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Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)

BACKGROUND: Cryptococcal antigen (CrAg) screening with fluconazole prophylaxis has been shown to prevent cryptococcal meningitis and mortality for people living with HIV (PLWH) with CD4 < 100 cells/mm(3). While cryptococcal meningitis occurs in individuals with CD4 100–200 cells/mm(3), there is l...

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Autores principales: Wykowski, James, Galagan, Sean R., Govere, Sabina, Wallis, Carole L., Moosa, Mahomed-Yunus, Celum, Connie, Drain, Paul K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971851/
https://www.ncbi.nlm.nih.gov/pubmed/31959112
http://dx.doi.org/10.1186/s12879-020-4798-1
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author Wykowski, James
Galagan, Sean R.
Govere, Sabina
Wallis, Carole L.
Moosa, Mahomed-Yunus
Celum, Connie
Drain, Paul K.
author_facet Wykowski, James
Galagan, Sean R.
Govere, Sabina
Wallis, Carole L.
Moosa, Mahomed-Yunus
Celum, Connie
Drain, Paul K.
author_sort Wykowski, James
collection PubMed
description BACKGROUND: Cryptococcal antigen (CrAg) screening with fluconazole prophylaxis has been shown to prevent cryptococcal meningitis and mortality for people living with HIV (PLWH) with CD4 < 100 cells/mm(3). While cryptococcal meningitis occurs in individuals with CD4 100–200 cells/mm(3), there is limited evidence that CrAg screening predicts cryptococcal meningitis or mortality among this group with moderate immunosuppression. Current IDSA and WHO clinical guidelines recommend restricting CrAg screening to PLWH with CD4 < 100 cells/mm(3). METHODS: We conducted a prospective cohort study of PLWH 18+ years who had not initiated ART in South Africa. We followed participants for 14 months to determine onset of cryptococcal meningitis or all-cause mortality. At study completion, we retrospectively tested stored serum samples for CrAg using an enzyme immunoassay (EIA). We calculated CD4-stratified incidence rates of outcomes and used Cox proportional hazards to measure associations between CrAg positivity and outcomes. RESULTS: We enrolled 2383 PLWH, and 1309 participants had serum samples tested by CrAg EIA. The median CD4 was 317 cells/mm(3) (interquartile range: 173–491 cells/mm(3)). By CD4 count at baseline, there were 209 individuals with a CD4 count of 100–200 cells/mm(3) and available CrAg test results. Of these, four (1.9%) tested positive. Two of four (IR: 58.8 per 100 person-years) CrAg+ participants and 11 of 205 (IR: 5.6 per 100 person-years) CrAg- participants developed cryptococcal meningitis or died for an overall rate of death or cryptococcal meningitis that was 10.0-times higher for those who were CrAg+ (95% confidence interval: 2.2–45.3). Among those with CD4 < 100 cell/mm(3) and CrAg EIA test results (N = 179), ten (5.6%) participants tested CrAg+. Among this group, seven of ten (IR: 137.6 per 100 person-years) CrAg+ participants and 26 of 169 (IR: 17.8 per 100 person-years) CrAg- participants developed cryptococcal meningitis or died, for a rate of death or cryptococcal meningitis that was 6.3-times higher for those who were CrAg+ (95% confidence interval: 2.7–14.6). CONCLUSIONS: Although few PLWH with moderate immunosuppression screened CrAg positive, a positive CrAg test was predictive of increased risk of cryptococcal meningitis or death. Similar to those with a CD4 < 100 cell/mm(3), systematic CrAg screening may reduce morbidity and mortality in PLWH with CD4 100–200 cells/mm(3).
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spelling pubmed-69718512020-01-27 Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3) Wykowski, James Galagan, Sean R. Govere, Sabina Wallis, Carole L. Moosa, Mahomed-Yunus Celum, Connie Drain, Paul K. BMC Infect Dis Research Article BACKGROUND: Cryptococcal antigen (CrAg) screening with fluconazole prophylaxis has been shown to prevent cryptococcal meningitis and mortality for people living with HIV (PLWH) with CD4 < 100 cells/mm(3). While cryptococcal meningitis occurs in individuals with CD4 100–200 cells/mm(3), there is limited evidence that CrAg screening predicts cryptococcal meningitis or mortality among this group with moderate immunosuppression. Current IDSA and WHO clinical guidelines recommend restricting CrAg screening to PLWH with CD4 < 100 cells/mm(3). METHODS: We conducted a prospective cohort study of PLWH 18+ years who had not initiated ART in South Africa. We followed participants for 14 months to determine onset of cryptococcal meningitis or all-cause mortality. At study completion, we retrospectively tested stored serum samples for CrAg using an enzyme immunoassay (EIA). We calculated CD4-stratified incidence rates of outcomes and used Cox proportional hazards to measure associations between CrAg positivity and outcomes. RESULTS: We enrolled 2383 PLWH, and 1309 participants had serum samples tested by CrAg EIA. The median CD4 was 317 cells/mm(3) (interquartile range: 173–491 cells/mm(3)). By CD4 count at baseline, there were 209 individuals with a CD4 count of 100–200 cells/mm(3) and available CrAg test results. Of these, four (1.9%) tested positive. Two of four (IR: 58.8 per 100 person-years) CrAg+ participants and 11 of 205 (IR: 5.6 per 100 person-years) CrAg- participants developed cryptococcal meningitis or died for an overall rate of death or cryptococcal meningitis that was 10.0-times higher for those who were CrAg+ (95% confidence interval: 2.2–45.3). Among those with CD4 < 100 cell/mm(3) and CrAg EIA test results (N = 179), ten (5.6%) participants tested CrAg+. Among this group, seven of ten (IR: 137.6 per 100 person-years) CrAg+ participants and 26 of 169 (IR: 17.8 per 100 person-years) CrAg- participants developed cryptococcal meningitis or died, for a rate of death or cryptococcal meningitis that was 6.3-times higher for those who were CrAg+ (95% confidence interval: 2.7–14.6). CONCLUSIONS: Although few PLWH with moderate immunosuppression screened CrAg positive, a positive CrAg test was predictive of increased risk of cryptococcal meningitis or death. Similar to those with a CD4 < 100 cell/mm(3), systematic CrAg screening may reduce morbidity and mortality in PLWH with CD4 100–200 cells/mm(3). BioMed Central 2020-01-20 /pmc/articles/PMC6971851/ /pubmed/31959112 http://dx.doi.org/10.1186/s12879-020-4798-1 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wykowski, James
Galagan, Sean R.
Govere, Sabina
Wallis, Carole L.
Moosa, Mahomed-Yunus
Celum, Connie
Drain, Paul K.
Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title_full Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title_fullStr Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title_full_unstemmed Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title_short Cryptococcal antigenemia is associated with meningitis or death in HIV-infected adults with CD4 100–200 cells/mm(3)
title_sort cryptococcal antigenemia is associated with meningitis or death in hiv-infected adults with cd4 100–200 cells/mm(3)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971851/
https://www.ncbi.nlm.nih.gov/pubmed/31959112
http://dx.doi.org/10.1186/s12879-020-4798-1
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