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Correlation between HIV-1 Viral Load Quantification Measured in Dried Blood Spots and Plasma Using 2 Commercial Assays
Carolina Garrido*, N Zahonero, V Soriano, and C de Mendoza
Hosp Carlos III, Madrid, Spain
Background: Viral load quantification is used for monitoring HIV infection in
clinical routine and is usually carried out in plasma specimens. However, it
can be made in other body fluids or in dried blood spots (DBS). The latter
sample format may be especially useful for monitoring patients living in
resource-poor settings.
Methods: Pairwise
plasma and DBS samples belonging to HIV-1-infected patients were quantified
using 2 different commercial assays: Nuclisens EasyQ®HIV-1 v1.1
(Biomerieux) and the m2000rt Real Time™HIV (Abbott). Nucleic acid extraction
was performed manually using the Nuclisens Isolation kit (Boom methodology) and
using the mSample Preparation kit (an iron particle based method). Statistical
correlations were performed using SPSS v13.0.
Results: A
total of 103 paired plasma and DBS samples were collected. Viral load
determinations could be made in 97 (94.2%) using Nuclisens and 81 (78.6%) using
m2000rt. The correlation between measures in plasma and DBS was good, although
better results were obtained using Nuclisens (R2 = 0.87, p
<0.001) than m2000rt (R2 = 0.70, p <0.001).
While the specificity was excellent and similar using both Nuclisens and
m2000rt (97.1% vs 100%), the sensitivity was better using Nuclisens than
m2000rt (75.8% vs 56.5%). Overall, viral load values in DBS tended to be lower
than in plasma with mean (SD) differences of 0.3 (0.5) logs and 0.76 (0.8) logs
using Nuclisens and m2000rt, respectively. The
agreement between measurements in plasma and DBS was also assessed using a
Bland-Altman plot for each assay. Nuclisens provided 95.9% of samples within
its defined limits (–0.65 to 1.26), while m2000rt provided 100% within its
limits (–0.8 to 2.33). However, the limit range for the latter is significantly
wider. When comparing viral load determinations with
Nuclisens and m2000rt, the correlation was good too, reaching R2 =
0.921 (p <0.001) for plasma samples and R2 = 0.714
(p <0.001) for DBS.
Conclusions: HIV-1 viral load can be quantified accurately using DBS with either Nuclisens
EasyQ HIV-1 or m2000rt Abbott RealTime HIV, although Nuclisens may outperform
m2000rt at least when nucleic acids are extracted manually.
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