The Journal of Urology
Volume 177, Issue 2 , Pages 610-614, February 2007

A Preliminary Study of JM-27: A Serum Marker That Can Specifically Identify Men With Symptomatic Benign Prostatic Hyperplasia

  • Grant W. Cannon

      Affiliations

    • James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland
  • ,
  • Chris Mullins

      Affiliations

    • National Institute of Diabetes and Digestive and Kidney Disease, National Institutes of Health, Bethesda, Maryland
  • ,
  • M. Scott Lucia

      Affiliations

    • Prostate Diagnostic Laboratory and MTOPS Prostate Samples Analysis Consortium Pathology Coordinating Center, Department of Pathology, University of Colorado, Denver and Health Sciences Center, Aurora, Colorado
  • ,
  • Simon W. Hayward

      Affiliations

    • Departments of Urologic Surgery and Cancer Biology, Vanderbilt University Medical Center, Nashville, Tennessee
  • ,
  • Victor Lin

      Affiliations

    • Department of Urology, The University of Texas Southwest Medical Center, Dallas, Texas
  • ,
  • Brian C.-S. Liu

      Affiliations

    • Molecular Urology Laboratory, Brigham and Women’s Hospital, Boston, Massachusetts
  • ,
  • Kevin Slawin

      Affiliations

    • Scott Department of Urology, Baylor College of Medicine, Houston, Texas
  • ,
  • Mark A. Rubin

      Affiliations

    • Harvard Medical School, Brigham and Women’s Hospital, Boston, Massachusetts
  • ,
  • Robert H. Getzenberg

      Affiliations

    • James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland
    • Corresponding Author InformationCorrespondence: The Brady Urological Institute, Johns Hopkins Hospital, Marburg 121, 600 North Wolfe St., Baltimore, Maryland 21287 (telephone: 410-502-3137; FAX: 410-502-9336).

Received 12 January 2006

Purpose

Benign prostatic hyperplasia is a common disease in men that until recently was considered a single disease with varying symptoms. Our recent analysis has revealed that a molecular marker, JM-27, is able to distinguish at the tissue level between highly symptomatic individuals and those with histological disease. The goal of these studies was to determine if a serum based assay to detect JM-27 could distinguish men with different forms of benign prostatic hyperplasia.

Materials and Methods

A serum based enzyme-linked immunosorbent assay was developed using a novel anti-JM-27 monoclonal antibody. The assay was sensitive, detecting JM-27 at the low ng/ml level within the serum. A quantitative measurement of serum JM-27 levels was performed in 68 patients. The patients consisted of 3 groups of 29 patients with asymptomatic benign prostatic hyperplasia (American Urological Association symptom score of 15 or less), 39 with symptomatic benign prostatic hyperplasia (American Urological Association symptom score 16 to 32) and 17 with confirmed prostate cancer. The assay cutoff was determined after a pilot run of samples and applied prospectively.

Results

Using the determined cutoff, serum levels of JM-27 can distinguish between symptomatic and asymptomatic patient sets. The sensitivity and specificity of the assay are 90% and 77%, respectively. The presence of prostate cancer in these men does not appear to alter the marker levels.

Conclusions

The present study is believed to represent the first characterization of a serum based marker for severe benign prostatic hyperplasia.

Key Words: prostatic hyperplasia, urinary tract, biological markers, immunoassay

Abbreviations and Acronyms: AUA, American Urological Association, BPH, benign prostatic hyperplasia, BSA, bovine serum albumin, CV, coefficient of variation, ELISA, enzyme-linked immunosorbent assay, LUTS, lower urinary tract symptoms, MTOPS, Medical Therapy of Prostatic Symptoms, PSA, prostate specific antigen, TBS, tris buffered saline

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 Study received institutional review board approval.

PII: S0022-5347(06)02518-3

doi:10.1016/j.juro.2006.09.023

The Journal of Urology
Volume 177, Issue 2 , Pages 610-614, February 2007