Prostate diseases are a major problem for aging men. Prostate cancer is the most commonly diagnosed cancer and the second leading cause of cancer deaths in U.S. men. Furthermore, benign prostate hypertrophy (BPH) affects most men by age 80. The Baltimore Longitudinal Study of Aging (BLSA)is defining anatomic and physiologic characteristics that distinguish normal prostate growth with age and the development of prostate disease; identifying hormonal changes important in the diseases; and characterizing markers(serum and genetic) that could identify high risk groups, and increasing knowledge regarding the development and progression of prostate disease, and lead to methods of disease prevention. The BLSA prostate study pioneered the use of prostate specific antigen (PSA) velocity to improve the specificity of PSA. testing. Less than 5% of men without prostate cancer have a rate of change in PSA exceeding 0.75ng/ml per year; while 70% of men with cancer have a rate of change in PSA that exceeds 0.75ng/ml per year. These data have now been confirmed in large prospective screening trials. The BLSA has recently analyzed free PSA levels using frozen sera from men with and without prostate cancer. Free PSA levels were significantly lower in cancer cases 10 years before diagnosis; while total PSA levels were significantly different 4 years before diagnosis. This finding could have important implications regarding early detection of prostate cancer. Human studies of androgen levels in men with and without prostate cancer have reported varying results. A preliminary case-control analysis in BLSA men with and without prostate cancer, found no significant differences in total and free testosterone levels at 0-5, 5-10, and 10-15 years before diagnosis of disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000633-07
Application #
2565738
Study Section
Special Emphasis Panel (LSB)
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
1996
Total Cost
Indirect Cost
Name
National Institute on Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Loeb, Stacy; Kettermann, Anna; Ferrucci, Luigi et al. (2008) The Optimal Application of Prostate-Specific Antigen (PSA) Velocity to Predict High-Risk Disease. Eur Urol 54:978-979
Carter, H Ballentine; Kettermann, Anna; Ferrucci, Luigi et al. (2007) Prostate-specific antigen velocity risk count assessment: a new concept for detection of life-threatening prostate cancer during window of curability. Urology 70:685-90
Carter, H Ballentine; Kettermann, Anna; Warlick, Christopher et al. (2007) Expectant management of prostate cancer with curative intent: an update of the Johns Hopkins experience. J Urol 178:2359-64;discussion 2364-5
Maggio, Marcello; Blackford, Amanda; Taub, Dennis et al. (2006) Circulating inflammatory cytokine expression in men with prostate cancer undergoing androgen deprivation therapy. J Androl 27:725-8
Carter, H Ballentine; Ferrucci, Luigi; Kettermann, Anna et al. (2006) Detection of life-threatening prostate cancer with prostate-specific antigen velocity during a window of curability. J Natl Cancer Inst 98:1521-7
Parsons, J Kellogg; Carter, H Ballentine; Partin, Alan W et al. (2006) Metabolic factors associated with benign prostatic hyperplasia. J Clin Endocrinol Metab 91:2562-8
Parsons, J Kellogg; Carter, H Ballentine; Platz, Elizabeth A et al. (2005) Serum testosterone and the risk of prostate cancer: potential implications for testosterone therapy. Cancer Epidemiol Biomarkers Prev 14:2257-60
Platz, Elizabeth A; Rohrmann, Sabine; Pearson, Jay D et al. (2005) Nonsteroidal anti-inflammatory drugs and risk of prostate cancer in the Baltimore Longitudinal Study of Aging. Cancer Epidemiol Biomarkers Prev 14:390-6
Berndt, Sonja I; Carter, H Ballentine; Landis, Patricia K et al. (2005) Prediagnostic plasma vitamin C levels and the subsequent risk of prostate cancer. Nutrition 21:686-90
Carter, H Ballentine; Landis, Patricia; Wright, E James et al. (2005) Can a baseline prostate specific antigen level identify men who will have lower urinary tract symptoms later in life? J Urol 173:2040-3

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