Breathing new life into the study of COPD with genes identified from genome-wide association studies

Eur Respir Rev. 2024 May 29;33(172):240019. doi: 10.1183/16000617.0019-2024. Print 2024 Apr 30.

Abstract

COPD is a major cause of morbidity and mortality globally. While the significance of environmental exposures in disease pathogenesis is well established, the functional contribution of genetic factors has only in recent years drawn attention. Notably, many genes associated with COPD risk are also linked with lung function. Because reduced lung function precedes COPD onset, this association is consistent with the possibility that derangements leading to COPD could arise during lung development. In this review, we summarise the role of leading genes (HHIP, FAM13A, DSP, AGER and TGFB2) identified by genome-wide association studies in lung development and COPD. Because many COPD genome-wide association study genes are enriched in lung epithelial cells, we focus on the role of these genes in the lung epithelium in development, homeostasis and injury.

Publication types

  • Review

MeSH terms

  • Animals
  • Genetic Markers
  • Genetic Predisposition to Disease*
  • Genome-Wide Association Study*
  • Humans
  • Lung* / physiopathology
  • Phenotype*
  • Prognosis
  • Pulmonary Disease, Chronic Obstructive* / diagnosis
  • Pulmonary Disease, Chronic Obstructive* / genetics
  • Pulmonary Disease, Chronic Obstructive* / physiopathology
  • Risk Factors

Substances

  • Genetic Markers