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The Effect of Medical Male Circumcision on Urogenital Mycoplasma genitalium among Men in Kisumu, Kenya

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posted on 2013-12-06, 00:00 authored by Supriya D. Mehta, Charlotte Gaydos, Ian Maclean, Elijah Odoyo-June, Stephen Moses, Lawrence Agunda, Nicole Quinn, Robert C. Bailey
Background: We determined the prevalence of urethral Mycoplasma genitalium (MG) infection and whether infection was associated with circumcision status, among men enrolled in the randomized trial of medical male circumcision to prevent HIV acquisition in Kisumu, Kenya. Methods: M. genitalium and Trichomonas vaginalis (TV) were detected in first void urine (FVU) by APTIMA transcription mediated amplification assay. FVU and urethral swabs were assessed for N. gonorrhoeae (NG) and C. trachomatis (CT) by polymerase chain reaction assay. HSV-2 antibodies were detected by IgG ELISA. Multivariable logistic regression identified factors associated with MG infection. Results: Specimens were collected between July and September 2010, and 52 [9.9%; 95% CI: 7.3-12.4%] MG infections were detected among 526 men. NG and TV were not associated with MG. CT co-infection was 5.8% in MG-infected men, and 0.8% among MG-uninfected men (p=0.02). MG infection was predominantly asymptomatic (98%). The prevalence of MG was 13.4% in uncircumcised men vs. 8.2% in circumcised men (p=0.06). Being circumcised nearly halved the odds of MG [adjusted OR=0.54; 95% CI: 0.29-0.99], adjusted for other variables significant at the p<0.05 level: HSV-2 infection [aOR=2.05; 95% CI: 1.05-4.00], CT infection [aOR=2.69; 95% CI: 1.44-5.02], and washing the penis <=1 hour after sex [aOR=0.47; 95% CI: 0.24-0.95]. Conclusions: MG infection was reduced among men who were circumcised, adding to the benefits of male circumcision in preventing several sexually transmitted infections.

Funding

This work was supported by grant number AI50440 from the Division of AIDS, National Institute of Allergies and Infectious Disease of the United States National Institutes of Health, AI50440-S (American Recovery and Reinvestment Act), and by grant number HCT 44180 from the Canadian Institutes of Health Research (CIHR). S Moses was supported by a CIHR Investigator Award.

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Publisher Statement

Post print version of article may differ from published version. The final publication is available at www.lww.com/; DOI:10.1097/OLQ.0b013e318240189c

Publisher

Lippincott, Williams & Wilkins

Language

  • en_US

issn

1537-4521

Issue date

2012-04-01

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