Fertility and Sterility
Volume 90, Issue 3 , Pages 513-520, September 2008

Mycoplasma genitalium, Chlamydia trachomatis, and tubal factor infertility—a prospective study

  • Helle Friis Svenstrup, M.Sc., Ph.D.

      Affiliations

    • Institute of Medical Microbiology and Immunology, University of Aarhus, Arhus, Denmark
    • Corresponding Author InformationReprint requests: Helle Friis Svenstrup, 68 Blackheath Park, London SE3 0ET, United Kingdom.
  • ,
  • Jens Fedder, M.D, Ph.D.

      Affiliations

    • Fertility Clinic and Scientific Unit, Braedstrup Hospital, Braedstrup, Denmark
  • ,
  • Sven Erik Kristoffersen, M.D.

      Affiliations

    • Department of Gynecology and Obstetrics, Horsens Hospital, Horsens, Denmark
  • ,
  • Birgitta Trolle, M.D.

      Affiliations

    • Department of Gynecology and Obstetrics, Holstebro Hospital, Holstebro, Denmark
  • ,
  • Svend Birkelund, M.D., D.M.Sc.

      Affiliations

    • Institute of Medical Microbiology and Immunology, University of Aarhus, Arhus, Denmark
  • ,
  • Gunna Christiansen, M.D., D.M.Sc.

      Affiliations

    • Institute of Medical Microbiology and Immunology, University of Aarhus, Arhus, Denmark

Received 28 September 2006; received in revised form 12 December 2006; accepted 12 December 2006. published online 04 June 2007.

Objective

To determine the presence of M. genitalium and C. trachomatis in women attending fertility clinics and to follow these women for the effects of previous infections or tubal damage on pregnancy rate and outcome.

Design

Prospective study.

Setting

Fertility clinics and university.

Patient(s)

Two hundred twelve couples attending fertility clinics.

Intervention(s)

Blood and cervical swab samples from the women. Tubal status was assessed by culdoscopy and/or laparoscopy.

Main Outcome Measure(s)

Presence of M. genitalium and C. trachomatis was determined by polymerase chain reaction. Serum samples were tested for antibodies against M. genitalium and C. trachomatis.

Result(s)

One swap sample was positive to C. trachomatis and none positive to M. genitalium. Thirty of the 194 women had tubal factor infertility (TFI); 23% and 17% of women with TFI had antibodies to C. trachomatis and M. genitalium, respectively, compared with 15% and 4%, respectively, of women with normal tubes; 36% and 14% of women with a self-reported history of pelvic inflammatory disease (PID) were seropositive to C. trachomatis and M. genitalium, respectively, compared with 10% and 6%, respectively, of women without past PID.

Conclusion(s)

A strong antibody response against M. genitalium or C. trachomatis but no sign of current or chronic infection was found in women with TFI, indicating that previous infections caused by these microorganisms may have resulted in permanent damage and occlusion of the fallopian tubes.

Key Words: Culdoscopy, LightCycler PCR, Mycoplasma genitalium, serology, tubal infertility

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 Supported by Vestdansk Sundhedsvidenskabeligt Forskningsforum, Denmark (journal no. 1999–043–33) and Vejle Amts Forskningsfond, Denmark (journal no. 2–16–4-27–01). Dr. Svenstrup received a Ph.D. stipend from the Faculty of Health Sciences, University of Aarhus, Denmark, to carry out the project. Dr. Christiansen and Birkelund developed the pELISA for Medac.

 Presented as a poster at the 16th International Congress of the International Organisation of Mycoplasmology, July 9–14, 2006, Cambridge, U.K.

PII: S0015-0282(07)00107-0

doi:10.1016/j.fertnstert.2006.12.056

Fertility and Sterility
Volume 90, Issue 3 , Pages 513-520, September 2008