Interstitial lung disease in patients with systemic scleroderma: approaches to predicting lesion volume
https://doi.org/10.17650/1818-8338-2023-17-3-K684
Abstract
Aim. To determine the factors that contribute to the prediction of the volume of pulmonary lesion in patients with systemic scleroderma (SSc).
Materials and methods. The analysis included patients with SSc observed in the Registry of Myositis, systemic sclerosis and mixed connective tissue disease (REMISSIS), who underwent high-resolution computed tomography (HRCT) of the lungs. For the immunological characteristic, all patients were tested for anti-topoisomerase (anti-Scl-70), and anti-centromeric (anti-CENP-B) antibodies, and anticentromere antibodies (anti-Pm-Scl).
Results. The study included 79 patients with SSc. There was 94.9 % women. Average age – 64.4 ± 11.5 years. Signs of interstitial lung disease (ILD), according to HRCT were detected in 50 patients. The largest extent of lung injury was noted in patients with SSc sine scleroderma (32.7 ± 29.3 %), a smaller extent in patients with diffuse form SSc (16.9 ± 17.1 %) and the lowest in patients with limited SSc (8.5 ± 14.2 %). In addition to the type of disease, the extent of lung injury in patients with SSc-ILD was statistically significantly higher in patients with arthralgia, dyspnea and the presence of antibodies to topoisomerase I and combined autoantibodies. Also, a statistically significant feedback was established with all indicators of the test with a 6-minute walk and forced vital capacity and a direct relationship with indicators of pulmonary artery systolic pressure. When evaluating the correlation between the extent of lung injury and the degree of dyspnea according to Borg, it was found that in patients who assessed dyspnea less than 3 points, the extent of lung injury was less than 25 %. Due to the high degree of correlation, a regression formula was created for the dependence of the extent of lung injury on the distance in the test with a 6-minute walk: extent of lung injury = (52.7–0.1) × distance 6MWT. A multivariate model was also obtained for predicting the extent of lung injury in SSc, in which the patient’s immunotype, distance in the 6-minute walk test, saturation after the 6-minute walk test, and the presence of dyspnea became the most effective.
About the Authors
D. V. KhorolskyRussian Federation
1 Ostrovityanov St., Moscow 117997
A. A. Klimenko
Russian Federation
1 Ostrovityanov St., Moscow 117997
E. S. Pershina
Russian Federation
Bld 2, 8 Trubetskaya St., Moscow 119991
N. M. Babadaeva
Russian Federation
1 Ostrovityanov St., Moscow 117997
A. A. Kondrashov
Russian Federation
1 Ostrovityanov St., Moscow 117997
N. A. Shostak
Russian Federation
1 Ostrovityanov St., Moscow 117997
E. P. Mikheeva
Russian Federation
1 Ostrovityanov St., Moscow 117997
M. P. Mezenova
Russian Federation
14 Plyushchikha St., Moscow 119121
E. V. Zhilyaev
Russian Federation
1 Ostrovityanov St., Moscow 117997
35 Schepkina St., Moscow 129090
2 / 1 Barricadnaya St., Moscow 125993
References
1. Bergamasco A., Hartmann N., Wallace L., Verpillat P. Epidemiology of systemic sclerosis and systemic sclerosis-associated interstitial lung disease. Clin Epidemiol 2019;11:257–3. DOI: 10.2147/CLEP.S191418
2. Tyndall A.J., Bannert B., Vonk M. et al. Causes and risk factors for death in systemic sclerosis: a study from the EULAR Scleroderma Trials and Research (EUSTAR) database. Ann Rheum Dis 2010;69(10):1809–15. DOI: 10.1136/ard.2009.114264
3. Raghu G., Remy-Jardin M., Richeldi L. et al. Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline. Am J Respir Crit Care Med 2022;205(9):e18– 47. doi:10.1164/rccm.202202-0399ST
4. Avdeev S.N., Chikina S.Yu., Tyurin I.E. et al. Chronic fibrosing progressing interstitial lung disease: a decision of Multidisciplinary Expert Board. Pul`monologiya = Pulmonology 2021;31(4):505–10. (In Russ.). DOI: 10.18093/0869-0189-2021-31-4-505-510
5. Dvornikov A.S., Khamaganova I.V., Skrlpkin Yu.K., Bogush P.G. The present-day approaches to localized scleroderma therapy. Vestnik Dermatologii i Venerologii = Bulletin of Dermatology and Venereology 2013;(3):96–100. (In Russ.).
6. Khorolsky D.V., Klimenko A.A., Pershina E.S. et al. Ways to predict interstitial lung disease in patients with systemic sclerosis: results of an observational study. Sovremennaya revmatologiya = Modern Rheumatology Journal 2023;17(4):57–63. (In Russ.). DOI: 10.14412/1996-7012-2023-4-57-63
7. Distler O., Assassi S., Cottin V. et al. Predictors of progression in systemic sclerosis patients with interstitial lung disease. Eur Respir J 2020;55(5):1902026. DOI: 10.1183/13993003.02026-2019
8. Le Gouellec N., Duhamel A., Perez T. et al. Predictors of lung function test severity and outcome in systemic sclerosis-associated interstitial lung disease. PloS One 2017;12(8):e0181692. DOI: 10.1371/journal.pone.0181692
9. Vandecasteele E., De Pauw M., De Keyser F. et al. Six-minute walk test in systemic sclerosis: A systematic review and meta-analysis. Int J Cardiol 2016;212:265–73. DOI: 10.1016/j.ijcard.2016.03.084
10. Van den Hoogen F., Khanna D., Fransen J. et al. 2013 classification criteria for systemic sclerosis: an American College of Rheumatology / European League against Rheumatism collaborative initiative. Arthritis Rheum 2013;65(11):2737–47. DOI: 10.1002/art.38098
11. Holland A.E., Spruit M.A., Troosters T. et al. An official European Respiratory Society / American Thoracic Society technical standard: field walking tests in chronic respiratory disease. Eur Respir J 2014;44(6):1428–46. doi:10.1183/09031936.00150314
12. Graham B.L., Steenbruggen I., Miller M.R. et al. Standardization of Spirometry 2019 Update. An Official American Thoracic Society and European Respiratory Society Technical Statement. Am J Respir Crit Care Med 2019;200(8):e70–e88. doi:10.1164/rccm.201908-1590ST
13. Wittram C., Mark E.J., McLoud T.C. CT-histologic correlation of the ATS/ERS 2002 classification of idiopathic interstitial pneumonias. Radiographics 2003;23(5):1057–71. DOI: 10.1148/rg.235035702
14. Nihtyanova S.I., Schreiber B.E., Ong V.H. et al. Prediction of pulmonary complications and long-term survival in systemic sclerosis. Arthritis Rheumatol 2014;66(6):1625–35. DOI: 10.1002/art.38390
15. Savarino E., Bazzica M., Zentilin P. et al. Gastroesophageal reflux and pulmonary fibrosis in scleroderma: a study using pHimpedance monitoring. Am J Respir Crit Care Med 2009;179(5):408–13. DOI: 10.1164/rccm.200808-1359OC
16. Assassi S., Sharif R., Lasky R.E. et al. Predictors of interstitial lung disease in early systemic sclerosis: a prospective longitudinal study of the GENISOS cohort. Arthritis Res Ther 2010;12(5):R166. DOI: 10.1186/ar3125
Review
For citations:
Khorolsky D.V., Klimenko A.A., Pershina E.S., Babadaeva N.M., Kondrashov A.A., Shostak N.A., Mikheeva E.P., Mezenova M.P., Zhilyaev E.V. Interstitial lung disease in patients with systemic scleroderma: approaches to predicting lesion volume. The Clinician. 2023;17(3):31-41. (In Russ.) https://doi.org/10.17650/1818-8338-2023-17-3-K684