The demographics of adverse outcomes in cystic fibrosis

Meghan E. McGarry*, Wadsworth A. Williams, Susanna A. McColley

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

49 Scopus citations

Abstract

Understanding variability in cystic fibrosis (CF) health outcomes requires an understanding of factors that go far beyond Cystic Fibrosis Transmembrane Receptor (CFTR) function caused by different gene mutations. Social and environmental factors that influence health have a significant influence on the trajectory of health in CF and in other chronic diseases. In this article, we review demographic factors associated with poorer health outcomes in CF, known and postulated biological mechanisms of these outcomes, and interventions that healthcare teams can implement that may reduce outcome disparities.

Original languageEnglish (US)
Pages (from-to)S74-S83
JournalPediatric Pulmonology
Volume54
Issue numberS3
DOIs
StatePublished - Nov 1 2019

Funding

MEM is supported by the NHLBI (1K23HL133437‐01A1) and Cystic Fibrosis Foundation Therapeutics (MCGARR16A0). SAM is supported by the Northwestern University Clinical and Translational Sciences Institute through the National Center for Advancing Translational Sciences (UL1TR001422).

Keywords

  • cystic fibrosis
  • epidemiology
  • social dimensions of pulmonary medicine

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Pediatrics, Perinatology, and Child Health

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