Determination of the yearly distribution of the incidence of Allergic Bronchopulmonary Aspergillosis (ABPA) in patients registered in the cystic fibrosis patient registry system of Turkey and identification of risk factors for its development

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Authors: Havva İpek Demir, Ebru Elmas Yalcin, Halime Nayır Büyükşahin, Suat Savaş, Velat Şen, Hadice Selimoğlu Şen, Azer Kılıç Başkan, Ayşe Ayzıt Kılınç, Hakan Yazan, Abdülhamit Çollak, Erkan Çakır, Hanife Tuğçe Çağlar
+42 more Fatih Ercan, Sevgi Pekcan, Merve Korkmaz, Yakup Canıtez, Bahar Girgin Dindar, Figen Gülen, Elif Pınar Arık, Özlem Keskin, Ali Özdemir Ersoy, Mehmet Faruk Kose, Mahir Serbes, Derya Ufuk Altıntaş, Ebru Çelebioğlu, Oğuz Karcıoğlu, Abdurrahman Erdem Başaran, Ayşen Bingöl, Zeynep İlkşen Hocoğlu, Ayşe Tana Aslan, Demet Polat Yuluğ, Ali Özdemir, Işıl Bilgiç, Gökçen Dilşa Tuğcu, K. Harmancı, Beste Özsezen, Pervin Korkmaz, Nazan Çobanoğlu, Hasan Yüksel, Sibel Doğru, Gönül Çaltepe, Melih Hangül, Z.G. Gayretli Aydın, Mehmet KILIC, Hamza Ogün, Mina Gharibzadeh Hızal, Ayşe Süleyman, Gizem Özcan, Aslı Görek Dilektaşlı, Tuğba Şişmanlar Eyüboğlu, Nagehan Emiralioğlu, Güzin Cinel, Uğur Özçelik, Deni̇z Doğru
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References: 24

Abstract

Background Allergic bronchopulmonary aspergillosis (ABPA), is a hypersensitivity reaction in the lung against the antigens of Aspergillus fumigatus. The aim of this study is to determine the incidence of ABPA, and to determine the risk factors leading to the development of ABPA. Methods The study was designed as a retrospective cohort study. Using the CF Registry System of Turkey data, the incidence of ABPA was determined and the clinical and demographic characteristics of 44 patients newly diagnosed with ABPA in 2022 and 132 patients with similar mutation weight and age range without ABPA diagnosis in that year were examined and compared. Also risk factors affecting the development of ABPA were determined. Results Low pulmonary function test values, having had at least one pulmonary exacerbation in that year, receiving intravenous antibiotic treatment, using inhaled antibiotics, having high number of pulmonary exacerbations, having Pseudomonas aeruginosa colonization, having low body mass index (BMI), having cystic fibrosis related diabetes mellitus were found to be among the risk factors for the development of ABPA. Conclusions Early recognition and treatment of ABPA is essential to prevent further damage to the lungs. Patients with frequent pulmonary exacerbations, low BMI and low pulmonary function test values, chronic colonization should definitely be considered for ABPA.

Fields of Study & Subjects

Cystic Fibrosis Research Advances

Publication details

Journal / source
Chronic Illness
Publisher
SAGE Publications
Volume
22
Issue
3
Pages
229–239
Publication date
30 May 2026
Language
EN