Hobbs M.M., Steiner M.J., Rich K.D., Gallo M.F., Alam A., Rahman M., Menezes P., Chipato T., Warner L., Macaluso M.
Department of Medicine, CB# 7031, UNC School of Medicine, Chapel Hill, NC 27599, United States; Family Health International, Research Triangle Park, NC, United States; Centers for Disease Control and Prevention, Atlanta, GA, United States; International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh; Department of Obstetrics and Gynecology, University of Zimbabwe, Harare, Zimbabwe
Hobbs, M.M., Department of Medicine, CB# 7031, UNC School of Medicine, Chapel Hill, NC 27599, United States; Steiner, M.J., Family Health International, Research Triangle Park, NC, United States; Rich, K.D., Department of Medicine, CB# 7031, UNC School of Medicine, Chapel Hill, NC 27599, United States; Gallo, M.F., Centers for Disease Control and Prevention, Atlanta, GA, United States; Alam, A., International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh; Rahman, M., International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh; Menezes, P., Department of Medicine, CB# 7031, UNC School of Medicine, Chapel Hill, NC 27599, United States; Chipato, T., Department of Obstetrics and Gynecology, University of Zimbabwe, Harare, Zimbabwe; Warner, L., Centers for Disease Control and Prevention, Atlanta, GA, United States; Macaluso, M., Centers for Disease Control and Prevention, Atlanta, GA, United States
BACKGROUND: Prostate-specific antigen (PSA) is a valid biomarker of semen exposure in women and has been used to assess reliability of self-reported sexual behavior as well as serve as a proxy measure for condom efficacy. Quantitative PSA tests are expensive and require specialized equipment. A simple, rapid, and inexpensive test for PSA would facilitate semen biomarker evaluation in a variety of research settings. This study evaluated the performance of a rapid PSA test compared with a quantitative assay to identify semen in vaginal swab specimens. METHODS: We tested 581 vaginal swabs collected from 492 women participating in 2 separate research studies in Bangladesh and Zimbabwe. PSA in vaginal secretions was detected using the quantitative IMx (Abbott Laboratories) assay and the ABAcard p30 (Abacus Diagnostics) rapid immunochromatographic strip test. RESULTS: The ABAcard test was 100% sensitive (95% confidence interval [CI], 98%-100%) and 96% specific (95% CI, 93%-97%) compared with the quantitative test in detecting >1.0 ng PSA/mL vaginal swab eluate. Rapid PSA results were semiquantitative and correlated well with PSA concentrations (κ = 0.88; 95% CI, 0.85-0.90). CONCLUSION: Rapid PSA detection requires no instrumentation and can be performed easily and economically. Having rapid PSA results available immediately following interview provides opportunities to explore discrepancies between the objective marker of recent semen exposure and self-reported behaviors. © Copyright 2009 American Sexually Transmitted Diseases Association.