Predictors of mortality in rheumatoid arthritis-associated interstitial lung disease. Issue 2 (19th November 2015)

• Record Type: Journal Article
• Authors: Solomon, Joshua J.; Chung, Jonathan H.; Cosgrove, Gregory P.; Demoruelle, M. Kristen; Fernandez-Perez, Evans R.; Fischer, Aryeh; Frankel, Stephen K.; Hobbs, Stephen B.; Huie, Tristan J.; Ketzer, Jill; Mannina, Amar; Olson, Amy L.; Russell, Gloria; Tsuchiya, Yutaka; Yunt, Zulma X.; Zelarney, Pearlanne T.; Brown, Kevin K.; Swigris, Jeffrey J.
• Is Part Of: European respiratory journal. Volume 47:Issue 2(2016)
• Page Start: 588
• Page End: 596
• Publication Date: 2015-11-19
• Subjects: Respiratory organs -- Diseases -- Periodicals; Respiration -- Periodicals; 616.2
• DOI: 10.1183/13993003.00357-2015
• Languages: English
• ISSNs: 0903-1936

Abstract

Interstitial lung disease (ILD) is a common pulmonary manifestation of rheumatoid arthritis. There is lack of clarity around predictors of mortality and disease behaviour over time in these patients. We identified rheumatoid arthritis-related interstitial lung disease (RA-ILD) patients evaluated at National Jewish Health (Denver, CO, USA) from 1995 to 2013 whose baseline high-resolution computed tomography (HRCT) scans showed either a nonspecific interstitial pneumonia (NSIP) or a "definite" or "possible" usual interstitial pneumonia (UIP) pattern. We used univariate, multivariate and longitudinal analytical methods to identify clinical predictors of mortality and to model disease behaviour over time. The cohort included 137 subjects; 108 had UIP on HRCT (RA-UIP) and 29 had NSIP on HRCT (RA-NSIP). Those with RA-UIP had a shorter survival time than those with RA-NSIP (log rank p=0.02). In a model controlling for age, sex, smoking and HRCT pattern, a lower baseline % predicted forced vital capacity (FVC % pred) (HR 1.46; p<0.0001) and a 10% decline in FVC % pred from baseline to any time during follow up (HR 2.57; p<0.0001) were independently associated with an increased risk of death. Data from this study suggest that in RA-ILD, disease progression and survival differ between subgroups defined by HRCT pattern; however, when controlling for potentially influential variables, pulmonary physiology, but not HRCT pattern, independently predicts mortality. In rheumatoid-arthritis associated interstitial lung disease, physiology, and not HRCT pattern, predicts mortality http://ow.ly/Uf1IF