Risk prediction model in rheumatoid arthritis-associated interstitial lung disease

被引:29
|
作者
Kim, Ho Cheol [1 ]
Lee, Jeong Seok [2 ]
Lee, Eun Young [2 ]
Ha, You-Jung [3 ]
Chae, Eun Jin [4 ]
Han, Minkyu [5 ]
Cross, Gary [6 ]
Barnett, Joseph [7 ]
Joseph, Jacob [8 ,9 ]
Song, Jin Woo [1 ]
机构
[1] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Pulm & Crit Care Med, 88,Olymp Ro 43 Gil, Seoul 05505, South Korea
[2] Seoul Natl Univ, Dept Internal Med, Div Rheumatol, Coll Med, Seoul, South Korea
[3] Seoul Natl Univ, Dept Internal Med, Div Rheumatol, Bundang Hosp, Seongnam, South Korea
[4] Univ Ulsan, Asan Med Ctr, Dept Radiol, Coll Med, Seoul, South Korea
[5] Asan Med Ctr, Clin Epidemiol & Biostat, Seoul, South Korea
[6] Royal Free London NHS Fdn Trust, Royal Free Hosp, Dept Radiol, London, England
[7] Royal Brompton & Hare Field NHS Fdn Trust, Royal Brompton Hosp, Dept Radiol, London, England
[8] UCL, Dept Resp Med, London, England
[9] UCL, Ctr Med Image Comp, London, England
基金
新加坡国家研究基金会;
关键词
diagnostic; interstitial lung disease; imaging; prognosis; rheumatoid arthritis; COMBINED PULMONARY-FIBROSIS; CLINICAL-FEATURES; EMPHYSEMA; PNEUMONIA; MORTALITY; SURVIVAL; STANDARDIZATION; SOCIETY;
D O I
10.1111/resp.13848
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background and objective RA-ILD has a variable clinical course, and its prognosis is difficult to predict. Moreover, risk prediction models for prognosis remain undefined. Methods The prediction model was developed using retrospective data from 153 patients with RA-ILD and validated in an independent RA-ILD cohort (n = 149). Candidate variables for the prediction models were screened using a multivariate Cox proportional hazard model. C-statistics were calculated to assess and compare the predictive ability of each model. Results In the derivation cohort, the median follow-up period was 54 months, and 38.6% of the subjects exhibited a UIP pattern on HRCT imaging. In multivariate Cox analysis, old age (>= 60 years, HR: 2.063), high fibrosis score (>= 20% of the total lung extent, HR: 4.585), a UIP pattern (HR: 1.899) and emphysema (HR: 2.596) on HRCT were significantly poor prognostic factors and included in the final model. The prediction model demonstrated good performance in the prediction of 5-year mortality (C-index: 0.780, P < 0.001); furthermore, patients at risk were divided into three groups with 1-year mortality rates of 0%, 5.1% and 24.1%, respectively. Predicted and observed mortalities at 1, 2 and 3 years were similar in the derivation cohort, and the prediction model was also effective in predicting prognosis of the validation cohort (C-index: 0.638, P < 0.001). Conclusion Our results suggest that a risk prediction model based on HRCT variables could be useful for patients with RA-ILD.
引用
收藏
页码:1257 / 1264
页数:8
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