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-Fetoprotein in Estimating Breast Cancer Risk1
Department of Epidemiology and Biostatistics, School of Rural Public Health, Texas A&M University System Health Science Center, College Station, Texas 77843-1266 [B. E. R.]; Department of Epidemiology, University of North Carolina at Chapel Hill, School of Public Health, Chapel Hill, North Carolina 27599-7400 [J. D. P.]; and School of Medicine, The University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229 [J. K. W.]
Data
from a nested case-control study were analyzed to examine high mean
arterial pressure (MAP), hypertension of pregnancy, and preeclampsia as
independent predictors and as surrogate markers for elevated
-fetoprotein (AFP) levels in evaluating breast cancer risk. Cases
(n = 205) were identified by the California Cancer
Registry from a cohort of pregnant women who were part of the Kaiser
Health Plan and took part in the Child Health and Development Studies
initiated by the University of California, Berkeley, from June 1959 to
September 1966. Controls (n = 337) were selected by
randomized recruitment from the same cohort probability matched to
cases by distribution of birth dates of cases. High MAP was associated
with breast cancer risk and is different across quartile of age at
first full-term pregnancy as is high AFP. Odds ratios (OR) across
quartiles for MAP were 0.24 [95% confidence interval (CI),
0.080.71], 0.84 (95% CI, 0.391.66), 1.00 (referent), and 2.50
(95% CI, 1.215.13), and for AFP were 0.34 (95% CI, 0.130.93),
0.77 (95% CI, 0.361.67), 1.00 (referent), and 2.38 (95% CI,
1.135.00). Neither diagnosed preeclampsia nor hypertension of
pregnancy showed any association with breast cancer risk. When both
high AFP and high MAP were entered into the same analysis, neither
changed the OR for the other more than 8%. Additionally, AFP level was
not a linear function of MAP. Although the pattern of ORs across
quartiles of age at first full-term pregnancy was similar for the two
variables, it cannot be concluded that high MAP is an adequate
surrogate for high levels of maternal serum AFP, but rather represents
some related process that is in and of itself a risk factor for breast
cancer.
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