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Original Studies |
Departments of Medicine (D.K.M., A.W.M.), Urology (R.A.S., R.G.M.), Pathology (J.T.W., A.W.M.), and Medical Informatics (A.B.), University of Utah School of Medicine and the ARUP Institute, Salt Lake City, Utah 84132
Address correspondence and requests for reprints to: A. Wayne Meikle, M.D., University of Utah School of Medicine, 50 North Medical Drive, Salt Lake City, Utah 84132.
Both benign prostatic hyperplasia and prostate-specific antigen (PSA)
have been shown to increase with age and with prostate volume in men,
but the influence of heredity on these relationships is not completely
understood. This study has two aims: 1) to investigate the
inter-relationships of age, PSA, and various zonal measurements in the
prostate; and 2) to assess the impact of heritable influences on total
PSA. Eighty-four monozygotic twin pairs and 83 dizygotic twin pairs
were studied, and serum total PSA, free PSA, and
PSA-
1-antichymotrypsin were measured. Their prostate
volumes [total (TV), transition zone (TZ), and peripheral zone) were
quantitated using transrectal ultrasound.
Total PSA is significantly correlated with all zonal prostate measurements (TZ, peripheral zone, TV, and TZ/TV) and with age. When linear regression was applied, only age and TZ were retained in the final model. The proportion of variability in total PSA explained by these two factors, however, is below 24%. In contrast, estimates of heritability show that approximately 45% of the variability in total PSA can be explained by inherited factors. Whereas age and TZ are linearly related to total PSA, their influence is much less than that of familial and genetic factors. It is uncertain whether these factors predispose also to prostate cancer or if they are independent of those, whether they confound the accuracy of using total serum PSA level as a diagnostic tool.
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