Journal of Clinical Virology
Volume 35, Issue 2 , Pages 197-200, February 2006

Increased levels of HIV RNA detected in samples with viral loads close to the detection limit collected in Plasma Preparation Tubes™ (PPT)

  • Brigitte P. Griffith

      Affiliations

    • VA CT Virology Reference Laboratory, VA Connecticut Healthcare System, West Haven, CT 06516, USA
    • Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA
    • Corresponding Author InformationCorresponding author at: VA CT Virology Reference Laboratory, VA Connecticut Healthcare System, 950 Campbell Avenue, West Haven, CT 06516, USA. Tel.: +1 203 932 5711x3504; fax: +1 203 937 3893.
  • ,
  • Donald R. Mayo

      Affiliations

    • VA CT Virology Reference Laboratory, VA Connecticut Healthcare System, West Haven, CT 06516, USA
    • Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA

Received 16 May 2005; received in revised form 1 August 2005; accepted 15 August 2005. published online 27 October 2005.

Abstract 

Background

The accurate and reliable quantification of HIV RNA is an essential part of the management of HIV infected individuals, and elucidation of factors that may affect HIV RNA measurements, such as the use of Vacutainer Plasma Preparation Tubes™ (PPT), is crucial.

Objectives

The objective of this study was to determine if plasma samples with viral loads close to the lower limit of the dynamic range of the assay collected in PPT tubes had increased levels of HIV RNA as compared to samples collected in standard EDTA tubes.

Study design

HIV RNA levels were compared in 112 paired plasma samples collected in PPT and standard EDTA tubes. All samples had been frozen prior to testing.

Results

Discrepancies between PPT and EDTA tubes did not occur for samples with high viral loads. However, in samples with viral loads close to the lower limit of the dynamic range, levels of HIV RNA detected were higher in a large proportion of PPT as compared to the corresponding EDTA plasma samples. Forty percent of plasma pairs had no detectable HIV RNA in the EDTA aliquot, but had low levels of HIV RNA in the corresponding PPT aliquot.

Conclusions

This prospective study underlines the need for cautious interpretation of small transient viral load changes in samples with values close to the detection limit.

Keywords: HIV-1 RNA, Plasma Preparation Tubes™, Standard EDTA tubes, Low viral loads

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PII: S1386-6532(05)00244-1

doi:10.1016/j.jcv.2005.08.008

Journal of Clinical Virology
Volume 35, Issue 2 , Pages 197-200, February 2006