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Published in: Respiratory Research 1/2010

Open Access 01-12-2010 | Review

Clinical use of biomarkers of survival in pulmonary fibrosis

Authors: Michiel Thomeer, Jan C Grutters, Wim A Wuyts, Stijn Willems, Maurits G Demedts

Published in: Respiratory Research | Issue 1/2010

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Abstract

Background

Biologic predictors or biomarkers of survival in pulmonary fibrosis with a worse prognosis, more specifically in idiopathic pulmonary fibrosis would help the clinician in deciding whether or not to treat since treatment carries a potential risk for adverse events. These decisions are made easier if accurate and objective measurements of the patients' clinical status can predict the risk of progression to death.

Method

A literature review is given on different biomarkers of survival in interstitial lung disease, mainly in IPF, since this disease has the worst prognosis.

Conclusion

Serum biomarkers, and markers measured by medical imaging as HRCT, pertechnegas, DTPA en FDG-PET are not ready for clinical use to predict mortality in different forms of ILD. A baseline FVC, a change of FVC of more than 10%, and change in 6MWD are clinically helpful predictors of survival.
Literature
1.
go back to reference Coultas DB, Zumwalt RE, Black WC, Sobonya RE: The epidemiology of interstitial lung diseases. Am J Respir Crit Care Med 1994, 150:967–972.CrossRefPubMed Coultas DB, Zumwalt RE, Black WC, Sobonya RE: The epidemiology of interstitial lung diseases. Am J Respir Crit Care Med 1994, 150:967–972.CrossRefPubMed
2.
3.
go back to reference American Thoracic Society (ATS) and the European Respiratory Society (ERS): Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. Am J Respir Crit Care Med 2000, 161:646–664.CrossRef American Thoracic Society (ATS) and the European Respiratory Society (ERS): Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. Am J Respir Crit Care Med 2000, 161:646–664.CrossRef
4.
go back to reference British Thoracic Society recommendations: The diagnosis, assessment and treatment of diffuse parenchymal lung disease in adults. Thorax 1999,54(Suppl 1):S1–30. British Thoracic Society recommendations: The diagnosis, assessment and treatment of diffuse parenchymal lung disease in adults. Thorax 1999,54(Suppl 1):S1–30.
5.
go back to reference Wilson JW, du Bois RM, King TE Jr: Challenges in pulmonary fibrosis: 8--The need for an international registry for idiopathic pulmonary fibrosis. Thorax 2008, 63:285–287.CrossRefPubMed Wilson JW, du Bois RM, King TE Jr: Challenges in pulmonary fibrosis: 8--The need for an international registry for idiopathic pulmonary fibrosis. Thorax 2008, 63:285–287.CrossRefPubMed
6.
go back to reference Martinez FJ, Safrin S, Weycker D, Starko KM, Bradford WZ, King TE Jr, et al.: The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005, 142:963–967.CrossRefPubMed Martinez FJ, Safrin S, Weycker D, Starko KM, Bradford WZ, King TE Jr, et al.: The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005, 142:963–967.CrossRefPubMed
7.
go back to reference Hosenpud JD, Bennett LE, Keck BM, Edwards EB, Novick RJ: Effect of diagnosis on survival benefit of lung transplantation for end-stage lung disease. Lancet 1998, 351:24–27.CrossRefPubMed Hosenpud JD, Bennett LE, Keck BM, Edwards EB, Novick RJ: Effect of diagnosis on survival benefit of lung transplantation for end-stage lung disease. Lancet 1998, 351:24–27.CrossRefPubMed
8.
go back to reference Prasse A, Probst C, Bargagli E, Zissel G, Toews GB, Flaherty KR, et al.: Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009, 179:717–723.CrossRefPubMed Prasse A, Probst C, Bargagli E, Zissel G, Toews GB, Flaherty KR, et al.: Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009, 179:717–723.CrossRefPubMed
9.
go back to reference Fung ET, Wright GL Jr, Dalmasso EA: Proteomic strategies for biomarker identification: progress and challenges. Curr Opin Mol Ther 2000, 2:643–650.PubMed Fung ET, Wright GL Jr, Dalmasso EA: Proteomic strategies for biomarker identification: progress and challenges. Curr Opin Mol Ther 2000, 2:643–650.PubMed
10.
go back to reference Wikipedia: Biomarker. 22–5-2009. 23–5-2009 Wikipedia: Biomarker. 22–5-2009. 23–5-2009
12.
go back to reference Greene KE, King TE Jr, Kuroki Y, Bucher-Bartelson B, Hunninghake GW, Newman LS, et al.: Serum surfactant proteins-A and -D as biomarkers in idiopathic pulmonary fibrosis. Eur Respir J 2002, 19:439–446.CrossRefPubMed Greene KE, King TE Jr, Kuroki Y, Bucher-Bartelson B, Hunninghake GW, Newman LS, et al.: Serum surfactant proteins-A and -D as biomarkers in idiopathic pulmonary fibrosis. Eur Respir J 2002, 19:439–446.CrossRefPubMed
13.
go back to reference Takahashi H, Fujishima TA, Koba H, Murakami S, Kurokawa K, Shibuya Y, 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, 162:1109–1114.CrossRefPubMed Takahashi H, Fujishima TA, Koba H, Murakami S, Kurokawa K, Shibuya Y, 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, 162:1109–1114.CrossRefPubMed
14.
go back to reference Kinder BW, Brown KK, McCormack FX, Ix JH, Kervitsky A, Schwarz MI, et al.: Serum Surfactant Protein-A Is a Strong Predictor of Early Mortality in Idiopathic Pulmonary Fibrosis. Chest 2009, 135:1557–1563.CrossRefPubMedPubMedCentral Kinder BW, Brown KK, McCormack FX, Ix JH, Kervitsky A, Schwarz MI, et al.: Serum Surfactant Protein-A Is a Strong Predictor of Early Mortality in Idiopathic Pulmonary Fibrosis. Chest 2009, 135:1557–1563.CrossRefPubMedPubMedCentral
15.
go back to reference Kohno N, Kyoizumi S, Awaya Y, Fukuhara H, Yamakido M, Akiyama M: New serum indicator of interstitial pneumonitis activity. Sialylated carbohydrate antigen KL-6. Chest 1989, 96:68–73.CrossRefPubMed Kohno N, Kyoizumi S, Awaya Y, Fukuhara H, Yamakido M, Akiyama M: New serum indicator of interstitial pneumonitis activity. Sialylated carbohydrate antigen KL-6. Chest 1989, 96:68–73.CrossRefPubMed
16.
go back to reference Snijdewint FG, von Mensdorff-Pouilly S, Karuntu-Wanamarta AH, Verstraeten AA, Livingston PO, Hilgers J, et al.: Antibody-dependent cell-mediated cytotoxicity can be induced by MUC1 peptide vaccination of breast cancer patients. Int J Cancer 2001, 93:97–106.CrossRefPubMed Snijdewint FG, von Mensdorff-Pouilly S, Karuntu-Wanamarta AH, Verstraeten AA, Livingston PO, Hilgers J, et al.: Antibody-dependent cell-mediated cytotoxicity can be induced by MUC1 peptide vaccination of breast cancer patients. Int J Cancer 2001, 93:97–106.CrossRefPubMed
17.
go back to reference Hirasawa Y, Kohno N, Yokoyama A, Kondo K, Hiwada K, Miyake M: Natural autoantibody to MUC1 is a prognostic indicator for non-small cell lung cancer. Am J Respir Crit Care Med 2000, 161:589–594.CrossRefPubMed Hirasawa Y, Kohno N, Yokoyama A, Kondo K, Hiwada K, Miyake M: Natural autoantibody to MUC1 is a prognostic indicator for non-small cell lung cancer. Am J Respir Crit Care Med 2000, 161:589–594.CrossRefPubMed
18.
go back to reference Hiraga Y, Tanaka S, Haruma K, Yoshihara M, Sumii K, Kajiyama G, et al.: Immunoreactive MUC1 expression at the deepest invasive portion correlates with prognosis of colorectal cancer. Oncology 1998, 55:307–319.CrossRefPubMed Hiraga Y, Tanaka S, Haruma K, Yoshihara M, Sumii K, Kajiyama G, et al.: Immunoreactive MUC1 expression at the deepest invasive portion correlates with prognosis of colorectal cancer. Oncology 1998, 55:307–319.CrossRefPubMed
19.
go back to reference Inoue Y, Nishimura K, Shiode M, Akutsu H, Hamada H, Fujioka S, et al.: Evaluation of serum KL-6 levels in patients with pulmonary tuberculosis. Tuber Lung Dis 1995, 76:230–233.CrossRefPubMed Inoue Y, Nishimura K, Shiode M, Akutsu H, Hamada H, Fujioka S, et al.: Evaluation of serum KL-6 levels in patients with pulmonary tuberculosis. Tuber Lung Dis 1995, 76:230–233.CrossRefPubMed
20.
go back to reference Yokoyama A, Kohno N, Hamada H, Sakatani M, Ueda E, Kondo K, et al.: Circulating KL-6 predicts the outcome of rapidly progressive idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998, 158:1680–1684.CrossRefPubMed Yokoyama A, Kohno N, Hamada H, Sakatani M, Ueda E, Kondo K, et al.: Circulating KL-6 predicts the outcome of rapidly progressive idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998, 158:1680–1684.CrossRefPubMed
21.
go back to reference Janssen R, Grutters JC, Sato H, van Velzen-Blad H, Zanen P, Kohno N, et al.: Analysis of KL-6 and SP-D as disease markers in bird fancier's lung. Sarcoidosis Vasc Diffuse Lung Dis 2005, 22:51–57.PubMed Janssen R, Grutters JC, Sato H, van Velzen-Blad H, Zanen P, Kohno N, et al.: Analysis of KL-6 and SP-D as disease markers in bird fancier's lung. Sarcoidosis Vasc Diffuse Lung Dis 2005, 22:51–57.PubMed
22.
go back to reference Nakashima T, Yokoyama A, Ohnishi H, Hamada H, Ishikawa N, Haruta Y, et al.: Circulating KL-6/MUC1 as an independent predictor for disseminated intravascular coagulation in acute respiratory distress syndrome. J Intern Med 2008, 263:432–439.CrossRefPubMed Nakashima T, Yokoyama A, Ohnishi H, Hamada H, Ishikawa N, Haruta Y, et al.: Circulating KL-6/MUC1 as an independent predictor for disseminated intravascular coagulation in acute respiratory distress syndrome. J Intern Med 2008, 263:432–439.CrossRefPubMed
23.
go back to reference Kohno N, Yokoyama A, Kondo K: KL-6 as a serum marker for amiodarone-induced pulmonary toxicity. Intern Med 2000, 39:1004–1005.CrossRefPubMed Kohno N, Yokoyama A, Kondo K: KL-6 as a serum marker for amiodarone-induced pulmonary toxicity. Intern Med 2000, 39:1004–1005.CrossRefPubMed
24.
go back to reference Cobben NA, Drent M, Schols AM, Lamers RJ, Wouters EF, Van Dieijen-Visser MP: Serum lactate dehydrogenase and its isoenzyme pattern in ex-coalminers. Respir Med 1997, 91:616–623.CrossRefPubMed Cobben NA, Drent M, Schols AM, Lamers RJ, Wouters EF, Van Dieijen-Visser MP: Serum lactate dehydrogenase and its isoenzyme pattern in ex-coalminers. Respir Med 1997, 91:616–623.CrossRefPubMed
25.
go back to reference Drent M, Cobben NA, Henderson RF, Wouters EF, van Dieijen-Visser M: Usefulness of lactate dehydrogenase and its isoenzymes as indicators of lung damage or inflammation. Eur Respir J 1996, 9:1736–1742.CrossRefPubMed Drent M, Cobben NA, Henderson RF, Wouters EF, van Dieijen-Visser M: Usefulness of lactate dehydrogenase and its isoenzymes as indicators of lung damage or inflammation. Eur Respir J 1996, 9:1736–1742.CrossRefPubMed
26.
go back to reference Drent M, Cobben NA, Van Dieijen-Visser MP, Braat SH, Wouters EF: Serum lactate dehydrogenase activity: indicator of the development of pneumonitis induced by amiodarone. Eur Heart J 1998, 19:969–970.CrossRefPubMed Drent M, Cobben NA, Van Dieijen-Visser MP, Braat SH, Wouters EF: Serum lactate dehydrogenase activity: indicator of the development of pneumonitis induced by amiodarone. Eur Heart J 1998, 19:969–970.CrossRefPubMed
27.
go back to reference Matusiewicz SP, Williamson IJ, Sime PJ, Brown PH, Wenham PR, Crompton GK, et al.: Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis? Eur Respir J 1993, 6:1282–1286.PubMed Matusiewicz SP, Williamson IJ, Sime PJ, Brown PH, Wenham PR, Crompton GK, et al.: Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis? Eur Respir J 1993, 6:1282–1286.PubMed
28.
go back to reference van Krugten M, Cobben NA, Lamers RJ, Van Dieijen-Visser MP, Wagenaar SS, Wouters EF, et al.: Serum LDH: a marker of disease activity and its response to therapy in idiopathic pulmonary fibrosis. Neth J Med 1996, 48:220–223.CrossRefPubMed van Krugten M, Cobben NA, Lamers RJ, Van Dieijen-Visser MP, Wagenaar SS, Wouters EF, et al.: Serum LDH: a marker of disease activity and its response to therapy in idiopathic pulmonary fibrosis. Neth J Med 1996, 48:220–223.CrossRefPubMed
29.
30.
go back to reference Prasse A, Pechkovsky DV, Toews GB, Jungraithmayr W, Kollert F, Goldmann T, et al.: A vicious circle of alveolar macrophages and fibroblasts perpetuates pulmonary fibrosis via CCL18. Am J Respir Crit Care Med 2006, 173:781–792.CrossRefPubMed Prasse A, Pechkovsky DV, Toews GB, Jungraithmayr W, Kollert F, Goldmann T, et al.: A vicious circle of alveolar macrophages and fibroblasts perpetuates pulmonary fibrosis via CCL18. Am J Respir Crit Care Med 2006, 173:781–792.CrossRefPubMed
31.
go back to reference Prasse A, Pechkovsky DV, Toews GB, Schafer M, Eggeling S, Ludwig C, et al.: CCL18 as an indicator of pulmonary fibrotic activity in idiopathic interstitial pneumonias and systemic sclerosis. Arthritis Rheum 2007, 56:1685–1693.CrossRefPubMed Prasse A, Pechkovsky DV, Toews GB, Schafer M, Eggeling S, Ludwig C, et al.: CCL18 as an indicator of pulmonary fibrotic activity in idiopathic interstitial pneumonias and systemic sclerosis. Arthritis Rheum 2007, 56:1685–1693.CrossRefPubMed
32.
go back to reference Thomeer MJ, Vansteenkiste J, Verbeken EK, Demedts M: Interstitial lung diseases: characteristics at diagnosis and mortality risk assessment. Respir Med 2004, 98:567–573.CrossRefPubMed Thomeer MJ, Vansteenkiste J, Verbeken EK, Demedts M: Interstitial lung diseases: characteristics at diagnosis and mortality risk assessment. Respir Med 2004, 98:567–573.CrossRefPubMed
33.
go back to reference Demedts M, Behr J, Buhl R, Costabel U, Dekhuijzen R, Jansen HM, et al.: High-dose acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med 2005, 353:2229–2242.CrossRefPubMed Demedts M, Behr J, Buhl R, Costabel U, Dekhuijzen R, Jansen HM, et al.: High-dose acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med 2005, 353:2229–2242.CrossRefPubMed
34.
go back to reference Raghu G, Brown KK, Bradford WZ, Starko K, Noble PW, Schwartz DA, et al.: A placebo-controlled trial of interferon gamma-1b in patients with idiopathic pulmonary fibrosis. N Engl J Med 2004, 350:125–133.CrossRefPubMed Raghu G, Brown KK, Bradford WZ, Starko K, Noble PW, Schwartz DA, et al.: A placebo-controlled trial of interferon gamma-1b in patients with idiopathic pulmonary fibrosis. N Engl J Med 2004, 350:125–133.CrossRefPubMed
35.
go back to reference Flaherty KR, Mumford JA, Murray S, Kazerooni EA, Gross BH, Colby TV, et al.: Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 2003, 168:543–548.CrossRefPubMed Flaherty KR, Mumford JA, Murray S, Kazerooni EA, Gross BH, Colby TV, et al.: Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 2003, 168:543–548.CrossRefPubMed
36.
go back to reference Erbes R, Schaberg T, Loddenkemper R: Lung function tests in patients with idiopathic pulmonary fibrosis. Are they helpful for predicting outcome? Chest 1997, 111:51–57.CrossRefPubMed Erbes R, Schaberg T, Loddenkemper R: Lung function tests in patients with idiopathic pulmonary fibrosis. Are they helpful for predicting outcome? Chest 1997, 111:51–57.CrossRefPubMed
37.
go back to reference Jezek V, Fucik J, Michaljanic A, Jezkova L: The prognostic significance of functional tests in cryptogenic fibrosing alveolitis. Bull Eur Physiopathol Respir 1980, 16:711–720.PubMed Jezek V, Fucik J, Michaljanic A, Jezkova L: The prognostic significance of functional tests in cryptogenic fibrosing alveolitis. Bull Eur Physiopathol Respir 1980, 16:711–720.PubMed
38.
go back to reference Schwartz DA, Helmers RA, Galvin JR, Van Fossen DS, Frees KL, Dayton CS, et al.: Determinants of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1994, 149:450–454.CrossRefPubMed Schwartz DA, Helmers RA, Galvin JR, Van Fossen DS, Frees KL, Dayton CS, et al.: Determinants of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1994, 149:450–454.CrossRefPubMed
39.
go back to reference Rudd RM, Haslam PL, Turner-Warwick M: Cryptogenic fibrosing alveolitis: Relationships of pulmonary physiology and bronchoalveolar lavage to response to treatment and prognosis. Am Rev Respir Dis 1981, 124:1–8.PubMed Rudd RM, Haslam PL, Turner-Warwick M: Cryptogenic fibrosing alveolitis: Relationships of pulmonary physiology and bronchoalveolar lavage to response to treatment and prognosis. Am Rev Respir Dis 1981, 124:1–8.PubMed
40.
go back to reference Mapel DW, Hunt WC, Utton R, Baumgartner KB, Samet JM, Coultas DB: Idiopathic pulmonary fibrosis: survival in population based and hospital based cohorts. Thorax 1998, 53:469–476.CrossRefPubMedPubMedCentral Mapel DW, Hunt WC, Utton R, Baumgartner KB, Samet JM, Coultas DB: Idiopathic pulmonary fibrosis: survival in population based and hospital based cohorts. Thorax 1998, 53:469–476.CrossRefPubMedPubMedCentral
41.
go back to reference Hanson D, Winterbauer RH, Kirtland S, Wu R: Changes in pulmonary function test: results after 1 year of therapy as predictors of survival in patients with pulmonary fibrosis. Chest 1995, 108:305–310.CrossRefPubMed Hanson D, Winterbauer RH, Kirtland S, Wu R: Changes in pulmonary function test: results after 1 year of therapy as predictors of survival in patients with pulmonary fibrosis. Chest 1995, 108:305–310.CrossRefPubMed
42.
go back to reference Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al.: Standardisation of spirometry. Eur Respir J 2005, 26:319–338.CrossRefPubMed Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates A, et al.: Standardisation of spirometry. Eur Respir J 2005, 26:319–338.CrossRefPubMed
43.
go back to reference Miller A, Elliott JC, Thornton JC, Warshaw R, Geiger M, Anderson H: Comparison of spirometry performed on the same subjects by two teams using similar instruments: an investigation of variability in prevalence of impairment. Environ Res 1980, 21:229–234.CrossRefPubMed Miller A, Elliott JC, Thornton JC, Warshaw R, Geiger M, Anderson H: Comparison of spirometry performed on the same subjects by two teams using similar instruments: an investigation of variability in prevalence of impairment. Environ Res 1980, 21:229–234.CrossRefPubMed
45.
go back to reference Schwartz DA, Van Fossen D, Davis C, Helmers RA, Dayton CS, Burmeister L, et al.: Determinants of progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1994, 149:444–449.CrossRefPubMed Schwartz DA, Van Fossen D, Davis C, Helmers RA, Dayton CS, Burmeister L, et al.: Determinants of progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1994, 149:444–449.CrossRefPubMed
46.
go back to reference Schwartz DA, Van Fossen D, Davis C, Helmers RA, Dayton CS, Burmeister L, et al.: Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the lung study group. Am J Respir Crit Care Med 1998, 158:220–225.CrossRef Schwartz DA, Van Fossen D, Davis C, Helmers RA, Dayton CS, Burmeister L, et al.: Colchicine versus prednisone in the treatment of idiopathic pulmonary fibrosis. A randomized prospective study. Members of the lung study group. Am J Respir Crit Care Med 1998, 158:220–225.CrossRef
47.
go back to reference Raghu G, DePaso WJ, Cain K, Hammar SP, Wetzel CE, Dreis DF, et al.: Azathioprine combined with prednisone in the treatment of idiopathic pulmonary fibrosis: a prospective, double-blind, randomized, placebo-controlled trial. Am Rev Respir Dis 1991, 144:291–296.CrossRefPubMed Raghu G, DePaso WJ, Cain K, Hammar SP, Wetzel CE, Dreis DF, et al.: Azathioprine combined with prednisone in the treatment of idiopathic pulmonary fibrosis: a prospective, double-blind, randomized, placebo-controlled trial. Am Rev Respir Dis 1991, 144:291–296.CrossRefPubMed
48.
go back to reference Raghu G, Craig JW, Lockhart D, Mageto Y: Treatment of idiopathic pulmonary fibrosis with a new antifibrotic agent, pirfenidone. Results of a prospective, open-label phase II study. Am J Respir Crit Care Med 1999, 159:1061–1069.CrossRefPubMed Raghu G, Craig JW, Lockhart D, Mageto Y: Treatment of idiopathic pulmonary fibrosis with a new antifibrotic agent, pirfenidone. Results of a prospective, open-label phase II study. Am J Respir Crit Care Med 1999, 159:1061–1069.CrossRefPubMed
49.
go back to reference Zanen P, van der LL, van der MT, van den Bosch JM: Reference values for alveolar membrane diffusion capacity and pulmonary capillary blood volume. Eur Respir J 2001, 18:764–769.CrossRefPubMed Zanen P, van der LL, van der MT, van den Bosch JM: Reference values for alveolar membrane diffusion capacity and pulmonary capillary blood volume. Eur Respir J 2001, 18:764–769.CrossRefPubMed
50.
go back to reference Aguilaniu B, Maitre J, Glenet S, Gegout-Petit A, Guenard H: European reference equations for CO and NO lung transfer. Eur Respir J 2008, 31:1091–1097.CrossRefPubMed Aguilaniu B, Maitre J, Glenet S, Gegout-Petit A, Guenard H: European reference equations for CO and NO lung transfer. Eur Respir J 2008, 31:1091–1097.CrossRefPubMed
51.
go back to reference O'Donnell D: Physiology of interstitial lung disease. In Interstitial lung disease. Edited by: Schwarz MI, King TE Jr. Hamilton, ON, Canada: Decker Inc; 1998:51–70. O'Donnell D: Physiology of interstitial lung disease. In Interstitial lung disease. Edited by: Schwarz MI, King TE Jr. Hamilton, ON, Canada: Decker Inc; 1998:51–70.
52.
go back to reference du Bois RM: Strategies for treating idiopathic pulmonary fibrosis. Nat Rev Drug Discov 2010, 9:129–140.CrossRefPubMed du Bois RM: Strategies for treating idiopathic pulmonary fibrosis. Nat Rev Drug Discov 2010, 9:129–140.CrossRefPubMed
53.
go back to reference King TE Jr, Albera C, Bradford WZ, Costabel U, Hormel P, Lancaster L, et al.: Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial. Lancet 2009, 374:222–228.CrossRefPubMed King TE Jr, Albera C, Bradford WZ, Costabel U, Hormel P, Lancaster L, et al.: Effect of interferon gamma-1b on survival in patients with idiopathic pulmonary fibrosis (INSPIRE): a multicentre, randomised, placebo-controlled trial. Lancet 2009, 374:222–228.CrossRefPubMed
54.
go back to reference Fleischmann R: Primer: establishing a clinical trial unit - regulations and infrastructure. Nat Clin Pract Rheumatol 2007, 3:234–239.CrossRefPubMed Fleischmann R: Primer: establishing a clinical trial unit - regulations and infrastructure. Nat Clin Pract Rheumatol 2007, 3:234–239.CrossRefPubMed
55.
go back to reference Swigris JJ, Wamboldt FS, Behr J, du Bois RM, King TE, Raghu G, et al.: The 6 minute walk in idiopathic pulmonary fibrosis: longitudinal changes and minimum important difference. Thorax 2010, 65:173–177.CrossRefPubMed Swigris JJ, Wamboldt FS, Behr J, du Bois RM, King TE, Raghu G, et al.: The 6 minute walk in idiopathic pulmonary fibrosis: longitudinal changes and minimum important difference. Thorax 2010, 65:173–177.CrossRefPubMed
56.
go back to reference Holland AE, Hill CJ, Conron M, Munro P, McDonald CF: Small changes in six-minute walk distance are important in diffuse parenchymal lung disease. Respir Med 2009, 103:1430–1435.CrossRefPubMed Holland AE, Hill CJ, Conron M, Munro P, McDonald CF: Small changes in six-minute walk distance are important in diffuse parenchymal lung disease. Respir Med 2009, 103:1430–1435.CrossRefPubMed
57.
go back to reference Lettieri CJ, Nathan SD, Browning RF, Barnett SD, Ahmad S, Shorr AF: The distance-saturation product predicts mortality in idiopathic pulmonary fibrosis. Respir Med 2006, 100:1734–1741.CrossRefPubMed Lettieri CJ, Nathan SD, Browning RF, Barnett SD, Ahmad S, Shorr AF: The distance-saturation product predicts mortality in idiopathic pulmonary fibrosis. Respir Med 2006, 100:1734–1741.CrossRefPubMed
58.
go back to reference Caminati A, Bianchi A, Cassandro R, Mirenda MR, Harari S: Walking distance on 6-MWT is a prognostic factor in idiopathic pulmonary fibrosis. Respir Med 2009, 103:117–123.CrossRefPubMed Caminati A, Bianchi A, Cassandro R, Mirenda MR, Harari S: Walking distance on 6-MWT is a prognostic factor in idiopathic pulmonary fibrosis. Respir Med 2009, 103:117–123.CrossRefPubMed
59.
go back to reference Hallstrand TS, Boitano LJ, Johnson WC, Spada CA, Hayes JG, Raghu G: The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis. Eur Respir J 2005, 25:96–103.CrossRefPubMed Hallstrand TS, Boitano LJ, Johnson WC, Spada CA, Hayes JG, Raghu G: The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis. Eur Respir J 2005, 25:96–103.CrossRefPubMed
60.
go back to reference Eaton T, Young P, Milne D, Wells AU: Six-minute walk, maximal exercise tests: reproducibility in fibrotic interstitial pneumonia. Am J Respir Crit Care Med 2005, 171:1150–1157.CrossRefPubMed Eaton T, Young P, Milne D, Wells AU: Six-minute walk, maximal exercise tests: reproducibility in fibrotic interstitial pneumonia. Am J Respir Crit Care Med 2005, 171:1150–1157.CrossRefPubMed
61.
go back to reference Lederer DJ, Arcasoy SM, Wilt JS, D'Ovidio F, Sonett JR, Kawut SM: Six-minute-walk distance predicts waiting list survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2006, 174:659–664.CrossRefPubMedPubMedCentral Lederer DJ, Arcasoy SM, Wilt JS, D'Ovidio F, Sonett JR, Kawut SM: Six-minute-walk distance predicts waiting list survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2006, 174:659–664.CrossRefPubMedPubMedCentral
62.
go back to reference du Bois RM, Albera C, Costabel U, Bradford WZ, Kartashov A, Noble PW, Szwarcberg J, Thomeer M, Valeyre D, Weycker D, King TE: 6 minute walk test distance is a reliable, valid and responsive outcome measure that predicts mortality in patients with IPF. Am J Respir Crit Care Med 2010, 181:A1103. du Bois RM, Albera C, Costabel U, Bradford WZ, Kartashov A, Noble PW, Szwarcberg J, Thomeer M, Valeyre D, Weycker D, King TE: 6 minute walk test distance is a reliable, valid and responsive outcome measure that predicts mortality in patients with IPF. Am J Respir Crit Care Med 2010, 181:A1103.
63.
go back to reference Wells AU, Hansell DM, Rubens MB, Cullinan P, Black CM, du Bois RM: The predictive value of appearances on thin-section computed tomography in fibrosing alveolitis. Am Rev Respir Dis 1993, 148:1076–1082.CrossRefPubMed Wells AU, Hansell DM, Rubens MB, Cullinan P, Black CM, du Bois RM: The predictive value of appearances on thin-section computed tomography in fibrosing alveolitis. Am Rev Respir Dis 1993, 148:1076–1082.CrossRefPubMed
64.
go back to reference Leung AN, Miller RR, Muller NL: Parenchymal opacification in chronic infiltrative lung diseases: CT-pathologic correlation. Radiology 1993, 188:209–214.CrossRefPubMed Leung AN, Miller RR, Muller NL: Parenchymal opacification in chronic infiltrative lung diseases: CT-pathologic correlation. Radiology 1993, 188:209–214.CrossRefPubMed
65.
go back to reference Lee JS, Im JG, Ahn JM, Kim YM, Han MC: Fibrosing alveolitis: prognostic implication of ground-glass attenuation at high-resolution CT. Radiology 1992, 184:451–454.CrossRefPubMed Lee JS, Im JG, Ahn JM, Kim YM, Han MC: Fibrosing alveolitis: prognostic implication of ground-glass attenuation at high-resolution CT. Radiology 1992, 184:451–454.CrossRefPubMed
66.
go back to reference Remy-Jardin M, Giraud F, Remy J, Copin MC, Gosselin B, Duhamel A: Importance of ground-glass attenuation in chronic diffuse infiltrative lung disease: pathologic-CT correlation. Radiology 1993, 189:693–698.CrossRefPubMed Remy-Jardin M, Giraud F, Remy J, Copin MC, Gosselin B, Duhamel A: Importance of ground-glass attenuation in chronic diffuse infiltrative lung disease: pathologic-CT correlation. Radiology 1993, 189:693–698.CrossRefPubMed
67.
go back to reference Hansell DM, Wells AU: CT evaluation of fibrosing alveolitis--applications and insights. J Thorac Imaging 1996, 11:231–249.CrossRefPubMed Hansell DM, Wells AU: CT evaluation of fibrosing alveolitis--applications and insights. J Thorac Imaging 1996, 11:231–249.CrossRefPubMed
68.
go back to reference Wells AU, Hansell DM, Corrin B, Harrison NK, Goldstraw P, Black CM, et al.: High resolution computed tomography as a predictor of lung histology in systemic sclerosis. Thorax 1992, 47:738–742.CrossRefPubMedPubMedCentral Wells AU, Hansell DM, Corrin B, Harrison NK, Goldstraw P, Black CM, et al.: High resolution computed tomography as a predictor of lung histology in systemic sclerosis. Thorax 1992, 47:738–742.CrossRefPubMedPubMedCentral
69.
go back to reference Gay SE, Kazerooni EA, Toews GB, Lynch JP III, Gross BH, Cascade PN, et al.: Idiopathic pulmonary fibrosis: predicting response to therapy and survival. Am J Respir Crit Care Med 1998, 157:1063–1072.CrossRefPubMed Gay SE, Kazerooni EA, Toews GB, Lynch JP III, Gross BH, Cascade PN, et al.: Idiopathic pulmonary fibrosis: predicting response to therapy and survival. Am J Respir Crit Care Med 1998, 157:1063–1072.CrossRefPubMed
70.
go back to reference Mouratidis B, Lising J, Nogrady S, Hurwitz M: Increased pertechnegas lung clearance in interstitial lung disease. Clin Nucl Med 1999, 24:105–108.CrossRefPubMed Mouratidis B, Lising J, Nogrady S, Hurwitz M: Increased pertechnegas lung clearance in interstitial lung disease. Clin Nucl Med 1999, 24:105–108.CrossRefPubMed
72.
go back to reference Barrowcliffe MP, Jones JG: Pulmonary clearance of 99m Tc-DTPA in the diagnosis and evolution of increased permeability pulmonary oedema. Anaesth Intensive Care 1989, 17:422–432.PubMed Barrowcliffe MP, Jones JG: Pulmonary clearance of 99m Tc-DTPA in the diagnosis and evolution of increased permeability pulmonary oedema. Anaesth Intensive Care 1989, 17:422–432.PubMed
73.
go back to reference Kon OM, Daniil Z, Black CM, du Bois RM: Clearance of inhaled technetium-99m-DTPA as a clinical index of pulmonary vascular disease in systemic sclerosis. Eur Respir J 1999, 13:133–136.CrossRefPubMed Kon OM, Daniil Z, Black CM, du Bois RM: Clearance of inhaled technetium-99m-DTPA as a clinical index of pulmonary vascular disease in systemic sclerosis. Eur Respir J 1999, 13:133–136.CrossRefPubMed
74.
go back to reference Thomeer MJ, Dehaes B, Mortelmans L, Demedts M: Pertechnegas lung clearance in different forms of interstitial lung disease. Eur Respir J 2002, 19:31–36.CrossRefPubMed Thomeer MJ, Dehaes B, Mortelmans L, Demedts M: Pertechnegas lung clearance in different forms of interstitial lung disease. Eur Respir J 2002, 19:31–36.CrossRefPubMed
75.
go back to reference Keijsers RG, Verzijlbergen FJ, Oyen WJ, van den Bosch JM, Ruven HJ, van Velzen-Blad H, et al.: 18F-FDG PET, genotype-corrected ACE and sIL-2R in newly diagnosed sarcoidosis. Eur J Nucl Med Mol Imaging 2009, 36:1131–1137.CrossRefPubMed Keijsers RG, Verzijlbergen FJ, Oyen WJ, van den Bosch JM, Ruven HJ, van Velzen-Blad H, et al.: 18F-FDG PET, genotype-corrected ACE and sIL-2R in newly diagnosed sarcoidosis. Eur J Nucl Med Mol Imaging 2009, 36:1131–1137.CrossRefPubMed
76.
go back to reference Langah R, Spicer K, Gebregziabher M, Gordon L: Effectiveness of prolonged fasting 18f-FDG PET-CT in the detection of cardiac sarcoidosis. J Nucl Cardiol 2009, 16:801–810.CrossRefPubMed Langah R, Spicer K, Gebregziabher M, Gordon L: Effectiveness of prolonged fasting 18f-FDG PET-CT in the detection of cardiac sarcoidosis. J Nucl Cardiol 2009, 16:801–810.CrossRefPubMed
77.
go back to reference Teirstein AS, Machac J, Almeida O, Lu P, Padilla ML, Iannuzzi MC: Results of 188 whole-body fluorodeoxyglucose positron emission tomography scans in 137 patients with sarcoidosis. Chest 2007, 132:1949–1953.CrossRefPubMed Teirstein AS, Machac J, Almeida O, Lu P, Padilla ML, Iannuzzi MC: Results of 188 whole-body fluorodeoxyglucose positron emission tomography scans in 137 patients with sarcoidosis. Chest 2007, 132:1949–1953.CrossRefPubMed
78.
go back to reference Ryu JH, Daniels CE, Hartman TE, Yi ES: Diagnosis of interstitial lung diseases. Mayo Clin Proc 2007, 82:976–986.CrossRefPubMed Ryu JH, Daniels CE, Hartman TE, Yi ES: Diagnosis of interstitial lung diseases. Mayo Clin Proc 2007, 82:976–986.CrossRefPubMed
Metadata
Title
Clinical use of biomarkers of survival in pulmonary fibrosis
Authors
Michiel Thomeer
Jan C Grutters
Wim A Wuyts
Stijn Willems
Maurits G Demedts
Publication date
01-12-2010
Publisher
BioMed Central
Published in
Respiratory Research / Issue 1/2010
Electronic ISSN: 1465-993X
DOI
https://doi.org/10.1186/1465-9921-11-89

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