TY - JOUR
T1 - Chronic obstructive pulmonary disease among lung cancer-free smokers
T2 - The importance of healthy controls
AU - Karpman, Michelle D.
AU - Eldridge, Ronald
AU - Follis, Jack L.
AU - Etzel, Carol J.
AU - Shete, Sanjay
AU - El-Zein, Randa A.
N1 - Publisher Copyright:
© 2017 The Japanese Respiratory Society
PY - 2018/1
Y1 - 2018/1
N2 - Background: The prevalence of chronic obstructive pulmonary disease (COPD) in smokers enrolled as “healthy” controls in studies is 10–50%. The COPD status of ideal smoker populations for lung cancer case-control studies should be checked via spirometry; however, this is often not feasible, because no medical indications exist for asymptomatic smokers to undergo spirometry prior to study enrollment. Therefore, there is an unmet need for robust, cost effective assays for identifying undiagnosed lung disease among asymptomatic smokers. Such assays would help excluding unhealthy smokers from lung cancer case-control studies. Methods: We used the cytokinesis-blocked micronucleus (CBMN) assay (a measure of genetic instability) to identify undiagnosed lung disease among asymptomatic smokers. We used a convenience population from an on-going lung cancer case-control study including smokers with lung cancer (n = 454), smoker controls (n = 797), and a self-reported COPD (n = 200) contingent within the smoker controls. Results: Significant differences for all CBMN endpoints were observed when comparing lung cancer to All controls (which included COPD) and Healthy controls (with no COPD). The risk ratio (RR) was increased in the COPD group vs. Healthy controls for nuclear buds (RR 1.28, 95% confidence interval 1.01–1.62), and marginally increased for micronuclei (RR 1.06, 0.98–1.89) and nucleoplasmic bridges (RR 1.07, 0.97–1.15). Conclusion: These findings highlight the importance of using truly healthy controls in studies geared toward assessment of lung cancer risk. Using genetic instability biomarkers would facilitate the identification of smokers susceptible to tobacco smoke carcinogens and therefore predisposed to either disease.
AB - Background: The prevalence of chronic obstructive pulmonary disease (COPD) in smokers enrolled as “healthy” controls in studies is 10–50%. The COPD status of ideal smoker populations for lung cancer case-control studies should be checked via spirometry; however, this is often not feasible, because no medical indications exist for asymptomatic smokers to undergo spirometry prior to study enrollment. Therefore, there is an unmet need for robust, cost effective assays for identifying undiagnosed lung disease among asymptomatic smokers. Such assays would help excluding unhealthy smokers from lung cancer case-control studies. Methods: We used the cytokinesis-blocked micronucleus (CBMN) assay (a measure of genetic instability) to identify undiagnosed lung disease among asymptomatic smokers. We used a convenience population from an on-going lung cancer case-control study including smokers with lung cancer (n = 454), smoker controls (n = 797), and a self-reported COPD (n = 200) contingent within the smoker controls. Results: Significant differences for all CBMN endpoints were observed when comparing lung cancer to All controls (which included COPD) and Healthy controls (with no COPD). The risk ratio (RR) was increased in the COPD group vs. Healthy controls for nuclear buds (RR 1.28, 95% confidence interval 1.01–1.62), and marginally increased for micronuclei (RR 1.06, 0.98–1.89) and nucleoplasmic bridges (RR 1.07, 0.97–1.15). Conclusion: These findings highlight the importance of using truly healthy controls in studies geared toward assessment of lung cancer risk. Using genetic instability biomarkers would facilitate the identification of smokers susceptible to tobacco smoke carcinogens and therefore predisposed to either disease.
KW - COPD
KW - Genetic instability
KW - Healthy controls
KW - Lung cancer
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U2 - 10.1016/j.resinv.2017.11.002
DO - 10.1016/j.resinv.2017.11.002
M3 - Article
C2 - 29325677
AN - SCOPUS:85035350201
SN - 2212-5345
VL - 56
SP - 28
EP - 33
JO - Respiratory Investigation
JF - Respiratory Investigation
IS - 1
ER -