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Predictors of lack of serological response to syphilis treatment in HIV-infected subjects
INTRODUCTION: The aim of this study was to determine factors associated with lack of serological response (LSR) to treatment of syphilis among HIV-infected subjects. MATERIALS AND METHODS: Retrospective, longitudinal study on HIV-infected subjects diagnosed and treated for syphilis and with an asses...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International AIDS Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224790/ https://www.ncbi.nlm.nih.gov/pubmed/25394158 http://dx.doi.org/10.7448/IAS.17.4.19654 |
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author | Spagnuolo, Vincenzo Poli, Andrea Galli, Laura Cernuschi, Massimo Nozza, Silvia Maillard, Myriam Gianotti, Nicola Hasson, Hamid Bossolasco, Simona Lazzarin, Adriano Castagna, Antonella |
author_facet | Spagnuolo, Vincenzo Poli, Andrea Galli, Laura Cernuschi, Massimo Nozza, Silvia Maillard, Myriam Gianotti, Nicola Hasson, Hamid Bossolasco, Simona Lazzarin, Adriano Castagna, Antonella |
author_sort | Spagnuolo, Vincenzo |
collection | PubMed |
description | INTRODUCTION: The aim of this study was to determine factors associated with lack of serological response (LSR) to treatment of syphilis among HIV-infected subjects. MATERIALS AND METHODS: Retrospective, longitudinal study on HIV-infected subjects diagnosed and treated for syphilis and with an assessable serological response between 1 January 2004 and 15 September 2013. LSR was defined as a <4-fold decline of rapid plasma reagin (RPR) titer or a failed reversion to nonreactive (if RPR ≤1:4 at diagnosis) after one year since treatment. Diagnoses of syphilis were staged in early syphilis (primary, secondary and early latent) or late syphilis (tertiary and late latent) according to clinical examination and patient's history. Syphilis was classified in new infections [NI: positive RPR and TPHA (Treponema pallidum Haemagglutination assay) titers in subjects without previous history of syphilis] or re-infections [ReI: a ≥4-fold increase of RPR titer in subjects previously successfully treated for syphilis]. Syphilis treatment was prescribed according to CDC guidelines. The crude incidence rates (IRs) of LSR were calculated per 1000-person months of follow-up (PMFU) as the total number of LSR episodes divided by the cumulative time contributed by all subjects (interval time since each syphilis diagnosis and the date of ascertainment of response). Results are described as median (IQR) or frequency (%). RESULTS: 565 diagnoses of syphilis with an assessable serological response in 421 patients; 458 (81%) were early syphilis, 189 (33%) were NI, 376 (67%) were ReI. At first, diagnosis of syphilis median age was 41 (36–47) years, 419 (99.5%) males, 391 (93%) MSM, HIV-infected since 7.7 (3.5–12.9) years, 75 (18%) HCV or HBV co-infected, 56 (13%) with a previous AIDS diagnosis, 82 (19%) antiretroviral treatment naïve, 102 (24%) with HIV-RNA ≥50 cp/mL, CD4+=576 (437–749) cells/mm(3), nadir CD4+=308 (194–406) cells/mm(3). LSRs were observed in 70/565 (12.4%) treated syphilis. Incidence of LSR decreased over time [2004–2008 IR=25.1 (17.2–33.1)/1000 PMFU; 2009–2010 IR=21.1 (12.3–29.9)/1000 PMFU; 2011–2013 IR=10.6 (5.1–18.2)/1000 PMFU; Poisson regression: p=0.001]. Results of univariate and multivariate analysis on the risk of LSR are reported in Table 1. CONCLUSIONS: In HIV-infected subjects we observed 12% of LSR to treatment of syphilis. LSR was associated with an older age, late syphilis, lower nadir CD4+ and detectable HIV viral load. |
format | Online Article Text |
id | pubmed-4224790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | International AIDS Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42247902014-11-13 Predictors of lack of serological response to syphilis treatment in HIV-infected subjects Spagnuolo, Vincenzo Poli, Andrea Galli, Laura Cernuschi, Massimo Nozza, Silvia Maillard, Myriam Gianotti, Nicola Hasson, Hamid Bossolasco, Simona Lazzarin, Adriano Castagna, Antonella J Int AIDS Soc Poster Sessions – Abstract P122 INTRODUCTION: The aim of this study was to determine factors associated with lack of serological response (LSR) to treatment of syphilis among HIV-infected subjects. MATERIALS AND METHODS: Retrospective, longitudinal study on HIV-infected subjects diagnosed and treated for syphilis and with an assessable serological response between 1 January 2004 and 15 September 2013. LSR was defined as a <4-fold decline of rapid plasma reagin (RPR) titer or a failed reversion to nonreactive (if RPR ≤1:4 at diagnosis) after one year since treatment. Diagnoses of syphilis were staged in early syphilis (primary, secondary and early latent) or late syphilis (tertiary and late latent) according to clinical examination and patient's history. Syphilis was classified in new infections [NI: positive RPR and TPHA (Treponema pallidum Haemagglutination assay) titers in subjects without previous history of syphilis] or re-infections [ReI: a ≥4-fold increase of RPR titer in subjects previously successfully treated for syphilis]. Syphilis treatment was prescribed according to CDC guidelines. The crude incidence rates (IRs) of LSR were calculated per 1000-person months of follow-up (PMFU) as the total number of LSR episodes divided by the cumulative time contributed by all subjects (interval time since each syphilis diagnosis and the date of ascertainment of response). Results are described as median (IQR) or frequency (%). RESULTS: 565 diagnoses of syphilis with an assessable serological response in 421 patients; 458 (81%) were early syphilis, 189 (33%) were NI, 376 (67%) were ReI. At first, diagnosis of syphilis median age was 41 (36–47) years, 419 (99.5%) males, 391 (93%) MSM, HIV-infected since 7.7 (3.5–12.9) years, 75 (18%) HCV or HBV co-infected, 56 (13%) with a previous AIDS diagnosis, 82 (19%) antiretroviral treatment naïve, 102 (24%) with HIV-RNA ≥50 cp/mL, CD4+=576 (437–749) cells/mm(3), nadir CD4+=308 (194–406) cells/mm(3). LSRs were observed in 70/565 (12.4%) treated syphilis. Incidence of LSR decreased over time [2004–2008 IR=25.1 (17.2–33.1)/1000 PMFU; 2009–2010 IR=21.1 (12.3–29.9)/1000 PMFU; 2011–2013 IR=10.6 (5.1–18.2)/1000 PMFU; Poisson regression: p=0.001]. Results of univariate and multivariate analysis on the risk of LSR are reported in Table 1. CONCLUSIONS: In HIV-infected subjects we observed 12% of LSR to treatment of syphilis. LSR was associated with an older age, late syphilis, lower nadir CD4+ and detectable HIV viral load. International AIDS Society 2014-11-02 /pmc/articles/PMC4224790/ /pubmed/25394158 http://dx.doi.org/10.7448/IAS.17.4.19654 Text en © 2014 Spagnuolo V et al; licensee International AIDS Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Sessions – Abstract P122 Spagnuolo, Vincenzo Poli, Andrea Galli, Laura Cernuschi, Massimo Nozza, Silvia Maillard, Myriam Gianotti, Nicola Hasson, Hamid Bossolasco, Simona Lazzarin, Adriano Castagna, Antonella Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title | Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title_full | Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title_fullStr | Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title_full_unstemmed | Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title_short | Predictors of lack of serological response to syphilis treatment in HIV-infected subjects |
title_sort | predictors of lack of serological response to syphilis treatment in hiv-infected subjects |
topic | Poster Sessions – Abstract P122 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224790/ https://www.ncbi.nlm.nih.gov/pubmed/25394158 http://dx.doi.org/10.7448/IAS.17.4.19654 |
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