Comparison of commercial and in-house Real-time PCR assays for quantification of Epstein-Barr virus (EBV) DNA in plasma
2007

Comparing PCR Tests for Epstein-Barr Virus DNA in Blood

Sample size: 199 publication Evidence: moderate

Author Information

Author(s): Francesca Perandin, Elisabetta Cariani, Caterina Patrizia Pollara, Nino Manca

Primary Institution: Department of Experimental and Applied Medicine, Section of Microbiology, University of Brescia

Hypothesis

The study aims to compare the performance of two real-time PCR assays for quantifying Epstein-Barr virus (EBV) DNA in plasma.

Conclusion

Both the commercial and the in-house assay may be appropriate for clinical use, but common standards are advisable for comparable absolute values.

Supporting Evidence

  • The clinical sensitivity of Q-EBV PCR was higher for samples with less than 1,000 EBV DNA copies/ml.
  • Both assays showed statistically correlated results (R2 = 0.7789; p < 0.0001).
  • 17 out of 199 plasma samples were positive for EBV DNA by both methods.

Takeaway

The study looked at two tests to measure a virus in blood and found they work similarly, but using the same standards would help make the results clearer.

Methodology

The study compared two real-time PCR assays using 199 plasma samples, evaluating their sensitivity, linearity, and precision.

Potential Biases

Potential bias due to differences in PCR efficiency between the assays.

Limitations

The study did not address the variability in EBV DNA load detected by different assays.

Participant Demographics

199 consecutive plasma samples received for EBV DNA quantification, including samples from healthy blood donors.

Statistical Information

P-Value

p<0.0001

Statistical Significance

p<0.0001

Digital Object Identifier (DOI)

10.1186/1471-2180-7-22

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