Evidence map›Paper›PMID 38993868›Full record

ArticleFrontiers in transplantation2023

Modern glucose-lowering drugs in liver transplant recipients: improvement in weight, glycemic control, and potentially allograft steatosis.

Srilakshmi Atthota, Kayla Joyal, Mariesa Cote, Riley Scalzo, Ruby Singh, Nikita Consul, Aoife Kilcoyne, Emily D Bethea, Leigh Anne Dageforde

Abstract read
In one paragraph

Article in Frontiers in transplantation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Review
  7. Empagliflozin as treatment in glycogen storage disease type IB patients.Molecular genetics and metabolism reports · 2025
    Article
  8. Review
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

9 authors.

Srilakshmi AtthotaDepartment of Surgery, Division of Transplantation, Massachusetts General Hospital, Boston, MA, United States.
Kayla JoyalDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States.
Mariesa CoteDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States.
Riley ScalzoDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, United States.
Ruby SinghDepartment of Surgery, Division of Transplantation, Massachusetts General Hospital, Boston, MA, United States.
Nikita ConsulDepartment of Radiology, Massachusetts General Hospital, Boston, MA, United States.
Aoife KilcoyneDepartment of Radiology, Massachusetts General Hospital, Boston, MA, United States.
Emily D BetheaDepartment of Medicine, Division of Transplant Hepatology, Massachusetts General Hospital, Boston, MA, United States.
Leigh Anne DagefordeDepartment of Surgery, Division of Transplantation, Massachusetts General Hospital, Boston, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Recurrent allograft steatosis occurs in one-third of transplanted livers. Antidiabetic agents like glucagon-like peptide-1 receptor agonists (GLP1RA) and sodium-glucose cotransporter type-2 (SGLT2) inhibitors are effective in the management of obesity and hepatic steatosis in the general population; however, there is limited evidence supporting their use in allograft steatosis. We aimed to evaluate their effects on steatosis, body weight, and glycemic control in liver transplant recipients at our institution. Methods: In this single-center retrospective cohort study of liver transplant recipients currently on a GLP1RA or SGLT2 inhibitor (transplanted 2015-2022), we compared clinical and radiological data before medication use and at follow-up. Differences were compared using Wilcoxon signed-rank test. Results: Thirty-seven liver transplant recipients were taking the agents. Diabetes was the most common indication ( Discussion: GLP1RA and SGLT-2 inhibitors are tolerated in transplant patients and result in weight loss and better glycemic control. They are promising agents to treat recurrent or de-novo liver allograft steatosis, but further research is needed to evaluate long-term outcomes in liver transplant recipients.

Indexed as

antidiabetic medicationglucose-lowering medicationliver transplantationmetabolic syndromeobesityweight loss

Identifiers

PMID38993868
PMCPMC11235220

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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.