Articles producció científica> Medicina i Cirurgia

Expanding HIV clinical monitoring: the role of CD4, CD8, and CD4/CD8 ratio in predicting non-AIDS events

  • Identification data

    Identifier: imarina:9333674
    Authors:
    Martínez-Sanz, JDiaz-alvarez, JRosas, MRon, RIribarren, JABernal, EGutiérrez, FSancho, ARCabello, NOlalla, JMoreno, SSerrano-Villar, S
    Abstract:
    Background While a low CD4/CD8 ratio during HIV treatment correlates with immunosenescence, its value in identifying patients at an increased risk for clinical events remains unclear.Methods We analyzed data from the CoRIS cohort to determine whether CD4 count, CD8 count, and CD4/CD8 ratio at year two of antiretroviral therapy (ART) could predict the risk of serious non-AIDS events (SNAEs) during the next five years. These included major adverse cardiovascular events, non-AIDS-defining malignancies, and non-accidental deaths. We used pooled logistic regression with inverse probability weighting to estimate the survival curves and cumulative risk of clinical events.Findings The study included 4625 participants, 83% male, of whom 200 (4.3%) experienced an SNAE during the follow-up period. A CD4/CD8 ratio <0.3 predicted an increased risk of SNAEs during the next five years (OR 1.63, 95% CI 1.03-2.58). The effect was stronger at a CD4/CD8 ratio cut-off of <0.2 (OR 3.09, 95% CI 1.57-6.07). Additionally, low CD4 count at cut-offs of <500 cells/mu L predicted an increased risk of clinical events. Among participants with a CD4 count >500 cells/mu L, a CD8 count >1500 cells/mu L or a CD4/CD8 ratio <0.4 predicted increased SNAE risk.Interpretation Our results support the use of the CD4/CD8 ratio and CD8 count as predictors of clinical progression. Patients with CD4/CD8 ratio <0.3 or CD8 count >1500/mu L, regardless of their CD4 count, may benefit from closer monitoring and targeted preventive interventions.Copyright (c) 2023 The Author(s). Published by Elsevier B.V.
  • Others:

    Author, as appears in the article.: Martínez-Sanz, J; Diaz-alvarez, J; Rosas, M; Ron, R; Iribarren, JA; Bernal, E; Gutiérrez, F; Sancho, AR; Cabello, N; Olalla, J; Moreno, S; Serrano-Villar, S
    Department: Medicina i Cirurgia
    URV's Author/s: Peraire Forner, José Joaquin
    Keywords: Risk Population Old Non-aids events Neoplasia Initiation Infected adults Individuals Hiv Hazards Cohort Cell counts Cd4/cd8 ratio Cardiovascular event Antiretroviral therapy
    Abstract: Background While a low CD4/CD8 ratio during HIV treatment correlates with immunosenescence, its value in identifying patients at an increased risk for clinical events remains unclear.Methods We analyzed data from the CoRIS cohort to determine whether CD4 count, CD8 count, and CD4/CD8 ratio at year two of antiretroviral therapy (ART) could predict the risk of serious non-AIDS events (SNAEs) during the next five years. These included major adverse cardiovascular events, non-AIDS-defining malignancies, and non-accidental deaths. We used pooled logistic regression with inverse probability weighting to estimate the survival curves and cumulative risk of clinical events.Findings The study included 4625 participants, 83% male, of whom 200 (4.3%) experienced an SNAE during the follow-up period. A CD4/CD8 ratio <0.3 predicted an increased risk of SNAEs during the next five years (OR 1.63, 95% CI 1.03-2.58). The effect was stronger at a CD4/CD8 ratio cut-off of <0.2 (OR 3.09, 95% CI 1.57-6.07). Additionally, low CD4 count at cut-offs of <500 cells/mu L predicted an increased risk of clinical events. Among participants with a CD4 count >500 cells/mu L, a CD8 count >1500 cells/mu L or a CD4/CD8 ratio <0.4 predicted increased SNAE risk.Interpretation Our results support the use of the CD4/CD8 ratio and CD8 count as predictors of clinical progression. Patients with CD4/CD8 ratio <0.3 or CD8 count >1500/mu L, regardless of their CD4 count, may benefit from closer monitoring and targeted preventive interventions.Copyright (c) 2023 The Author(s). Published by Elsevier B.V.
    Thematic Areas: Saúde coletiva Medicine, research & experimental Medicine (miscellaneous) Medicine (all) Medicina iii Medicina ii Medicina i General medicine General biochemistry,genetics and molecular biology Ciências biológicas ii Biotecnología Biochemistry, genetics and molecular biology (miscellaneous) Biochemistry, genetics and molecular biology (all)
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    Author's mail: joaquim.peraire@urv.cat
    Author identifier: 0000-0001-7808-5479
    Record's date: 2024-08-03
    Papper version: info:eu-repo/semantics/publishedVersion
    Link to the original source: https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(23)00339-0/fulltext#%20
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Papper original source: Ebiomedicine. 95
    APA: Martínez-Sanz, J; Diaz-alvarez, J; Rosas, M; Ron, R; Iribarren, JA; Bernal, E; Gutiérrez, F; Sancho, AR; Cabello, N; Olalla, J; Moreno, S; Serrano-Vil (2023). Expanding HIV clinical monitoring: the role of CD4, CD8, and CD4/CD8 ratio in predicting non-AIDS events. Ebiomedicine, 95(), -. DOI: 10.1016/j.ebiom.2023.104773
    Article's DOI: 10.1016/j.ebiom.2023.104773
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2023
    Publication Type: Journal Publications
  • Keywords:

    Biochemistry, Genetics and Molecular Biology (Miscellaneous),Medicine (Miscellaneous),Medicine, Research & Experimental
    Risk
    Population
    Old
    Non-aids events
    Neoplasia
    Initiation
    Infected adults
    Individuals
    Hiv
    Hazards
    Cohort
    Cell counts
    Cd4/cd8 ratio
    Cardiovascular event
    Antiretroviral therapy
    Saúde coletiva
    Medicine, research & experimental
    Medicine (miscellaneous)
    Medicine (all)
    Medicina iii
    Medicina ii
    Medicina i
    General medicine
    General biochemistry,genetics and molecular biology
    Ciências biológicas ii
    Biotecnología
    Biochemistry, genetics and molecular biology (miscellaneous)
    Biochemistry, genetics and molecular biology (all)
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