Cargando…

Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals

OBJECTIVES: Among antiretroviral therapy (ART)-naive individuals, viral load levels tend to increase and CD4(+) cell counts decline over time. We sought to explore the rate of change and influence of other factors associated with these markers of HIV progression. DESIGN: An observational cohort coll...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032217/
https://www.ncbi.nlm.nih.gov/pubmed/24959963
http://dx.doi.org/10.1097/QAD.0000000000000224
_version_ 1782317609917612032
collection PubMed
description OBJECTIVES: Among antiretroviral therapy (ART)-naive individuals, viral load levels tend to increase and CD4(+) cell counts decline over time. We sought to explore the rate of change and influence of other factors associated with these markers of HIV progression. DESIGN: An observational cohort collaboration study. METHODS: A total of 158 385 pairs of consecutive viral load and CD4(+) cell count simultaneously measured from 34 384 ART-naive individuals in the COHERE database were analysed. Annual changes and factors associated with these changes were estimated using generalized estimating equations. RESULTS: Viral load continued to rise at a mean [95% confidence interval (CI)] rate of 0.091 (0.086–0.096) log(10) copies/ml per year. A faster rise in viral load was significantly associated with older age, such that for every 10 years older, it was a mean 0.022 log(10) copies/ml per year greater. The mean (95% CI) CD4(+) cell count change was −78.0 (−80.1 to −76.0) cell/μl per year and it was strongly associated with a higher current viral load: for every 1 log(10) copies/ml higher, CD4(+) cell count declined by an additional 37.6 cells/μl per year (P < 0.001). Current viral load was a stronger predictor of CD4(+) cell count depletion than baseline viral load. Neither sex, race nor transmission by injecting drug use was associated with change in either the viral load or CD4(+) cell count. DISCUSSION: We found that in ART-naive individuals, viral load continues to increase over time and more sharply in those who are older. Our results also suggest that higher current viral load is strongly associated with ongoing rate of CD4(+) cell count depletion.
format Online
Article
Text
id pubmed-4032217
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-40322172014-05-27 Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals AIDS Epidemiology and Social: CONCISE COMMUNICATIONS OBJECTIVES: Among antiretroviral therapy (ART)-naive individuals, viral load levels tend to increase and CD4(+) cell counts decline over time. We sought to explore the rate of change and influence of other factors associated with these markers of HIV progression. DESIGN: An observational cohort collaboration study. METHODS: A total of 158 385 pairs of consecutive viral load and CD4(+) cell count simultaneously measured from 34 384 ART-naive individuals in the COHERE database were analysed. Annual changes and factors associated with these changes were estimated using generalized estimating equations. RESULTS: Viral load continued to rise at a mean [95% confidence interval (CI)] rate of 0.091 (0.086–0.096) log(10) copies/ml per year. A faster rise in viral load was significantly associated with older age, such that for every 10 years older, it was a mean 0.022 log(10) copies/ml per year greater. The mean (95% CI) CD4(+) cell count change was −78.0 (−80.1 to −76.0) cell/μl per year and it was strongly associated with a higher current viral load: for every 1 log(10) copies/ml higher, CD4(+) cell count declined by an additional 37.6 cells/μl per year (P < 0.001). Current viral load was a stronger predictor of CD4(+) cell count depletion than baseline viral load. Neither sex, race nor transmission by injecting drug use was associated with change in either the viral load or CD4(+) cell count. DISCUSSION: We found that in ART-naive individuals, viral load continues to increase over time and more sharply in those who are older. Our results also suggest that higher current viral load is strongly associated with ongoing rate of CD4(+) cell count depletion. Lippincott Williams & Wilkins 2014-06-01 2014-05-14 /pmc/articles/PMC4032217/ /pubmed/24959963 http://dx.doi.org/10.1097/QAD.0000000000000224 Text en © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins http://creativecommons.org/licenses/by-nc-nd/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivitives 3.0 License, 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.
spellingShingle Epidemiology and Social: CONCISE COMMUNICATIONS
Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title_full Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title_fullStr Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title_full_unstemmed Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title_short Factors associated with short-term changes in HIV viral load and CD4(+) cell count in antiretroviral-naive individuals
title_sort factors associated with short-term changes in hiv viral load and cd4(+) cell count in antiretroviral-naive individuals
topic Epidemiology and Social: CONCISE COMMUNICATIONS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032217/
https://www.ncbi.nlm.nih.gov/pubmed/24959963
http://dx.doi.org/10.1097/QAD.0000000000000224