Frontiers in Immunology (Aug 2017)

Multivariate Analysis As a Support for Diagnostic Flowcharts in Allergic Bronchopulmonary Aspergillosis: A Proof-of-Concept Study

  • Joana Vitte,
  • Joana Vitte,
  • Stéphane Ranque,
  • Stéphane Ranque,
  • Ania Carsin,
  • Ania Carsin,
  • Carine Gomez,
  • Carine Gomez,
  • Thomas Romain,
  • Carole Cassagne,
  • Carole Cassagne,
  • Marion Gouitaa,
  • Mélisande Baravalle-Einaudi,
  • Nathalie Stremler-Le Bel,
  • Martine Reynaud-Gaubert,
  • Martine Reynaud-Gaubert,
  • Jean-Christophe Dubus,
  • Jean-Christophe Dubus,
  • Jean-Louis Mège,
  • Jean-Louis Mège,
  • Jean Gaudart

DOI
https://doi.org/10.3389/fimmu.2017.01019
Journal volume & issue
Vol. 8

Abstract

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Molecular-based allergy diagnosis yields multiple biomarker datasets. The classical diagnostic score for allergic bronchopulmonary aspergillosis (ABPA), a severe disease usually occurring in asthmatic patients and people with cystic fibrosis, comprises succinct immunological criteria formulated in 1977: total IgE, anti-Aspergillus fumigatus (Af) IgE, anti-Af “precipitins,” and anti-Af IgG. Progress achieved over the last four decades led to multiple IgE and IgG(4) Af biomarkers available with quantitative, standardized, molecular-level reports. These newly available biomarkers have not been included in the current diagnostic criteria, either individually or in algorithms, despite persistent underdiagnosis of ABPA. Large numbers of individual biomarkers may hinder their use in clinical practice. Conversely, multivariate analysis using new tools may bring about a better chance of less diagnostic mistakes. We report here a proof-of-concept work consisting of a three-step multivariate analysis of Af IgE, IgG, and IgG4 biomarkers through a combination of principal component analysis, hierarchical ascendant classification, and classification and regression tree multivariate analysis. The resulting diagnostic algorithms might show the way for novel criteria and improved diagnostic efficiency in Af-sensitized patients at risk for ABPA.

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