ABO phenotypes and inflammation-related predictors of lung cancer mortality: the Copenhagen Male Study - a 16-year follow-up
Inflammation and genetic susceptibility influence the risk of lung cancer. Previous studies suggest that the inflammatory response may depend upon ABO phenotype. The hypothesis that the association with lung cancer mortality risk of lifestyle and occupational factors previously linked to inflammatio...
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Veröffentlicht in: | The European respiratory journal 2007-07, Vol.30 (1), p.13-20 |
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description | Inflammation and genetic susceptibility influence the risk of lung cancer. Previous studies suggest that the inflammatory response may depend upon ABO phenotype. The hypothesis that the association with lung cancer mortality risk of lifestyle and occupational factors previously linked to inflammation would depend upon ABO phenotype was tested in a long-term follow-up of 3,346 male subjects aged 53-74 yrs. During a 16-yr period, 170 (5.1%) of the male subjects died due to lung cancer; 84 (5.9%) of phenotype O, 70 (4.9%) of phenotype A and 16 (3.2%) of phenotype B/AB. In addition to cumulative tobacco consumption, high salt intake long-term occupational dust exposure, high fat intake and consumption of alcohol were significantly predictive of lung cancer mortality for phenotype O subjects. After multivariable adjustment, the hazard ratios associated with the first three of these factors were 2.31, 2.08 and 1.67, respectively. Compared with abstainers, the hazard ratios for males drinking 1-10 wine drinks x week(-1) and males drinking >10 wine drinks x week(-1) were 1.65 and 2.02, respectively. Among phenotype A subjects, only cumulative tobacco consumption was associated with lung cancer mortality risk. The predictive role of inflammation-related risk factors for lung cancer mortality was significantly stronger among males of phenotype O than A. |
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O ; Gyntelberg, F</creator><creatorcontrib>Suadicani, P ; Hein, H. O ; Gyntelberg, F</creatorcontrib><description>Inflammation and genetic susceptibility influence the risk of lung cancer. Previous studies suggest that the inflammatory response may depend upon ABO phenotype. The hypothesis that the association with lung cancer mortality risk of lifestyle and occupational factors previously linked to inflammation would depend upon ABO phenotype was tested in a long-term follow-up of 3,346 male subjects aged 53-74 yrs. During a 16-yr period, 170 (5.1%) of the male subjects died due to lung cancer; 84 (5.9%) of phenotype O, 70 (4.9%) of phenotype A and 16 (3.2%) of phenotype B/AB. In addition to cumulative tobacco consumption, high salt intake long-term occupational dust exposure, high fat intake and consumption of alcohol were significantly predictive of lung cancer mortality for phenotype O subjects. After multivariable adjustment, the hazard ratios associated with the first three of these factors were 2.31, 2.08 and 1.67, respectively. Compared with abstainers, the hazard ratios for males drinking 1-10 wine drinks x week(-1) and males drinking >10 wine drinks x week(-1) were 1.65 and 2.02, respectively. Among phenotype A subjects, only cumulative tobacco consumption was associated with lung cancer mortality risk. 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O</creatorcontrib><creatorcontrib>Gyntelberg, F</creatorcontrib><title>ABO phenotypes and inflammation-related predictors of lung cancer mortality: the Copenhagen Male Study - a 16-year follow-up</title><title>The European respiratory journal</title><addtitle>Eur Respir J</addtitle><description>Inflammation and genetic susceptibility influence the risk of lung cancer. Previous studies suggest that the inflammatory response may depend upon ABO phenotype. The hypothesis that the association with lung cancer mortality risk of lifestyle and occupational factors previously linked to inflammation would depend upon ABO phenotype was tested in a long-term follow-up of 3,346 male subjects aged 53-74 yrs. During a 16-yr period, 170 (5.1%) of the male subjects died due to lung cancer; 84 (5.9%) of phenotype O, 70 (4.9%) of phenotype A and 16 (3.2%) of phenotype B/AB. In addition to cumulative tobacco consumption, high salt intake long-term occupational dust exposure, high fat intake and consumption of alcohol were significantly predictive of lung cancer mortality for phenotype O subjects. After multivariable adjustment, the hazard ratios associated with the first three of these factors were 2.31, 2.08 and 1.67, respectively. Compared with abstainers, the hazard ratios for males drinking 1-10 wine drinks x week(-1) and males drinking >10 wine drinks x week(-1) were 1.65 and 2.02, respectively. Among phenotype A subjects, only cumulative tobacco consumption was associated with lung cancer mortality risk. The predictive role of inflammation-related risk factors for lung cancer mortality was significantly stronger among males of phenotype O than A.</description><subject>ABO Blood-Group System</subject><subject>Addictive behaviors</subject><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>Alcohol Drinking</subject><subject>Alcoholism</subject><subject>Alcoholism and acute alcohol poisoning</subject><subject>Biological and medical sciences</subject><subject>Denmark</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lung Neoplasms - blood</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Phenotype</subject><subject>Pneumology</subject><subject>Prospective Studies</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Risk Factors</subject><subject>Smoking</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0903-1936</issn><issn>1399-3003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1v1DAQhi0EokvhB3BBPgC3FNuTOAm3dsWXVNQDcLYcZ7xx5cTBdlRF4seT1W7V0xzmeV_NPIS85eyK8wY-sZYBb0FeMcakqJh8RnYc2rYAxuA52R33xRG4IK9SumeMyxL4S3LBa2gFCLEj_65v7ug84BTyOmOieuqpm6zX46izC1MR0euMPZ0j9s7kEBMNlvplOlCjJ4ORjiFm7V1eP9M8IN2HGadBH3CiP7VH-isv_UoLqimXxYo6Uhu8Dw_FMr8mL6z2Cd-c5yX58_XL7_334vbu24_99W1hSsZzIUsLjagRsLJl0wA0WDNjGiY41JXFHtu-qzqupRGmqhiUputq01ddB9aICi7Jx1PvHMPfBVNWo0sGvdcThiWpmslSCgkbyE-giSGliFbN0Y06roozdVSuHpWrR-Vb5t25fOlG7J8SZ8cb8OEM6GS0t3HT5tIT12wvNU27ce9P3OAOw4OLqNKovd9qucJ4D9sFigP8B-yWlds</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Suadicani, P</creator><creator>Hein, H. O</creator><creator>Gyntelberg, F</creator><general>Eur Respiratory Soc</general><general>Maney</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070701</creationdate><title>ABO phenotypes and inflammation-related predictors of lung cancer mortality: the Copenhagen Male Study - a 16-year follow-up</title><author>Suadicani, P ; Hein, H. O ; Gyntelberg, F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-64f3827e3e5f488338e70cc8021375fede9db5b1a6c2c55034cbb7cd5bb3fc253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>ABO Blood-Group System</topic><topic>Addictive behaviors</topic><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>Alcohol Drinking</topic><topic>Alcoholism</topic><topic>Alcoholism and acute alcohol poisoning</topic><topic>Biological and medical sciences</topic><topic>Denmark</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Lung Neoplasms - blood</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Phenotype</topic><topic>Pneumology</topic><topic>Prospective Studies</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Risk Factors</topic><topic>Smoking</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suadicani, P</creatorcontrib><creatorcontrib>Hein, H. O</creatorcontrib><creatorcontrib>Gyntelberg, F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The European respiratory journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suadicani, P</au><au>Hein, H. O</au><au>Gyntelberg, F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ABO phenotypes and inflammation-related predictors of lung cancer mortality: the Copenhagen Male Study - a 16-year follow-up</atitle><jtitle>The European respiratory journal</jtitle><addtitle>Eur Respir J</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>30</volume><issue>1</issue><spage>13</spage><epage>20</epage><pages>13-20</pages><issn>0903-1936</issn><eissn>1399-3003</eissn><abstract>Inflammation and genetic susceptibility influence the risk of lung cancer. Previous studies suggest that the inflammatory response may depend upon ABO phenotype. The hypothesis that the association with lung cancer mortality risk of lifestyle and occupational factors previously linked to inflammation would depend upon ABO phenotype was tested in a long-term follow-up of 3,346 male subjects aged 53-74 yrs. During a 16-yr period, 170 (5.1%) of the male subjects died due to lung cancer; 84 (5.9%) of phenotype O, 70 (4.9%) of phenotype A and 16 (3.2%) of phenotype B/AB. In addition to cumulative tobacco consumption, high salt intake long-term occupational dust exposure, high fat intake and consumption of alcohol were significantly predictive of lung cancer mortality for phenotype O subjects. After multivariable adjustment, the hazard ratios associated with the first three of these factors were 2.31, 2.08 and 1.67, respectively. Compared with abstainers, the hazard ratios for males drinking 1-10 wine drinks x week(-1) and males drinking >10 wine drinks x week(-1) were 1.65 and 2.02, respectively. Among phenotype A subjects, only cumulative tobacco consumption was associated with lung cancer mortality risk. The predictive role of inflammation-related risk factors for lung cancer mortality was significantly stronger among males of phenotype O than A.</abstract><cop>Leeds</cop><pub>Eur Respiratory Soc</pub><pmid>17392322</pmid><doi>10.1183/09031936.00062506</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ABO Blood-Group System Addictive behaviors Adult and adolescent clinical studies Aged Alcohol Drinking Alcoholism Alcoholism and acute alcohol poisoning Biological and medical sciences Denmark Genetic Predisposition to Disease Humans Inflammation Lung Neoplasms - blood Lung Neoplasms - genetics Lung Neoplasms - pathology Male Medical sciences Middle Aged Phenotype Pneumology Prospective Studies Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Risk Factors Smoking Time Factors Toxicology Tumors of the respiratory system and mediastinum |
title | ABO phenotypes and inflammation-related predictors of lung cancer mortality: the Copenhagen Male Study - a 16-year follow-up |
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