ASSOCIATION OF INCIDENT LUNG-CANCER WITH FAMILY HISTORY OF FEMALE REPRODUCTIVE CANCERS - THE IOWA-WOMENS-HEALTH-STUDY

被引:50
作者
SELLERS, TA
POTTER, JD
FOLSOM, AR
机构
[1] Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis, Minnesota
[2] The Institute of Human Genetics, University of Minnesota, Minneapolis, Minnesota
关键词
LUNG CANCER; FAMILY HISTORY; CASE-CONTROL; REPRODUCTIVE CANCERS;
D O I
10.1002/gepi.1370080306
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A number of studies have documented the familial aggregation of lung cancer; there is at least one report that female reproductive cancers are also increased in these families. To determine if the risk exists for all reproductive cancer sites, we conducted a nested case-control study of lung cancer incidence in a cohort of 41,837 women ages 55-69 years. Women were recruited by mail and asked to provide information on education, occupation, smoking habits, physical activity, and family history of specific cancer sites among female relatives. Four year follow-up for cancer incidence was conducted using a state-wide tumor registry. Compared to random controls (n = 1900), cases (n = 152) were more likely to have reported at baseline a sister affected with cancer of the uterus [crude odds ratio (OR) = 3.4, 95% Cl = 1.7-7.0, P < 0.01], cervix (OR = 3.2, 95% Cl 1.2-8.6, P < 0.05), or cancer at any site (OR = 1.6, 95% Cl 1.1-2.4, P < 0.05). A family history of an affected mother with a female reproductive cancer was also more common among the cases, but not statistically significant. Cases were less educated, more likely to work in a technical/industrial setting, less physically active, more likely to smoke, and to smoke for a longer period of time than the controls (all P < 0.01). These differences reduced the magnitude of the family history risk indicators; only the combined category of reproductive cancer at all sites remained statistically significant. Additional family studies should be done to assess environmental factors in the relatives of the cases and controls to disentangle the influence of shared genes and shared environmental factors in these associations.
引用
收藏
页码:199 / 208
页数:10
相关论文
共 61 条
[1]   RISK OF CANCER IN WOMEN RECEIVING HORMONE REPLACEMENT THERAPY [J].
ADAMI, HO ;
PERSSON, I ;
HOOVER, R ;
SCHAIRER, C ;
BERGKVIST, L .
INTERNATIONAL JOURNAL OF CANCER, 1989, 44 (05) :833-839
[2]   PHYSICAL-ACTIVITY AND RISK OF CANCER IN THE NHANES-I POPULATION [J].
ALBANES, D ;
BLAIR, A ;
TAYLOR, PR .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1989, 79 (06) :744-750
[3]   METABOLIC OXIDATION PHENOTYPES AS MARKERS FOR SUSCEPTIBILITY TO LUNG-CANCER [J].
AYESH, R ;
IDLE, JR ;
RITCHIE, JC ;
CROTHERS, MJ ;
HETZEL, MR .
NATURE, 1984, 312 (5990) :169-170
[4]  
BALE S J, 1984, Genetic Epidemiology, V1, P53, DOI 10.1002/gepi.1370010108
[5]   MOLECULAR ANALYSIS OF THE SHORT ARM OF CHROMOSOME-3 IN SMALL-CELL AND NON-SMALL-CELL CARCINOMA OF THE LUNG [J].
BRAUCH, H ;
JOHNSON, B ;
HOVIS, J ;
YANO, T ;
GAZDAR, A ;
PETTENGILL, OS ;
GRAZIANO, S ;
SORENSON, GD ;
POIESZ, BJ ;
MINNA, J ;
LINEHAN, M ;
ZBAR, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1987, 317 (18) :1109-1113
[6]   CIGARETTE-SMOKING AND INVASIVE CERVICAL-CANCER [J].
BRINTON, LA ;
SCHAIRER, C ;
HAENSZEL, W ;
STOLLEY, P ;
LEHMAN, HF ;
LEVINE, R ;
SAVITZ, DA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1986, 255 (23) :3265-3269
[7]  
BRISMAN R, 1967, CANCER, V20, P2048, DOI 10.1002/1097-0142(196711)20:11<2048::AID-CNCR2820201134>3.0.CO
[8]  
2-A
[9]  
BROBECH O, 1949, HEREDITY UTERINE CAN
[10]  
CASAGRANDE JT, 1979, LANCET, V2, P170