Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease - Risk to relatives for airflow obstruction and chronic bronchitis

被引:288
|
作者
Silverman, EK
Chapman, HA
Drazen, JM
Weiss, ST
Rosner, B
Campbell, EJ
O'Donnell, WJ
Reilly, JJ
Ginns, L
Mentzer, S
Wain, J
Speizer, FE
机构
[1] Brigham & Womens Hosp, Channing Lab, Boston, MA 02115 USA
[2] Brigham & Womens Hosp, Dept Med, Div Pulm & Crit Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Surg, Div Thorac Surg, Boston, MA 02115 USA
[4] Massachusetts Gen Hosp, Dept Med, Pulm & Crit Care Unit, Boston, MA 02114 USA
[5] Massachusetts Gen Hosp, Dept Surg, Div Gen Thorac Surg Serv, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Boston, MA USA
[7] Univ Utah, Hlth Sci Ctr, Dept Internal Med, Salt Lake City, UT USA
关键词
D O I
10.1164/ajrccm.157.6.9706014
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Severe alpha-l-antitrypsin deficiency is the only proven genetic risk factor for chronic obstructive pulmonary disease (COPD). We have assembled a cohort of 44 probands with severe, early-onset COPD, who do not have severe alpha-l-antitrypsin deficiency. A surprisingly high prevalence of females (79.6%) was found. Assessment of the risk to relatives of these early-onset COPD probands for airflow obstruction and chronic bronchitis was performed to determine whether significant familial aggregation for COPD, independent of alpha-l-antitrypsin deficiency, could be demonstrated. First-degree relatives of early-onset COPD probands had significantly lower FEV1 and FEV1/FVC values than control subjects (p < 0.01), despite similar pack-years of smoking. Reduced spirometric values in first-degree relatives of early-onset COPD probands were found only in current or ex-cigarette smokers. The mean FEV1 in current or ex-smoking first-degree relatives was 76.1 +/- 20.9% predicted compared to 89.2 +/- 14.4% predicted in current or ex-smoking control subjects (p < 0.01); in lifelong nonsmokers, the mean FEV1 was 93.4% predicted for both control subjects and first-degree relatives of early-onset COPD probands. Generalized estimating equations, adjusting for age and pack-years of smoking, demonstrated increased odds of reduced FEV1 and chronic bronchitis in current or ex-smoking first-degree relatives of early-onset COPD probands. Using a new method to estimate relative risk from relative odds, we estimate that the relative risks for FEV1 below 60%, FEV1 below 80%, and chronic bronchitis are each approximately three in current or ex-smoking first-degree relatives of early-onset COPD probands. The increased risk to relatives of early-onset COPD probands for reduced FEV1 and chronic bronchitis, limited to current or ex-smokers, suggests genetic risk factor(s) for COPD that are expressed in response to cigarette smoking.
引用
收藏
页码:1770 / 1778
页数:9
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