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C FTR variants are associated with chronic bronchitis in smokers.
Saferali, Aabida; Qiao, Dandi; Kim, Wonji; Raraigh, Karen; Levy, Hara; Diaz, Alejandro A; Cutting, Garry R; Cho, Michael H; Hersh, Craig P.
Affiliation
  • Saferali A; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Qiao D; Harvard Medical School, Boston, MA, USA.
  • Kim W; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Raraigh K; Harvard Medical School, Boston, MA, USA.
  • Levy H; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Diaz AA; Harvard Medical School, Boston, MA, USA.
  • Cutting GR; Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Cho MH; Division of Pulmonary Medicine, Dept of Pediatrics, National Jewish Health, Denver, CO, USA.
  • Hersh CP; Harvard Medical School, Boston, MA, USA.
Eur Respir J ; 60(2)2022 08.
Article in En | MEDLINE | ID: mdl-34996830
ABSTRACT

INTRODUCTION:

Loss-of-function variants in both copies of the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF); however, there is evidence that reduction in CFTR function due to the presence of one deleterious variant can have clinical consequences. Here, we hypothesise that CFTR variants in individuals with a history of smoking are associated with chronic obstructive pulmonary disease (COPD) and related phenotypes.

METHODS:

Whole-genome sequencing was performed through the National Heart, Lung, and Blood Institute TOPMed (TransOmics in Precision Medicine) programme in 8597 subjects from the COPDGene (Genetic Epidemiology of COPD) study, an observational study of current and former smokers. We extracted clinically annotated CFTR variants and performed single-variant and variant-set testing for COPD and related phenotypes. Replication was performed in 2118 subjects from the ECLIPSE (Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints) study.

RESULTS:

We identified 301 coding variants within the CFTR gene boundary 147 of these have been reported in individuals with CF, including 36 CF-causing variants. We found that CF-causing variants were associated with chronic bronchitis in variant-set testing in COPDGene (one-sided p=0.0025; OR 1.53) and in meta-analysis of COPDGene and ECLIPSE (one-sided p=0.0060; OR 1.52). Single-variant testing revealed that the F508del variant was associated with chronic bronchitis in COPDGene (one-sided p=0.015; OR 1.47). In addition, we identified 32 subjects with two or more CFTR variants on separate alleles and these subjects were enriched for COPD cases (p=0.010).

CONCLUSIONS:

Cigarette smokers who carry one deleterious CFTR variant have higher rates of chronic bronchitis, while presence of two CFTR variants may be associated with COPD. These results indicate that genetically mediated reduction in CFTR function contributes to COPD related phenotypes, in particular chronic bronchitis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis / Bronchitis, Chronic / Pulmonary Disease, Chronic Obstructive Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Eur Respir J Year: 2022 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cystic Fibrosis / Bronchitis, Chronic / Pulmonary Disease, Chronic Obstructive Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Eur Respir J Year: 2022 Document type: Article Affiliation country: United States