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Primary respiratory disease in patients with systemic lupus erythematosus: data from the Spanish rheumatology society lupus registry (RELESSER) cohort
Authors:Javier?Narváez  Helena?Borrell  Fernando?Sánchez-Alonso  I?igo?Rúa-Figueroa  Francisco?Javier?López-Longo  María?Galindo-Izquierdo  Jaime?Calvo-Alén  Antonio?Fernández-Nebro  Alejandro?Olivé  José?Luis?Andreu  Víctor?Martínez-Taboada  Joan?Miquel?Nolla  José?María?Pego-Reigosa
Affiliation:1.Department of Rheumatology (Planta 10-2), Servicio de Reumatología,Hospital Universitario de Bellvitge,Barcelona,Spain;2.Unidad de Investigación, Sociedad Espa?ola de Reumatología,Madrid,Spain;3.Hospital Universitario Doctor Negrín,Las Palmas de,Spain;4.Hospital Universitario Gregorio Mara?ón,Madrid,Spain;5.Hospital Universitario 12 de Octubre,Madrid,Spain;6.Hospital Universitario Araba,Vitoria,Spain;7.Hospital Universitario de Málaga,Málaga,Spain;8.Hospital Germans Trias i Pujol,Barcelona,Spain;9.Hospital Universitario Puerta de Hierro,Madrid,Spain;10.Hospital Universitario Marqués de Valdecilla,Santander,Spain;11.Complexo Hospitalario Universitario de Vigo,Vigo,Spain
Abstract:

Background

The purpose of this study was to assess the prevalence, associated factors, and impact on mortality of primary respiratory disease in a large systemic lupus erythematosus (SLE) retrospective cohort.

Methods

All adult patients in the RELESSER-TRANS (Registry of Systemic Lupus Erythematosus Patients of the Spanish Society of Rheumatology [SER], cross-sectional phase) registry were retrospectively investigated for the presence of primary pleuropulmonary manifestations.

Results

In total 3215 patients were included. At least one pleuropulmonary manifestation was present in 31% of patients. The most common manifestation was pleural disease (21%), followed by lupus pneumonitis (3.6%), pulmonary thromboembolism (2.9%), primary pulmonary hypertension (2.4%), diffuse interstitial lung disease (2%), alveolar hemorrhage (0.8%), and shrinking lung syndrome (0.8%).In the multivariable analysis, the variables associated with the development of pleuropulmonary manifestation were older age at disease onset (odds ratio (OR) 1.03, 95% confidence interval (CI) 1.02–1.04), higher SLEDAI (Systemic Lupus Erythematosus Disease Activity Index) scores (OR 1.03, 95% CI 1.00–1.07), the presence of Raynaud’s phenomenon (OR 1.41, 95% CI 1.09–1.84), secondary antiphospholipid syndrome (OR 2.20, 95% CI 1.63–2.97), and the previous or concomitant occurrence of severe lupus nephritis, (OR 1.48, 95% CI 1.12–1.95) neuropsychiatric manifestations (OR 1.49, 95% CI 1.11–2.02), non-ischemic cardiac disease (OR 2.91, 95% CI 1.90–4.15), vasculitis (OR 1.81, 95% CI 1.25–2.62), hematological manifestations (OR 1.31, 95% CI 1.00–1.71), and gastrointestinal manifestations, excluding hepatitis (OR 2.05, 95% CI 1.14–3.66). Anti-RNP positivity had a clear tendency to significance (OR 1.32, 95% CI 1.00–1.75; P = 0.054).The development of pleuropulmonary manifestations independently contributes to a diminished survival (hazard ratio of 3.13). However, not all complications will influence the prognosis in the same way. Whereas the occurrence of pleural disease or pulmonary thromboembolism has a minimal impact on the survival of these patients, the remaining manifestations have a major impact on mortality.

Conclusion

Except for pleural disease, the remaining respiratory manifestations are very uncommon in SLE (<4%). Pleuropulmonary manifestations independently contributed to a decreased survival in these patients.
Keywords:
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