Key result
The CMV pp67 mRNA assay demonstrated a positive predictive value of 60% and a negative predictive value of 76% for predicting the development of CMV disease in liver transplant recipients.
Why the study?
Do molecular biology assays (quantitative PCR and qualitative NASBA) improve the detection of CMV infection and prediction of CMV disease compared to pp65 antigenemia in liver transplant recipients?
Observational (n=10)
No
Do molecular biology assays (quantitative PCR and qualitative NASBA) improve the detection of CMV infection and prediction of CMV disease compared to pp65 antigenemia in liver transplant recipients?
The concomitant use of antigenemia and pp67 mRNA assays may provide the best identification of liver transplant patients at risk of developing CMV disease.
Antigenemia cutoff may aid CMV risk stratification post-liver transplant; leaves open whether combined molecular assays improve prediction in larger cohorts.
BACKGROUND: CMV is a major clinical problem in transplant recipients. Thus, it is important to use sensitive and specific diagnostic techniques to rapidly and accurately detect CMV infection and identify patients at risk of developing CMV disease. In the present study, CMV infection after liver transplantation was monitored retrospectively by two molecular biology assays - a quantitative PCR assay and a qualitative NASBA assay. The results were compared with those obtained by prospective pp65 antigenemia determinations. MATERIALS AND METHODS: 87 consecutive samples from 10 liver transplanted patients were tested for CMV by pp65 antigenemia, and CMV monitor and NASBA pp67 mRNA assay. RESULTS: CMV infection was detected in all patients by antigenemia and CMV monitor, whereas NASBA assay identified only 8/10 patients with viremia. Furthermore, CMV infection was never detected earlier by molecular biology assays than by antigenemia. Only 5/10 patients with CMV infection developed CMV disease. Using a cut off value of 8 cells/50,000, antigenemia was found to be the assay that better identified patients at risk of developing CMV disease. However, the kinetics of the onset of infection detected by NASBA and CMV monitor seemed to have better identified patients at risk of developing CMV disease. Furthermore, before onset of disease, CMV pp67 mRNA was found to have similar or better negative and positive predictive values for the development of CMV disease. CONCLUSIONS: The present data, suggests that the concomitant use of antigenemia and pp67 mRNA assay gives the best identification of patients at risk of developing CMV disease.
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Amorim et al. (2001) conducted an observational in CMV infection in liver transplant recipients (n=10). CMV pp67 mRNA and CMV monitor assays vs. pp65 antigenemia was evaluated on Prediction of CMV disease development before onset. The CMV pp67 mRNA assay demonstrated a positive predictive value of 60% and a negative predictive value of 76% for predicting the development of CMV disease in liver transplant recipients.
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