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Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model

BACKGROUND: HIV infected patients may experience many intermediate events including between-event transition throughout their follow up. Through modelling these transitions, we can gain a deeper understanding of HIV disease process and progression and of factors that influence the disease process an...

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Autores principales: Dessie, Zelalem G., Zewotir, Temesgen, Mwambi, Henry, North, Delia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310520/
https://www.ncbi.nlm.nih.gov/pubmed/32571361
http://dx.doi.org/10.1186/s12976-020-00128-5
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author Dessie, Zelalem G.
Zewotir, Temesgen
Mwambi, Henry
North, Delia
author_facet Dessie, Zelalem G.
Zewotir, Temesgen
Mwambi, Henry
North, Delia
author_sort Dessie, Zelalem G.
collection PubMed
description BACKGROUND: HIV infected patients may experience many intermediate events including between-event transition throughout their follow up. Through modelling these transitions, we can gain a deeper understanding of HIV disease process and progression and of factors that influence the disease process and progression pathway. In this work, we present transition-specific parametric multi-state models to describe HIV disease process and progression. METHODS: The data is from an ongoing prospective cohort study conducted amongst adult women who were HIV-infected in KwaZulu-Natal, South Africa. Participants were enrolled during the acute HIV infection phase and then followed up during chronic infection, up to ART initiation. RESULTS: Transition specific distributions for multi-state models, including a variety of accelerated failure time (AFT) models and proportional hazards (PH) models, were presented and compared in this study. The analysis revealed that women enrolling with a CD4 count less than 350 cells/mm(3) (severe and advanced disease stages) had a far lower chance of immune recovery, and a considerably higher chance of immune deterioration, compared to women enrolling with a CD4 count of 350 cells/mm(3) or more (normal and mild disease stages). Our analyses also showed that older age, higher educational levels, higher scores for red blood cell counts, higher mononuclear scores, higher granulocytes scores, and higher physical health scores, all had a significant effect on a shortened time to immunological recovery, while women with many sex partners, higher viral load and larger family size had a significant effect on accelerating time to immune deterioration. CONCLUSION: Multi-state modelling of transition-specific distributions offers a flexible tool for the study of demographic and clinical characteristics’ effects on the entire disease progression pathway. It is hoped that the article will help applied researchers to familiarize themselves with the models, including interpretation of results.
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spelling pubmed-73105202020-06-23 Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model Dessie, Zelalem G. Zewotir, Temesgen Mwambi, Henry North, Delia Theor Biol Med Model Research BACKGROUND: HIV infected patients may experience many intermediate events including between-event transition throughout their follow up. Through modelling these transitions, we can gain a deeper understanding of HIV disease process and progression and of factors that influence the disease process and progression pathway. In this work, we present transition-specific parametric multi-state models to describe HIV disease process and progression. METHODS: The data is from an ongoing prospective cohort study conducted amongst adult women who were HIV-infected in KwaZulu-Natal, South Africa. Participants were enrolled during the acute HIV infection phase and then followed up during chronic infection, up to ART initiation. RESULTS: Transition specific distributions for multi-state models, including a variety of accelerated failure time (AFT) models and proportional hazards (PH) models, were presented and compared in this study. The analysis revealed that women enrolling with a CD4 count less than 350 cells/mm(3) (severe and advanced disease stages) had a far lower chance of immune recovery, and a considerably higher chance of immune deterioration, compared to women enrolling with a CD4 count of 350 cells/mm(3) or more (normal and mild disease stages). Our analyses also showed that older age, higher educational levels, higher scores for red blood cell counts, higher mononuclear scores, higher granulocytes scores, and higher physical health scores, all had a significant effect on a shortened time to immunological recovery, while women with many sex partners, higher viral load and larger family size had a significant effect on accelerating time to immune deterioration. CONCLUSION: Multi-state modelling of transition-specific distributions offers a flexible tool for the study of demographic and clinical characteristics’ effects on the entire disease progression pathway. It is hoped that the article will help applied researchers to familiarize themselves with the models, including interpretation of results. BioMed Central 2020-06-23 /pmc/articles/PMC7310520/ /pubmed/32571361 http://dx.doi.org/10.1186/s12976-020-00128-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Dessie, Zelalem G.
Zewotir, Temesgen
Mwambi, Henry
North, Delia
Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title_full Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title_fullStr Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title_full_unstemmed Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title_short Modelling HIV disease process and progression in seroconversion among South Africa women: using transition-specific parametric multi-state model
title_sort modelling hiv disease process and progression in seroconversion among south africa women: using transition-specific parametric multi-state model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310520/
https://www.ncbi.nlm.nih.gov/pubmed/32571361
http://dx.doi.org/10.1186/s12976-020-00128-5
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