ArticleCureus2026
Association Between Mucosal Cytomegalovirus DNA Load and Short-Term Clinical Outcomes in Acute Severe Ulcerative Colitis.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
14 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background Whether cytomegalovirus (CMV) infection is a cause or consequence of relapse or therapeutic refractoriness in patients with ulcerative colitis (UC) remains debatable. This study aimed to evaluate the frequency of CMV infection and the association between mucosal CMV DNA load and medical management failure in patients with acute severe ulcerative colitis (ASUC). Methods Consecutive patients with ASUC admitted between May 2023 and November 2024 were included. All patients received intravenous (IV) hydrocortisone and ganciclovir when quantitative CMV DNA real-time polymerase chain reaction (RT-PCR) levels were >250 copies/mg and/or histopathology demonstrated CMV infection. The primary outcome was to determine the frequency of CMV infection and to evaluate the association between quantitative CMV PCR levels from biopsy samples obtained during sigmoidoscopy and the risk of medical management failure (IV steroids ± ganciclovir). The secondary outcome was medical management failure, defined as the need for rescue therapy. Results CMV infection was detected in 70 (64.8%) patients with ASUC (44 by RT-PCR alone, one by inclusion bodies alone, and 25 by both methods). Patients with medical management failure had a significantly higher CMV DNA load than responders (44,990,045.76 copies/mg (0-754,359,454.0) vs. 249,720.95 copies/mg (0-9,729,500.00); p < 0.05) and a higher proportion of CMV DNA titres >250 and >1000 copies/mg (p < 0.05). Eight patients developed toxic megacolon, among whom seven (87.5%) had CMV infection. Overall, 17 (15.7%) of the 108 patients with ASUC experienced medical management failure. Conclusion Higher mucosal CMV DNA load was associated with medical management failure in patients with ASUC. Patients with higher CMV DNA loads also had higher frequencies of rescue therapy, toxic megacolon, and mortality.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.