JRI 
Vol. 1, Issue 1, / January-March 2000
(Review Article, pages 36-43)

Mahmood Jeddi-Tehrani Corresponding Author
- Nanobiotechnology Research Center, Avicenna Research Institute (ACECR), Tehran, Iran

Received: 1/11/2000 Accepted: 3/2/2000 - Publisher : Avicenna Research Institute

Related Articles

 

Other Format

 


Abstract

Chlamydia trachomatis is the most prevalent sexually transmitted bacterial infection, with an estimated annual worldwide incidence of 50 million cases. A large Proportion of those infected, particularly women, are asymptomatic, and these individuals serve as a major reservoir of infection. Women are also at risk for serious reproductive tract complications with significant morbidity. In an effort to prevent spread of these infections, increased attention is being paid to early diagnosis and treatment. The introduction of sensitive and highly specific nucleic acid amplification tests for detection of C. trachomatis has made the use of noninvasive testing feasible in women. Recent studies have found that nucleic acid amplification tests are sufficiently sensitive to detect C. trachomatis in first-void urine in women. Sensitivities have exceeded 95% in most studies when compared to detection with non culture tests of endocervical specimens as a standard, while at the same time preserving high specificities



Keywords:


To cite this article:


References

  1. Qyubb TC. Recent advances in the diagnosis of sexually transmitted diseases. Sex transm Des. 1994;24: (wuppl 2): S 19-S 27.
  2. Centers for Disease Control and prevention. Ten leading nationally notifiable infectious diseases-US. MMWR Morb Mortal Wkly Rep. 1996;45:883-884.
  3. Centers for disease control and prevention recommendations for the prevention and management of Chlamydia trachomatis infections, 1993. MMWR Morb Mortal Wkly Rep. 1993; 42: (RR-12): 1-39.
  4. Hammerschlag MR. Chlamydia trachomatis trachomatis in children pediatr Ann, 1994; 23:349-353.
  5. pate SP, Hook EW. Laboratory to laboratory variation in Chlamydia trachomatis culture practices. Sex transm Dis. 1995;22:322-326.
  6. Tam M.R., Stamm W.E., Handsfield H.H., et al. Culture independent diagnosis of Chlamydia trachomatis infection using monoclonal antibodies. N. Engl J Med. 1984;310:1146-1150.
  7. Black CM. Current methods of laboratory diagnosis of Chlamydia trachomatis infection. Clin Microbiol Rev. 1997;10:160-184.
  8. An Q, Olive DM. Molecular cloning and nucleic acid sequencing of Chlamydia trachomatis 16s-RNA from patient samples lacking the cryptic plasmid. Mol Cell Probes. 1994; 8:429-435.
  9. Mahoney J, Chong S, Jang D, et al. Urine speciments from pregnant and nonpregnant women inhibitory to amplification of Chlamydia trachoma is nucleic acel by PCR, ligase chain reaction, and transcription mediated-amplification: identification of urinary substances associated with inhibition and removal of inhibitory activity. J Clin Microbiol.1998;36:3122-3126.
  10. Mouton JW, Verkoonyen R, Vandermeijden WI, et al. Detection of Chlamydia trachomatis in male and female urine specimens by using the amplified Chlamydia trachomatis test. J Clin Microbiol. 1997;35:1369:1372.
  11. Quinn TC, Welsh L, Lentz A, et al. Diagnosis by AMPLICOR PCR of Chlamydia trachoma is infection in urine samples from women and men attending sexually transmitted disease clinics. J Clin Microbiol. 1996; 34:1401-1406.
  12. Pasternack R, Vuorinen P, Kuukankorpi A, Pitkajarvi T, Miettinen A. Detection of Chlamydia trachoma is infections in women by amplictor PCR: comparison of diagnostic performance with urine and cervical specimens. J Clin Microbiol. 1996; 34:995-998.
  13. Puolakkainen M, Hiltunen-Back, Reunula T, et al. Comparison of performances of two commercially available tests, a PCR assay and a ligase chain reaction test, in detection of urogenital Chlamydia trachomatis infection. J Clin Microbiol. 1998;36:1489-1493.
  14. Vincelette J, Schirm J, Bogard M, et al. Multicenter evaluation of the fully automated COBAS AMPLICOR PCR test for detection of Chlamydia trachomatis in urogenital speciments. H Clin Microbiol. 1999;37:74-80.
  15. Lee HH, Chernesky MA, Schacher J, et al. Diagnosis of Chlamydia trachomatis genitourinary tract infection in women by ligase chain reaction assay of urine. Lancet. 1995; 345:213-216.
  16. Stary A, Schuh E, Kerschenbaumer M, G tz B, Lee H. Performance of transcription-mediated amplification and ligase chain reaction assays for detection of Chlamydia infection in urogenital samples obtained by invasive and noninvasive methods. J Clin Microbiol. 1998;36:2666-2670.
  17. Crotchfelt KA, Pare B, Gaydos C, Quinn TC. Detection of Chlamydia trachomatis by the Gen-Prob AMPLIFIED Chlamydia trachomatis assay (AMP CT) in urine specimens from men and women and endocervical speciments from women. J Clin Microbiol. 1998; 36:391-394.
  18. Ferrero DV, Meyers HN, Schultz DE, Willis SA, Performance of the Gen Probe AMPLIFIED Chlamydia trachomatis assay in detecting Chlamydia trachomatis in endocervical and urine speciments from women and urethral and urine specimens from men attending sexually transmitted disease and family planning clinics. J Clin Microbiol. 1998;3230-3233.
  19. Gaydos CA, Crotchfelt KA, Howell MR, Kralian S, Hauptman P, Quinn TC. Molecular amplification assays to detect Chlamydia infection in urine specimens from high school female students and to monitor the persistence of chlomydial DNA after therapy. J Infect Dis. 1998;417-424.

COPE
SID
NLM
AJMB
IJBMLE
IJBMLE

Home | About Us | Current Issue | Past Issues | Submit a Manuscript | Instructions for Authors | Subscribe | Search | Contact Us

"Journal of Reproduction & Infertility" is owned, published, and managed by Avicenna Research Institute .
Creative Commons License

This work is licensed under a Creative Commons Attribution –NonCommercial 4.0 International License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.

Journal of Reproductoin and Infertility (JRI) is a member of COMMITTEE ON PUBLICATION ETHICS . Verify here .

©2024 - eISSN : 2251-676X, ISSN : 2228-5482, For any comments and questions please contact us.