Observational studyBMC nephrology2025
Ethnic differences in early blood tacrolimus concentrations after kidney transplantation: a retrospective observational study.
Observational study in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- A Novel Laboratory-Developed Test Using Multiplex qPCR to Further Personalize Tacrolimus Dosing.International journal of molecular sciences · 2026Article
- Kidney transplantation in obese Black patients: Strategies to improve access and outcomes.World journal of nephrology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDespite evidence of variation in CYP3A5 expressor status between different ethnic groups, many transplant centres operate a 'one size fits all' immunosuppression policy in which all kidney transplant recipients receive the same weight-adjusted daily dose of tacrolimus, adjusted subsequently to achieve target blood concentrations.
methodsWe evaluated retrospective blood tacrolimus concentrations and tacrolimus doses in 382 patients based on self-described ethnicity.
resultsMedian tacrolimus concentrations were lower in Black patients than those from other ethnic groups for the first four weeks following transplantation. More than 70% of measurements in Black patients were below target in the first and second weeks, and Black ethnicity was strongly associated with early subtherapeutic tacrolimus concentrations (odds ratio 3.49, p < 0.001). There were no significant differences in transplant outcomes between ethnic groups, although the rate of acute rejection was higher in Black patients, despite greater use of anti-thymocyte globulin induction therapy in these patients. DISCUSSION: There is emerging evidence to support either prescribing based on CYP3A5 genotyping, or the empirical use of higher starting doses in Black patients. However, notwithstanding the complexities inherent in our understanding of ethnic identity, we advocate an approach where clinicians act proactively to avoid under-dosing in Black patients. CLINICAL TRIAL NUMBER: Not applicable. Bart's Health NHS Trust audit number: 13,204.
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