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β 2 -Adrenergic genotypes and risk of severe exacerbations in COPD: a prospective cohort study.
- Source :
-
Thorax [Thorax] 2019 Oct; Vol. 74 (10), pp. 934-940. Date of Electronic Publication: 2019 Sep 03. - Publication Year :
- 2019
-
Abstract
- Background: Individual susceptibility to exacerbations in chronic obstructive pulmonary disease (COPD) is likely influenced by genetic factors; however, most such variance is unexplained. We hypothesised that β <subscript>2</subscript> -adrenergic receptor genotypes, Gly16Arg (rs1042713, c.46G>A) and Gln27Glu (rs1042714, c.79C>G) influence risk of severe exacerbations in COPD.<br />Methods: Among 96 762 individuals in the Copenhagen General Population Study, we identified 5262 with COPD (forced expiratory volume in one second divided by forced vital capacity, FEV <subscript>1</subscript> /FVC, below 0.7, FEV <subscript>1</subscript> less than 80% of predicted value, age above 40 years and no asthma) who had genotyping performed. Severe exacerbations were defined as acute admissions due to COPD during 5 years of follow-up (mean 3.4 years). 923 individuals with COPD diagnosed similarly in the Copenhagen City Heart Study (CCHS) were used for replication analyses.<br />Results: We recorded 461 severe exacerbations in 5262 subjects. The HRs for severe exacerbations were 1.62 (95% CI 1.30 to 2.03, p=0.00002) for 16Gly/Arg heterozygotes and 1.41 (1.04 to 1.91, p=0.03) for 16Arg homozygotes, compared with 16Gly homozygotes. HRs were 1.35 (1.03 to 1.76, p=0.03) for 27Gln/Glu heterozygotes and 1.49 (1.12 to 1.98, p=0.006) for 27Gln homozygotes, compared with 27Glu homozygotes. Similar trends were observed in the CCHS. Among 27Gln homozygotes only, HRs were 5.20 (1.81 to 14.9, p=0.002) for 16Gly/Arg heterozygotes and 4.03 (1.40 to 11.6, p=0.01) for 16Arg homozygotes, compared with 16Gly homozygotes.<br />Conclusion: Common β <subscript>2</subscript> -adrenergic receptor genotypes influence risk of severe exacerbations in COPD, potentially mainly by genetic influence of the 16Arg allele in rs1042713.<br />Competing Interests: Competing interests: TSI has received a fee for speaking from AstraZeneca. JV has received honoraria from Chiesi, GlaxoSmithKline, Almirall, AstraZeneca, Boehringer-Ingelheim, and Novartis for consulting and for presenting at meetings and symposia, none of it related to the topic of this study. LR and JLM: none to declare. PL has received honoraria from AstraZeneca, Boehringer Ingelheim, Chiesi, Novartis, Teva, and GlaxoSmithKline for presenting at meetings and symposia, none of it related to the topic of this study. BGN: none to declare.<br /> (© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Adult
Aged
Alleles
Disease Progression
Female
Follow-Up Studies
Forced Expiratory Volume physiology
Genotype
Humans
Male
Middle Aged
Prospective Studies
Pulmonary Disease, Chronic Obstructive diagnosis
Pulmonary Disease, Chronic Obstructive physiopathology
Receptors, Adrenergic, beta-2 metabolism
Recurrence
Severity of Illness Index
Forecasting
Polymorphism, Genetic
Pulmonary Disease, Chronic Obstructive genetics
Receptors, Adrenergic, beta-2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1468-3296
- Volume :
- 74
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Thorax
- Publication Type :
- Academic Journal
- Accession number :
- 31481635
- Full Text :
- https://doi.org/10.1136/thoraxjnl-2018-212340