Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers

被引:51
作者
Antoniou, Antonis C.
Shenton, Andrew
Maher, Eamonn R.
Watson, Emma
Woodward, Emma
Lalloo, Fiona
Easton, Douglas F.
Evans, D. Gareth [1 ]
机构
[1] St Marys Hosp, Acad Unit Med Genet & Reg Genet Serv, Manchester M13 0JH, Lancs, England
[2] Univ Cambridge, CR UK Genet Epidemiol Unit, Strangeways Res Lab, Dept Publ Hlth & Primary Care, Cambridge CB1 8RN, England
[3] St Marys Hosp, Dept Clin Genet, SM2, Manchester M13 0JH, Lancs, England
[4] Univ Birmingham, Sch Med, Div Med Genet, Birmingham B15 2TT, W Midlands, England
关键词
D O I
10.1186/bcr1630
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Increasing parity and age at first full-term pregnancy are established risk factors for breast cancer in the general population. However, their effects among BRCA1 and BRCA2 mutation carriers is still under debate. We used retrospective data on BRCA1 and BRCA2 mutation carriers from the UK to assess the effects of parity-related variables on breast cancer risk. Methods The data set included 457 mutation carriers who developed breast cancer (cases) and 332 healthy mutation carriers (controls), ascertained through families seen in genetic clinics. Hazard ratios were estimated by using a weighted cohort approach. Results Parous BRCA1 and BRCA2 mutation carriers were at a significantly lower risk of developing breast cancer ( hazard ratio 0.54, 95% confidence interval 0.37 to 0.81; p = 0.002). The protective effect was observed only among carriers who were older than 40 years. Increasing age at first live birth was associated with an increased breast cancer risk among BRCA2 mutation carriers (p trend = 0.002) but not BRCA1 carriers. However, the analysis by age at first live birth was based on small numbers. Conclusion The results suggest that the relative risks of breast cancer associated with parity among BRCA1 and BRCA2 mutation carriers may be similar to those in the general population and that reproductive history may be used to improve risk prediction in carriers.
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页数:6
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共 23 条
[1]   Pregnancies, breast-feeding, and breast cancer risk in the international BRCA1/2 carrier cohort study (IBCCS) [J].
Andrieu, Nadine ;
Goldgar, David E. ;
Easton, Douglas F. ;
Rookus, Matti ;
Brohet, Richard ;
Antoniou, Antonis C. ;
Peock, Susan ;
Evans, Gareth ;
Eccles, Diana ;
Douglas, Fiona ;
Nogues, Catherine ;
Gauthier-Villars, Marion ;
Chompret, Agnes ;
van Leeuwen, Flora E. ;
Kluijt, Irina ;
Benitez, Javier ;
Arver, Brita ;
Olah, Edith ;
Chang-Claude, Jenny .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (08) :535-544
[2]  
[Anonymous], [No title captured]
[3]   Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies [J].
Antoniou, A ;
Pharoah, PDP ;
Narod, S ;
Risch, HA ;
Eyfjord, JE ;
Hopper, JL ;
Loman, N ;
Olsson, H ;
Johannsson, O ;
Borg, Å ;
Pasini, B ;
Radice, P ;
Manoukian, S ;
Eccles, DM ;
Tang, N ;
Olah, E ;
Anton-Culver, H ;
Warner, E ;
Lubinski, J ;
Gronwald, J ;
Gorski, B ;
Tulinius, H ;
Thorlacius, S ;
Eerola, H ;
Nevanlinna, H ;
Syrjäkoski, K ;
Kallioniemi, OP ;
Thompson, D ;
Evans, C ;
Peto, J ;
Lalloo, F ;
Evans, DG ;
Easton, DF .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) :1117-1130
[4]   A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes [J].
Antoniou, AC ;
Pharoah, PDP ;
McMullan, G ;
Day, NE ;
Stratton, MR ;
Peto, J ;
Ponder, BJ ;
Easton, DF .
BRITISH JOURNAL OF CANCER, 2002, 86 (01) :76-83
[5]   A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes [J].
Antoniou, AC ;
Goldgar, DE ;
Andrieu, N ;
Chang-Claude, J ;
Brohet, R ;
Rookus, MA ;
Easton, DF .
GENETIC EPIDEMIOLOGY, 2005, 29 (01) :1-11
[6]   Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50 302 women with breast cancer and 96 973 women without the disease [J].
Beral, V ;
Bull, D ;
Doll, R ;
Peto, R ;
Reeves, G ;
La Vecchia, C ;
Magnusson, C ;
Miller, T ;
Peterson, B ;
Pike, M ;
Thomas, D ;
van Leeuwen, F .
LANCET, 2002, 360 (9328) :187-195
[7]   CHILDBEARING, ORAL-CONTRACEPTIVE USE, AND BREAST-CANCER [J].
BERAL, V ;
REEVES, G .
LANCET, 1993, 341 (8852) :1102-1102
[8]   Modifying effect of reproductive risk factors on the age at onset of breast cancer for German BRCA1 mutation carriers [J].
ChangClaude, J ;
Becher, H ;
Eby, N ;
Bastert, G ;
Wahrendorf, J ;
Hamann, U .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1997, 123 (05) :272-279
[9]   Differential effects of reproductive factors on the risk of pre- and postmenopausal breast cancer. Results from a large cohort of French women [J].
Clavel-Chapelon, F .
BRITISH JOURNAL OF CANCER, 2002, 86 (05) :723-727
[10]   Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers [J].
Cullinane, CA ;
Lubinski, J ;
Neuhausen, SL ;
Ghadirian, P ;
Lynch, HT ;
Isaacs, C ;
Weber, B ;
Moller, P ;
Offit, K ;
Kim-Sing, C ;
Friedman, E ;
Randall, S ;
Pasini, B ;
Ainsworth, P ;
Gershoni-Baruch, R ;
Foulkes, WD ;
Klijn, J ;
Tung, N ;
Rennert, G ;
Olopade, O ;
Couch, F ;
Wagner, T ;
Olsson, H ;
Sun, P ;
Weitzel, JN ;
Narod, SA .
INTERNATIONAL JOURNAL OF CANCER, 2005, 117 (06) :988-991