The Journal of Urology
Volume 176, Issue 4 , Pages 1299-1306, October 2006

Prevention of Benign Prostatic Hyperplasia Disease

  • Leonard S. Marks

      Affiliations

    • Urological Sciences Research Foundation and Department of Urology, Geffen School of Medicine, University of California-Los Angeles, Los Angeles, California
    • Corresponding Author InformationCorrespondence: Urological Sciences Research Foundation, 3831 Hughes Ave., Suite 701, Culver City, California 90232 (telephone: 310-559-9800; FAX: 310-559-7821).
    • Financial interest and/or other relationship with Merck, Beckman-Coulter, Pfizer, Sanofi, Watson, Gen-Probe, GlaxoSmithKline and Diagnostic Ultrasound.
  • ,
  • Claus G. Roehrborn

      Affiliations

    • Department of Urology, University of Texas Southwestern Medical Center, Dallas, Texas
  • ,
  • Gerald L. Andriole

      Affiliations

    • Division of Urologic Surgery, Washington University School of Medicine, St. Louis, Missouri

Received 19 September 2005

Purpose

We reviewed the evidence that benign prostatic hyperplasia is a progressive condition and men at risk for benign prostatic hyperplasia disease can be identified, treated and protected to a meaningful extent regardless of symptom status.

Materials and Methods

The MEDLINE database was searched in 4 areas of interest relating to benign prostatic hyperplasia, including 1) progression of clinical manifestations with age, especially in regard to baseline symptom status, 2) the incidence of complications due to disease progression, 3) the use of predictive factors that may help identify men at risk for disease progression and 4) the prevention of benign prostatic hyperplasia disease with medical therapy.

Results

Tissue changes in the prostate (benign prostatic hyperplasia) are inevitable consequences of aging. However, benign prostatic hyperplasia disease, which we define as a life altering urinary condition requiring medical intervention, is predictable and preventable. Benign prostatic hyperplasia disease progression is associated with increasing prostate volume, decreasing urinary flow, symptomatic deterioration often to the point of major life-style interference and serious complications, eg acute urinary retention and the need for surgery. The risk of benign prostatic hyperplasia disease progression was found to be directly related to prostate volume and its surrogate marker, serum prostate specific antigen, after prostate cancer is excluded. Other factors, eg baseline symptoms and the flow rate, were found to be less relevant compared with prostate specific antigen greater than 1.5 ng/ml for predicting benign prostatic hyperplasia disease morbidity.

Conclusions

Men at risk for benign prostatic hyperplasia disease can be identified using prostate specific antigen greater than 1.5 ng/ml as a surrogate marker of prostate volume. In men at risk with prostate specific antigen greater than 1.5 ng/ml 5α-reductase inhibitors have potential value for benign prostatic hyperplasia disease prevention regardless of symptom status.

Key Words:  prostate , prostatic hyperplasia , 5 alpha-reductase , dutasteride , finasteride

Abbreviation and Acronyms:  5AR, 5α-reductase , 5ARI, 5AR inhibitor , AUA, American Urological Association , AUR, acute urinary retention , BPH, benign prostatic hyperplasia , DHT, dihydrotestosterone , HGCaP, high grade prostate cancer , MTOPS, Medical Therapy of Prostatic Symptoms , PCPT, Prostate Cancer Prevention Trial , PLESS, Proscar® Long-Term Evaluation of Symptoms Study , PSA, prostate specific antigen

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 Supported by an unrestricted educational grant from GlaxoSmithKline, Philadelphia, Pennsylvania.

PII: S0022-5347(06)01390-5

doi:10.1016/j.juro.2006.06.022

The Journal of Urology
Volume 176, Issue 4 , Pages 1299-1306, October 2006