Peer-Reviewed Journal Details
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Ronan, Nicola J.; Einarsson, Gisli G.; Twomey, Maria; Mooney, Denver; Mullane, David; Ní Chroinin, Muireann; O’Callaghan, Grace; Shanahan, Fergus; Murphy, Desmond M.; O’Connor, Owen J.; Shortt, Cathy A.; Tunney, Michael M.; Eustace, Joseph A.; Maher, Michael M.; Elborn, J. Stuart; Plant, Barry J.
2017
Unknown
Chest
CORK Study in Cystic Fibrosis: Sustained Improvements in Ultra-Low-Dose Chest CT Scores After CFTR Modulation With Ivacaftor
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Cystic fibrosis Ivacaftor G551D Low-dose chest CT imaging
Ivacaftor produces significant clinical benefit in patients with cystic fibrosis (CF) with the G551D mutation. Prevalence of this mutation at the Cork CF Centre is 23%. This study assessed the impact of CFTR modulation on multiple modalities of patient assessment. Thirty-three patients with the G551D mutation were assessed at baseline and prospectively every 3 months for 1 year after initiation of ivacaftor. Change in ultra-low-dose chest CT scans, blood inflammatory mediators, and the sputum microbiome were assessed. Significant improvements in FEV1, BMI, and sweat chloride levels were observed post-ivacaftor treatment. Improvement in ultra-low-dose CT imaging scores were observed after treatment, with significant mean reductions in total Bhalla score (P < .01), peribronchial thickening (P = .035), and extent of mucous plugging (P < .001). Reductions in circulating inflammatory markers, including interleukin (IL)-1ß, IL-6, and IL-8 were demonstrated. There was a 30% reduction in the relative abundance of Pseudomonas species and an increase in the relative abundance of bacteria associated with more stable community structures. Posttreatment community richness increased significantly (P = .03). Early and sustained improvements on ultra-low-dose CT scores suggest it may be a useful method of evaluating treatment response. It paralleled improvement in symptoms, circulating inflammatory markers, and changes in the lung microbiota.
0012-3692
http://www.sciencedirect.com/science/article/pii/S0012369217328969
https://doi.org/10.1016/j.chest.2017.10.005
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