Progressive Decline of Lung Function in Rheumatoid Arthritis-Associated Interstitial Lung Disease.
Progressive Decline of Lung Function in Rheumatoid Arthritis-Associated Interstitial Lung Disease.
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DOI:
10.1002/art.39971
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发表时间:
2017-03
期刊:
影响因子:
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通讯作者:
Matteson EL
中科院分区:
文献类型:
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作者:
Zamora-Legoff JA;Krause ML;Crowson CS;Ryu JH;Matteson EL
Interstitial lung disease (ILD) is associated with substantial morbidity in rheumatoid arthritis (RA), but very little is known about its long-term progression. All patients with RA-ILD seen at Mayo Clinic in 1998-2014 with at least 4 weeks follow-up and at least 1 pulmonary function test (PFT) were identified and manually screened for study inclusion. Progression was defined as a diffusing capacity for carbon monoxide (DLCO) <40% predicted or too ill to perform, or a forced vital capacity (FVC) <50% predicted. Time to progression was analyzed using Kaplan-Meier methods. Of 167 included patients, 81 (49%) were female with mean age of 67 years (standard deviation: 10) at ILD diagnosis. Median follow-up time from ILD diagnosis was 3.3 (range: 0.01-14.8) years. A third of patients required supplemental oxygen, 40% developed DLCO <40% predicted and 22% developed FVC <50% predicted by 5 years after ILD diagnosis. Risk factors for DLCO progression were usual interstitial pneumonia (UIP) vs. nonspecific interstitial pneumonia (NSIP) (hazard ratio [HR]: 3.29; 95% confidence interval [CI]: 1.28, 8.41). Lower percent predicted DLCO and FVC at baseline increased the risk for progression to DLCO <40% and FVC<50% predicted, and higher rates of change in the first 6 months also increased the risk of progression. Progressive loss of pulmonary function is common in RA-ILD and worse in patients with UIP than NSIP. Predictors of progression in patients with RA-ILD may aid clinicians in identifying patients at highest risk for progression of ILD.