Genetic ancestry and the relationship of cigarette smoking to lung function and per cent emphysema in four race/ethnic groups: a cross-sectional study. Issue 7 (12th April 2013)

• Record Type: Journal Article
• Authors: Powell, Rhea; Davidson, Duncan; Divers, Jasmin; Manichaikul, Ani; Carr, J Jeffrey; Detrano, Robert; Hoffman, Eric A; Jiang, Rui; Kronmal, Richard A; Liu, Kiang; Punjabi, Naresh M; Shahar, Eyal; Watson, Karol E; Rotter, Jerome I; Taylor, Kent D; Rich, Stephen S; Barr, R Graham
• Is Part Of: Thorax. Volume 68:Issue 7(2013)
• Page Start: 634
• Page End: 642
• Publication Date: 2013-04-12
• Subjects: COPD epidemiology -- Tobacco and the lung -- Emphysema; Chest -- Diseases -- Periodicals; Thorax; Chest -- Diseases; Periodicals; Periodicals; 617.54
• DOI: 10.1136/thoraxjnl-2012-202116
• Languages: English
• ISSNs: 0040-6376

Abstract

Abstract : Background: Cigarette smoking is the major cause of chronic obstructive pulmonary disease and emphysema. Recent studies suggest that susceptibility to cigarette smoke may vary by race/ethnicity; however, they were generally small and relied on self-reported race/ethnicity. Objective: To test the hypothesis that relationships of smoking to lung function and per cent emphysema differ by genetic ancestry and self-reported race/ethnicity among Caucasians, African-Americans, Hispanics and Chinese-Americans. Design: Cross-sectional population-based study of adults age 45–84 years in the USA. Measurements: Principal components of genetic ancestry and continental ancestry estimated from one million genome-wide single nucleotide polymorphisms; pack-years of smoking; spirometry measured for 3344 participants; and per cent emphysema on computed tomography for 8224 participants. Results: The prevalence of ever-smoking was: Caucasians, 57.6%; African-Americans, 56.4%; Hispanics, 46.7%; and Chinese-Americans, 26.8%. Every 10 pack-years was associated with −0.73% (95% CI −0.90% to −0.56%) decrement in the forced expiratory volume in 1 s to forced vital capacity (FEV1 to FVC) and a 0.23% (95% CI 0.08% to 0.38%) increase in per cent emphysema. There was no evidence that relationships of pack-years to the FEV1 to FVC, airflow obstruction and per cent emphysema varied by genetic ancestry (all p>0.10), self-reported race/ethnicity (all p>0.10) or, among African-Americans, African ancestry. There were small differences in relationships of pack-years to the FEV1 among male Chinese-Americans and to the FEV1 to FVC ratio with African and Native American ancestry among male Hispanics only. Conclusions: In this large cohort, there was little to no evidence that the associations of smoking to lung function and per cent emphysema differed by genetic ancestry or self-reported race/ethnicity.