Evidence map›Paper›PMID 42403167›Full record

Observational studyThe Journal of international medical research2026

Tacrolimus intrapatient variability and latent virus reactivation after kidney transplantation: A retrospective study comparing prolonged-release and immediate-release tacrolimus formulations.

Sibel Ersan, Gulin Kavakalan, Gursel Ersan, Gozde Buhur Sari, Sibel Akkurt, Mehmet Tanrisev

Abstract readObservational StudyComparative Study
In one paragraph

Observational study in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sibel ErsanDepartment of Internal Medicine, Division of Nephrology, Health Sciences University, Izmir Medical School, Tepecik Training and Research Hospital, Turkey.ORCID 0000-0002-9381-5262
Gulin KavakalanDepartment of Internal Medicine, Health Sciences University, Tepecik Training and Research Hospital, Turkey.
Gursel ErsanDepartment of Infectious Diseases and Clinical Microbiology, Health Sciences University, Izmir Medical School, Tepecik Training and Research Hospital, Turkey.ORCID 0000-0002-1859-7066
Gozde Buhur SariDepartment of Internal Medicine, Division of Nephrology, Health Sciences University, Tepecik Training and Research Hospital, Turkey.
Sibel AkkurtDepartment of Internal Medicine, Health Sciences University, Tepecik Training and Research Hospital, Turkey.ORCID 0000-0002-0915-9005
Mehmet TanrisevDepartment of Internal Medicine, Division of Nephrology, Health Sciences University, Izmir Medical School, Tepecik Training and Research Hospital, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveThis study explored the differences in intrapatient variability of tacrolimus between prolonged-release and immediate-release formulations and evaluated the association between tacrolimus intrapatient variability and reactivation of BK virus and cytomegalovirus in kidney transplant recipients.MethodsThis retrospective observational study included 270 kidney transplant recipients receiving either prolonged-release tacrolimus or immediate-release tacrolimus. Receiver operating characteristic curve analysis identified tacrolimus intrapatient variability cutoff values associated with viral reactivation. Logistic regression analyses identified predictors of BK virus and cytomegalovirus reactivation.ResultsThe prolonged-release tacrolimus group had significantly lower tacrolimus intrapatient variability than the immediate-release tacrolimus group (p < 0.001). No significant differences were observed in BK virus and cytomegalovirus reactivation rates. Receiver operating characteristic curve analysis identified tacrolimus intrapatient variability cutoffs of 0.268 for BK virus and 0.261 for cytomegalovirus. High tacrolimus intrapatient variability was significantly associated with increased BK virus and cytomegalovirus reactivation. Logistic regression showed that high tacrolimus intrapatient variability was significantly associated with BK virus and cytomegalovirus reactivation. Multivariate analysis confirmed an independent association between high tacrolimus intrapatient variability and cytomegalovirus reactivation.ConclusionsTacrolimus intrapatient variability may predict reactivation of latent viral infection after kidney transplantation. Although viral reactivation rates were similar between tacrolimus formulations, prolonged-release tacrolimus showed lower tacrolimus intrapatient variability levels, suggesting that fluctuations in tacrolimus exposure might increase the risk of viral reactivation.

Indexed as

Cytomegalovirus InfectionsGraft RejectionImmunosuppressive AgentsKidney TransplantationPolyomavirus InfectionsTacrolimusVirus ActivationAdultBK VirusCytomegalovirusDelayed-Action PreparationsFemaleHumansMaleMiddle AgedRetrospective StudiesDelayed-Action PreparationsImmunosuppressive AgentsTacrolimusBK viruscytomegalovirusKidney transplantationlatent viral infectionstacrolimus formulationstacrolimus intrapatient variability

Identifiers

PMID42403167
PMCPMC13338517

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Registered trials

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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.