Abstract:Early age at first intercourse, increased number of sexual partners, lack of circumcision and history of sexually transmitted diseases (STDs) are associated with prostate cancer. There has been no investigation of the effect of these factors on prostate health at an early age. Previously collected serum samples from STD clinic attendees were tested retrospectively for anti-chlamydial antibodies, and prostate specific antigen (PSA) concentration. Patients at an STD clinic were interviewed regarding age of first… Show more
“…2,3 Interestingly, in the first of these studies, men's convalescent PSA concentrations remained elevated for at least several months after diagnosis and effective antibiotic therapy, raising the possibility of a longer-term influence of STIs on the prostate. 2 These findings are consistent with those from cross-sectional studies of Chlamydia trachomatis (CT) 4 and human herpesvirus type 8 serology 5,6 that observed positive results with PSA, as well as those from longitudinal studies of men treated for febrile urinary tract infections (UTIs) that observed large PSA rises sustained over several months. 7,8 In addition to genitourinary infections, non-genitourinary and systemic infections have also been found to contribute to elevated serum PSA.…”
While PSA has been previously shown to rise during acute infection, these findings demonstrate that PSA remains elevated over a longer period. Additionally, the overall infection burden, rather than solely genitourinary-specific infection burden, contributed to these long-term changes, possibly implying a role for the cumulative burden of infections in prostate cancer risk.
“…2,3 Interestingly, in the first of these studies, men's convalescent PSA concentrations remained elevated for at least several months after diagnosis and effective antibiotic therapy, raising the possibility of a longer-term influence of STIs on the prostate. 2 These findings are consistent with those from cross-sectional studies of Chlamydia trachomatis (CT) 4 and human herpesvirus type 8 serology 5,6 that observed positive results with PSA, as well as those from longitudinal studies of men treated for febrile urinary tract infections (UTIs) that observed large PSA rises sustained over several months. 7,8 In addition to genitourinary infections, non-genitourinary and systemic infections have also been found to contribute to elevated serum PSA.…”
While PSA has been previously shown to rise during acute infection, these findings demonstrate that PSA remains elevated over a longer period. Additionally, the overall infection burden, rather than solely genitourinary-specific infection burden, contributed to these long-term changes, possibly implying a role for the cumulative burden of infections in prostate cancer risk.
“…Viewing our findings in the context of the longer‐term or cumulative influences of current and/or resolved infections rather than the acute influences of infection, our nonsignificant findings are consistent with those from previous cross‐sectional studies of nonlifelong infections ( T. vaginalis and syphilis) that observed null associations with PSA, but differ from those from other cross‐sectional and longitudinal studies that observed positive findings for C. trachomatis serostatus and histories of medical record–confirmed chlamydia and NCNGU diagnoses with PSA concentration and trajectories in younger men . However, in the latter study, positive associations were observed only when PSA trajectories were examined and not when only one PSA measurement was used (% with PSA ≥0.7 ng/mL = 38.3 for chlamydia, 39.6 for gonorrhea, and 31.7 for NCNGU vs 37.1 for controls without these infections; P = 0.772, 0.639, and 0.659, respectively).…”
Background: The protist
Trichomonas vaginalis causes a common, sexually transmitted infection and has been proposed to contribute to the development of chronic prostate conditions, including benign prostatic hyperplasia and prostate cancer. However, few studies have investigated the extent to which it involves the prostate in the current antimicrobial era. We addressed this question by investigating the relation between
T. vaginalis antibody serostatus and serum prostate‐specific antigen (PSA) concentration, a marker of prostate infection, inflammation, and/or cell damage, in young, male, US military members.
Methods: We measured
T. vaginalis serum IgG antibodies and serum total PSA concentration in a random sample of 732 young, male US active duty military members. Associations between
T. vaginalis serostatus and PSA were investigated by linear regression.
Results: Of the 732 participants, 341 (46.6%) had a low
T. vaginalis seropositive score and 198 (27.0%) had a high score, with the remainder seronegative. No significant differences were observed in the distribution of PSA by
T. vaginalis serostatus. However, slightly greater, nonsignificant differences were observed when men with high
T. vaginalis seropositive scores were compared with seronegative men, and when higher PSA concentrations were examined (≥0.70 ng/mL). Specifically, 42.5% of men with high seropositive scores had a PSA concentration greater than or equal to 0.70 ng/mL compared with 33.2% of seronegative men (adjusted
P = .125).
Conclusions: Overall, our findings do not provide strong support for prostate involvement during
T. vaginalis infection, although our suggestive positive findings for higher PSA concentrations do not rule out this possibility entirely. These suggestive findings may be relevant for prostate condition development because higher early‐ to mid‐life PSA concentrations have been found to predict greater prostate cancer risk later in life.
“…Accepting PSA as a marker of prostate inflammation, we postulate that the association between HHV-8 seropositivity and elevated PSA signifies either the effects of HHV-8 infection on prostate inflammation [19] or the effects of prostate inflammation on HHV-8 reactivation. PSA elevation has been observed in relation to other infectious disease agents [36,37]. …”
BackgroundWe previously reported a cross-sectional association between the presence of human herpesvirus 8 (HHV-8) serum antibodies and screen-detected prostate cancer in men living in Tobago. In the same study population, we examined the association between HHV-8 seropositivity and incident prostate cancer discovered at later screenings.MethodsIn 40-81 year-old men without prostate cancer discovered at initial digital rectal examination (DRE) and prostate-specific antigen (PSA) screening, a case-cohort design measured the association between baseline HHV-8 seropositivity (modified immunofluorescence assay for antibodies against HHV-8 lytic antigens) and incident prostate cancer detected at DRE and PSA screenings three or five years later.ResultsAnalyses included 486 unique individuals, 96 incident prostate cancer cases, and 415 randomly selected subjects representing an at-risk cohort. By design, the random sub-cohort contained 25 incident prostate cancer cases. In the sub-cohort, the frequency of HHV-8 seropositivity increased across age groupings (40-49 years: 3.5%, 50-59 years: 13.6%, and ≥ 60 years: 22.9%). HHV-8 seropositivity was higher in men with elevated (≥ 4.0 ng/mL) than men with non-elevated PSA at initial screening (30.4% vs. 9.9% seropositive; crude odds ratio (OR) 3.96, 95% confidence interval (CI) 1.53-10.2; age-adjusted OR 2.42, 95% CI 0.91-6.47). HHV-8 seropositivity did not increase incident prostate cancer risk (age-adjusted hazard ratio (HR) 0.88, 95% CI 0.46-1.69).ConclusionsCase-cohort analysis did not identify association between HHV-8 seropositivity and incident prostate cancer. However, analyses uncovered possible association between HHV-8 and PSA (a marker of prostate inflammation). Co-occurrence of HHV-8 seropositivity and PSA elevation may explain cross-sectional association between HHV-8 and PSA screen-detected prostate cancer.
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