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Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease: Risk to relatives for airflow obstruction and chronic bronchitis
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...
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Published in: | American journal of respiratory and critical care medicine 1998-06, Vol.157 (6), p.1770-1778 |
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creator | SILVERMAN, E. K CHAPMAN, H. A WAIN, J SPEIZER, F. E DRAZEN, J. M WEISS, S. T ROSNER, B CAMPBELL, E. J O'DONNELL, W. J REILLY, J. J GINNS, L MENTZER, S |
description | 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. |
doi_str_mv | 10.1164/ajrccm.157.6.9706014 |
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K ; CHAPMAN, H. A ; WAIN, J ; SPEIZER, F. E ; DRAZEN, J. M ; WEISS, S. T ; ROSNER, B ; CAMPBELL, E. J ; O'DONNELL, W. J ; REILLY, J. J ; GINNS, L ; MENTZER, S</creator><creatorcontrib>SILVERMAN, E. K ; CHAPMAN, H. A ; WAIN, J ; SPEIZER, F. E ; DRAZEN, J. M ; WEISS, S. T ; ROSNER, B ; CAMPBELL, E. J ; O'DONNELL, W. J ; REILLY, J. J ; GINNS, L ; MENTZER, S</creatorcontrib><description>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.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/ajrccm.157.6.9706014</identifier><identifier>PMID: 9620904</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>alpha 1-Antitrypsin Deficiency - complications ; Biological and medical sciences ; Bronchitis - etiology ; Bronchitis - genetics ; Chronic Disease ; Chronic obstructive pulmonary disease, asthma ; Female ; Forced Expiratory Volume ; Humans ; Lung Diseases, Obstructive - etiology ; Lung Diseases, Obstructive - genetics ; Lung Diseases, Obstructive - physiopathology ; Male ; Medical sciences ; Middle Aged ; Pneumology ; Risk Factors ; Smoking - adverse effects ; Vital Capacity</subject><ispartof>American journal of respiratory and critical care medicine, 1998-06, Vol.157 (6), p.1770-1778</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c280t-4cd90608f539a4300f9a1b804202fca5328207b7d3c96e35ad760f050cbfc9d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2300670$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9620904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SILVERMAN, E. K</creatorcontrib><creatorcontrib>CHAPMAN, H. A</creatorcontrib><creatorcontrib>WAIN, J</creatorcontrib><creatorcontrib>SPEIZER, F. E</creatorcontrib><creatorcontrib>DRAZEN, J. M</creatorcontrib><creatorcontrib>WEISS, S. T</creatorcontrib><creatorcontrib>ROSNER, B</creatorcontrib><creatorcontrib>CAMPBELL, E. J</creatorcontrib><creatorcontrib>O'DONNELL, W. J</creatorcontrib><creatorcontrib>REILLY, J. J</creatorcontrib><creatorcontrib>GINNS, L</creatorcontrib><creatorcontrib>MENTZER, S</creatorcontrib><title>Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease: Risk to relatives for airflow obstruction and chronic bronchitis</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>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.</description><subject>alpha 1-Antitrypsin Deficiency - complications</subject><subject>Biological and medical sciences</subject><subject>Bronchitis - etiology</subject><subject>Bronchitis - genetics</subject><subject>Chronic Disease</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Female</subject><subject>Forced Expiratory Volume</subject><subject>Humans</subject><subject>Lung Diseases, Obstructive - etiology</subject><subject>Lung Diseases, Obstructive - genetics</subject><subject>Lung Diseases, Obstructive - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pneumology</subject><subject>Risk Factors</subject><subject>Smoking - adverse effects</subject><subject>Vital Capacity</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNpFkVFrFTEQhYMotVb_gUIexCf3Otlkk41vpWgVCoIo-Bay2YlNzW6uyW7l_g7_sCl3uT5NwnznwJlDyEsGO8akeGfvsnPTjnVqJ3dagQQmHpFz1vGuEfX_uL5B8UYI_eMpeVbKHQBrewZn5EzLFjSIc_L3GmdcgqO4DyNOIcX080CTpwXvMeNbijbHQ5Pmggt1tznNlU1DWfLqlnCPdL_GKc02H-gYCtqC7-nXUH7RJdGM0T4whfqUqQ3Zx_TnvzjN1M7jyXSow92GJZTn5Im3seCLbV6Q7x8_fLv61Nx8uf58dXnTuLaHpRFu1DV07zuureAAXls29CBaaL2zHW_7FtSgRu60RN7ZUUnw0IEbvNNjzy_Im6PvPqffK5bFTKE4jNHOmNZilNZtrySroDiCLqdSMnqzz2GqmQ0D89CFOXZhahdGmq2LKnu1-a_DhONJtB2_7l9ve1ucjT7b2YVywtoaSSrg_wD-OpdA</recordid><startdate>19980601</startdate><enddate>19980601</enddate><creator>SILVERMAN, E. 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K</creatorcontrib><creatorcontrib>CHAPMAN, H. A</creatorcontrib><creatorcontrib>WAIN, J</creatorcontrib><creatorcontrib>SPEIZER, F. E</creatorcontrib><creatorcontrib>DRAZEN, J. M</creatorcontrib><creatorcontrib>WEISS, S. T</creatorcontrib><creatorcontrib>ROSNER, B</creatorcontrib><creatorcontrib>CAMPBELL, E. J</creatorcontrib><creatorcontrib>O'DONNELL, W. J</creatorcontrib><creatorcontrib>REILLY, J. 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J</au><au>GINNS, L</au><au>MENTZER, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease: Risk to relatives for airflow obstruction and chronic bronchitis</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>1998-06-01</date><risdate>1998</risdate><volume>157</volume><issue>6</issue><spage>1770</spage><epage>1778</epage><pages>1770-1778</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>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.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>9620904</pmid><doi>10.1164/ajrccm.157.6.9706014</doi><tpages>9</tpages></addata></record> |
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subjects | alpha 1-Antitrypsin Deficiency - complications Biological and medical sciences Bronchitis - etiology Bronchitis - genetics Chronic Disease Chronic obstructive pulmonary disease, asthma Female Forced Expiratory Volume Humans Lung Diseases, Obstructive - etiology Lung Diseases, Obstructive - genetics Lung Diseases, Obstructive - physiopathology Male Medical sciences Middle Aged Pneumology Risk Factors Smoking - adverse effects Vital Capacity |
title | Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease: Risk to relatives for airflow obstruction and chronic bronchitis |
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