Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function. Academic Article uri icon

Overview

abstract

  • Genome-wide association studies have identified numerous common genetic variants associated with spirometric measures of pulmonary function, including forced expiratory volume in one second (FEV1), forced vital capacity, and their ratio. However, variants with lower minor allele frequencies are less explored. We conducted a large-scale gene-smoking interaction meta-analysis on exonic rare and low-frequency variants involving 44,429 individuals of European ancestry in the discovery stage and sought replication in the UK BiLEVE study with 45,133 European ancestry samples and UK Biobank study with 59,478 samples. We leveraged data on cigarette smoking, the major environmental risk factor for reduced lung function, by testing gene-by-smoking interaction effects only and simultaneously testing the genetic main effects and interaction effects. The most statistically significant signal that replicated was a previously reported low-frequency signal in GPR126, distinct from common variant associations in this gene. Although only nominal replication was obtained for a top rare variant signal rs142935352 in one of the two studies, interaction and joint tests for current smoking and PDE3B were significantly associated with FEV1. This study investigates the utility of assessing gene-by-smoking interactions and underscores their effects on potential pulmonary function.

authors

publication date

  • September 29, 2021

Research

keywords

  • Cigarette Smoking
  • Forced Expiratory Volume
  • Gene-Environment Interaction

Identity

PubMed Central ID

  • PMC8481467

Scopus Document Identifier

  • 85116338038

Digital Object Identifier (DOI)

  • 10.1002/gepi.21703

PubMed ID

  • 34588469

Additional Document Info

volume

  • 11

issue

  • 1