Recent Biomarker-Confirmed Unprotected Vaginal Sex, But Not Self-reported Unprotected Sex, Is Associated With Recurrent Bacterial Vaginosis.

Abigail Norris Turner, Patricia Carr Reese, Margaret Christine Snead, Karen Fields, Melissa Ervin, Athena P Kourtis, Mark A Klebanoff, Maria F Gallo
Author Information
  1. Abigail Norris Turner: From the *Division of Infectious Diseases, College of Medicine, Ohio State University, Columbus, OH; †School of Medicine and Health Sciences, George Washington University, Washington, DC; ‡Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention, Atlanta, GA; §Sexual Health Clinic, Columbus Public Health, Columbus, OH; ¶The Research Institute at Nationwide Children's Hospital, Columbus, OH; and ∥Department of Pediatrics, Ohio State University, Columbus, OH; and **Division of Epidemiology, College of Public Health, Ohio State University, Columbus, OH.

Abstract

BACKGROUND: Self-reported unprotected vaginal sex seems to increase risk of bacterial vaginosis (BV). However, the validity of self-reports is questionable, given their inconsistency with more objective measures of recent semen exposure such as detection of prostate-specific antigen (PSA). We examined whether recent unprotected sex, as measured both by PSA detection on vaginal swabs and by self-report, was associated with increased BV recurrence.
METHODS: We analyzed randomized trial data from nonpregnant, BV-positive adult women recruited from a sexually transmitted disease clinic. Participants received BV therapy at enrollment and were scheduled to return after 4, 12, and 24 weeks. Bacterial vaginosis (by Nugent score) and PSA were measured at each visit. We used Cox proportional hazards models to examine the association between PSA positivity and recurrent BV. We also evaluated associations between self-reported unprotected sex (ever/never since the last visit and in the last 48 hours, analyzed separately) and recurrent BV.
RESULTS: Prostate-specific antigen and BV results were available for 96 women who contributed 226 follow-up visits. Prostate-specific antigen positivity was associated with increased BV recurrence (adjusted hazard ratio [aHR], 2.32; 95% confidence interval [CI], 1.28-4.21). In contrast, we observed no significant increase in BV recurrence among women self-reporting unprotected sex since the last visit (aHR, 1.63; 95% CI, 0.77-3.43) or in the last 48 hours (aHR, 1.28; 95% CI, 0.70-2.36).
CONCLUSIONS: Estimates from earlier studies linking self-reported unprotected sex and BV may be biased by misclassification. Biomarkers can improve measurement of unprotected sex, a critical exposure variable in sexual health research.

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Grants

  1. UL1 TR001070/NCATS NIH HHS
  2. 8UL1TR000090-05/NCATS NIH HHS
  3. UL1 TR000090/NCATS NIH HHS
  4. R21 AI095987/NIAID NIH HHS
  5. R21AI095987/NIAID NIH HHS
  6. KL2RR025754/NCRR NIH HHS
  7. KL2 RR025754/NCRR NIH HHS

MeSH Term

Adolescent
Adult
Biomarkers
Female
Health Knowledge, Attitudes, Practice
Humans
Middle Aged
Prostate-Specific Antigen
Randomized Controlled Trials as Topic
Recurrence
Risk Factors
Self Report
Semen
United States
Unsafe Sex
Vagina
Vaginosis, Bacterial

Chemicals

Biomarkers
Prostate-Specific Antigen

Word Cloud

Created with Highcharts 10.0.0BVunprotectedsexPSAlastantigenrecurrencewomenvisit95%1Self-reportedvaginalincreasevaginosisrecentexposuredetectionmeasuredassociatedincreasedanalyzedBacterialpositivityrecurrentself-reportedsince48hoursProstate-specificaHRCI0UnprotectedSexBACKGROUND:seemsriskbacterialHowevervalidityself-reportsquestionablegiveninconsistencyobjectivemeasuressemenprostate-specificexaminedwhetherswabsself-reportMETHODS:randomizedtrialdatanonpregnantBV-positiveadultrecruitedsexuallytransmitteddiseaseclinicParticipantsreceivedtherapyenrollmentscheduledreturn41224weeksNugentscoreusedCoxproportionalhazardsmodelsexamineassociationalsoevaluatedassociationsever/neverseparatelyRESULTS:resultsavailable96contributed226follow-upvisitsadjustedhazardratio[aHR]232confidenceinterval[CI]28-421contrastobservedsignificantamongself-reporting6377-3432870-236CONCLUSIONS:EstimatesearlierstudieslinkingmaybiasedmisclassificationBiomarkerscanimprovemeasurementcriticalvariablesexualhealthresearchRecentBiomarker-ConfirmedVaginalAssociatedRecurrentVaginosis

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