| Literature DB >> 30547383 |
Katharina Schütz1, Diana Alecsandru2,3, Bodo Grimbacher3,4, Jamanda Haddock5, Annemarie Bruining6, Gertjan Driessen7,8, Esther de Vries9,10, Peter M van Hagen11, Ieneke Hartmann12, Francesco Fraioli13,14, Cinzia Milito15, Milica Mitrevski15, Isabella Quinti15, Goffredo Serra13, Peter Kelleher16, Michael Loebinger17, Jiri Litzman18, Vera Postranecka19, Vojtech Thon18,20, Judith Babar21, Alison M Condliffe21, Andrew Exley22, Dinakantha Kumararatne23, Nick Screaton24, Alison Jones25, Maria P Bondioni26, Vassilios Lougaris27, Alessandro Plebani27, Annarosa Soresina28, Cesare Sirignano29, Giuseppe Spadaro30, Nermeen Galal31, Luis I Gonzalez-Granado2, Sabine Dettmer32, Robert Stirling33, Helen Chapel34, Mary Lucas34, Smita Patel34, Claire-Michele Farber35, Isabelle Meyts36, Arpan K Banerjee37, Scott Hackett38, John R Hurst39, Klaus Warnatz4, Benjamin Gathmann40, Ulrich Baumann41.
Abstract
Studies of chest computed tomography (CT) in patients with primary antibody deficiency syndromes (ADS) suggest a broad range of bronchial pathology. However, there are as yet no multicentre studies to assess the variety of bronchial pathology in this patient group. One of the underlying reasons is the lack of a consensus methodology, a prerequisite to jointly document chest CT findings. We aimed to establish an international platform for the evaluation of bronchial pathology as assessed by chest CT and to describe the range of bronchial pathologies in patients with antibody deficiency. Ffteen immunodeficiency centres from 9 countries evaluated chest CT scans of patients with ADS using a predefined list of potential findings including an extent score for bronchiectasis. Data of 282 patients with ADS were collected. Patients with common variable immunodeficiency disorders (CVID) comprised the largest subgroup (232 patients, 82.3%). Eighty percent of CVID patients had radiological evidence of bronchial pathology including bronchiectasis in 61%, bronchial wall thickening in 44% and mucus plugging in 29%. Bronchiectasis was detected in 44% of CVID patients aged less than 20 years. Cough was a better predictor for bronchiectasis than spirometry values. Delay of diagnosis as well as duration of disease correlated positively with presence of bronchiectasis. The use of consensus diagnostic criteria and a pre-defined list of bronchial pathologies allows for comparison of chest CT data in multicentre studies. Our data suggest a high prevalence of bronchial pathology in CVID due to late diagnosis or duration of disease.Entities:
Keywords: CVID; Chest CT; bronchial pathology; bronchiectasis; primary antibody deficiency
Mesh:
Year: 2018 PMID: 30547383 DOI: 10.1007/s10875-018-0577-9
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317