The Association Between Age at Diagnosis and Disease Characteristics and Damage in Patients With ANCA‐Associated Vasculitis

Author:

Bloom Jessica L.1ORCID,Pickett‐Nairn Kaci1,Silveira Lori1,Fuhlbrigge Robert C.1,Cuthbertson David2,Akuthota Praveen3,Corbridge Thomas C.4,Khalidi Nader A.5,Koening Curry L.6,Langford Carol A.7,McAlear Carol A.8,Monach Paul A.9ORCID,Moreland Larry W.1,Pagnoux Christian10,Rhee Rennie L.8ORCID,Seo Philip11,Silver Jared4,Specks Ulrich12,Warrington Kenneth J.12,Wechsler Michael E.13,Merkel Peter A.8ORCID,

Affiliation:

1. University of Colorado Denver

2. University of South Florida Tampa

3. University of California San Diego La Jolla

4. US Medical Affairs‐Respiratory GSK Durham North Carolina

5. St. Joseph's Healthcare Hamilton McMaster University Ontario Canada

6. University of Utah Salt Lake City

7. Cleveland Clinic Cleveland Ohio

8. University of Pennsylvania Philadelphia

9. Brigham and Women's Hospital Boston Massachusetts

10. Mount Sinai Hospital Toronto Canada

11. Johns Hopkins University Baltimore Maryland

12. Mayo Clinic Rochester Minnesota

13. National Jewish Health Denver Colorado

Abstract

ObjectiveThis study examined the relationship between age at diagnosis and disease characteristics and damage in patients with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV).MethodsAnalysis of a prospective longitudinal cohort of patients with granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic GPA (EGPA) in the Vasculitis Clinical Research Consortium (2013–2021). Disease cohorts were divided by age at diagnosis (years): children (<18), young adults (18–40), middle‐aged adults (41–65), and older adults (>65). Data included demographics, ANCA type, clinical characteristics, Vasculitis Damage Index (VDI) scores, ANCA Vasculitis Index of Damage (AVID) scores, and novel disease‐specific and non‐disease‐specific damage scores built from VDI and AVID items.ResultsAnalysis included data from 1020 patients with GPA/MPA and 357 with EGPA. Female predominance in GPA/MPA decreased with age at diagnosis. AAV in childhood was more often GPA and proteinase 3‐ANCA positive. Children with GPA/MPA experienced more subglottic stenosis and alveolar hemorrhage; children and young adults with EGPA experienced more alveolar hemorrhage, need for intubation, and gastrointestinal involvement. Older adults (GPA/MPA) had more neurologic manifestations. After adjusting for disease duration, medications, tobacco, and ANCA, all damage scores increased with age at diagnosis for GPA/MPA (P < 0.001) except the disease‐specific damage score, which did not differ (P = 0.44). For EGPA, VDI scores increased with age at diagnosis (P < 0.009), whereas all other scores were not significantly different.ConclusionAge at diagnosis is associated with clinical characteristics in AAV. Although VDI and AVID scores increase with age at diagnosis, this is driven by non‐disease‐specific damage items.image

Funder

GlaxoSmithKline

National Center for Advancing Translational Sciences

National Center for Research Resources

National Institute of Arthritis and Musculoskeletal and Skin Diseases

Vasculitis Foundation

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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