Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection

• Jessica E. Pittman ,

  * E-mail: pittman_j@kids.wustl.edu

  Affiliation Washington University School of Medicine, Division of Pediatric Allergy, Immunology, and Pulmonary Medicine, St. Louis, MO, United States of America

  http://orcid.org/0000-0003-3789-1241

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• Hannah Noah,

  Affiliation University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC, United States of America

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• Hollin E. Calloway,

  Affiliation Stanford University School of Medicine, Department of Otolaryngology Head & Neck Surgery, Palo Alto, CA, United States of America

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• Stephanie D. Davis,

  Affiliation Indiana University School of Medicine/Riley Hospital for Children, Section of Pediatric Pulmonology, Allergy, and Sleep Medicine, Indianapolis, IN, United States of America

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• Margaret W. Leigh,

  Affiliations University of North Carolina at Chapel Hill, Department of Pediatrics, Chapel Hill, NC, United States of America, University of North Carolina at Chapel Hill, Marisco Lung Institute, Chapel Hill, NC, United States of America

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• Mitchell Drumm,

  Affiliation Departments of Pediatrics and Genetics and Genome Sciences, Case Western Reserve University, Cleveland, OH, United States of America

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• Scott D. Sagel,

  Affiliation Department of Pediatrics, Children’s Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, United States of America

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• Frank J. Accurso,

  Affiliation Department of Pediatrics, Children’s Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, United States of America

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• Michael R. Knowles,

  Affiliation University of North Carolina at Chapel Hill, Marisco Lung Institute, Chapel Hill, NC, United States of America

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• Marci K. Sontag

  Affiliation Department of Pediatrics, Children’s Hospital Colorado and University of Colorado School of Medicine, Aurora, CO, United States of America

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