Evidence mapPaperPMID 40471368Full record

ReviewMolecular biology reports2025

Metabolic resilience: liraglutide's potential in alleviating depressive symptoms.

Omar Gammoh, Esam Qnais, Alaa A A Aljabali, Taher Hatahet, Abdelrahim Alqudah

Erratum issuedAbstract readReview
In one paragraph

Review in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Omar GammohDepartment of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmacy, Yarmouk University, PO BOX 566, Irbid, 21163, Jordan.
Esam QnaisDepartment of Biology and Biotechnology, Faculty of Science, The Hashemite University, Zarqa, Jordan.
Alaa A A AljabaliFaculty of Pharmacy, Department of Pharmaceutics & Pharmaceutical Technology, Yarmouk University, Irbid, 21163, Jordan.
Taher HatahetNorth Wales Medical School, Bangor University, Brigantia Building, Penrallt Road, Bangor, Gwynedd, Wales, LL57 2AS, UK. t.hatahet@bangor.ac.uk.
Abdelrahim AlqudahDepartment of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, The Hashemite University, Zarqa, Jordan.

Funding

Yarmouk University 2/2024
6 · The paper itself

Abstract

Research in psychiatry requires substantial resources and interdisciplinary collaboration. The investigation of liraglutide's potential to reduce depressive symptoms is a pioneering and novel approach. that ventures into underexplored mechanisms bridging metabolic and psychiatric domains. Originally approved for the management of type 2 diabetes, it has increasingly emerged as a potential therapeutic candidate in the complex landscape of mental health disorders. being examined for its ability to modulate depressive symptomatology, acting as a glucagon-like peptide-1 (GLP-1) receptor agonist. However, its action extends beyond traditional monoaminergic pathways, also influencing neuroplasticity, synaptic remodeling, and neuroinflammatory processes. Recent studies have shown preclinical and early-phase clinical insights into how liraglutide modulates mood-related neural circuits. These findings suggest mechanistic distinctions from conventional antidepressant pharmacotherapies. This manuscript presents a research gap. Specifically, it addresses gaps in both mechanistic understanding and translational potential, where liraglutide's dual impact bridges the traditional divide between psychiatric and metabolic medicine. Liraglutide has demonstrated benefits in improving both glycemic control and depressive symptoms. These integrated effects position it as a candidate for dual-purpose interventions in patients with comorbid metabolic and psychiatric disorders. Scientists have shown details of how liraglutide affects depression. Emerging evidence remains preliminary yet promising, encouraging researchers to explore, question, and refine current psychiatric treatment models. In an era prioritizing biologically integrated therapeutics, liraglutide exemplifies the evolution of psychiatric drug development. In a field where innovation is key, liraglutide is a testament to evolving science. It provides a model for how metabolic agents may contribute to the future landscape of mental health therapeutics.

Indexed as

DepressionLiraglutideAnimalsAntidepressive AgentsDiabetes Mellitus, Type 2Glucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsHumansAntidepressive AgentsGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsLiraglutideClinical trialsDepressionGlucagon-like peptide-1 receptor agonistLiraglutideMetabolic healthNeurobiological mechanisms

Identifiers

PMID40471368
PMCPMC12141419

What Socratic holds

Texttitle and abstract
LicenceCC BY
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 Socratic graph.