Your browser doesn't support javascript.
loading
Identification of distinct immunophenotypes in chronic pulmonary aspergillosis using cluster analysis.
Sehgal, Inderpaul S; Dhooria, Sahajal; Muthu, Valliappan; Rudramurthy, Shivaprakash M; Prasad, Kuruswamy T; Chakrabarti, Arunaloke; Aggarwal, Ashutosh N; Agarwal, Ritesh.
Afiliación
  • Sehgal IS; Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Dhooria S; Department of Medical Microbiology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Muthu V; Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Rudramurthy SM; Department of Medical Microbiology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Prasad KT; Director, Doodhadhari Burfani Hospital, Haridwar, Uttarakhand, India.
  • Chakrabarti A; Department of Pulmonary Medicine, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
  • Aggarwal AN; Director, Doodhadhari Burfani Hospital, Haridwar, Uttarakhand, India.
  • Agarwal R; Director, Doodhadhari Burfani Hospital, Haridwar, Uttarakhand, India.
Mycoses ; 66(4): 299-303, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36504459
ABSTRACT

BACKGROUND:

Whether chronic pulmonary aspergillosis (CPA) has different immunophenotypes remains unknown.

OBJECTIVE:

To identify different CPA immunophenotypes using cluster analysis.

METHODS:

We used a subject-centred multivariate clustering approach without prior assumptions to identify CPA phenotypes. We retrospectively included the data of treatment-naïve subjects with CPA and excluded subjects with asthma and allergic bronchopulmonary aspergillosis (ABPA). We performed a scalable two-step cluster analysis using the log-likelihood distance measures to identify CPA phenotypes based on the blood immunological profile (total IgE, eosinophil count and Aspergillus-specific IgE and IgG).

RESULTS:

We included 351 CPA subjects and found two clusters. Cluster 2 (n = 118) had significantly higher serum total IgE, peripheral blood eosinophil count, and serum A. fumigatus-specific IgE and IgG than cluster 1 (n = 233). Cluster 2 subjects had a lower FEV1FVC ratio on spirometry and were more likely to have a fungal ball (88 [74.6%] vs. 145 (62.2%), p = .023) on the CT thorax than cluster 1. After treatment discontinuation, cluster 2 had a longer median (interquartile range) time to relapse than cluster 1 (11.5 [7.3-27.4] vs. 4 [1.1-8.9] months, p = .005).

CONCLUSION:

We identified two distinct CPA phenotypes, type-2 dominant and non-type-2, with different clinical and radiological findings and treatment outcomes. Future studies should confirm our findings and investigate different treatment strategies based on CPA phenotypes.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Aspergilosis Broncopulmonar Alérgica / Aspergilosis Pulmonar Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Mycoses Asunto de la revista: MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Aspergilosis Broncopulmonar Alérgica / Aspergilosis Pulmonar Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Mycoses Asunto de la revista: MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: India