CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.

<h4>Objectives</h4>Immune non-responders (INR) have poor CD4 recovery and are associated with increased risk of serious events despite antiretroviral therapy (ART). A clinically relevant definition for INR is lacking.<h4>Methods</h4>We conducted a retrospective analysis of th...

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Main Authors: Sol Aldrete, Jeong Hoon Jang, Kirk A Easley, Jason Okulicz, Tian Dai, Yi No Chen, Maria Pino, Brian K Agan, Ryan C Maves, Mirko Paiardini, Vincent C Marconi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0227124&type=printable
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author Sol Aldrete
Jeong Hoon Jang
Kirk A Easley
Jason Okulicz
Tian Dai
Yi No Chen
Maria Pino
Brian K Agan
Ryan C Maves
Mirko Paiardini
Vincent C Marconi
author_facet Sol Aldrete
Jeong Hoon Jang
Kirk A Easley
Jason Okulicz
Tian Dai
Yi No Chen
Maria Pino
Brian K Agan
Ryan C Maves
Mirko Paiardini
Vincent C Marconi
author_sort Sol Aldrete
collection DOAJ
description <h4>Objectives</h4>Immune non-responders (INR) have poor CD4 recovery and are associated with increased risk of serious events despite antiretroviral therapy (ART). A clinically relevant definition for INR is lacking.<h4>Methods</h4>We conducted a retrospective analysis of three large cohorts: Infectious Disease Clinic at the Atlanta Veterans Affairs Medical Center, the US Military HIV Natural History Study and Infectious Disease Program of the Grady Health System in Atlanta, Georgia. Two-stage modeling and joint model (JM) approaches were used to evaluate the association between CD4 (or CD4/CD8 ratio) slope within two years since ART initiation and a composite endpoint (AIDS, serious non-AIDS events and death) after two years of ART. We compared the predictive capacity of four CD4 count metrics (estimated CD4 slope, estimated CD4/CD8 ratio slope during two years following ART initiation and CD4 at 1 and 2 years following ART initiation) using Cox regression models.<h4>Results</h4>We included 2,422 patients. Mean CD4 slope (±standard error) during two years of ART was 102 ± 2 cells/μl/year (95% confidence interval: 98-106 cells/μl/year), this increase was uniform among the three cohorts (p = 0.80). There were 267 composite events after two years on ART. Using the JM approach, a CD4 slope ≥100 cells/μL/year or CD4/CD8 ratio slope >0.1 higher rate per year were associated with lower composite endpoint rates (adjusted hazard ratio [HR] = 0.80, p = 0.04 and HR = 0.75 p<0.01, respectively). All four CD4 metrics showed modest predictive capacity.<h4>Conclusions</h4>Using a complex JM approach, CD4 slope and CD4/CD8 ratio slope the first two years after ART initiation were associated with lower rates of the composite outcome. Moreover, the uniformity observed in the mean CD4 slope regardless of the cohort suggests a common CD4 response pattern independent of age or CD4 nadir. Given the consistency observed with CD4 slope, availability and ease of interpretation, this study provides strong rationale for using CD4 gains <100 cells/μl/year to identify patients at risk for adverse events.
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spelling doaj-art-5f91485c6cc44210a490afaa6b954a672025-08-20T02:17:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01151e022712410.1371/journal.pone.0227124CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.Sol AldreteJeong Hoon JangKirk A EasleyJason OkuliczTian DaiYi No ChenMaria PinoBrian K AganRyan C MavesMirko PaiardiniVincent C Marconi<h4>Objectives</h4>Immune non-responders (INR) have poor CD4 recovery and are associated with increased risk of serious events despite antiretroviral therapy (ART). A clinically relevant definition for INR is lacking.<h4>Methods</h4>We conducted a retrospective analysis of three large cohorts: Infectious Disease Clinic at the Atlanta Veterans Affairs Medical Center, the US Military HIV Natural History Study and Infectious Disease Program of the Grady Health System in Atlanta, Georgia. Two-stage modeling and joint model (JM) approaches were used to evaluate the association between CD4 (or CD4/CD8 ratio) slope within two years since ART initiation and a composite endpoint (AIDS, serious non-AIDS events and death) after two years of ART. We compared the predictive capacity of four CD4 count metrics (estimated CD4 slope, estimated CD4/CD8 ratio slope during two years following ART initiation and CD4 at 1 and 2 years following ART initiation) using Cox regression models.<h4>Results</h4>We included 2,422 patients. Mean CD4 slope (±standard error) during two years of ART was 102 ± 2 cells/μl/year (95% confidence interval: 98-106 cells/μl/year), this increase was uniform among the three cohorts (p = 0.80). There were 267 composite events after two years on ART. Using the JM approach, a CD4 slope ≥100 cells/μL/year or CD4/CD8 ratio slope >0.1 higher rate per year were associated with lower composite endpoint rates (adjusted hazard ratio [HR] = 0.80, p = 0.04 and HR = 0.75 p<0.01, respectively). All four CD4 metrics showed modest predictive capacity.<h4>Conclusions</h4>Using a complex JM approach, CD4 slope and CD4/CD8 ratio slope the first two years after ART initiation were associated with lower rates of the composite outcome. Moreover, the uniformity observed in the mean CD4 slope regardless of the cohort suggests a common CD4 response pattern independent of age or CD4 nadir. Given the consistency observed with CD4 slope, availability and ease of interpretation, this study provides strong rationale for using CD4 gains <100 cells/μl/year to identify patients at risk for adverse events.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0227124&type=printable
spellingShingle Sol Aldrete
Jeong Hoon Jang
Kirk A Easley
Jason Okulicz
Tian Dai
Yi No Chen
Maria Pino
Brian K Agan
Ryan C Maves
Mirko Paiardini
Vincent C Marconi
CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
PLoS ONE
title CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
title_full CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
title_fullStr CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
title_full_unstemmed CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
title_short CD4 rate of increase is preferred to CD4 threshold for predicting outcomes among virologically suppressed HIV-infected adults on antiretroviral therapy.
title_sort cd4 rate of increase is preferred to cd4 threshold for predicting outcomes among virologically suppressed hiv infected adults on antiretroviral therapy
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0227124&type=printable
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