Journal
CLINICAL INFECTIOUS DISEASES
Volume 63, Issue 5, Pages 583-589Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciw370
Keywords
cytomegalovirus; international standard; result harmonization; viral load
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Background. Interassay harmonization of cytomegalovirus (CMV) DNA measurement is important for infection management. Uncertainty exists regarding the result harmonization achievable in patient plasma samples using quantitative polymerase chain reaction (qPCR) assays with calibrators now traceable to the First World Health Organization International Standard (IS) for CMV DNA. Method. Serial dilutions of the IS and a blinded panel of 40 genotyped CMV DNA-positive pooled plasma samples and 10 negative plasma samples were tested by 6 laboratories using 10 qPCR assays calibrated to the IS. Each clinical sample was constructed using plasma from a single unique transplant recipient. Results. The variance for individual CMV DNA-positive samples was greater for clinical samples (median, 1.50 [range, 1.22-2.82] log(10) IU/mL) than for IS dilutions (median, 0.94 [range, 0.69-1.35] log(10) IU/mL) (P < .001); 58.9% of all clinical sample results and 93.6% of IS dilution results fell within +/- 0.5 log(10) IU/mL of the mean viral load of each sample. Result variability was not impacted by either genotype or quantitative levels of CMV DNA. Testing procedure differences can significantly influence results, even when analyte-specific reagents are identical. For clinical samples, all assays demonstrated result bias (P < .008). Assays with amplicon sizes <= 86 bp had significantly higher results compared to assays with larger amplicon sizes (>= 105 bp) (P < .001). Conclusions. The variability in CMV DNA results reported on individual samples has been reduced by the IS, but ongoing clinically relevant variability persists, preventing meaningful interassay result comparison.
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