Back to Search Start Over

Clinical differences among patients with myeloperoxidase–antineutrophil cytoplasmic antibody–positive interstitial lung disease.

Authors :
Yamaguchi, Koichi
Yamaguchi, Aya
Ito, Masashi
Wakamatsu, Ikuo
Itai, Miki
Muto, Sohei
Uno, Shogo
Aikawa, Masaki
Kouno, Shunichi
Takemura, Masao
Yatomi, Masakiyo
Aoki-Saito, Haruka
Koga, Yasuhiko
Hara, Kenichiro
Motegi, Shinsuke
Tsukida, Mayuko
Ota, Fumie
Tsukada, Yoshito
Motegi, Mitsuru
Nakasatomi, Masao
Source :
Clinical Rheumatology; Feb2023, Vol. 42 Issue 2, p479-488, 10p
Publication Year :
2023

Abstract

Introduction: Patients with antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis and idiopathic interstitial lung diseases (IIPs) are positive for myeloperoxidase (MPO)–ANCA. MPO–ANCA-positive vasculitis mainly comprises microscopic polyangiitis (MPA) and unclassifiable vasculitis. These diseases are frequently complicated by interstitial lung disease (ILD). Few studies have reported the clinical differences between the subtypes of MPO–ANCA-positive ILD. Therefore, this study aimed to examine the clinical findings and courses of MPO–ANCA-positive ILD. Method: This retrospective study enrolled 100 patients with MPO–ANCA-positive ILD who were categorized into three groups: MPA (n = 44), unclassifiable vasculitis (n = 29), and IIP (n = 27). Our study compared the clinical findings and prognosis of these patients and analyzed the poor prognostic factors. Furthermore, we assessed the association between the patients with and without acute exacerbation of ILD (AE-ILD). Results: Our study found clinical differences in serum markers, clinical symptoms, and treatment regimens among the three groups. ILD complications, as the main cause of death, differed among the three groups (P = 0.04). Patients with unclassifiable vasculitis showed higher survival rates than those with IIP (P = 0.046). Patients with AE-ILD showed fewer general symptoms (P = 0.02) and lower survival rates (P < 0.01) than those without AE-ILD. In multivariate analysis, AE-ILD development was a strong poor prognostic factor for MPO–ANCA-positive ILD. Conclusions: The subtypes of MPO–ANCA-positive ILD have different clinical features and prognoses. Patients who develop AE-ILD require careful evaluation of clinical courses. Key Points • In myeloperoxidase (MPO)–antineutrophil cytoplasmic antibody (ANCA)–positive interstitial lung disease (ILD), patients with unclassifiable vasculitis showed a better prognosis than those with idiopathic ILD.. • Development of acute exacerbation in ILD was a strong poor prognostic factor in patients with MPO–ANCA-positive ILD.. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07703198
Volume :
42
Issue :
2
Database :
Complementary Index
Journal :
Clinical Rheumatology
Publication Type :
Academic Journal
Accession number :
161486763
Full Text :
https://doi.org/10.1007/s10067-022-06388-5