Aspergillus fumigatus colonization in cystic fibrosis: implications for lung function?
A M M de Vrankrijker1, C K van der Ent, F T van Berkhout
1Department of Paediatric Respiratory Medicine, University Medical Centre Utrecht, Utrecht, The Netherlands. a.m.m.devrankrijker@umcutrecht.nl
Summary
Aspergillus fumigatus colonization in cystic fibrosis (CF) patients without allergic bronchopulmonary aspergillosis (ABPA) was not linked to worse lung function. This finding suggests CF lung health is not significantly impacted by this specific fungal presence.
Area of Science:
- Medical Research
- Pulmonology
- Infectious Diseases
Background:
- Aspergillus fumigatus is frequently detected in respiratory secretions of cystic fibrosis (CF) patients.
- Allergic bronchopulmonary aspergillosis (ABPA) is known to worsen CF lung function.
- The impact of A. fumigatus colonization without ABPA on CF lung function remains unclear.
Purpose of the Study:
- To investigate the clinical characteristics associated with A. fumigatus colonization in CF patients without ABPA.
- To determine the effect of A. fumigatus colonization on lung function and its decline over time in this patient group.
Main Methods:
- Cross-sectional and retrospective cohort analyses were conducted on 259 CF patients (adults and children) without ABPA.
- A. fumigatus colonization was defined by >50% positive respiratory cultures annually.
- Longitudinal lung function data from 2002-2007 were analyzed using linear mixed models.
Main Results:
- Sixty-one patients (23.6%) showed intermittent or persistent A. fumigatus colonization.
- Colonization was associated with increased patient age and use of inhaled antibiotics.
- No significant differences in lung function or lung function decline were observed between colonized and non-colonized patients over a 5-year period, even when stratified by colonization duration.
Conclusions:
- Despite an association with more severe lung disease and higher treatment burden, A. fumigatus colonization is not an independent predictor of reduced lung function or accelerated lung function decline in CF patients without ABPA.
- These findings differentiate the impact of colonization from ABPA in CF management.
Related Concept Videos
Cystic Fibrosis: Pathogenesis
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Cystic Fibrosis: Management
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic sinusitis...
Sinus disease and chronic sinusitis...
Cryptococcal Meningitis
Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...
Fungal Phylum Ascomycota
Phylum Ascomycota, a major division within the subkingdom Dikarya, comprises a diverse range of fungal species, including both unicellular yeasts and filamentous molds such as Aspergillus and Penicillium. These fungi thrive in a variety of habitats, from aquatic ecosystems to terrestrial environments, playing crucial ecological and economic roles.Morphology and ReproductionThe defining characteristic of Ascomycetes, commonly referred to as sac fungi, is the ascus—a sac-like structure that...
Chronic Obstructive Pulmonary Disease III: Chronic Bronchitis Features
Chronic bronchitis is a key phenotype of chronic obstructive pulmonary disease (COPD), characterized by airway-centered inflammation and mucus overproduction. It develops from long-term exposure to harmful particles or gases, most commonly cigarette smoke, which triggers a persistent inflammatory response.Cellular and Structural ChangesInflammation initially affects the large bronchi and later the smaller airways, with infiltration by immune cells, including neutrophils, macrophages, and...
Fungal Group Zygomycota
Zygomycota, previously classified as a distinct fungal group, are primarily terrestrial, saprophytic molds that play a crucial role as decomposers. Recent phylogenetic studies have revealed that these fungi are now divided into two major clades — Mucoromycota, which includes many symbiotic species, and Zoopagomycota, which primarily consists of parasitic and pathogenic fungi. These groups exhibit distinct ecological roles and reproductive strategies while sharing key structural and...


