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Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4
OBJECTIVES: We studied the frequency and risk factors for loss of long-term non-progressor (LTNP) and HIV controller (HIC) status among patients identified as such in 2005 in the French Hospital Database on HIV (FHDH-ANRS CO4). METHODS: We selected patients who were treatment-naïve and asymptomatic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624574/ https://www.ncbi.nlm.nih.gov/pubmed/28968404 http://dx.doi.org/10.1371/journal.pone.0184441 |
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author | Grabar, Sophie Selinger-Leneman, Hana Abgrall, Sophie Pialoux, Gilles Weiss, Laurence Costagliola, Dominique |
author_facet | Grabar, Sophie Selinger-Leneman, Hana Abgrall, Sophie Pialoux, Gilles Weiss, Laurence Costagliola, Dominique |
author_sort | Grabar, Sophie |
collection | PubMed |
description | OBJECTIVES: We studied the frequency and risk factors for loss of long-term non-progressor (LTNP) and HIV controller (HIC) status among patients identified as such in 2005 in the French Hospital Database on HIV (FHDH-ANRS CO4). METHODS: We selected patients who were treatment-naïve and asymptomatic in 2005 (baseline). Those with ≥8 years of known HIV infection and a CD4 cell nadir ≥500/mm(3) were classified as LTNP and those with ≥10 years of known HIV infection and 90% of plasma viral load (VL) values ≤500 copies/ml in the absence of cART as HIC. cART initiation without loss of status and death from non AIDS-defining causes were considered as competing events. RESULTS: After 5 years of follow-up, 33% (95%CI; 27–42) of 171 LTNP patients and 17% (95%CI; 10–30) of 72 HIC patients had lost their status. In multivariable analyses, loss of LTNP status was associated with lower baseline CD4 cell counts and CD4/CD8 ratios. Only VL was significantly associated with loss of HIC status after adjustment for the baseline CD4 cell count, the CD4/CD8 ratio, and concomitant LTNP status. The hazard ratio for loss of HIC status was 5.5 (95%CI, 1.5–20.1) for baseline VL 50–500 vs ≤50 cp/mL, after adjustment for the baseline CD4 cell count. CONCLUSIONS: One-third of LTNP and one-fifth of HIC patients lost their status after 5 years of follow-up, raising questions as to the possible benefits and timing of ART initiation in these populations. |
format | Online Article Text |
id | pubmed-5624574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56245742017-10-17 Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 Grabar, Sophie Selinger-Leneman, Hana Abgrall, Sophie Pialoux, Gilles Weiss, Laurence Costagliola, Dominique PLoS One Research Article OBJECTIVES: We studied the frequency and risk factors for loss of long-term non-progressor (LTNP) and HIV controller (HIC) status among patients identified as such in 2005 in the French Hospital Database on HIV (FHDH-ANRS CO4). METHODS: We selected patients who were treatment-naïve and asymptomatic in 2005 (baseline). Those with ≥8 years of known HIV infection and a CD4 cell nadir ≥500/mm(3) were classified as LTNP and those with ≥10 years of known HIV infection and 90% of plasma viral load (VL) values ≤500 copies/ml in the absence of cART as HIC. cART initiation without loss of status and death from non AIDS-defining causes were considered as competing events. RESULTS: After 5 years of follow-up, 33% (95%CI; 27–42) of 171 LTNP patients and 17% (95%CI; 10–30) of 72 HIC patients had lost their status. In multivariable analyses, loss of LTNP status was associated with lower baseline CD4 cell counts and CD4/CD8 ratios. Only VL was significantly associated with loss of HIC status after adjustment for the baseline CD4 cell count, the CD4/CD8 ratio, and concomitant LTNP status. The hazard ratio for loss of HIC status was 5.5 (95%CI, 1.5–20.1) for baseline VL 50–500 vs ≤50 cp/mL, after adjustment for the baseline CD4 cell count. CONCLUSIONS: One-third of LTNP and one-fifth of HIC patients lost their status after 5 years of follow-up, raising questions as to the possible benefits and timing of ART initiation in these populations. Public Library of Science 2017-10-02 /pmc/articles/PMC5624574/ /pubmed/28968404 http://dx.doi.org/10.1371/journal.pone.0184441 Text en © 2017 Grabar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Grabar, Sophie Selinger-Leneman, Hana Abgrall, Sophie Pialoux, Gilles Weiss, Laurence Costagliola, Dominique Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title | Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title_full | Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title_fullStr | Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title_full_unstemmed | Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title_short | Loss of long-term non-progressor and HIV controller status over time in the French Hospital Database on HIV - ANRS CO4 |
title_sort | loss of long-term non-progressor and hiv controller status over time in the french hospital database on hiv - anrs co4 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5624574/ https://www.ncbi.nlm.nih.gov/pubmed/28968404 http://dx.doi.org/10.1371/journal.pone.0184441 |
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