» Articles » PMID: 8552144

Changes in Plasma HIV-1 RNA and CD4+ Lymphocyte Counts and the Risk of Progression to AIDS. Veterans Affairs Cooperative Study Group on AIDS

Overview
Journal N Engl J Med
Specialty General Medicine
Date 1996 Feb 15
PMID 8552144
Citations 154
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Clinical trials of antiretroviral drugs can take years to complete because the outcomes measured are progression to the acquired immunodeficiency syndrome (AIDS) or death. Trials could be accelerated by the use of end points such as changes in CD4+ lymphocyte counts and plasma levels of human immunodeficiency virus type 1 (HIV-1) RNA and beta 2-microglobulin, but there is uncertainty about whether these surrogate measures are valid predictors of disease progression.

Methods: We analyzed data from the Veterans Affairs Cooperative Study on AIDS, which compared immediate with deferred zidovudine therapy. Patients' plasma levels of HIV-1 RNA and beta 2-microglobulin were measured in stored plasma.

Results: Among the 129 patients in the immediate-treatment group, 34 had disease that progressed to AIDS, as compared with 57 of the 141 patients in the deferred-treatment group (P = 0.03). Progression to AIDS correlated strongly with base-line CD4+ lymphocyte counts (P = 0.001) and plasma levels of HIV-1 RNA (P < 0.001), but not with base-line levels of beta 2-microglobulin (P = 0.14). A decrease of at least 75 percent in the plasma level of HIV-1 RNA over the first six months of zidovudine therapy accounted for 59 percent of the benefit of treatment, defined as the absence of progression to AIDS (95 percent confidence interval, 13 to 112 percent). Plasma beta 2-microglobulin levels and CD4+ lymphocyte counts explained less of the effect of treatment. A 75 percent decrease in the plasma HIV-1 RNA level plus a 10 percent increase in the CD4+ lymphocyte count could explain 79 percent of the treatment effect (95 percent confidence interval, 27 to 145 percent).

Conclusions: Treatment-induced changes in the plasma HIV-1 RNA level and the CD4+ lymphocyte count, taken together, are valid predictors of the clinical progression of HIV-related disease and can be used to assess the efficacy of zidovudine and possibly other antiretroviral drugs as well.

Citing Articles

A General Framework to Assess Complex Heterogeneity in the Strength of a Surrogate Marker.

Knowlton R, Tian L, Parast L Stat Med. 2025; 44(5):e70001.

PMID: 39915898 PMC: 11835199. DOI: 10.1002/sim.70001.


HIV-1 control in vivo is related to the number but not the fraction of infected cells with viral unspliced RNA.

Capoferri A, Wiegand A, Hong F, Jacobs J, Spindler J, Musick A Proc Natl Acad Sci U S A. 2024; 121(36):e2405210121.

PMID: 39190360 PMC: 11388345. DOI: 10.1073/pnas.2405210121.


Long-term HIV care outcomes under universal HIV treatment guidelines: A retrospective cohort study in 25 countries.

Brazier E, Tymejczyk O, Wools-Kaloustian K, Jiamsakul A, Torres M, Lee J PLoS Med. 2024; 21(3):e1004367.

PMID: 38498589 PMC: 10962811. DOI: 10.1371/journal.pmed.1004367.


Effectiveness of intensive adherence counselling in achieving an undetectable viral load among people on antiretroviral therapy with low-level viraemia in Uganda.

Nanyeenya N, Nakanjako D, Makumbi F, Nakigozi G, Nalugoda F, Kigozi G HIV Med. 2023; 25(2):245-253.

PMID: 37853605 PMC: 11047222. DOI: 10.1111/hiv.13568.


Contribution of the HIV-1 Envelope Glycoprotein to AIDS Pathogenesis and Clinical Progression.

Valenzuela-Fernandez A, Cabrera-Rodriguez R, Casado C, Perez-Yanes S, Pernas M, Garcia-Luis J Biomedicines. 2022; 10(9).

PMID: 36140273 PMC: 9495913. DOI: 10.3390/biomedicines10092172.