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The Effect of Benign Lower Urinary Tract Symptoms on Subsequent Prostate Cancer Testing and Diagnosis
Authors:Christopher J Weight  Simon P Kim  Debra J Jacobson  Michaela E McGree  Stephen A Boorjian  R Houston Thompson  Bradley C Leibovich  R Jeffrey Karnes  Jennifer St Sauver
Institution:1. University of Minnesota, Department of Urology, Minneapolis, MN, USA;2. Mayo Clinic, Department of Urology, Rochester, MN, USA;3. Mayo Clinic, Department of Health Sciences Research, Rochester, MN, USA
Abstract:

Background

Lower urinary tract symptoms (LUTS) are common and have been associated with the subsequent diagnosis of prostate cancer (PCa) in population cohorts.

Objective

To determine whether the association between LUTS and PCa is due to the intensity of PCa testing after LUTS diagnosis.

Design, setting, and participants

We prospectively followed a representative, population-based cohort of 1922 men, aged 40–79 yr, from 1990 until 2010 with interviews, questionnaires, and abstracting of medical records for prostate outcomes. Men were excluded if they had a previous prostate biopsy or PCa diagnosis. Self-reported LUTS was defined as an American Urological Association symptom index score >7 (n = 621). Men treated for LUTS (n = 168) were identified from review of medical records and/or self report. Median follow-up was 11.8 yr (interquartile range: 10.7–12.3).

Outcome measurements and statistical analysis

Associations between self-reported LUTS, or treatment for LUTS, and risk of subsequent prostate biopsy and PCa were estimated using Cox proportional hazard models.

Results and limitations

Fifty-five percent of eligible men enrolled in the study. Men treated for LUTS were more likely to undergo a prostate biopsy (hazard ratio HR]: 2.4; 95% confidence interval CI], 1.7–3.3). Men younger than 65 yr who were treated for LUTS were more likely to be diagnosed with PCa (HR: 2.3, 95% CI, 1.5–3.5), while men aged >65 yr were not (HR: 0.89, 95% CI, 0.35–1.9). Men with self-reported LUTS were not more likely to be biopsied or diagnosed with PCa. Neither definition of LUTS was associated with subsequent intermediate- to high-risk cancer. The study is limited by lack of histologic or prostate-specific antigen level data for the cohort.

Conclusions

These results indicate that a possible cause of the association between LUTS and PCa is increased diagnostic intensity among men whose LUTS come to the attention of physicians. Increased symptoms themselves were not associated with intensity of testing or diagnosis.
Keywords:Prostate Cancer  Benign Prostatic Hypertrophy  Cohort Study  PSA screening
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