ArticleJournal of medical virology2025
Cytomegalovirus-RNA Accurately Identifies Clinically Significant Infection Needing Preemptive Therapy in Liver Transplanted Children: A Proof-of-Concept Study.
Article in Journal of medical virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07286461 (VIROMARKERS GA n.101194735 - CMV and TTV Biomarkers Study Protocol), which is not on this map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
VIROMARKERS GA n.101194735 - CMV and TTV Biomarkers Study Protocol
Who cites it
1 citing paper in PubMed.
- Article
Corrections and comments
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Authors and funding
16 authors.
Funding
Abstract
Preemptive therapy (PET) is safe and effective in controlling Cytomegalovirus (CMV) infection after pediatric liver transplantation (LT) and allows to observe the kinetics of quantitative CMV-DNA viral load till it reaches the treatment thresholds. While early detection of low-to-moderate CMV-DNA levels may not indicate active viral replication, awaiting the viral load to exceed the treatment threshold may lead to viremic breakthroughs and CMV disease. We assessed the capacity of quantitative CMV-RNA (UL21.5 mRNA) to identify active viral replication and its accuracy in identifying clinically significant CMV infection (csCMVi) needing PET in LT children. One-hundred and forty-four comparative quantitative CMV-RNA and CMV-DNA determinations were obtained from 12 children followed prospectically for 6 months after LT. Of 52 CMV-DNA-positive specimens, 17 (32%) were also CMV-RNA-positive, while CMV-RNA was undetectable in CMV-DNA-negative specimens. All children with csCMVi had early detectable CMV-RNA, peaking simultaneously to CMV-DNA (median CMV-DNA: 65 906 cp/mL; median CMV-RNA: 767 cp/mL); conversely, none of those with persistently low DNAemia proved CMV-RNA-positive. In this first pilot study, CMV-RNA had 100% sensitivity and specificity in identifying children needing PET after pediatric LT. The early detection of CMV-RNA marks significant CMV infection/reactivation, thus allowing to avoid unnecessary antiviral treatment.
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Registered trials
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