Rationale: Airway wall thickness (AWT) is affected by both environmental and genetic factors and is strongly associated with airflow limitation in smaller airways.
Objectives: To investigate the genetic component of AWT.
Methods: AWT was measured on low-dose computed tomography scans in male heavy smokers participating in a lung cancer screening study (n = 2,640). Genome-wide association studies on AWT were performed under an additive model using linear regression (adjusted for pack-years, lung volume), followed by metaanalysis. An independent cohort was used for validation of the most strongly associated single-nucleotide polymorphisms (SNP). The functional relevance of significant SNPs was evaluated.
Measurements and Main Results: Three significant loci on chromosomes 2q (rs734556; P = 6.2 X 10(-7)) and 10q (rs10794108, P = 8.6 X 10(-8); rs7078439, P = 2.3 X 10(-7)) were associated with AWT and confirmed in the metaanalysis in cohorts with comparable lung function: P values = 4.6 X 10(-8), 7.4 X 10(-8), and 7.5 X 10(-8), respectively. SNP rs734556 was associated with decreased lung tissue expression of SERPINE2, a susceptibility gene for emphysema. Two nominally significant SNPs showed effects with similar direction: rs10251504 in MAGI2 (P = 5.8 X 10(-7)) and rs4796712 in NT5C3B (P = 3.1 X 10(-6)). Higher MAGI2 expression in bronchial biopsies of patients with chronic obstructive pulmonary disease was significantly associated with fewer inflammatory cells. The presence of the NT5C3B risk allele was associated with higher lung tissue expression (P = 1.09 X 10(-41)).
Conclusions: Genetic variants contribute to AWT. Among others, the identified genes are also involved in emphysema, airway obstruction, and bronchial inflammation.
|Tijdschrift||American Journal of Respiratory and Critical Care Medicine|
|Nummer van het tijdschrift||5|
|Status||Published - 1-mrt-2015|