Subglottic stenosis and endobronchial disease in granulomatosis with polyangiitis

Author:

Quinn Kaitlin A12,Gelbard Alexander3,Sibley Cailin4,Sirajuddin Arlene5,Ferrada Marcela A2,Chen Marcus5,Cuthbertson David6,Carette Simon7,Khalidi Nader A8,Koening Curry L9,Langford Carol A10,McAlear Carol A11,Monach Paul A12,Moreland Larry W13,Pagnoux Christian7,Seo Philip14,Specks Ulrich15,Sreih Antoine G11,Ytterberg Steven R16,Merkel Peter A17,Grayson Peter C2

Affiliation:

1. Division of Rheumatology, MedStar Georgetown University Hospital, Washington, DC, USA

2. Systemic Autoimmunity Branch, National Institutes of Health, NIAMS, Bethesda, MD, USA

3. Department of Otolaryngology – Head and Neck Surgery, Vanderbilt University, Nashville, TN, USA

4. Division of Arthritis & Rheumatic Diseases, Oregon Health & Science University, Portland, OR, USA

5. National Institutes of Health, NHLBI, Bethesda, MD, USA

6. Biostatistics and Informatics, University of South Florida, Tampa, FL, USA

7. Division of Rheumatology, Mount Sinai Hospital, Toronto, Canada

8. Division of Rheumatology, McMaster University, Hamilton, ON, Canada

9. Division of Rheumatology, University of Utah, Salt Lake City, UT, USA

10. Department of Rheumatic and Immunologic Diseases, Cleveland Clinic, Cleveland, OH, USA

11. Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, USA

12. Division of Rheumatology, Brigham and Women’s Hospital, Boston, MA, USA

13. Division of Rheumatology, University of Pittsburgh, Pittsburgh, PA, USA

14. Division of Rheumatology, Johns Hopkins University, Baltimore, MD, USA

15. Division of Pulmonary and Critical Care Medicine, MN, USA

16. Division of Rheumatology, Mayo Clinic College of Medicine, Rochester, MN, USA

17. Division of Rheumatology and Department of Biostatistics, Epidemiology, and Informatics, University of Pennsylvania, Philadelphia, PA, USA

Abstract

Abstract Objectives To describe tracheobronchial disease in patients with granulomatosis with polyangiitis (GPA) and evaluate the utility of dynamic expiratory CT to detect large-airway disease. Methods Demographic and clinical features associated with the presence of subglottic stenosis (SGS) or endobronchial involvement were assessed in a multicentre, observational cohort of patients with GPA. A subset of patients with GPA from a single-centre cohort underwent dynamic chest CT to evaluate the airways. Results Among 962 patients with GPA, SGS and endobronchial disease were identified in 95 (10%) and 59 (6%) patients, respectively. Patients with SGS were more likely to be female (72% vs 53%, P < 0.01), younger at time of diagnosis (36 vs 49 years, P < 0.01), and have saddle-nose deformities (28% vs 10%, P < 0.01), but were less likely to have renal involvement (39% vs 62%, P < 0.01). Patients with endobronchial disease were more likely to be PR3-ANCA positive (85% vs 66%, P < 0.01), with more ENT involvement (97% vs 77%, P < 0.01) and less renal involvement (42% vs 62%, P < 0.01). Disease activity in patients with large-airway disease was commonly isolated to the subglottis/upper airway (57%) or bronchi (32%). Seven of 23 patients screened by dynamic chest CT had large-airway pathology, including four patients with chronic, unexplained cough, discovered to have tracheobronchomalacia. Conclusion SGS and endobronchial disease occur in 10% and 6% of patients with GPA, respectively, and may occur without disease activity in other organs. Dynamic expiratory chest CT is a potential non-invasive screening test for large-airway involvement in GPA.

Funder

AbbVie

NIH

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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