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Randomized Controlled Trial
. 2013 Jan 2;27(1):59-68.
doi: 10.1097/QAD.0b013e32835a104d.

Platelet count kinetics following interruption of antiretroviral treatment

Collaborators, Affiliations
Randomized Controlled Trial

Platelet count kinetics following interruption of antiretroviral treatment

Eva Zetterberg et al. AIDS. .

Abstract

Objectives: To investigate the mechanisms of platelet kinetics in the Strategies for Management of Antiretroviral Therapy (SMART) study that demonstrated excess mortality with CD4 guided episodic antiretroviral therapy (ART) drug conservation compared with continuous treatment viral suppression. Follow-up analyses of stored plasma samples demonstrated increased activation of both inflammatory and coagulation pathways after stopping ART.

Design: SMART patients from sites that determined platelets routinely.

Methods: Platelet counts were retrospectively collected from 2206 patients from visits at study entry, and during follow-up. D-dimer levels were measured at study entry, month 1, and 2.

Results: Platelet levels decreased in the drug conservation group following randomization, but remained stable in the viral suppression group [median (IQR) decline from study entry to month 4: -24 000/μl (-54 000 to 4000) vs. 3000 (-22 000 to 24 000), respectively, P < 0.0001)] and the rate of developing thrombocytopenia (<100 000/μl) was significantly higher in the drug conservation vs. the viral suppression arm (unadjusted drug conservation/viral suppression [HR (95%CI) = 1.8 (1.2-2.7)]. The decline in platelet count among drug conservation participants on fully suppressive ART correlated with the rise in D-dimer from study entry to either month 1 or 2 (r = -0.41; P = 0.02). Among drug conservation participants who resumed ART 74% recovered to their study entry platelet levels.

Conclusion: Interrupting ART increases the risk of thrombocytopenia, but reinitiation of ART typically reverses it. Factors contributing to declines in platelets after interrupting ART may include activation of coagulation pathways or HIV-1 replication itself. The contribution of platelets in HIV-related procoagulant activity requires further study.

Trial registration: ClinicalTrials.gov NCT00027352.

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Conflict of interest statement

Conflicts of interest

There are no conflicts of interest.

Figures

Fig. 1
Fig. 1
Mean (±2 SE) log platelet change from study entry.
Fig. 2
Fig. 2. Kinetic changes in platelet count according to change in D-dimer and HIV-RNA
(a) Drug conservation group, change in D-dimer level by change in platelet level participants on ART at study entry. (b) Median (IQR) change in platelet levels to month 4 by Month 4 HIV-RNA: drug conservation group on ART with HIV-RNA 400 or less at study entry.

References

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