pressure-overloaded mouse hearts. J Clin Invest 2010;120:242-53. https://doi.org/10.1172/JCI39942
- Ohkita M, Takaoka M, Shiota Y, Nojiri R, Matsumura Y. Nitric oxide inhibits endothelin-1 production through the suppression of nuclear factor kappa B. Clin Sci (Lond) 2002;103 Suppl 48:68S-71S. https://doi.org/10.1042/CS103S068S
- Rudolph V, Andrie RP, Rudolph TK, et al. Myeloperoxidase acts as a profibrotic mediator of atrial fibrillation. Nat Med 2010;16:470-4. https://doi.org/10.1038/nm.2124
- Park JH, Pak HN, Lee S, Park HK, Seo JW, Chang BC. The clinical significance of the atrial subendocardial smooth muscle layer and cardiac myofibroblasts in human atrial tissue with valvular atrial fibrillation. Cardiovasc Pathol 2013;22:58-64. https://doi.org/10.1016/j.carpath.2012.05.001
- Mortazavi A, Williams BA, McCue K, Schaeffer L, Wold B. Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods 2008;5:621-8. https://doi.org/10.1038/nmeth.1226
- De Caterina R, Libby P, Peng HB, et al. Nitric oxide decreases cytokineinduced endothelial activation. Nitric oxide selectively reduces endothelial expression of adhesion molecules and proinflammatory cytokines. J Clin Invest 1995;96:60-8. https://doi.org/10.1172/JCI118074
- Turu MM, Slevin M, Matou S, et al. C-reactive protein exerts angiogenic effects on vascular endothelial cells and modulates associated signalling pathways and gene expression. BMC Cell Biol 2008;9:47. https://doi.org/10.1186/1471-2121-9-47
- Burstein B, Libby E, Calderone A, Nattel S. Differential behaviors of atrial versus ventricular fibroblasts: a potential role for platelet-derived growth factor in atrial-ventricular remodeling differences. Circulation 2008;117:1630-41. https://doi.org/10.1161/CIRCULATIONAHA.107.748053
- Goldsmith I, Kumar P, Carter P, Blann AD, Patel RL, Lip GY. Atrial endocardial changes in mitral valve disease: a scanning electron microscopy study. Am Heart J 2000;140:777-84. https://doi.org/10.1067/mhj.2000.110284
- Modrego J, Maroto L, Tamargo J, et al. Comparative expression of proteins in left and right atrial appendages from patients with mitral valve disease at sinus rhythm and atrial fibrillation. J Cardiovasc Electrophysiol 2010;21:859-68.
- Fuster V, Ryden LE, Asinger RW, et al. ACC/AHA/ESC guidelines for the management of patients with atrial fibrillation: executive summary. A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines and Policy Conferences (Committee to Develop Guidelines for the Management of Patients With Atrial Fibrillation): developed in Collaboration With the North American Society of Pacing and Electrophysiology. J Am Coll Cardiol 2001;38:1231-66. https://doi.org/10.1016/S0735-1097(01)01587-X
- Franco D, Campione M. The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases. Trends Cardiovasc Med 2003;13:157-63. https://doi.org/10.1016/S1050-1738(03)00039-2
- King T, Bland Y, Webb S, Barton S, Brown NA. Expression of Peg1 (Mest) in the developing mouse heart: involvement in trabeculation. Dev Dyn 2002;225:212-5. https://doi.org/10.1002/dvdy.10142
- Corradi D, Maestri R, Macchi E, Callegari S. The atria: from morphology to function. J Cardiovasc Electrophysiol 2011;22:223-35.
- Ho SY, McCarthy KP. Anatomy of the left atrium for interventional electrophysiologists. Pacing Clin Electrophysiol 2010;33:620-7.
- Subramaniam B, Riley MF, Panzica PJ, Manning WJ. Transesophageal echocardiographic assessment of right atrial appendage anatomy and function: comparison with the left atrial appendage and implications for local thrombus formation. J Am Soc Echocardiogr 2006;19:429-33. https://doi.org/10.1016/j.echo.2005.10.013
피인용 문헌
- Valvular atrial fibrillation: rheumatic mitral valve disease vol.18, pp.4, 2016, https://doi.org/10.1093/europace/euv065
- Differences in atrial fibrillation-associated proteins between the left and right atrial appendages from patients with rheumatic mitral valve disease: A comparative proteomic analysis vol.14, pp.5, 2016, https://doi.org/10.3892/mmr.2016.5776
- Gender differences in fibrosis remodeling in patients with long-standing persistent atrial fibrillation vol.8, pp.32, 2014, https://doi.org/10.18632/oncotarget.16342
- The Next 10 Years in Atrial Fibrillation vol.13, pp.1, 2019, https://doi.org/10.15420/usc.2018.21.2
- Factors relevant to atrial 18 F-fluorodeoxyglucose uptake in atrial fibrillation vol.27, pp.5, 2014, https://doi.org/10.1007/s12350-018-1387-4
- Atrial Fibrillation in Valvular Heart Disease vol.13, pp.1, 2014, https://doi.org/10.1016/j.ccep.2020.11.007
- Calcium Regulation on the Atrial Regional Difference of Collagen Production Activity in Atrial Fibrogenesis vol.9, pp.6, 2014, https://doi.org/10.3390/biomedicines9060686
- Regional Diversities in Fibrogenesis Weighed as a Key Determinant for Atrial Arrhythmogenesis vol.9, pp.12, 2014, https://doi.org/10.3390/biomedicines9121900