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Clinical Characteristics of EGPA Patients in Comparison to GPA Subgroup with Increased Blood Eosinophilia from POLVAS Registry.
- Source :
-
Journal of immunology research [J Immunol Res] 2024 Apr 25; Vol. 2024, pp. 4283928. Date of Electronic Publication: 2024 Apr 25 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Objective: To characterize the eosinophilic granulomatosis with polyangiitis (EGPA) population from the POLVAS registry depending on ANCA status and diagnosis onset, including their comparison with the granulomatosis with polyangiitis (GPA) subset with elevated blood eosinophilia (min. 400/ μ l) (GPA HE) to develop a differentiating strategy.<br />Methods: A retrospective analysis of the POLVAS registry.<br />Results: The EGPA group comprised 111 patients. The ANCA-positive subset ( n = 45 [40.54%]) did not differ from the ANCA-negative one in clinics. Nevertheless, cardiovascular manifestations were more common in ANCA-negative patients than in those with anti-myeloperoxidase (MPO) antibodies (46.97% vs. 26.92%, p = 0.045). Patients diagnosed before 2012 ( n = 70 [63.06%]) were younger (median 41 vs. 49 years, p < 0.01), had higher blood eosinophilia at diagnosis (median 4,946 vs. 3,200/ μ l, p < 0.01), and more often ear/nose/throat (ENT) and cardiovascular involvement. GPA HE comprised 42 (13.00%) out of 323 GPA cases with reported blood eosinophil count. Both GPA subsets had a lower prevalence of respiratory, cardiovascular, and neurologic manifestations but more often renal and ocular involvement than EGPA. EGPA also had cutaneous and gastrointestinal signs more often than GPA with normal blood eosinophilia (GPA NE) but not GPA HE. The model differentiating EGPA from GPA HE, using ANCA status and clinical manifestations, had an AUC of 0.92, sensitivity of 96%, and specificity of 95%.<br />Conclusion: Cardiovascular symptoms were more prevalent in the ANCA-negative subset than in the MPO-ANCA-positive one. Since EGPA and GPE HE share similarities in clinics, diagnostic misleading may result in an inappropriate therapeutic approach. Further studies are needed to optimize their differentiation and tailored therapy, including biologics.<br />Competing Interests: All authors have declared no conflicts of interest.<br /> (Copyright © 2024 Anna Drynda et al.)
- Subjects :
- Humans
Male
Middle Aged
Female
Adult
Retrospective Studies
Granulomatosis with Polyangiitis diagnosis
Granulomatosis with Polyangiitis immunology
Aged
Churg-Strauss Syndrome diagnosis
Churg-Strauss Syndrome immunology
Churg-Strauss Syndrome epidemiology
Peroxidase immunology
Eosinophils immunology
Registries
Eosinophilia diagnosis
Eosinophilia immunology
Eosinophilia blood
Antibodies, Antineutrophil Cytoplasmic blood
Antibodies, Antineutrophil Cytoplasmic immunology
Subjects
Details
- Language :
- English
- ISSN :
- 2314-7156
- Volume :
- 2024
- Database :
- MEDLINE
- Journal :
- Journal of immunology research
- Publication Type :
- Academic Journal
- Accession number :
- 38699219
- Full Text :
- https://doi.org/10.1155/2024/4283928