rs113897301 - ADAM19
Magnitude 2.2 · 1 study on file
Reported associations
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Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis - Unknown journal (n.d.) · Unknown authors · PubMed 28166215
[INTRO] Chronic obstructive pulmonary disease (COPD) is a leading cause of mortality worldwide. We performed a genetic association in 15,256 cases and 47,936 controls, with replication of select top results (P < 5×10−6) in 9,498 cases and 9,748 controls. In the combined meta-analysis, we identified 22 loci at genome-wide significance, including 13 new associations with COPD. Nine of these 13 loci have been associated with lung function in general population samples; however, 4 (EEFSEC, DSP, MTCL1, and SFTPD) are novel. We noted 2 loci shared with pulmonary fibrosis (FAM13A and DSP) but with opposite risk alleles for COPD. None of our loci overlapped with genome-wide associations for asthma; however, one locus has been implicated in the joint susceptibility to asthma and obesity. We also
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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Genetic COPD susceptibility and prevention strategy Moderate
ADAM19 variant increases COPD risk independent of smoking status; personalized risk assessment and prevention approach recommended
Lifestyle
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Smoking and secondhand smoke exposure Moderate
Smoking is primary COPD risk factor; genetic variant confers additive independent risk, making avoidance critically important
If current smoker, prioritize cessation support; minimize secondhand smoke and occupational respiratory hazard exposure
Screening
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Spirometry (lung function testing for FEV1/FVC) Moderate
ADAM19 variant associated with 20-23% increased COPD odds; early detection of airflow limitation enables timely intervention
Discuss with healthcare provider about baseline spirometry at age 40-45 or earlier if smoking exposure or respiratory symptoms present