Cigarette smoking and lung cancer - Modeling effect modification of total exposure and intensity

被引:72
作者
Lubin, Jay H.
Caporaso, Neil
Wichmann, H. Erich
Schaffrath-Rosario, Angelika
Alavanja, Michael C. R.
机构
[1] NCI, Biostat Branch, Div Canc Epidemiol & Genet, Rockville, MD 20852 USA
[2] NCI, Genet Epidemiol Branch, Div Canc Epidemiol & Genet, Rockville, MD USA
[3] GSF, Natl Res Ctr Environm & Hlth, Neuherberg, Germany
[4] Abt Epidemiol & Gesundheitsberichterstattung, Robert Koch Inst, Berlin, Germany
[5] NCI, Div Canc Epidemiol & Genet, Occupat & Environm Epidemiol Branch, Rockville, MD USA
关键词
D O I
10.1097/EDE.0b013e31812717fe
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: A recent analysis indicates that the excess odds ratio for lung cancer by smoking is described by a function that is linear in pack-years and exponential in the logarithm of smoking intensity and its square (Cancer Epidemiol Biomarkers Prev. 2006;15:517i, s i, 52 he model suggests that below 15-20 cigarettes per day there a direct exposure rate" effect, ie, the excess odds ratio per pack-year for higher intensity (and shorter duration) smokers is greater than for lower-intensity (and longer duration) smokers. Above 20 cigarettes per day, there is an "inverse-exposure-rate" effect, ie, the excess odds ratio per pack-year for higher intensity smokers is smaller than for lower-intensity smokers. Methods: Using pooled data from 2 large case-control studies of lung cancer (the European Smoking and Health Study and the German Radon Study), we evaluated effect modification of the association between smoking and lung cancer. Results: Interaction effects are very specific. Variations in risk of lung cancer with years since cessation of smoking, age, method of inhalation, and type of cigarette result from interactions with smoking intensity, and not total pack-years. In contrast, risk variations by sex result from the interaction with total pack-years, while intensity effects are homogeneous. Risk variations by age at which smoking started result from interactions with both total pack-years and intensity. All intensity interactions are homogeneous across studies. Conclusions: The specificity of the interactions may provide clues for the molecular basis of the smoking and lung cancer relationship.
引用
收藏
页码:639 / 648
页数:10
相关论文
共 47 条
[11]   Gender differences in genetic damage induced by the tobacco-specific nitrosamine NNKand the influence of the Thr241Met polymorphism in the XRCC3 gene [J].
Hill, CE ;
Affatato, AA ;
Wolfe, KJ ;
Lopez, MS ;
Hallberg, CK ;
Canistro, D ;
Abdel-Rahman, SZ .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2005, 46 (01) :22-29
[12]  
HOOVER DR, 1994, AM J EPIDEMIOL, V140, P186, DOI 10.1093/oxfordjournals.aje.a117230
[13]   Large-scale investigation of base excision repair genetic polymorphisms and lung cancer risk in a multicenter study [J].
Hung, RJ ;
Brennan, P ;
Canzian, F ;
Szeszenia-Dabrowska, N ;
Zaridze, D ;
Lissowska, J ;
Rudnai, P ;
Fabianova, E ;
Mates, D ;
Foretova, L ;
Janout, V ;
Bencko, V ;
Chabrier, A ;
Borel, S ;
Hall, J ;
Boffetta, P .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (08) :567-576
[14]   The changing epidemiology of lung cancer in Europe [J].
Janssen-Heijnen, MLG ;
Coebergh, JWW .
LUNG CANCER, 2003, 41 (03) :245-258
[15]   Relationships between cigarette consumption and biomarkers of tobacco toxin exposure [J].
Joseph, AM ;
Hecht, SS ;
Murphy, SE ;
Carmella, SG ;
Le, CT ;
Zhang, Y ;
Han, SM ;
Hatsukami, DK .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2005, 14 (12) :2963-2968
[16]  
KREIENBROCK L, 2001, AM J EPIDEMIOL, V13, P42
[17]   Residential radon and risk of lung cancer in Eastern Germany [J].
Kreuzer, M ;
Heinrich, J ;
Wölke, G ;
Rosario, AS ;
Gerken, M ;
Wellmann, J ;
Keller, G ;
Kreienbrock, L ;
Wichmann, HE .
EPIDEMIOLOGY, 2003, 14 (05) :559-568
[18]   The dose-response relationship between cigarette consumption, biochemical markers and risk of lung cancer [J].
Law, MR ;
Morris, JK ;
Watt, HC ;
Wald, NJ .
BRITISH JOURNAL OF CANCER, 1997, 75 (11) :1690-1693
[19]   Cotinine levels and self-reported smoking status in patients attending a bronchoscopy clinic [J].
Lewis, SJ ;
Cherry, NM ;
Niven, RM ;
Barber, PV ;
Wilde, K ;
Povey, AC .
BIOMARKERS, 2003, 8 (3-4) :218-228
[20]   Air pollution exposure DNA adduct dosimetry in humans and rodents: evidence for non-linearity at high doses [J].
Lewtas, J ;
Walsh, D ;
Williams, R ;
Dobias, L .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1997, 378 (1-2) :51-63