Silverman E K, Chapman H A, Drazen J M, Weiss S T, Rosner B, Campbell E J, O'DONNELL W J, Reilly J J, Ginns L, Mentzer S, Wain J, Speizer F E
Channing Laboratory, Brigham and Women's Hospital, Boston, MA 02115, USA.
Am J Respir Crit Care Med. 1998 Jun;157(6 Pt 1):1770-8. doi: 10.1164/ajrccm.157.6.9706014.
Severe alpha-1-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-1-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-1-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.
严重的α-1抗胰蛋白酶缺乏症是慢性阻塞性肺疾病(COPD)唯一已证实的遗传危险因素。我们组建了一个由44名患有严重早发性COPD且无严重α-1抗胰蛋白酶缺乏症的先证者组成的队列。结果发现女性患病率出奇地高(79.6%)。对这些早发性COPD先证者的亲属患气流阻塞和慢性支气管炎的风险进行评估,以确定是否能证明存在与α-1抗胰蛋白酶缺乏症无关的COPD显著家族聚集性。早发性COPD先证者的一级亲属尽管吸烟包年数相似,但FEV1和FEV1/FVC值显著低于对照组(p<0.01)。早发性COPD先证者的一级亲属中肺功能测定值降低仅见于当前或既往吸烟者。当前或既往吸烟的一级亲属的平均FEV1为预测值的76.1±20.9%,而当前或既往吸烟的对照者为预测值的89.2±14.4%(p<0.01);在终身不吸烟者中,对照者和早发性COPD先证者的一级亲属的平均FEV1均为预测值的93.4%。采用广义估计方程,对年龄和吸烟包年数进行校正,结果显示早发性COPD先证者当前或既往吸烟的一级亲属FEV1降低和患慢性支气管炎的几率增加。使用一种从相对比值估计相对风险的新方法,我们估计早发性COPD先证者当前或既往吸烟的一级亲属中FEV1低于60%、FEV1低于80%以及患慢性支气管炎的相对风险均约为3。早发性COPD先证者的亲属中FEV1降低和患慢性支气管炎的风险增加,且仅限于当前或既往吸烟者,这表明存在因吸烟而表达的COPD遗传危险因素。