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Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection

OBJECTIVE: We compiled the largest dataset of seroconverter cohorts to date from 25 countries across Africa, North America, Europe, and Southeast/East (SE/E) Asia to simultaneously estimate transition rates between CD4(+) cell stages and death, in antiretroviral therapy (ART)-naive HIV-1-infected in...

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Autor principal: Mangal, Tara D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414573/
https://www.ncbi.nlm.nih.gov/pubmed/28301424
http://dx.doi.org/10.1097/QAD.0000000000001437
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author Mangal, Tara D.
author_facet Mangal, Tara D.
author_sort Mangal, Tara D.
collection PubMed
description OBJECTIVE: We compiled the largest dataset of seroconverter cohorts to date from 25 countries across Africa, North America, Europe, and Southeast/East (SE/E) Asia to simultaneously estimate transition rates between CD4(+) cell stages and death, in antiretroviral therapy (ART)-naive HIV-1-infected individuals. DESIGN: A hidden Markov model incorporating a misclassification matrix was used to represent natural short-term fluctuations and measurement errors in CD4(+) cell counts. Covariates were included to estimate the transition rates and survival probabilities for each subgroup. RESULTS: The median follow-up time for 16 373 eligible individuals was 4.1 years (interquartile range 1.7–7.1), and the mean age at seroconversion was 31.1 years (SD 8.8). A total of 14 525 individuals had recorded CD4(+) cell counts pre-ART, 1885 died, and 6947 initiated ART. Median (interquartile range) survival for men aged 20 years at seroconversion was 13.0 (12.4–13.4), 11.6 (10.9–12.3), and 8.3 years (7.9–8.9) in Europe/North America, Africa, and SE/E Asia, respectively. Mortality rates increase with age (hazard ratio 2.22, 95% confidence interval 1.84–2.67 for >45 years compared with <25 years) and vary by region (hazard ratio 2.68, 1.75–4.12 for Africa and 1.88, 1.50–2.35 for Asia compared with Europe/North America). CD4(+) cell decline was significantly faster in Asian cohorts compared with Europe/North America (hazard ratio 1.45, 1.36–1.54). CONCLUSION: Mortality and CD4(+) cell progression rates exhibited regional and age-specific differences, with decreased survival in African and SE/E Asian cohorts compared with Europe/North America and in older age groups. This extensive dataset reveals heterogeneities between regions and ages, which should be incorporated into future HIV models.
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spelling pubmed-54145732017-05-10 Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection Mangal, Tara D. AIDS Basic Science OBJECTIVE: We compiled the largest dataset of seroconverter cohorts to date from 25 countries across Africa, North America, Europe, and Southeast/East (SE/E) Asia to simultaneously estimate transition rates between CD4(+) cell stages and death, in antiretroviral therapy (ART)-naive HIV-1-infected individuals. DESIGN: A hidden Markov model incorporating a misclassification matrix was used to represent natural short-term fluctuations and measurement errors in CD4(+) cell counts. Covariates were included to estimate the transition rates and survival probabilities for each subgroup. RESULTS: The median follow-up time for 16 373 eligible individuals was 4.1 years (interquartile range 1.7–7.1), and the mean age at seroconversion was 31.1 years (SD 8.8). A total of 14 525 individuals had recorded CD4(+) cell counts pre-ART, 1885 died, and 6947 initiated ART. Median (interquartile range) survival for men aged 20 years at seroconversion was 13.0 (12.4–13.4), 11.6 (10.9–12.3), and 8.3 years (7.9–8.9) in Europe/North America, Africa, and SE/E Asia, respectively. Mortality rates increase with age (hazard ratio 2.22, 95% confidence interval 1.84–2.67 for >45 years compared with <25 years) and vary by region (hazard ratio 2.68, 1.75–4.12 for Africa and 1.88, 1.50–2.35 for Asia compared with Europe/North America). CD4(+) cell decline was significantly faster in Asian cohorts compared with Europe/North America (hazard ratio 1.45, 1.36–1.54). CONCLUSION: Mortality and CD4(+) cell progression rates exhibited regional and age-specific differences, with decreased survival in African and SE/E Asian cohorts compared with Europe/North America and in older age groups. This extensive dataset reveals heterogeneities between regions and ages, which should be incorporated into future HIV models. Lippincott Williams & Wilkins 2017-05-15 2017-04-25 /pmc/articles/PMC5414573/ /pubmed/28301424 http://dx.doi.org/10.1097/QAD.0000000000001437 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Basic Science
Mangal, Tara D.
Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title_full Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title_fullStr Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title_full_unstemmed Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title_short Joint estimation of CD4(+) cell progression and survival in untreated individuals with HIV-1 infection
title_sort joint estimation of cd4(+) cell progression and survival in untreated individuals with hiv-1 infection
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414573/
https://www.ncbi.nlm.nih.gov/pubmed/28301424
http://dx.doi.org/10.1097/QAD.0000000000001437
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