Evidence map›Paper›PMID 40893105›Full record

ArticleJMIR AI2025

AI-Driven Tacrolimus Dosing in Transplant Care: Cohort Study.

Mingjia Huo, Sean Perez, Linda Awdishu, Janice S Kerr, Pengtao Xie, Adnan Khan, Kristin Mekeel, Shamim Nemati

Abstract read
In one paragraph

Article in JMIR AI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
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

8 authors.

Mingjia HuoDepartment of Electrical and Computer Engineering, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0000-0003-1636-3933
Sean PerezDepartment of Surgery, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0000-0003-3196-629X
Linda AwdishuSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0000-0002-3187-3264
Janice S KerrSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0009-0007-7311-7524
Pengtao XieDepartment of Electrical and Computer Engineering, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0000-0003-0521-174X
Adnan KhanDepartment of Medicine, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093-0881, United States, 1 4058504751.ORCID http://orcid.org/0000-0001-6622-702X
Kristin MekeelDepartment of Surgery, University of California San Diego, La Jolla, CA, United States.ORCID http://orcid.org/0000-0002-8870-1287
Shamim NematiDepartment of Medicine, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093-0881, United States, 1 4058504751.ORCID http://orcid.org/0000-0002-0520-4948

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Tacrolimus forms the backbone of immunosuppressive therapy in solid organ transplantation, requiring precise dosing due to its narrow therapeutic range. Maintaining therapeutic tacrolimus levels in the postoperative period is challenging due to diverse patient characteristics, donor organ factors, drug interactions, and evolving perioperative physiology. Objective: The aim of this study is to design a machine learning model to predict the next-day tacrolimus trough concentrations (C0) and guide dosing to prevent persistent under- or overdosing. Methods: We used retrospective data from 1597 adult recipients of kidney and liver transplants at UC San Diego Health to develop a long short-term memory (LSTM) model to predict next-day tacrolimus C0 in an inpatient setting. Predictors included transplant type, demographics, comorbidities, vital signs, laboratory parameters, ordered diet, and medications. Permutation feature importance was evaluated for the model. We further implemented a classification task to evaluate the model's ability to identify underdosing, therapeutic dosing, and overdosing. Finally, we generated next-day dose recommendations that would achieve tacrolimus C0 within the target ranges. Results: The LSTM model provided a mean absolute error of 1.880 ng/mL when predicting next-day tacrolimus C0. Top predictive features included the recent tacrolimus C0, tacrolimus doses, transplant organ type, diet, and interactive drugs. When predicting underdosing, therapeutic dosing, and overdosing using a 3-class classification task, the model achieved a microaverage F1-score of 0.653. For dose recommendations, the best clinical outcomes were achieved when the actual total daily dose closely aligned with the model's recommended dose (within 3 mg). Conclusions: Ours is one of the largest studies to apply artificial intelligence to tacrolimus dosing, and our LSTM model effectively predicts tacrolimus C0 and could potentially guide accurate dose recommendations. Further prospective studies are needed to evaluate the model's performance in real-world dose adjustments.

Indexed as

clinical decision-makingmachine learningorgan transplantationpersonalized medicinetacrolimus

Identifiers

PMID40893105
PMCPMC12404564

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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.