Prostate-specific antigen is an androgen-regulated serine protease produced by both prostatic luminal epithelial cells and prostate cancer cells (
17). Prostate biopsies are often performed to determine the cause of elevated PSA levels. Reports indicate that biopsies showed no evidence of prostate cancer in 47% of men with PSA levels above 10 ng/mL (
18). Besides prostate cancer, any damage to the barrier provided by the basal layer and basement membranes within the normal gland may increase PSA levels in the blood (
8).
Acute urinary retention is a condition characterized by a sudden inability to empty the bladder, which can be distressing for patients and often requires immediate medical intervention. The etiology of AUR is poorly understood, but prostate inflammation has been suggested as a possible underlying cause (
19,
20). Catheterization is a common intervention performed in these patients to relieve urinary obstruction and has been associated with prostatic inflammation. Consequently, it is expected that patients with BPH who undergo catheterization due to AUR will have elevated PSA levels (
21-
23). However, a study conducted by Anand and Gupta on 80 patients with AUR who underwent catheterization found that PSA levels did not increase following AUR and showed no changes after catheterization (
14). On the other hand, Aliasgari et al. (
23) reported that the average PSA at the time of AUR and 2 weeks after bladder catheterization was 9.8 and 5, respectively, indicating that AUR can cause an approximately 2-fold increase in serum PSA levels.
In our study, we demonstrated that in patients with urinary retention due to BPH, an increase in PSA levels occurs prior to catheterization, and there was no significant change in PSA levels after urethral catheter insertion. This indicates that atraumatic catheterization has no effect on PSA levels.
The exact reason for the increase in PSA levels in patients with AUR before catheterization is not well-defined. Many researchers consider inflammation as the primary cause of elevated PSA levels (
22,
24). Kefi et al. (
22), in a retrospective case-control study, found chronic prostatic inflammation in 56% of transurethral resection of the prostate (TURP) specimens from AUR patients and 37% from non-AUR patients. In the AUR group, patients with prostatic inflammation had significantly higher mean PSA levels compared to those without, suggesting that prostatic inflammation significantly contributes to AUR. Conversely, Antunes et al. (
25) argued that prostatitis cannot be the main factor in PSA elevation in patients with AUR. In their study, only 1.5% and 24.7% of patients showed acute and chronic prostatitis, respectively, in histological diagnoses. However, it should be noted that this study only examined prostate biopsy samples, which are fewer in number compared to surgical prostate samples. Furthermore, while some consider catheterization alone to contribute to inflammation and increasing PSA levels, others believe that this procedure does not contribute to the increase, and the main cause of elevated PSA is AUR itself. Supporting this view are data indicating an increase in PSA levels prior to catheterization and a subsequent decrease after a few days (
21,
23,
26). Our findings also confirm the results of these studies.
In the present study, PSA levels in the group with a normal baseline PSA value (≤ 4.0 ng/mL) remained within the normal range throughout the measurement period after catheterization without any significant difference (P = 0.37). Also, no statistically significant changes were noted in serum PSA levels in the group with baseline PSA above 4 ng/mL.
Consistent with the results of our study, Matzkin et al. (
27), in a prospective study with a mean catheter duration of 5.5 days, showed that changes in PSA following prolonged catheterization were not clinically significant, neither in men with a normal baseline PSA nor in those with an above-normal baseline PSA. However, Faris et al. (
28) observed that catheterization in patients with AUR due to BPH only increases PSA levels in patients who had a higher baseline PSA level, and in individuals with normal baseline PSA, it does not cause a significant change.
In a study investigating the relationship between AUR and PSA concentration conducted on 34 patients who underwent suprapubic cystostomy, a dramatic increase in serum PSA levels was observed following urinary retention, with a subsequent reduction of over 50% after 48 hours. This study also indicates that the increase in PSA occurs during the process of urinary retention, given that none of the patients underwent urethral catheterization (
26). However, in our study, PSA levels did not show a significant change after 3 days, suggesting the hypothesis that urethral catheterization may slow down the rate of PSA decline following urinary retention.
We also examined the effects of age, prostate volume, and UOAC on the serum PSA level in our study. Our findings showed that baseline PSA in patients with AUR is not affected by age, prostate volume, or UOAC. Although a positive correlation between serum PSA, age, and prostate volume has been confirmed (
29,
30), it seems that elevated PSA before catheterization in patients with AUR is not influenced by age or prostate volume.
This study had some potential limitations. First, we were unable to determine whether PSA levels return to normal after catheter insertion and how long it would take to normalize. It has been reported that the effect of increased PSA due to urinary retention can persist for up to 2 weeks (
23,
31). Second, the small sample size is a severe limitation of our study, although it was estimated to be sufficient with 85% power and a 5% significance level. Therefore, further studies are necessary to confirm these results.
5.1. Conclusions
In this study, we demonstrated that in patients with BPH who underwent urethral catheterization due to AUR, there is an initial elevation in PSA levels. However, no significant changes in total PSA levels or the free/total PSA ratio were observed after catheterization. Additionally, prostate volume, age, and UOAC did not influence the baseline PSA levels.