Citation: 孙迪, 叶俏. 肺纤维化合并肺气肿定义为“综合征”的研究进展. Chinese Journal of Respiratory and Critical Care Medicine, 2023, 22(10): 749-754. doi: 10.7507/1671-6205.202304062 Copy
1. | Wiggins J, Strickland B, Turner-Warwick M. Combined cryptogenic fibrosing alveolitis and emphysema: the value of high resolution computed tomography in assessment. Respir Med, 1990, 84(5): 365-369. |
2. | Cottin V, Nunes H, Brillet PY, et al. Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity. Eur Respir J, 2005, 26(4): 586-593. |
3. | Scadding JG. Health and disease: what can medicine do for philosophy? J Med Ethics, 1988, 14(3): 118-124. |
4. | Cottin V, Selman M, Inoue Y, et al. Syndrome of Combined Pulmonary Fibrosis and Emphysema: An Official ATS/ERS/JRS/ALAT Research Statement. Am J Respir Crit Care Med, 2022, 206(4): e7-e41. |
5. | Chae KJ, Jin GY, Han YM, et al. Prevalence and progression of combined pulmonary fibrosis and emphysema in asymptomatic smokers: A case-control study. Eur Radiol, 2015, 25(8): 2326-2334. |
6. | 马江伟, 李振华, 许慧, 等. 特发性肺间质纤维化合并肺气肿与未合并肺气肿患者的临床对比研究. 中华结核和呼吸杂志, 2013, 36(3): 173-176. |
7. | Lai RS, Chen CF, Chu KA, et al. The effect of emphysema on survival in patients with idiopathic pulmonary fibrosis: a retrospective study in Taiwan. J Chin Med Assoc, 2019, 82(12): 922-928. |
8. | Ryerson C J, Hartman T, Elicker BM, et al. Clinical features and outcomes in combined pulmonary fibrosis and emphysema in idiopathic pulmonary fibrosis. Chest, 2013, 144(1): 234-240. |
9. | Sangani R, Ghio A, Culp S, et al. Combined pulmonary fibrosis emphysema: role of cigarette smoking and pulmonary hypertension in a rural cohort. Int J Chron Obstruct Pulmon Dis, 2021, 16: 1873-1885. |
10. | Kim HJ, Snyder LD, Neely ML, et al. Clinical outcomes of patients with combined idiopathic pulmonary fibrosis and emphysema in the IPF-PRO Registry. Lung, 2022, 200(1): 21-29. |
11. | Akagi T, Matsumoto T, Harada T, et al. Coexistent emphysema delays the decrease of vital capacity in idiopathic pulmonary fibrosis. Respir Med, 2009, 103(8): 1209-1215. |
12. | Kurashima K, Takayanagi N, Tsuchiya N, et al. The effect of emphysema on lung function and survival in patients with idiopathic pulmonary fibrosis. Respirology, 2010, 15(5): 843-848. |
13. | Nemoto M, Nei Y, Bartholmai B, et al. Automated computed tomography quantification of fibrosis predicts prognosis in combined pulmonary fibrosis and emphysema in a real-world setting: a single-centre, retrospective study. Respir Res, 2020, 21(1): 275. |
14. | Alsumrain M, De Giacomi F, Nasim F, et al. Combined pulmonary fibrosis and emphysema as a clinicoradiologic entity: characterization of presenting lung fibrosis and implications for survival. Respir Med, 2019, 146: 106-112. |
15. | 吴苏佶, 魏毅, 石俊青, 等. 肺纤维化合并肺气肿综合征的临床特征与危险因素分析. 中国呼吸与危重监护杂志, 2021, 20(01): 4-11. |
16. | Liu Q, Sun D, Wang Y, et al. Use of machine learning models to predict prognosis of combined pulmonary fibrosis and emphysema in a Chinese population. BMC Pulm Med, 2022, 22(1): 327. |
17. | Zhang LJ, Zhang CL, Dong FS, et al. Combined pulmonary fibrosis and emphysema: a retrospective analysis of clinical characteristics, treatment and prognosis. BMC Pulm Med, 2016, 16(1): 137. |
18. | Yuan XT, Jin J, Xu XM. Development of a nomogram for predicting the presence of combined pulmonary fibrosis and emphysema. BMC Pulm Med, 2021, 21(1): 349. |
19. | Mori K, Shirai T, Mikamo M, et al. Respiratory mechanics measured by forced oscillation technique in combined pulmonary fibrosis and emphysema. Respir Physiol Neurobiol, 2013, 185(2): 235-240. |
20. | Sugino K, Ishida F, Kikuchi N, et al. Comparison of clinical characteristics and prognostic factors of combined pulmonary fibrosis and emphysema versus idiopathic pulmonary fibrosis alone. Respirology, 2014, 19(2): 239-245. |
21. | Yamamoto Y, Hirata H, Shiroyama T, et al. Respiratory impedance is associated with ventilation and diffusing capacity in patients with idiopathic pulmonary fibrosis combined with emphysema. Int J Chron Obstruct Pulmon Dis, 2022, 17: 1495-1506. |
22. | Kitaguchi Y, Fujimoto K, Hanaoka M, et al. Clinical characteristics of combined pulmonary fibrosis and emphysema. Respirology, 2010, 15(2): 265-271. |
23. | Kishaba T, Shimaoka Y, Fukuyama H, et al. A cohort study of mortality predictors and characteristics of patients with combined pulmonary fibrosis and emphysema. BMJ Open, 2012, 2(3): e000988. |
24. | Schmidt SL, Nambiar AM, Tayob N, et al. Pulmonary function measures predict mortality differently in IPF versus combined pulmonary fibrosis and emphysema. Eur Respir J, 2011, 38(1): 176-183. |
25. | Mejia M, Carrillo G, Rojas-Serrano J, et al. Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension. Chest, 2009, 136(1): 10-15. |
26. | Champtiaux N, Cottin V, Chassagnon G, et al. Combined pulmonary fibrosis and emphysema in systemic sclerosis: a syndrome associated with heavy morbidity and mortality. Semin Arthritis Rheum, 2019, 49(1): 98-104. |
27. | Tomioka H, Mamesaya N, Yamashita S, et al. Combined pulmonary fibrosis and emphysema: effect of pulmonary rehabilitation in comparison with chronic obstructive pulmonary disease. BMJ Open Respir Res, 2016, 3(1): e000099. |
28. | 林敏杰, 张英为, 陈露露, 等. 肺纤维化合并肺气肿与特发性肺纤维化临床特点的比较. 中国呼吸与危重监护杂志, 2020, 19(06): 548-553. |
29. | Jankowich MD, Rounds S. Combined pulmonary fibrosis and emphysema alters physiology but has similar mortality to pulmonary fibrosis without emphysema. Lung, 2010, 188(5): 365-373. |
30. | Kim YS, Jin GY, Chae KJ, et al. Visually stratified CT honeycombing as a survival predictor in combined pulmonary fibrosis and emphysema. Br J Radiol, 2015, 88(1055): 20150545. |
31. | Lee CH, Kim HJ, Park CM, et al. The impact of combined pulmonary fibrosis and emphysema on mortality. Int J Tuberc Lung Dis, 2011, 15(8): 1111-1116. |
32. | Sato S, Tanino Y, Misa K, et al. Identification of clinical phenotypes in idiopathic interstitial pneumonia with pulmonary emphysema. Intern Med, 2016, 55(12): 1529-1535. |
33. | Yoon HY, Kim TH, Seo JB, et al. Effects of emphysema on physiological and prognostic characteristics of lung function in idiopathic pulmonary fibrosis. Respirology, 2019, 24(1): 55-62. |
34. | Tzouvelekis A, Zacharis G, Oikonomou A, et al. Increased incidence of autoimmune markers in patients with combined pulmonary fibrosis and emphysema. BMC Pulm Med, 2013, 13: 31. |
35. | Tasaka S, Mizoguchi K, Funatsu Y, et al. Cytokine profile of bronchoalveolar lavage fluid in patients with combined pulmonary fibrosis and emphysema. Respirology, 2012, 17(5): 814-820. |
36. | Cottin V, Hansell DM, Sverzellati N, et al. Effect of emphysema extent on serial lung function in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2017, 196(9): 1162-1171. |
37. | Ando K, Sekiya M, Tobino K, et al. Relationship between quantitative CT metrics and pulmonary function in combined pulmonary fibrosis and emphysema. Lung, 2013, 191(6): 585-591. |
38. | Kitaguchi Y, Fujimoto K, Hayashi R, et al. Annual changes in pulmonary function in combined pulmonary fibrosis and emphysema: over a 5-year follow-up. Respir Med, 2013, 107(12): 1986-1992. |
39. | Poncot-Mongars R, Zysman M, Regent D, et al. [Combined pulmonary fibrosis and emphysema: the natural history of the disease.The chronological evolution of clinical features, respiratory function and the CT scan]. Rev Mal Respir, 2013, 30(3): 222-226. |
40. | Mori K, Shirai T, Mikamo M, et al. Colored 3-dimensional analyses of respiratory resistance and reactance in COPD and asthma. COPD, 2011, 8(6): 456-463. |
41. | Hage R, Gautschi F, Steinack C, et al. Combined pulmonary fibrosis and emphysema (CPFE) clinical features and management. Int J Chron Obstruct Pulmon Dis, 2021, 16: 167-177. |
42. | Du Bois RM, Weycker D, Albera C, et al. Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2011, 184(4): 459-466. |
43. | Moll M, Sakornsakolpat P, Shrine N, et al. Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts. Lancet Respir Med, 2020, 8(7): 696-708. |
44. | Lynch DA, Austin JH, Hogg JC, et al. CT-definable subtypes of chronic obstructive pulmonary disease: a statement of the Fleischner Society. Radiology, 2015, 277(1): 192-205. |
45. | Inomata M, Ikushima S, Awano N, et al. An autopsy study of combined pulmonary fibrosis and emphysema: correlations among clinical, radiological, and pathological features. BMC Pulm Med, 2014, 14: 104. |
46. | Cottin V, Cordier JF. Combined pulmonary fibrosis and emphysema in connective tissue disease. Curr Opin Pulm Med, 2012, 18(5): 418-427. |
47. | Cottin V, Brillet PY, Nunes H, et al. [Combined pulmonary fibrosis and emphysema]. Presse Med, 2007, 36(6 Pt 2): 936-944. |
48. | Kinoshita Y, Watanabe K, Ishii H, et al. Distribution of emphysema and fibrosis in idiopathic pulmonary fibrosis with coexisting emphysema. Histopathology, 2019, 74(7): 1103-1108. |
49. | Antoniou KM, Walsh SL, Hansell DM, et al. Smoking-related emphysema is associated with idiopathic pulmonary fibrosis and rheumatoid lung. Respirology, 2013, 18(8): 1191-1196. |
50. | Weiss W. Smoking and pulmonary fibrosis. J Occup Med, 1988, 30(1): 33-39. |
51. | Bellou V, Belbasis L, Evangelou E. Tobacco smoking and risk for pulmonary fibrosis: a prospective cohort study from the UK Biobank. Chest, 2021, 160(3): 983-993. |
52. | Foronjy R, D'armiento J. The effect of cigarette smoke-derived oxidants on the inflammatory response of the lung. Clin Appl Immunol Rev, 2006, 6(1): 53-72. |
53. | Hubbard R, Lewis S, Richards K, et al. Occupational exposure to metal or wood dust and aetiology of cryptogenic fibrosing alveolitis. Lancet, 1996, 347(8997): 284-289. |
54. | Iwai K, Mori T, Yamada N, et al. Idiopathic pulmonary fibrosis. Epidemiologic approaches to occupational exposure. Am J Respir Crit Care Med, 1994, 150(3): 670-675. |
55. | Walsh SL, Wells AU, Sverzellati N, et al. Relationship between fibroblastic foci profusion and high resolution CT morphology in fibrotic lung disease. BMC Med, 2015, 13: 241. |
56. | Kusko RL, Brothers JF, 2nd, Tedrow J, et al. Integrated genomics reveals convergent transcriptomic networks underlying chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2016, 194(8): 948-960. |
57. | Halu A, Liu SK, Baek SH, et al. Exploring the cross-phenotype network region of disease modules reveals concordant and discordant pathways between chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. Hum Mol Genet, 2019, 28(14): 2352-2364. |
58. | Collum SD, Molina JG, Hanmandlu A, et al. Adenosine and hyaluronan promote lung fibrosis and pulmonary hypertension in combined pulmonary fibrosis and emphysema. Dis Model Mech, 2019, 12(5): dmm038711. |
59. | Lundblad LK, Thompson-Figueroa J, Leclair T, et al. Tumor necrosis factor-α overexpression in lung disease: a single cause behind a complex phenotype. Am J Respir Crit Care Med, 2005, 171(12): 1363-1370. |
60. | Houghton AM. Matrix metalloproteinases in destructive lung disease. Matrix Biol, 2015, 44-46: 167-174. |
61. | Pardo A, Cabrera S, Maldonado M, et al. Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis. Respir Res, 2016, 17: 23. |
62. | Mattey DL, Nixon NB, Dawes PT. Association of circulating levels of MMP-8 with mortality from respiratory disease in patients with rheumatoid arthritis. Arthritis Res Ther, 2012, 14(5): R204. |
63. | Andersen GN, Nilsson K, Pourazar J, et al. Bronchoalveolar matrix metalloproteinase 9 relates to restrictive lung function impairment in systemic sclerosis. Respir Med, 2007, 101(10): 2199-2206. |
64. | Rogliani P, Mura M, Mattia P, et al. HRCT and histopathological evaluation of fibrosis and tissue destruction in IPF associated with pulmonary emphysema. Respir Med, 2008, 102(12): 1753-1761. |
65. | Roake CM, Artandi SE. Control of cellular aging, tissue function, and cancer by p53 downstream of telomeres. Cold Spring Harb Perspect Med, 2017, 7(5): a026088. |
66. | Alder JK, Chen JJ, Lancaster L, et al. Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proc Natl Acad Sci U S A, 2008, 105(35): 13051-13056. |
67. | Cronkhite JT, Xing C, Raghu G, et al. Telomere shortening in familial and sporadic pulmonary fibrosis. Am J Respir Crit Care Med, 2008, 178(7): 729-737. |
68. | Alder JK, Guo N, Kembou F, et al. Telomere length is a determinant of emphysema susceptibility. Am J Respir Crit Care Med, 2011, 184(8): 904-912. |
69. | Tsuji T, Aoshiba K, Nagai A. Alveolar cell senescence in patients with pulmonary emphysema. Am J Respir Crit Care Med, 2006, 174(8): 886-893. |
70. | Povedano JM, Martinez P, Flores JM, et al. Mice with pulmonary fibrosis driven by telomere dysfunction. Cell Rep, 2015, 12(2): 286-299. |
71. | Wijsenbeek M, Cottin V. Spectrum of fibrotic lung diseases. N Engl J Med, 2020, 383(10): 958-968. |
72. | Cottin V, Bonniaud P, Cadranel J, et al. French practical guidelines for the diagnosis and management of idiopathic pulmonary fibrosis - 2021 update. Full-length version. Respir Med Res, 2023, 83: 100948. |
73. | Wongkarnjana A, Scallan C, Kolb MRJ. Progressive fibrosing interstitial lung disease: treatable traits and therapeutic strategies. Curr Opin Pulm Med, 2020, 26(5): 436-442. |
74. | Agusti A, Bel E, Thomas M, et al. Treatable traits: toward precision medicine of chronic airway diseases. Eur Respir J, 2016, 47(2): 410-419. |
75. | Dong FS, Zhang YM, Chi FZ, et al. Clinical efficacy and safety of ICS/LABA in patients with combined idiopathic pulmonary fibrosis and emphysema. Int J Clin Exp Med, 2015, 8(6): 8617-8625. |
76. | Flaherty KR, Wells AU, Cottin V, et al. Nintedanib in progressive fibrosing interstitial lung diseases. N Engl J Med, 2019, 381(18): 1718-1727. |
77. | Cottin V, Azuma A, Raghu G, et al. Therapeutic effects of nintedanib are not influenced by emphysema in the INPULSIS trials. Eur Respir J, 2019, 53(4): 1801655. |
78. | Jankowich MD, Rounds SIS. Combined pulmonary fibrosis and emphysema syndrome: a review. Chest, 2012, 141(1): 222-231. |
79. | Jiang CG, Fu Q, Zheng CM. Prognosis of combined pulmonary fibrosis and emphysema: comparison with idiopathic pulmonary fibrosis alone. Ther Adv Respir Dis, 2019, 13: 1753466619888119. |
80. | Jacob J, Bartholmai BJ, Rajagopalan S, et al. Functional and prognostic effects when emphysema complicates idiopathic pulmonary fibrosis. Eur Respir J, 2017, 50(1): 1700379. |
81. | Zhao A, Gudmundsson E, Mogulkoc N, et al. Mortality in combined pulmonary fibrosis and emphysema patients is determined by the sum of pulmonary fibrosis and emphysema. ERJ Open Res, 2021, 7(3): 00316-2021. |
82. | Jacob J, Bartholmai BJ, Rajagopalan S, et al. Predicting outcomes in idiopathic pulmonary fibrosis using automated computed tomographic analysis. Am J Respir Crit Care Med, 2018, 198(6): 767-776. |
83. | Zantah M, Dotan Y, Dass C, et al. Acute exacerbations of COPD versus IPF in patients with combined pulmonary fibrosis and emphysema. Respir Res, 2020, 21(1): 164. |
- 1. Wiggins J, Strickland B, Turner-Warwick M. Combined cryptogenic fibrosing alveolitis and emphysema: the value of high resolution computed tomography in assessment. Respir Med, 1990, 84(5): 365-369.
- 2. Cottin V, Nunes H, Brillet PY, et al. Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity. Eur Respir J, 2005, 26(4): 586-593.
- 3. Scadding JG. Health and disease: what can medicine do for philosophy? J Med Ethics, 1988, 14(3): 118-124.
- 4. Cottin V, Selman M, Inoue Y, et al. Syndrome of Combined Pulmonary Fibrosis and Emphysema: An Official ATS/ERS/JRS/ALAT Research Statement. Am J Respir Crit Care Med, 2022, 206(4): e7-e41.
- 5. Chae KJ, Jin GY, Han YM, et al. Prevalence and progression of combined pulmonary fibrosis and emphysema in asymptomatic smokers: A case-control study. Eur Radiol, 2015, 25(8): 2326-2334.
- 6. 马江伟, 李振华, 许慧, 等. 特发性肺间质纤维化合并肺气肿与未合并肺气肿患者的临床对比研究. 中华结核和呼吸杂志, 2013, 36(3): 173-176.
- 7. Lai RS, Chen CF, Chu KA, et al. The effect of emphysema on survival in patients with idiopathic pulmonary fibrosis: a retrospective study in Taiwan. J Chin Med Assoc, 2019, 82(12): 922-928.
- 8. Ryerson C J, Hartman T, Elicker BM, et al. Clinical features and outcomes in combined pulmonary fibrosis and emphysema in idiopathic pulmonary fibrosis. Chest, 2013, 144(1): 234-240.
- 9. Sangani R, Ghio A, Culp S, et al. Combined pulmonary fibrosis emphysema: role of cigarette smoking and pulmonary hypertension in a rural cohort. Int J Chron Obstruct Pulmon Dis, 2021, 16: 1873-1885.
- 10. Kim HJ, Snyder LD, Neely ML, et al. Clinical outcomes of patients with combined idiopathic pulmonary fibrosis and emphysema in the IPF-PRO Registry. Lung, 2022, 200(1): 21-29.
- 11. Akagi T, Matsumoto T, Harada T, et al. Coexistent emphysema delays the decrease of vital capacity in idiopathic pulmonary fibrosis. Respir Med, 2009, 103(8): 1209-1215.
- 12. Kurashima K, Takayanagi N, Tsuchiya N, et al. The effect of emphysema on lung function and survival in patients with idiopathic pulmonary fibrosis. Respirology, 2010, 15(5): 843-848.
- 13. Nemoto M, Nei Y, Bartholmai B, et al. Automated computed tomography quantification of fibrosis predicts prognosis in combined pulmonary fibrosis and emphysema in a real-world setting: a single-centre, retrospective study. Respir Res, 2020, 21(1): 275.
- 14. Alsumrain M, De Giacomi F, Nasim F, et al. Combined pulmonary fibrosis and emphysema as a clinicoradiologic entity: characterization of presenting lung fibrosis and implications for survival. Respir Med, 2019, 146: 106-112.
- 15. 吴苏佶, 魏毅, 石俊青, 等. 肺纤维化合并肺气肿综合征的临床特征与危险因素分析. 中国呼吸与危重监护杂志, 2021, 20(01): 4-11.
- 16. Liu Q, Sun D, Wang Y, et al. Use of machine learning models to predict prognosis of combined pulmonary fibrosis and emphysema in a Chinese population. BMC Pulm Med, 2022, 22(1): 327.
- 17. Zhang LJ, Zhang CL, Dong FS, et al. Combined pulmonary fibrosis and emphysema: a retrospective analysis of clinical characteristics, treatment and prognosis. BMC Pulm Med, 2016, 16(1): 137.
- 18. Yuan XT, Jin J, Xu XM. Development of a nomogram for predicting the presence of combined pulmonary fibrosis and emphysema. BMC Pulm Med, 2021, 21(1): 349.
- 19. Mori K, Shirai T, Mikamo M, et al. Respiratory mechanics measured by forced oscillation technique in combined pulmonary fibrosis and emphysema. Respir Physiol Neurobiol, 2013, 185(2): 235-240.
- 20. Sugino K, Ishida F, Kikuchi N, et al. Comparison of clinical characteristics and prognostic factors of combined pulmonary fibrosis and emphysema versus idiopathic pulmonary fibrosis alone. Respirology, 2014, 19(2): 239-245.
- 21. Yamamoto Y, Hirata H, Shiroyama T, et al. Respiratory impedance is associated with ventilation and diffusing capacity in patients with idiopathic pulmonary fibrosis combined with emphysema. Int J Chron Obstruct Pulmon Dis, 2022, 17: 1495-1506.
- 22. Kitaguchi Y, Fujimoto K, Hanaoka M, et al. Clinical characteristics of combined pulmonary fibrosis and emphysema. Respirology, 2010, 15(2): 265-271.
- 23. Kishaba T, Shimaoka Y, Fukuyama H, et al. A cohort study of mortality predictors and characteristics of patients with combined pulmonary fibrosis and emphysema. BMJ Open, 2012, 2(3): e000988.
- 24. Schmidt SL, Nambiar AM, Tayob N, et al. Pulmonary function measures predict mortality differently in IPF versus combined pulmonary fibrosis and emphysema. Eur Respir J, 2011, 38(1): 176-183.
- 25. Mejia M, Carrillo G, Rojas-Serrano J, et al. Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension. Chest, 2009, 136(1): 10-15.
- 26. Champtiaux N, Cottin V, Chassagnon G, et al. Combined pulmonary fibrosis and emphysema in systemic sclerosis: a syndrome associated with heavy morbidity and mortality. Semin Arthritis Rheum, 2019, 49(1): 98-104.
- 27. Tomioka H, Mamesaya N, Yamashita S, et al. Combined pulmonary fibrosis and emphysema: effect of pulmonary rehabilitation in comparison with chronic obstructive pulmonary disease. BMJ Open Respir Res, 2016, 3(1): e000099.
- 28. 林敏杰, 张英为, 陈露露, 等. 肺纤维化合并肺气肿与特发性肺纤维化临床特点的比较. 中国呼吸与危重监护杂志, 2020, 19(06): 548-553.
- 29. Jankowich MD, Rounds S. Combined pulmonary fibrosis and emphysema alters physiology but has similar mortality to pulmonary fibrosis without emphysema. Lung, 2010, 188(5): 365-373.
- 30. Kim YS, Jin GY, Chae KJ, et al. Visually stratified CT honeycombing as a survival predictor in combined pulmonary fibrosis and emphysema. Br J Radiol, 2015, 88(1055): 20150545.
- 31. Lee CH, Kim HJ, Park CM, et al. The impact of combined pulmonary fibrosis and emphysema on mortality. Int J Tuberc Lung Dis, 2011, 15(8): 1111-1116.
- 32. Sato S, Tanino Y, Misa K, et al. Identification of clinical phenotypes in idiopathic interstitial pneumonia with pulmonary emphysema. Intern Med, 2016, 55(12): 1529-1535.
- 33. Yoon HY, Kim TH, Seo JB, et al. Effects of emphysema on physiological and prognostic characteristics of lung function in idiopathic pulmonary fibrosis. Respirology, 2019, 24(1): 55-62.
- 34. Tzouvelekis A, Zacharis G, Oikonomou A, et al. Increased incidence of autoimmune markers in patients with combined pulmonary fibrosis and emphysema. BMC Pulm Med, 2013, 13: 31.
- 35. Tasaka S, Mizoguchi K, Funatsu Y, et al. Cytokine profile of bronchoalveolar lavage fluid in patients with combined pulmonary fibrosis and emphysema. Respirology, 2012, 17(5): 814-820.
- 36. Cottin V, Hansell DM, Sverzellati N, et al. Effect of emphysema extent on serial lung function in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2017, 196(9): 1162-1171.
- 37. Ando K, Sekiya M, Tobino K, et al. Relationship between quantitative CT metrics and pulmonary function in combined pulmonary fibrosis and emphysema. Lung, 2013, 191(6): 585-591.
- 38. Kitaguchi Y, Fujimoto K, Hayashi R, et al. Annual changes in pulmonary function in combined pulmonary fibrosis and emphysema: over a 5-year follow-up. Respir Med, 2013, 107(12): 1986-1992.
- 39. Poncot-Mongars R, Zysman M, Regent D, et al. [Combined pulmonary fibrosis and emphysema: the natural history of the disease.The chronological evolution of clinical features, respiratory function and the CT scan]. Rev Mal Respir, 2013, 30(3): 222-226.
- 40. Mori K, Shirai T, Mikamo M, et al. Colored 3-dimensional analyses of respiratory resistance and reactance in COPD and asthma. COPD, 2011, 8(6): 456-463.
- 41. Hage R, Gautschi F, Steinack C, et al. Combined pulmonary fibrosis and emphysema (CPFE) clinical features and management. Int J Chron Obstruct Pulmon Dis, 2021, 16: 167-177.
- 42. Du Bois RM, Weycker D, Albera C, et al. Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2011, 184(4): 459-466.
- 43. Moll M, Sakornsakolpat P, Shrine N, et al. Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts. Lancet Respir Med, 2020, 8(7): 696-708.
- 44. Lynch DA, Austin JH, Hogg JC, et al. CT-definable subtypes of chronic obstructive pulmonary disease: a statement of the Fleischner Society. Radiology, 2015, 277(1): 192-205.
- 45. Inomata M, Ikushima S, Awano N, et al. An autopsy study of combined pulmonary fibrosis and emphysema: correlations among clinical, radiological, and pathological features. BMC Pulm Med, 2014, 14: 104.
- 46. Cottin V, Cordier JF. Combined pulmonary fibrosis and emphysema in connective tissue disease. Curr Opin Pulm Med, 2012, 18(5): 418-427.
- 47. Cottin V, Brillet PY, Nunes H, et al. [Combined pulmonary fibrosis and emphysema]. Presse Med, 2007, 36(6 Pt 2): 936-944.
- 48. Kinoshita Y, Watanabe K, Ishii H, et al. Distribution of emphysema and fibrosis in idiopathic pulmonary fibrosis with coexisting emphysema. Histopathology, 2019, 74(7): 1103-1108.
- 49. Antoniou KM, Walsh SL, Hansell DM, et al. Smoking-related emphysema is associated with idiopathic pulmonary fibrosis and rheumatoid lung. Respirology, 2013, 18(8): 1191-1196.
- 50. Weiss W. Smoking and pulmonary fibrosis. J Occup Med, 1988, 30(1): 33-39.
- 51. Bellou V, Belbasis L, Evangelou E. Tobacco smoking and risk for pulmonary fibrosis: a prospective cohort study from the UK Biobank. Chest, 2021, 160(3): 983-993.
- 52. Foronjy R, D'armiento J. The effect of cigarette smoke-derived oxidants on the inflammatory response of the lung. Clin Appl Immunol Rev, 2006, 6(1): 53-72.
- 53. Hubbard R, Lewis S, Richards K, et al. Occupational exposure to metal or wood dust and aetiology of cryptogenic fibrosing alveolitis. Lancet, 1996, 347(8997): 284-289.
- 54. Iwai K, Mori T, Yamada N, et al. Idiopathic pulmonary fibrosis. Epidemiologic approaches to occupational exposure. Am J Respir Crit Care Med, 1994, 150(3): 670-675.
- 55. Walsh SL, Wells AU, Sverzellati N, et al. Relationship between fibroblastic foci profusion and high resolution CT morphology in fibrotic lung disease. BMC Med, 2015, 13: 241.
- 56. Kusko RL, Brothers JF, 2nd, Tedrow J, et al. Integrated genomics reveals convergent transcriptomic networks underlying chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. Am J Respir Crit Care Med, 2016, 194(8): 948-960.
- 57. Halu A, Liu SK, Baek SH, et al. Exploring the cross-phenotype network region of disease modules reveals concordant and discordant pathways between chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis. Hum Mol Genet, 2019, 28(14): 2352-2364.
- 58. Collum SD, Molina JG, Hanmandlu A, et al. Adenosine and hyaluronan promote lung fibrosis and pulmonary hypertension in combined pulmonary fibrosis and emphysema. Dis Model Mech, 2019, 12(5): dmm038711.
- 59. Lundblad LK, Thompson-Figueroa J, Leclair T, et al. Tumor necrosis factor-α overexpression in lung disease: a single cause behind a complex phenotype. Am J Respir Crit Care Med, 2005, 171(12): 1363-1370.
- 60. Houghton AM. Matrix metalloproteinases in destructive lung disease. Matrix Biol, 2015, 44-46: 167-174.
- 61. Pardo A, Cabrera S, Maldonado M, et al. Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis. Respir Res, 2016, 17: 23.
- 62. Mattey DL, Nixon NB, Dawes PT. Association of circulating levels of MMP-8 with mortality from respiratory disease in patients with rheumatoid arthritis. Arthritis Res Ther, 2012, 14(5): R204.
- 63. Andersen GN, Nilsson K, Pourazar J, et al. Bronchoalveolar matrix metalloproteinase 9 relates to restrictive lung function impairment in systemic sclerosis. Respir Med, 2007, 101(10): 2199-2206.
- 64. Rogliani P, Mura M, Mattia P, et al. HRCT and histopathological evaluation of fibrosis and tissue destruction in IPF associated with pulmonary emphysema. Respir Med, 2008, 102(12): 1753-1761.
- 65. Roake CM, Artandi SE. Control of cellular aging, tissue function, and cancer by p53 downstream of telomeres. Cold Spring Harb Perspect Med, 2017, 7(5): a026088.
- 66. Alder JK, Chen JJ, Lancaster L, et al. Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proc Natl Acad Sci U S A, 2008, 105(35): 13051-13056.
- 67. Cronkhite JT, Xing C, Raghu G, et al. Telomere shortening in familial and sporadic pulmonary fibrosis. Am J Respir Crit Care Med, 2008, 178(7): 729-737.
- 68. Alder JK, Guo N, Kembou F, et al. Telomere length is a determinant of emphysema susceptibility. Am J Respir Crit Care Med, 2011, 184(8): 904-912.
- 69. Tsuji T, Aoshiba K, Nagai A. Alveolar cell senescence in patients with pulmonary emphysema. Am J Respir Crit Care Med, 2006, 174(8): 886-893.
- 70. Povedano JM, Martinez P, Flores JM, et al. Mice with pulmonary fibrosis driven by telomere dysfunction. Cell Rep, 2015, 12(2): 286-299.
- 71. Wijsenbeek M, Cottin V. Spectrum of fibrotic lung diseases. N Engl J Med, 2020, 383(10): 958-968.
- 72. Cottin V, Bonniaud P, Cadranel J, et al. French practical guidelines for the diagnosis and management of idiopathic pulmonary fibrosis - 2021 update. Full-length version. Respir Med Res, 2023, 83: 100948.
- 73. Wongkarnjana A, Scallan C, Kolb MRJ. Progressive fibrosing interstitial lung disease: treatable traits and therapeutic strategies. Curr Opin Pulm Med, 2020, 26(5): 436-442.
- 74. Agusti A, Bel E, Thomas M, et al. Treatable traits: toward precision medicine of chronic airway diseases. Eur Respir J, 2016, 47(2): 410-419.
- 75. Dong FS, Zhang YM, Chi FZ, et al. Clinical efficacy and safety of ICS/LABA in patients with combined idiopathic pulmonary fibrosis and emphysema. Int J Clin Exp Med, 2015, 8(6): 8617-8625.
- 76. Flaherty KR, Wells AU, Cottin V, et al. Nintedanib in progressive fibrosing interstitial lung diseases. N Engl J Med, 2019, 381(18): 1718-1727.
- 77. Cottin V, Azuma A, Raghu G, et al. Therapeutic effects of nintedanib are not influenced by emphysema in the INPULSIS trials. Eur Respir J, 2019, 53(4): 1801655.
- 78. Jankowich MD, Rounds SIS. Combined pulmonary fibrosis and emphysema syndrome: a review. Chest, 2012, 141(1): 222-231.
- 79. Jiang CG, Fu Q, Zheng CM. Prognosis of combined pulmonary fibrosis and emphysema: comparison with idiopathic pulmonary fibrosis alone. Ther Adv Respir Dis, 2019, 13: 1753466619888119.
- 80. Jacob J, Bartholmai BJ, Rajagopalan S, et al. Functional and prognostic effects when emphysema complicates idiopathic pulmonary fibrosis. Eur Respir J, 2017, 50(1): 1700379.
- 81. Zhao A, Gudmundsson E, Mogulkoc N, et al. Mortality in combined pulmonary fibrosis and emphysema patients is determined by the sum of pulmonary fibrosis and emphysema. ERJ Open Res, 2021, 7(3): 00316-2021.
- 82. Jacob J, Bartholmai BJ, Rajagopalan S, et al. Predicting outcomes in idiopathic pulmonary fibrosis using automated computed tomographic analysis. Am J Respir Crit Care Med, 2018, 198(6): 767-776.
- 83. Zantah M, Dotan Y, Dass C, et al. Acute exacerbations of COPD versus IPF in patients with combined pulmonary fibrosis and emphysema. Respir Res, 2020, 21(1): 164.
-
Previous Article
脓毒症相关性急性呼吸窘迫综合征生物标志物研究进展 -
Next Article
肺泡上皮细胞与新型冠状病毒肺炎后肺纤维化的关系研究进展