Evidence map›Paper›PMID 42882521›Full record

ReviewCells2026

GDF-15/GFRAL Axis Dynamics and Vulnerability Windows in Bariatric Surgery: Pathophysiological, Microbiomic, and Pharmacological Perspectives.

Alin Constantin Pînzariu, Ionela Lăcrămioara Șerban, Radu Petru Soroceanu, Vlad Ionuț Vlăsceanu, Madalina Maxim, Ancuta Andreea Miler, Sebastian Marian Leonte, Carmen Atodiresei, Mihaela Moscalu, Lorena Mihaela Manole and 3 more

Abstract readReview
In one paragraph

Review in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

13 authors.

Alin Constantin PînzariuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0000-0001-5730-1662
Ionela Lăcrămioara ȘerbanGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.
Radu Petru SoroceanuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.
Vlad Ionuț VlăsceanuGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0009-0004-9984-0292
Madalina MaximGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.
Ancuta Andreea MilerGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0009-0001-0709-6899
Sebastian Marian LeonteGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0009-0009-3449-2983
Carmen AtodireseiGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.
Mihaela MoscaluGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0000-0002-8899-8594
Lorena Mihaela ManoleGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0009-0003-6798-9984
Laura Mihaela TrandafirGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0000-0002-8326-7610
Dragomir Nicolae ȘerbanGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0000-0001-6642-105X
Daniel Vasile TimofteGrigore T. Popa University of Medicine and Pharmacy Iasi, 700115 Iasi, Romania.ORCID 0000-0002-6604-874X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bariatric surgery (BS) and new pharmacological treatments cause significant neurometabolic changes. However, the pathways linking peripheral stress to central metabolic control remain poorly understood. This review highlights the GDF-15/GFRAL/RET complex as a key integrator of multiorgan-to-brain stress signals that shape systemic metabolic adaptation after surgical and pharmacological interventions. Based on a structured search across PubMed, Embase, Scopus, Google Scholar, and Web of Science covering 2020-2026 alongside foundational studies, we integrated translational evidence from peer-reviewed human trials and mechanistic animal models to map the GDF-15/GFRAL/RET axis across bariatric and incretin domains. We examined the neurobiology of the GDF-15/GFRAL axis to clarify variability in metabolic and behavioral outcomes after BS. This axis links metabolic stress signals from the gut, liver, and adipose tissue to the hindbrain and hypothalamic regulation of energy balance. Changes in the gut microbiome and SCFA-FFAR2/FFAR3 signaling after surgery interact with GDF-15 and incretin pathways. Future studies should critically compare BS with synergistic or alternative non-invasive neurometabolic approaches such as incretin mimetics, exogenous GDF-15 therapies, and high-protein diets.

Indexed as

Bariatric SurgeryGlial Cell Line-Derived Neurotrophic Factor ReceptorsGrowth Differentiation Factor 15AnimalsGastrointestinal MicrobiomeHumansObesitySignal TransductionGlial Cell Line-Derived Neurotrophic Factor ReceptorsGrowth Differentiation Factor 15bariatric surgeryfood aversionGDF-15/GFRAL/RET axisGLP-1-based pharmacotherapygut–brain axisgut microbiotaincretin-based therapiesMT1-MMPSCFAssemaglutide

Identifiers

PMID42882521
PMCPMC13664289

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.