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      Comparing the harmful effects of nontuberculous mycobacteria and Gram negative bacteria on lung function in patients with cystic fibrosis

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          Abstract

          Background

          To better understand the relative effects of infection with nontuberculous mycobacteria and Gram negative bacteria on lung function decline in cystic fibrosis, we assessed the impact of each infection in a Danish setting.

          Methods

          Longitudinal registry study of 432 patients with cystic fibrosis contributing 53,771 lung function measures between 1974 and 2014. We used a mixed effects model with longitudinally structured correlation, while adjusting for clinically important covariates.

          Results

          Infections with a significant impact on rate of decline in %FEV1 were Mycobacterium abscessus complex with − 2.22% points per year (95% CI − 3.21 to − 1.23), Burkholderia cepacia complex − 1.95% (95% CI − 2.51 to − 1.39), Achromobacter xylosoxidans − 1.55% (95% CI − 2.21 to − 0.90), and Pseudomonas aeruginosa − 0.95% (95% CI − 1.24 to − 0.66). Clearing M. abscessus complex was associated with a change to a slower decline, similar in magnitude to the pre-infection slope.

          Conclusions

          In a national population we have demonstrated the impact on lung function of each chronic CF pathogen. M. abscessus complex was associated with the worst impact on lung function. Eradication of M. abscessus complex may significantly improve lung function.

          Graphical abstract

          Effect on lung function of chronic infection from onset to end stage lung disease in Danish cystic fibrosis patients.

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          Most cited references43

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          Standardisation of spirometry.

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            An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases.

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              THE ENVIRONMENT AND DISEASE: ASSOCIATION OR CAUSATION?

              A. B. Hill (1965)
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                Author and article information

                Contributors
                Journal
                J Cyst Fibros
                J. Cyst. Fibros
                Journal of Cystic Fibrosis
                Elsevier
                1569-1993
                1873-5010
                1 May 2016
                May 2016
                : 15
                : 3
                : 380-385
                Affiliations
                [a ]Copenhagen Cystic Fibrosis Center, Department of Infectious Diseases, Rigshospitalet, Copenhagen University, Denmark
                [b ]Department of Public Health and Policy, University of Liverpool, Liverpool, UK
                [c ]Department of Medical Informatics, Biometry and Epidemiology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany
                [d ]Aarhus Cystic Fibrosis Center, Department of Pediatrics, University Hospital Skejby, Aarhus, Denmark
                [e ]Copenhagen Cystic Fibrosis Center, Department of Pediatrics, Rigshospitalet, Copenhagen University, Denmark
                [f ]Copenhagen Cystic Fibrosis Center, Department of Clinical Microbiology, Rigshospitalet, Copenhagen University, Denmark
                [g ]Institute of Child Health, University College London, London, UK
                [h ]Faculty of Medicine, Lancaster University, Lancaster, UK
                Author notes
                [* ]Corresponding author at: Department of Public Health and Policy, Whelan Building, University of Liverpool, Liverpool, UK.Department of Public Health and PolicyWhelan BuildingUniversity of LiverpoolLiverpoolUK david.taylor-robinson@ 123456liverpool.ac.uk
                [1]

                Contributed equally.

                Article
                S1569-1993(15)00215-5
                10.1016/j.jcf.2015.09.007
                4893021
                26482717
                ccd338a1-391c-45cb-9dbf-8a6b04fd80c0
                © 2015 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 July 2015
                : 27 August 2015
                : 18 September 2015
                Categories
                Original Article

                Genetics
                ats, american thoracic society,cf, cystic fibrosis,cfrd, cystic fibrosis related diabetes,ci, confidence interval,%fev1, forced expiratory volume in 1 s expressed as % of predicted,idsa, infectious disease society of america,mabsc, mycobacterium abscessus complex,mac, mycobacterium avium complex,ntm, nontuberculous mycobacteria.,lung function,abscessus,ntm,gram negative,cf

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