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Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis

Treponema pallidum subsp. pallidum is a fastidious spirochete and the etiologic agent of syphilis, a sexually transmitted infection (STI). Syphilis diagnoses and disease staging are based on clinical findings and serologic testing. Moreover, according to most international guidelines, PCR analysis o...

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Autores principales: Flipse, Jacky, Niekamp, Anne-Marie, Dirks, Anne, Dukers-Muijrers, Nicole H. T. M., Hoebe, Christian J. P. A., Wolffs, Petra, van Loo, Inge H. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281170/
https://www.ncbi.nlm.nih.gov/pubmed/37222630
http://dx.doi.org/10.1128/jcm.00112-23
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author Flipse, Jacky
Niekamp, Anne-Marie
Dirks, Anne
Dukers-Muijrers, Nicole H. T. M.
Hoebe, Christian J. P. A.
Wolffs, Petra
van Loo, Inge H. M.
author_facet Flipse, Jacky
Niekamp, Anne-Marie
Dirks, Anne
Dukers-Muijrers, Nicole H. T. M.
Hoebe, Christian J. P. A.
Wolffs, Petra
van Loo, Inge H. M.
author_sort Flipse, Jacky
collection PubMed
description Treponema pallidum subsp. pallidum is a fastidious spirochete and the etiologic agent of syphilis, a sexually transmitted infection (STI). Syphilis diagnoses and disease staging are based on clinical findings and serologic testing. Moreover, according to most international guidelines, PCR analysis of swab samples from genital ulcers is included in the screening algorithm where possible. It has been suggested that PCR might be omitted from the screening algorithm due to low added value. As an alternative to PCR, IgM serology might be used. In this study, we wanted to establish the added value of PCR and IgM serology for diagnosing primary syphilis. Added value was defined as finding more cases of syphilis, preventing overtreatment, or limiting the extent of partner notification to more recent partners. We found that both PCR and IgM immunoblotting could aid the timely diagnosis of early syphilis in ~24% to 27% of patients. PCR has the greatest sensitivity and can be applied to cases with an ulcer with suspected reinfection or primary infection. In the absence of lesions, the IgM immunoblot could be used. However, the IgM immunoblot has better performance in cases with suspected primary infection than in reinfections. The target population, testing algorithm, time pressures, and costs should determine whether either test provides sufficient value to be implemented in clinical practice.
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spelling pubmed-102811702023-06-21 Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis Flipse, Jacky Niekamp, Anne-Marie Dirks, Anne Dukers-Muijrers, Nicole H. T. M. Hoebe, Christian J. P. A. Wolffs, Petra van Loo, Inge H. M. J Clin Microbiol Bacteriology Treponema pallidum subsp. pallidum is a fastidious spirochete and the etiologic agent of syphilis, a sexually transmitted infection (STI). Syphilis diagnoses and disease staging are based on clinical findings and serologic testing. Moreover, according to most international guidelines, PCR analysis of swab samples from genital ulcers is included in the screening algorithm where possible. It has been suggested that PCR might be omitted from the screening algorithm due to low added value. As an alternative to PCR, IgM serology might be used. In this study, we wanted to establish the added value of PCR and IgM serology for diagnosing primary syphilis. Added value was defined as finding more cases of syphilis, preventing overtreatment, or limiting the extent of partner notification to more recent partners. We found that both PCR and IgM immunoblotting could aid the timely diagnosis of early syphilis in ~24% to 27% of patients. PCR has the greatest sensitivity and can be applied to cases with an ulcer with suspected reinfection or primary infection. In the absence of lesions, the IgM immunoblot could be used. However, the IgM immunoblot has better performance in cases with suspected primary infection than in reinfections. The target population, testing algorithm, time pressures, and costs should determine whether either test provides sufficient value to be implemented in clinical practice. American Society for Microbiology 2023-05-24 /pmc/articles/PMC10281170/ /pubmed/37222630 http://dx.doi.org/10.1128/jcm.00112-23 Text en Copyright © 2023 Flipse et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Bacteriology
Flipse, Jacky
Niekamp, Anne-Marie
Dirks, Anne
Dukers-Muijrers, Nicole H. T. M.
Hoebe, Christian J. P. A.
Wolffs, Petra
van Loo, Inge H. M.
Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title_full Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title_fullStr Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title_full_unstemmed Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title_short Refining Timely Diagnosis of Early Syphilis by Using Treponema pallidum PCR or IgM Immunoblotting Next to Conventional Serology for Syphilis
title_sort refining timely diagnosis of early syphilis by using treponema pallidum pcr or igm immunoblotting next to conventional serology for syphilis
topic Bacteriology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281170/
https://www.ncbi.nlm.nih.gov/pubmed/37222630
http://dx.doi.org/10.1128/jcm.00112-23
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