Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (17)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Tavani, A
Right arrow Articles by Franceschi, S
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tavani, A
Right arrow Articles by Franceschi, S
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

International Journal of Epidemiology 2000;29:799-802
© International Epidemiological Association 2000

Influence of menstrual and reproductive factors on ovarian cancer risk in women with and without family history of breast or ovarian cancer

A Tavania, E Riccia, C La Vecchiaa,b, M Suracea, G Benzic, F Parazzinic and S Franceschid

a Istituto di Ricerche Farmacologiche ‘Mario Negri’, Milan, Italy.
b Istituto Statistica Medica e Biometria, Università degli Studi di Milano, 20133 Milan, Italy.
c Prima Clinica Ostetrico-ginecologica, Università di Milano, 20122 Milan, Italy.
d Centro di Riferimento Oncologico, 33081 Aviano (PN), Italy.

Reprint requests to: Alessandra Tavani, Istituto di Ricerche Farmacologiche ‘Mario Negri’, Via Eritrea 62, 20157 Milano, Italy. E-mail: tavani{at}irfmn.mnegri.it

Background As women with a family history of ovarian and/or breast cancer possibly inherit genetic changes that alter their risk of ovarian cancer, other established risk factors for ovarian cancer may influence the risk differently in women with and without a family history of the disease.

Methods Case-control study conducted between 1983 and 1991 in Northern Italy. Cases were 971 women, under 75 years, with incident, histologically confirmed epithelial ovarian cancer, and controls were 2758 women, under 75 years, admitted to hospitals for non-malignant, non-hormone-related conditions, who had not undergone bilateral oophorectomy. Of these, 93 cases and 139 controls had a family history of ovarian and/or breast cancer.

Results The risk of ovarian cancer increased with irregular menstrual cycles, late age at menopause, natural menopause, nulliparity, never use of oral contraceptives and use of hormone replacement therapy. We computed an ‘adult life risk score’ (ALRS) considering the combined effect of these factors. Compared to women without a family history and a low ALRS, the OR was 1.7 for women without family history and high ALRS, 1.4 for women with a family history and low ALRS, and 3.5 for women with a family history and high ALRS.

Conclusions Intervention on selected hormonal risk factors for ovarian cancer might be important for women with a family history of the disease.

Keywords Breast cancer, case-control study, family history, hormone replacement therapy, menstrual factors, oral contraceptives, ovarian cancer, reproductive factors, risk factors

Accepted 13 March 2000


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Endocr Relat CancerHome page
J.-H. Choi, K.-C. Choi, N. Auersperg, and P. C K Leung
Gonadotropins upregulate the epidermal growth factor receptor through activation of mitogen-activated protein kinases and phosphatidyl-inositol-3-kinase in human ovarian surface epithelial cells
Endocr. Relat. Cancer, June 1, 2005; 12(2): 407 - 421.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
J.-H. Choi, K.-C. Choi, N. Auersperg, and P. C. K. Leung
Overexpression of Follicle-Stimulating Hormone Receptor Activates Oncogenic Pathways in Preneoplastic Ovarian Surface Epithelial Cells
J. Clin. Endocrinol. Metab., November 1, 2004; 89(11): 5508 - 5516.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
V. McGuire, A. Felberg, M. Mills, K. L. Ostrow, R. DiCioccio, E. M. John, D. W. West, and A. S. Whittemore
Relation of Contraceptive and Reproductive History to Ovarian Cancer Risk in Carriers and Noncarriers of BRCA1 Gene Mutations
Am. J. Epidemiol., October 1, 2004; 160(7): 613 - 618.
[Abstract] [Full Text] [PDF]


Home page
CMAJHome page
C. N. Wathen, D. S. Feig, J. W. Feightner, B. L. Abramson, and A. M. Cheung
Hormone replacement therapy for the primary prevention of chronic diseases: recommendation statement from the Canadian Task Force on Preventive Health Care
Can. Med. Assoc. J., May 11, 2004; 170(10): 1535 - 1537.
[Full Text] [PDF]


Home page
Am J EpidemiolHome page
K.-H. Tung, M. T. Goodman, A. H. Wu, K. McDuffie, L. R. Wilkens, A. M. Y. Nomura, and L. N. Kolonel
Aggregation of Ovarian Cancer with Breast, Ovarian, Colorectal, and Prostate Cancer in First-degree Relatives
Am. J. Epidemiol., April 15, 2004; 159(8): 750 - 758.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
S. L. Crawford, C. B. Johannes, and R. K. Stellato
Assessment of Digit Preference in Self-reported Year at Menopause: Choice of an Appropriate Reference Distribution
Am. J. Epidemiol., October 1, 2002; 156(7): 676 - 683.
[Abstract] [Full Text] [PDF]


Home page
CA Cancer J ClinHome page
M. N. Barnes, W. E. Grizzle, C. J. Grubbs, and E. E. Partridge
Paradigms for Primary Prevention of Ovarian Carcinoma
CA Cancer J Clin, July 1, 2002; 52(4): 216 - 225.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.