Evidence map›Paper›PMID 39925909›Full record

ArticleHepatobiliary surgery and nutrition2025

Plasma GLP-1 and metabolic dynamics during human liver regeneration and their association with posthepatectomy liver failure.

Markus Ammann, Jan Philipp Jonas, David Pereyra, Jonas Santol, Hubert Hackl, Tamara Kalchbrenner, Johannes Laengle, Vanja Podrascanin, Florian Lehner, Istvan Levente Viragos-Toth and 7 more

Abstract read
In one paragraph

Article in Hepatobiliary surgery and nutrition, 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.

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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

17 authors.

Markus AmmannDepartment of Surgery, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Jan Philipp JonasDepartment of Surgery, HPB Centre, Viennese Health Network, Clinic Favoriten and Sigmund Freud Private University, Vienna, Austria.
David PereyraDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, Vienna, Austria.
Jonas SantolDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Hubert HacklInstitute of Bioinformatics, Biocenter, Medical University of Innsbruck, Innsbruck, Austria.
Tamara KalchbrennerDepartment of Pathology, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Johannes LaengleDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, Vienna, Austria.
Vanja PodrascaninDepartment of Surgery, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Florian LehnerDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, Vienna, Austria.
Istvan Levente Viragos-TothDepartment of Surgery, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Wolfgang HullaDepartment of Pathology, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Verena RusoInstitute for Medical-Chemical and Molecular Biological Laboratory Diagnostics, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Rory SmootDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Friedrich LaengleDepartment of Surgery, State Hospital Wiener Neustadt, Wiener Neustadt, Austria.
Thomas GruenbergerDepartment of Surgery, HPB Centre, Viennese Health Network, Clinic Favoriten and Sigmund Freud Private University, Vienna, Austria.
Alice AssingerInstitute of Vascular Biology and Thrombosis Research, Center for Physiology and Pharmacology, Medical University of Vienna, Vienna, Austria.
Patrick P StarlingerDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.

Funding

Novel coagulation-dependent mechanisms of liver regeneration to detect and prevent liver dysfunction after partial hepatectomyR01DK122813 · NIDDK · MICHIGAN STATE UNIVERSITY · PI LUYENDYK, JAMES P · 2020 to 2024
$2.0M
NIDDK NIH HHS R01 DK122813
6 · The paper itself

Abstract

Background: Metabolic regulation is critical during liver regeneration in rodents, but human data are limited. We investigated perioperative dynamics of circulating metabolites and plasma levels of glucagon-like peptide-1 (GLP-1) and GLP-2, in patients undergoing liver resections, exploring their associations with the histological phenotype of metabolic dysfunction-associated steatotic liver disease (MASLD) and posthepatectomy liver failure (PHLF). Methods: Eighty-one and 75 patients from two centers between 2012 and 2023 were studied. Targeted quantitative metabolomic assay of 180 circulating metabolites, perioperative GLP-1, GLP-2, and standard lipid parameter level evaluation was employed. An exploratory PHLF prediction model was developed, including GLP-1 as a metabolic parameter. Results: Significant alterations of 44 metabolites by postoperative day (POD) 1 and 40 by POD5 were observed, mainly among phospholipid species. Unsupervised clustering identified two metabolic clusters, with one encompassing 93% of PHLF patients by POD5 (P<0.001). Standard plasma lipid parameters displayed consistent decrease after hepatectomy, independent from MASLD phenotype, with the lowest levels in PHLF patients. Postoperative GLP-1 and GLP-2 dynamics displayed a reciprocal pattern, indicating adaptive change in secretion. Preoperative GLP-1 levels were significantly increased in PHLF (P=0.02). Furthermore, incorporation of GLP-1 into the established aspartate aminotransferase to platelet ratio index (APRI) + albumin-bilirubin (ALBI) score, improved PHLF prediction [area under the curve (AUC): 0.833, 95% confidence interval (CI): 0.660-0.964]. Conclusions: Significant metabolic changes occur during human liver resection, particularly in phospholipid metabolism, along with distinct perioperative dynamics of GLP-1 and GLP-2, closely linked to PHLF and independent of the histological phenotype of MASLD. Additionally, we provide exploratory results on the predictive value of GLP-1 for PHLF, emphasizing a holistic model of liver function assessment highlighting the metabolic component of human liver regeneration.

Indexed as

glucagon-like peptide-1 (GLP-1)lipid metabolismLiver regenerationmetabolic dysfunction-associated steatotic liver disease (MASLD)posthepatectomy liver failure (PHLF)

Identifiers

PMID39925909
PMCPMC11806138

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LicenceCC BY-NC-ND
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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.