Key result
Previously treated CMV infection significantly decreased the likelihood of low-level DNAemia progression to high viral load (OR 0.081), while lung transplant recipients had higher risk (OR 3.09).
Why the study?
Low-level CMV DNAemia is common and can progress or spontaneously resolve, but clinical predictors of progression and spontaneous viral clearance are not well defined.
What are the clinical predictors of progression to high viral load in solid organ transplant recipients with untreated low-level CMV DNAemia?
Cohort (n=297)
What are the clinical predictors of progression to high viral load in solid organ transplant recipients with untreated low-level CMV DNAemia?
Odds Ratio: 0.081
Previous CMV infection significantly decreases the likelihood of low-level DNAemia progression in solid organ transplant recipients, suggesting a protective role for CMV immunity.
May inform risk stratification for monitoring in lung recipients; leaves open whether immunity-guided strategies alter progression.
BACKGROUND: Low-level CMV DNAemia is common and in the absence of treatment may either progress to higher viral loads that require therapy, or may spontaneously resolve. The clinical predictors of progression and spontaneous viral clearance are not well defined. METHODS: We performed a retrospective cohort study of organ transplant recipients who had untreated low-level CMV DNAemia (<1000 IU/mL). Outcomes were evaluated for 8 weeks after initial viral detection, and progression to CMV high viral load was defined as CMV viral load ≥1000 IU/mL. CMV DNAemia doubling time was calculated for a subset of patients with sufficient viral load timepoints. RESULTS: Of the 297 patients analyzed, 118/297 (39.7%) patients progressed to a high viral load and the remaining cleared DNAemia spontaneously (46.8%) or remained at low level (13.4%). In multivariate analysis, progression was significantly more likely in lung transplant recipients (odds ratio 3.09) and less likely in those with an episode of previously treated CMV infection (odds ratio 0.081). In a subset of 27 patients with progression, the doubling time for CMV DNAemia was a median of 6.1 days (range 2.4-21.8). CONCLUSION: We found that previous CMV infection significantly decreased the likelihood of low-level DNAemia progression suggesting that CMV immunity plays a role in progression vs spontaneous clearance.
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Natori et al. (2019) conducted a cohort in Low-level CMV DNAemia in solid organ transplant recipients (n=297). Previously treated CMV infection vs. No previously treated CMV infection was evaluated on Progression to CMV high viral load (≥1000 IU/mL) (OR 0.081). Previously treated CMV infection significantly decreased the likelihood of low-level DNAemia progression to high viral load (OR 0.081), while lung transplant recipients had higher risk (OR 3.09).
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