Urology
Volume 54, Issue 6 , Pages 1022-1027, December 1999

Serum prostate-specific antigen levels (PSA) in men without clinical evidence of prostate cancer: age-specific reference ranges for total PSA, free PSA, and percent free PSA

This study was presented in part at the 32nd Annual Meeting of the Society for Epidemiologic Research, Baltimore, Maryland, June 10 to 12, 1999.

  • Leslie A Kalish

      Affiliations

    • New England Research Institutes, Watertown, Massachusetts, USA
    • Corresponding Author InformationReprint requests: Leslie A. Kalish, Sc.D., New England Research Institutes, 9 Galen Street, Watertown, MA 02472
  • ,
  • John B McKinlay

      Affiliations

    • New England Research Institutes, Watertown, Massachusetts, USA

Received 7 May 1999; received in revised form 30 June 1999; accepted 30 June 1999.

Abstract 

Objectives. To investigate the relationship between age and total prostate-specific antigen (tPSA), free PSA (fPSA), and percent free PSA (%fPSA) in men 48 to 79 years old without clinical evidence of prostate cancer. We determined age-specific ranges for each parameter and compared the results with previously published studies in similar populations.

Methods. Nine hundred eighty-three men (96% white) from the random-sample community-based Massachusetts Male Aging Study were analyzed. Men with PSA 4.1 ng/mL or greater were referred for biopsy and those with positive biopsies or with medical record, cancer registry, or self-reported evidence of prostate cancer were excluded.

Results. The median tPSA increased 38.6% per decade (95% confidence interval 28.7% to 49.3%). Because of the greater variability at older ages, the 95th percentile increased faster than the median, leading to the following age-specific upper limits of normal: 2.84 for 50 to 59 years, 5.87 for 60 to 69 years, and 9.03 for 70 to 79 years. The pattern of association between fPSA and age was similar to tPSA. The 50th and 5th percentiles of %fPSA were 25.3% and 13.2%, respectively, regardless of age.

Conclusions. Establishing age-specific screening cutoffs based on the age-specific upper limits of normal will ensure low false-positive biopsy rates but may also lead to low true positive rates (ie, low sensitivity) in older age groups. Both sensitivity and specificity should be considered when counseling patients. The independence of %fPSA with age confirms others’ findings.

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 This investigation was supported by grant DK-51345 awarded by the National Institute of Diabetes and Digestive and Kidney Diseases.

PII: S0090-4295(99)00349-0

Urology
Volume 54, Issue 6 , Pages 1022-1027, December 1999