Evidence map›Paper›PMID 36979755›Full record

ArticleBiomedicines2023

EGPA Phenotyping: Not Only ANCA, but Also Eosinophils.

Andrea Matucci, Emanuele Vivarelli, Margherita Perlato, Valentina Mecheri, Matteo Accinno, Lorenzo Cosmi, Paola Parronchi, Oliviero Rossi, Alessandra Vultaggio

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Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.4field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  8. Article
  9. Article
  10. Immunological Markers Associated with Skin Manifestations of EGPA.International journal of molecular sciences · 2025
    Observational
  11. Review
  12. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Andrea MatucciImmunoallergology Unit, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy.
Emanuele VivarelliImmunology and Cellular Therapy Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.
Margherita PerlatoImmunology and Cellular Therapy Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.
Valentina MecheriImmunology and Cellular Therapy Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.
Matteo AccinnoImmunoallergology Unit, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy.
Lorenzo CosmiImmunoallergology Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0002-8150-8177
Paola ParronchiImmunology and Cellular Therapy Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.ORCID 0000-0002-9184-5089
Oliviero RossiImmunoallergology Unit, Careggi University Hospital, Largo Brambilla 3, 50134 Florence, Italy.
Alessandra VultaggioImmunoallergology Unit, Department of Experimental and Clinical Medicine, Careggi University Hospital, 50134 Florence, Italy.
Azienda Ospedaliero-Universitaria Careggi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEosinophilic Granulomatosis with Polyangiitis (EGPA) is a small-vessel necrotizing vasculitis. The anti-neutrophil cytoplasmic antibodies' (ANCA) role in defining clinical EGPA phenotypes is well established. Although the role of eosinophils in disease pathogenesis has been clearly demonstrated, the value of blood eosinophil count (BEC) as a biomarker of disease phenotypes is currently uncertain.

methodsWe retrospectively analyzed EGPA patients referred to our Immunology Clinic. Demographic, laboratory and clinical features were retrieved from clinical records, and a Logistic Regression was fitted to evaluate the predictive power of all baseline clinical and laboratory features to define EGPA phenotypes.

results168 patients were recruited. BEC ≤ 1500 cells/mL was predictive of a clinical involvement characterized by asthma, chronic rhinosinusitis with nasal polyps (CRSwNP) and lung opacities (OR 0.18, 95% CI 0.07-0.43; respiratory-limited phenotype); BEC > 3500/mL was predictive of extrapulmonary organ involvement (OR 3.5, 95% CI 1.7-7.1; systemic phenotype). BEC was also predictive of peripheral nervous system (PNS) involvement, with a positive trend with increasing BEC (<1500/mL: OR 0.17, 95%CI, 0.06-0.47; >3500/mL: OR 2.8, 95% CI, 1.5-5.28). ANCA positivity was also predictive of extrapulmonary involvement (OR 4.7, 95% CI 1.9-11.99).

conclusionsaccording to BEC and irrespective of the ANCA status, two EGPA phenotypes could be identified, named systemic and respiratory-limited phenotypes, with different organ involvement and possibly different prognoses.

Indexed as

ANCAEGPAeosinophilsphenotypevasculitis

Identifiers

PMID36979755
PMCPMC10045549
OpenAlexW4323311692

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.