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

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https://hdl.handle.net/20.500.12080/50991
dc.contributor.author Cervero, Miguel
dc.contributor.author Martínez-Sanz, Javier
dc.contributor.author Díaz-Álvarez, Jorge
dc.contributor.author Rosas, Marta
dc.contributor.author Ron, Raquel
dc.contributor.author Iribarren, José Antonio
dc.contributor.author Bernal, Enrique
dc.contributor.author Gutiérrez, Félix
dc.contributor.author Ruiz Sancho, Andrés
dc.contributor.author Cabello, Noemi
dc.contributor.author Olalla, Julián
dc.contributor.author Moreno, Santiago
dc.contributor.author Serrano-Villar, Sergio
dc.date.accessioned 2025-11-19T11:50:17Z
dc.date.available 2025-11-19T11:50:17Z
dc.date.created 2023
dc.date.issued 2023
dc.identifier.uri https://hdl.handle.net/20.500.12080/50991
dc.description.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/¿L predicted an increased risk of clinical events. Among participants with a CD4 count ¿500 cells/¿L, a CD8 count ¿1500 cells/¿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/¿L, regardless of their CD4 count, may benefit from closer monitoring and targeted preventive interventions. Funding This work was supported by CIBER (CB 2021), Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación and Unión Europea¿NextGenerationEU; by the Spanish AIDS Research Network (RIS) RD16/0025/ 0001 project as part of the Plan Nacional R + D + I, and cofinanced by Instituto de Salud Carlos III (ISCIII)- Subdirección General de Evaluación y el Fondo Europeo de Desarrollo Regional (FEDER), ISCIII projects PI18/00154, PI21/00141, and ERDF, ¿A way to make Europe¿, ICI20/00058. es_ES
dc.format application/pdf es_ES
dc.language eng es_ES
dc.publisher The Lancet Publishing Group . es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.source The Lancet es_ES
dc.title Expanding HIV clinical monitoring: the role of CD4, CD8, and CD4/CD8 ratio in predicting non-AIDS events es_ES
dc.type Artículo es_ES
dc.description.curso 2023 es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.dl 2023
dc.identifier.location N/A es_ES


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