Factors related to inflammation of the ovarian epithelium and risk of ovarian cancer

被引:284
作者
Ness, RB
Grisso, JA
Cottreau, C
Klapper, J
Vergona, R
Wheeler, JE
Morgan, M
Schlesselman, JJ
机构
[1] Univ Miami, Sylvester Comprehens Canc Ctr, Coral Gables, FL 33124 USA
[2] Univ Penn, Dept Obstet & Gynecol, Pittsburgh, PA USA
[3] Univ Penn, Dept Pathol & Lab Med, Pittsburgh, PA USA
[4] Univ Penn, Grad Sch Publ Hlth, Pittsburgh, PA USA
[5] Univ Penn, Ctr Clin Epidemiol & Biostat, Pittsburgh, PA USA
关键词
ovarian cancer; endometriosis; oral contraceptives; talc; tubal ligation;
D O I
10.1097/00001648-200003000-00006
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Previous epidemiologic observations consistently suggest that suppression of ovulation, tubal ligation, and hysterectomy reduce the risk of ovarian cancer and that perineal talc use increases the risk. We examined these and other risk factors in the context of a new hypothesis: that inflammation may play a role in ovarian cancer risk. Ovulation entails ovarian epithelial inflammation; talc, endometriosis, cysts, and hyperthyroidism may be associated with inflammatory responses of the ovarian epithelium; gynecologic surgery may preclude irritants from reaching the ovaries via ascension from the lower genital tract. We evaluated these risk factors in a population-based case-control study. Cases 20-69 years of age with a recent diagnosis of epithelial ovarian cancer (767) were compared with community controls (1367). We found that a number of reproductive and contraceptive factors that suppress ovulation, including gravidity, breast feeding, and oral contraception, reduced the risk of ovarian cancer. Environmental factors and medical conditions that increased risk included talc use, endometriosis, ovarian cysts, and hyperthyroidism. Gynecologic surgery including hysterectomy and tubal ligation were protective. Tubal ligation afforded a risk reduction even 20 or more years after the surgery. The spectrum of associations provides support for the hypothesis that inflammation may mediate ovarian cancer risk.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 58 条
[1]  
ACHESON ED, 1982, BRIT J IND MED, V39, P344
[2]  
AITOKALLIOTALLBERG AM, 1988, CANCER RES, V48, P2396
[3]   THE CAUSES AND PREVENTION OF CANCER [J].
AMES, BN ;
GOLD, LS ;
WILLETT, WC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5258-5265
[4]  
[Anonymous], 1982, CASE CONTROL STUDIES
[5]  
Auersperg N, 1997, J CELL PHYSIOL, V173, P261, DOI 10.1002/(SICI)1097-4652(199711)173:2<261::AID-JCP32>3.0.CO
[6]  
2-G
[7]  
Auersperg N, 1998, SEMIN ONCOL, V25, P281
[8]   RISK-FACTORS FOR OVARIAN-CANCER - A CASE CONTROL STUDY [J].
BOOTH, M ;
BERAL, V ;
SMITH, P .
BRITISH JOURNAL OF CANCER, 1989, 60 (04) :592-598
[9]   Cancer risk after a hospital discharge diagnosis of endometriosis [J].
Brinton, LA ;
Gridley, G ;
Persson, I ;
Baron, J ;
Bergqvist, A .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1997, 176 (03) :572-579
[10]  
Chang S, 1997, CANCER, V79, P2396, DOI 10.1002/(SICI)1097-0142(19970615)79:12<2396::AID-CNCR15>3.0.CO