| 15) Smith-Warner SA. (2001) | Pooled Analysis of 5 Cohort Studies. | 240,947 | 5-10 | 4,491? | Invasive breast cancer risk | Brussels sprouts |
INCLUSION CRITERIA:
- 1) A published prospective study with at least 200 incident breast cancer cases.
- 2) Assessment of usual dietary intake.
- 3) A validation study of the diet assessment method or a closely related instrument.
INCLUDED STUDIES (Follow-up years/No. of breast cancer cases):
- The Canadian National Breast Screening Study (1982-1987/419).
Rohan TE, Howe GR, Friedenreich CM, Jain M, Miller AB. Dietary fiber, vitamins A, C, and E, and risk of breast cancer: a cohort study. Cancer Causes Control. 1993 Jan;4(1):29-37. Abstract
- The Iowa Women's Health Study (1986-1995/1130).
Kushi LH, Fee RM, Sellers TA, Zheng W, Folsom AR. Intake of vitamins A, C, and E and postmenopausal breast cancer. The Iowa Women's Health Study. Am J Epidemiol. 1996 Jul 15;144(2):165-74. Full text
- The Netherlands Cohort Study (1986-1992/937).
Verhoeven DT, Assen N, Goldbohm RA, Dorant E, van 't Veer P, Sturmans F. Vitamins C and E, retinol, beta-carotene and dietary fibre in relation to breast cancer risk: a prospective cohort study. Br J Cancer. 1997;75(1):149-55. Abstract
- The New York State Cohort (1980-1987/367).
Graham S, Zielezny M, Marshall J, Priore R, Freudenheim J, Brasure J. Diet in the epidemiology of postmenopausal breast cancer in the New York State Cohort. Am J Epidemiol. 1992 Dec 1;136(11):1327-37. Abstract
- The Nurses' Health Study B (1986-1996/1638).
Zhang S, Hunter DJ, Forman MR, Rosner BA, Speizer FE, Colditz GA. Dietary carotenoids and vitamins A, C, and E and risk of breast cancer. J Natl Cancer Inst. 1999 Mar 17;91(6):547-56. Full text
RELATIVE RISK:
No significant association: RR = 0.67 (0.35-1.27) per 100 g/day increment.
P for heterogeneity in results across studies = 0.12.
Menopausal status at follow-up did not modify the associations (no data shown).
| Age at menarche, interaction between parity and age at birth of first child, oral contraceptive use (ever/never), history of benign breast disease, menopausal status at follow-up, postmenopausal hormone use, family history of breast cancer, smoking status (ever/never), education, BMI, BMI-menopausal status interaction, height, alcohol intake, and energy intake. |