The effects of interaction between familial and reproductive factors on breast cancer risk:: a combined analysis of seven case-control studies

被引:17
作者
Andrieu, N
Smith, T
Duffy, S
Zaridze, DG
Renaud, R
Rohan, T
Gerber, M
Luporsi, E
Lê, M
Lee, HP
Lifanova, Y
Day, NE
机构
[1] Inst Gustave Roussy, INSERM, U351, F-94805 Villejuif, France
[2] Univ Forvie Site, Inst Publ Hlth, MRC, Biostat Unit, Cambridge CB2 2SR, England
[3] Russian Acad Sci, Ctr Canc Res, Dept Epidemiol, Moscow 115478, Russia
[4] Hospices Civils Strasbourg, Dept Obstet Gynecol, F-67000 Strasbourg, France
[5] Univ Toronto, Epidemiol Unit, Toronto, ON M5S 1A8, Canada
[6] CNRS, INSERM, CRLC, Ctr Rech Cancerol,Grp Epidemiol Metab, F-34094 Montpellier 5, France
[7] Ctr Alexis Vautrin, F-54511 Vandoeuvre Les Nancy, France
[8] Natl Univ Singapore, Dept Community Occupat & Family Med, Singapore 117548, Singapore
关键词
breast cancer; familial risk; reproductive life factor; interactions;
D O I
10.1038/bjc.1998.251
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this paper, a combined analysis was performed to study the interaction between familial risk and reproductive life factors. In particular, the interaction between familial risk and breast cell mitotic activity (BCMA), as assessed by duration of ovarian activity, was investigated because of the potential importance of mitotic activity on genetically susceptible cells. The present analysis included 3152 cases and 4404 controls in seven case-control studies from four countries. The interaction effect was estimated in each study separately, then combined using two different methods: a multivariate weighted average and a Bayesian random-effects model. The main effects of reproductive life factors on the risk of breast cancer were in agreement with the previous findings. In particular, an increased duration of BCMA before the first childbirth and over life was found to increase the risk of breast cancer (P < 0.001). Slightly increasing but non-significant, familiar risks were observed with increasing number of children (P = 0.17), increasing age at first childbirth (P > 0.2) and increasing duration of BCMA (P > 0.2). There was no modification in familial risk with age at menarche and no clear pattern with menopause characteristics. A weak influence of reproductive and menstrual factors on the familial risk emerged from the present study.
引用
收藏
页码:1525 / 1536
页数:12
相关论文
共 46 条
[1]   FAMILIALITY IN BREAST-CANCER - A CASE-CONTROL STUDY IN A SWEDISH POPULATION [J].
ADAMI, HO ;
HANSEN, J ;
JUNG, B ;
RIMSTEN, A .
BRITISH JOURNAL OF CANCER, 1980, 42 (01) :71-77
[2]  
ANDERSON TJ, 1982, BRIT J CANCER, V46, P676
[3]   FAMILIAL RISK, ABORTION AND THEIR INTERACTIVE EFFECT ON THE RISK OF BREAST-CANCER - A COMBINED ANALYSIS OF 6 CASE-CONTROL STUDIES [J].
ANDRIEU, N ;
DUFFY, SW ;
ROHAN, TE ;
LE, MG ;
LUPORSI, E ;
GERBER, M ;
RENAUD, R ;
ZARIDZE, DG ;
LIFANOVA, Y ;
DAY, NE .
BRITISH JOURNAL OF CANCER, 1995, 72 (03) :744-751
[4]   VARIATIONS IN THE RISK OF BREAST-CANCER ASSOCIATED WITH A FAMILY HISTORY OF BREAST-CANCER ACCORDING TO AGE AT ONSET AND REPRODUCTIVE FACTORS [J].
ANDRIEU, N ;
CLAVEL, F ;
AUQUIER, A ;
LE, MG ;
GAIRARD, B ;
PIANA, L ;
BREMOND, A ;
LANSAC, J ;
FLAMANT, R ;
RENAUD, R .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1993, 46 (09) :973-980
[5]   GENETIC-ANALYSIS OF HUMAN-BREAST CANCER - IMPLICATIONS FOR FAMILY STUDY DESIGNS [J].
ANDRIEU, N ;
DEMENAIS, F ;
MARTINEZ, M .
GENETIC EPIDEMIOLOGY, 1988, 5 (04) :225-233
[6]  
BAIN C, 1980, AM J EPIDEMIOL, V111, P301, DOI 10.1093/oxfordjournals.aje.a112901
[7]  
BRINTON LA, 1982, J NATL CANCER I, V69, P817
[8]  
Byrne C, 1991, Epidemiology, V2, P276, DOI 10.1097/00001648-199107000-00007
[9]  
CLAUS EB, 1991, AM J HUM GENET, V48, P232
[10]   ORAL-CONTRACEPTIVES AND BREAST-CANCER - A FRENCH CASE-CONTROL STUDY [J].
CLAVEL, F ;
ANDRIEU, N ;
GAIRARD, B ;
BREMOND, A ;
PIANA, L ;
LANSAC, J ;
BREART, G ;
RUMEAUROUQUETTE, C ;
FLAMANT, R ;
RENAUD, R .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1991, 20 (01) :32-38