메뉴 건너뛰기




Volumn 309, Issue 21, 2013, Pages 2232-2239

Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis

(22)  Peljto, Anna L a   Zhang, Yingze a   Fingerlin, Tasha E a   Shwu Fan, Ma d   Garcia, Joe G N e   Richards, Thomas J f   Silveira, Lori J c   Lindell, Kathleen O f   Steele, Mark P g   Loyd, James E g   Gibson, Kevin F f   Seibold, Max A c   Brown, Kevin K c   Talbert, Janet L c   Markin, Cheryl g   Kossen, Karl h   Seiwert, Scott D h   Murphy, Elissa b   Noth, Imre d   Schwarz, Marvin I b   more..


Author keywords

[No Author keywords available]

Indexed keywords

GAMMA1B INTERFERON; MATRILYSIN; MUCIN 5B;

EID: 84878600828     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2013.5827     Document Type: Article
Times cited : (382)

References (29)
  • 2
    • 37549060070 scopus 로고    scopus 로고
    • Accelerated variant of idiopathic pulmonary fibrosis: Clinical behavior and gene expression pattern
    • Selman M, Carrillo G, Estrada A, et al. Accelerated variant of idiopathic pulmonary fibrosis: clinical behavior and gene expression pattern. PLoS One. 2007;2(5):e482.
    • (2007) PLoS One , vol.2 , Issue.5
    • Selman, M.1    Carrillo, G.2    Estrada, A.3
  • 3
    • 20544443765 scopus 로고    scopus 로고
    • The clinical course of patients with idiopathic pulmonary fibrosis
    • IPF Study Group
    • Martinez FJ, Safrin S, Weycker D, et al IPF Study Group. The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med . 2005;142(12 pt 1):963-967.
    • (2005) Ann Intern Med , vol.142 , Issue.12 PART 1 , pp. 963-967
    • Martinez, F.J.1    Safrin, S.2    Weycker, D.3
  • 6
    • 65249160219 scopus 로고    scopus 로고
    • Serum CCchemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis
    • Prasse A, Probst C, Bargagli E, et al. Serum CCchemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2009;179(8):717-723.
    • (2009) Am J Respir Crit Care Med , vol.179 , Issue.8 , pp. 717-723
    • Prasse, A.1    Probst, C.2    Bargagli, E.3
  • 7
    • 0033825445 scopus 로고    scopus 로고
    • Serum surfactant proteins A and D as prognostic factors in idiopathic pulmonary fibrosis and their relationship to disease extent
    • Takahashi H, Fujishima T, Koba H, et al. Serum surfactant proteins A and D as prognostic factors in idiopathic pulmonary fibrosis and their relationship to disease extent. Am J Respir Crit Care Med. 2000;162(3 pt 1):1109-1114.
    • (2000) Am J Respir Crit Care Med , vol.162 , Issue.3 PART 1 , pp. 1109-1114
    • Takahashi, H.1    Fujishima, T.2    Koba, H.3
  • 8
    • 84855264195 scopus 로고    scopus 로고
    • Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis
    • Richards TJ, Kaminski N, Baribaud F, et al. Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2012;185(1):67-76.
    • (2012) Am J Respir Crit Care Med , vol.185 , Issue.1 , pp. 67-76
    • Richards, T.J.1    Kaminski, N.2    Baribaud, F.3
  • 10
    • 0035931973 scopus 로고    scopus 로고
    • A mutation in the surfactant protein C gene associated with familial interstitial lung disease
    • DOI 10.1056/NEJM200102223440805
    • Nogee LM, Dunbar AE III, Wert SE, Askin F, Hamvas A, Whitsett JA. A mutation in the surfactant protein C gene associated with familial interstitial lung disease. N Engl J Med. 2001;344(8):573-579. (Pubitemid 32167871)
    • (2001) New England Journal of Medicine , vol.344 , Issue.8 , pp. 573-579
    • Nogee, L.M.1    Dunbar, A.E.2    Wert, S.E.3    Askin, F.4    Hamvas, A.5    Whitsett, J.A.6
  • 11
    • 58149159548 scopus 로고    scopus 로고
    • Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer
    • Wang Y, Kuan PJ, Xing C, et al. Genetic defects in surfactant protein A2 are associated with pulmonary fibrosis and lung cancer. Am J Hum Genet. 2009;84(1):52-59.
    • (2009) Am J Hum Genet , vol.84 , Issue.1 , pp. 52-59
    • Wang, Y.1    Kuan, P.J.2    Xing, C.3
  • 12
    • 79955146233 scopus 로고    scopus 로고
    • A common MUC5B promoter polymorphism and pulmonary fibrosis
    • Seibold MA, Wise AL, Speer MC, et al. A common MUC5B promoter polymorphism and pulmonary fibrosis. N Engl J Med . 2011;364(16):1503-1512.
    • (2011) N Engl J Med , vol.364 , Issue.16 , pp. 1503-1512
    • Seibold, M.A.1    Wise, A.L.2    Speer, M.C.3
  • 13
    • 79955144623 scopus 로고    scopus 로고
    • A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis
    • Zhang Y, Noth I, Garcia JG, Kaminski N. A variant in the promoter of MUC5B and idiopathic pulmonary fibrosis. N Engl J Med. 2011;364(16):1576-1577.
    • (2011) N Engl J Med , vol.364 , Issue.16 , pp. 1576-1577
    • Zhang, Y.1    Noth, I.2    Garcia, J.G.3    Kaminski, N.4
  • 14
    • 67650349068 scopus 로고    scopus 로고
    • Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): A multicentre, randomised, placebo-controlled trial
    • INSPIRE Study Group
    • King TE Jr, Albera C, Bradford WZ, et al INSPIRE Study Group. Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial. Lancet . 2009;374(9685):222-228.
    • (2009) Lancet , vol.374 , Issue.9685 , pp. 222-228
    • King Jr., T.E.1    Albera, C.2    Bradford, W.Z.3
  • 15
    • 15044357936 scopus 로고    scopus 로고
    • Survival model predictive accuracy and ROC curves
    • DOI 10.1111/j.0006-341X.2005.030814.x
    • Heagerty PJ, Zheng Y. Survival model predictive accuracy and ROC curves. Biometrics . 2005;61(1):92-105. (Pubitemid 40380968)
    • (2005) Biometrics , vol.61 , Issue.1 , pp. 92-105
    • Heagerty, P.J.1    Zheng, Y.2
  • 16
    • 84876281787 scopus 로고    scopus 로고
    • The MUC5B promoter polymorphism is associated with a less severe pathological form of familial interstitial pneumonia (FIP)
    • abstract
    • Cosgrove GP, Groshong SD, Peljto AL, et al. The MUC5B promoter polymorphism is associated with a less severe pathological form of familial interstitial pneumonia (FIP) [abstract]. Am J Respir Crit Care Med. 2012;185:A6865.
    • (2012) Am J Respir Crit Care Med , vol.185
    • Cosgrove, G.P.1    Groshong, S.D.2    Peljto, A.L.3
  • 17
    • 84876281483 scopus 로고    scopus 로고
    • Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis
    • doi:10.1136/thoraxjnl-2012-201786
    • Stock CJ, Sato H, Fonseca C, et al. Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis. Thorax. 2013;68(5):436-441. doi:10.1136/thoraxjnl-2012-201786.
    • (2013) Thorax , vol.68 , Issue.5 , pp. 436-441
    • Stock, C.J.1    Sato, H.2    Fonseca, C.3
  • 19
    • 84861162888 scopus 로고    scopus 로고
    • A multi-dimensional index and staging system for idiopathic pulmonary fibrosis
    • Ley B, Ryerson CJ, Vittinghoff E, et al. A multi-dimensional index and staging system for idiopathic pulmonary fibrosis. Ann Intern Med . 2012;156(10):684-691.
    • (2012) Ann Intern Med , vol.156 , Issue.10 , pp. 684-691
    • Ley, B.1    Ryerson, C.J.2    Vittinghoff, E.3
  • 20
    • 84455168726 scopus 로고    scopus 로고
    • Forced vital capacity in patients with idiopathic pulmonary fibrosis: test properties and minimal clinically important difference
    • du Bois RM, Weycker D, Albera C, et al. Forced vital capacity in patients with idiopathic pulmonary fibrosis: test properties and minimal clinically important difference. Am J Respir Crit Care Med. 2011;184(12):1382-1389.
    • (2011) Am J Respir Crit Care Med , vol.184 , Issue.12 , pp. 1382-1389
    • Du Bois, R.M.1    Weycker, D.2    Albera, C.3
  • 21
    • 77951170794 scopus 로고    scopus 로고
    • Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis
    • Zappala CJ, Latsi PI, Nicholson AG, et al. Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis. Eur Respir J. 2010;35(4):830-836.
    • (2010) Eur Respir J , vol.35 , Issue.4 , pp. 830-836
    • Zappala, C.J.1    Latsi, P.I.2    Nicholson, A.G.3
  • 24
    • 82755161052 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis
    • King TE Jr, Pardo A, Selman M. Idiopathic pulmonary fibrosis. Lancet . 2011;378(9807):1949-1961.
    • (2011) Lancet , vol.378 , Issue.9807 , pp. 1949-1961
    • King Jr., T.E.1    Pardo, A.2    Selman, M.3
  • 25
    • 84865132003 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: new evidence and an improved standard of care in 2012
    • Raghu G. Idiopathic pulmonary fibrosis: new evidence and an improved standard of care in 2012. Lancet. 2012;380(9842):699-701.
    • (2012) Lancet , vol.380 , Issue.9842 , pp. 699-701
    • Raghu, G.1
  • 26
    • 84878686854 scopus 로고    scopus 로고
    • Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
    • published online April 14, doi: 10.1038/ng.2609
    • Fingerlin TE, Murphy E, Zhang W, et al. Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis [published online April 14, 2013]. Nat Genet. doi: 10.1038/ng.2609.
    • (2013) Nat Genet
    • Fingerlin, T.E.1    Murphy, E.2    Zhang, W.3
  • 27
  • 28
    • 64649089804 scopus 로고    scopus 로고
    • Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF)
    • Boon K, Bailey NW, Yang J, et al. Molecular phenotypes distinguish patients with relatively stable from progressive idiopathic pulmonary fibrosis (IPF). PLoS One. 2009;4(4):e5134.
    • (2009) PLoS One , vol.4 , Issue.4
    • Boon, K.1    Bailey, N.W.2    Yang, J.3
  • 29
    • 43249084804 scopus 로고    scopus 로고
    • MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis
    • Rosas IO, Richards TJ, Konishi K, et al. MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis. PLoS Med . 2008;5(4):e93.
    • (2008) PLoS Med , vol.5 , Issue.4
    • Rosas, I.O.1    Richards, T.J.2    Konishi, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.