Are Total Prostate-specific Antigen Serum Levels in Cirrhotic Men Different From Those in Normal Men?

Urology ◽  
2009 ◽  
Vol 73 (5) ◽  
pp. 1032-1035 ◽  
Author(s):  
Fabio C. Vicentini ◽  
Luiz A.A. Botelho ◽  
Marcelo Hisano ◽  
Gustavo X. Ebaid ◽  
Marcos Lucon ◽  
...  
2017 ◽  
Vol 84 (3) ◽  
pp. 158-164 ◽  
Author(s):  
Alessandro Sciarra ◽  
Martina Maggi ◽  
Andrea Fasulo ◽  
Stefano Salciccia ◽  
Vincenzo Gentile ◽  
...  

Introduction The aim of this study was to analyze the significance of an increase in total prostate-specific antigen (PSA) serum levels despite dutasteride treatment as a predictor of prostate cancer (PC) at biopsy. We focused our attention on the rate of the first PSA increase and on the influence of prostatic inflammation. Methods From 2011 to 2016, 365 men with a previous negative prostate biopsy and persistent elevated PSA levels received dutasteride treatment. The population was followed for a range of 12-48 months. Results One hundred twelve cases with a confirmed PSA increase >0.5 ng/ml over the nadir value during the follow-up were included in Group A and underwent a new prostate biopsy. In Group A, the PSA increase was associated with PC at the re-biopsy in 66% of cases. The percentage of PSA reduction after 6 months of treatment was not a significant indicator of the risk for PC. The distribution of inflammatory infiltrates significantly (p<00.01) varied from positive to negative prostate biopsies. The relative risk for PC at biopsy significantly increased according to PSA level during dutasteride. Conclusions Treatment with dutasteride can help to analyze PSA kinetic. A persistent prostatic inflammation is a factor able to reduce the performance of PSA kinetic during dutasteride treatment.


2006 ◽  
Vol 13 (7) ◽  
pp. 947-950 ◽  
Author(s):  
RONAN LONG ◽  
SUBHASIS GIRI ◽  
SEAN DIVER ◽  
LORNA DUDDY ◽  
DECLAN MCKEOWN ◽  
...  

1999 ◽  
Vol 36 (5) ◽  
pp. 409-412 ◽  
Author(s):  
Yoko Kubota ◽  
Isoji Sasagawa ◽  
Haruhide Sinzawa ◽  
Takuya Kunii ◽  
Keiichi Itoh ◽  
...  

2004 ◽  
Vol 45 (2) ◽  
pp. 160-165 ◽  
Author(s):  
Gunnar Aus ◽  
Charlotte Becker ◽  
Stefan Franzén ◽  
Hans Lilja ◽  
Pär Lodding ◽  
...  

2006 ◽  
Vol 91 (10) ◽  
pp. 3850-3856 ◽  
Author(s):  
Stephanie T. Page ◽  
Daniel W. Lin ◽  
Elahe A. Mostaghel ◽  
David L. Hess ◽  
Lawrence D. True ◽  
...  

Abstract Context: The impact of serum androgen manipulation on prostate tissue hormone levels in normal men is unknown. Studies of men with prostate cancer have suggested that prostatic androgens are preserved in the setting of castration. Tissue androgens might stimulate prostate growth, producing adverse clinical consequences. Objective: The objective of the study was to determine the effect of serum androgen manipulation on intraprostatic androgens in normal men. Design: Thirteen male volunteers ages 35–55 yr (prostate-specific antigen &lt; 2.0 ng/ml; normal transrectal ultrasound) were randomly assigned to: 1) a long-acting GnRH-antagonist, acyline, every 2 wk; 2) acyline plus testosterone (T) gel (10 mg/d); or 3) placebo for 28 d. Serum hormones were assessed weekly. Prostate biopsies were obtained on d 28. Extracted androgens were measured by RIA, and immunohistochemistry for androgen-regulated proteins was performed. Results: The mean decrease in serum T was 94%, whereas prostatic T and dihydrotestosterone levels were 70 and 80% lower, respectively, in subjects receiving acyline alone compared with controls (P &lt; 0.05). Despite this decrease in prostate androgens, there were no detectable differences in prostate epithelial proliferation, apoptosis, prostate-specific antigen, and androgen receptor expression. Conclusion: In this small study of healthy subjects, despite a 94% decrease in serum T with medical castration, intraprostatic T and dihydrotestosterone levels remained 20–30% of control values, and prostate cell proliferation, apoptosis, and androgen-regulated protein expression were unaffected. Our data highlight the importance of assessing tissue hormone levels. The source of persistent prostate androgens associated with medical castration and their potential role in supporting prostate metabolism deserves further study.


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