Evidence mapPaperPMID 40272771Full record

ReviewMolecular neurobiology2025

Linking Metabolic Syndrome to Neurodegeneration Mechanisms and Potential Treatments.

Amina Džidić-Krivić, Almir Fajkić, Esma Karahmet Farhat, Lana Lekić, Amira Ejubović, Samra Kadić Vukas, Malik Ejubović, Orhan Lepara, Emina Karahmet Sher

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
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  4. Article
  5. Article
  6. Review
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  10. 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.

Amina Džidić-KrivićDepartment of Neurology, Cantonal Hospital Zenica, 72000, Zenica, Bosnia and Herzegovina.
Almir FajkićDepartment of Pathophysiology, Faculty of Medicine, University of Sarajevo, 71000, Sarajevo, Bosnia and Herzegovina.
Esma Karahmet FarhatFaculty of Food Technology, Juraj Strossmayer University of Osijek, 31000, Osijek, Croatia.
Lana LekićFaculty of Health Studies, University of Sarajevo, 71000, Sarajevo, Bosnia and Herzegovina.
Amira EjubovićDepartment of Internal Medicine, Cantonal Hospital Zenica, 72000, Zenica, Bosnia and Herzegovina.
Samra Kadić VukasDepartment of Neurology, Cantonal Hospital Zenica, 72000, Zenica, Bosnia and Herzegovina.
Malik EjubovićDepartment of Internal Medicine, Cantonal Hospital Zenica, 72000, Zenica, Bosnia and Herzegovina.
Orhan LeparaDepartment of Human Physiology, Faculty of Medicine, University of Sarajevo, 71000, Sarajevo, Bosnia and Herzegovina.
Emina Karahmet SherInternational Society of Engineering Science and Technology, Nottingham, UK. emina.sher@isest.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global rise in both metabolic syndrome (MetS) and neurodegenerative diseases (NDs), particularly dementia and Alzheimer's disease (AD) poses a growing health and socioeconomic burden. MetS affects approximately 25% of the global adult population and is associated with insulin resistance, hypertension, dyslipidemia, and obesity, factors increasingly linked to cognitive impairment and brain atrophy. This review explores the shared pathophysiological mechanisms between MetS and NDs, including neuroinflammation, oxidative stress, insulin resistance in the brain, blood-brain barrier (BBB) dysfunction, mitochondrial damage, gut microbiota dysbiosis, and alterations in the renin-angiotensin system. In terms of substance, MetS patients are four times more likely to develop dementia, with increased markers such as CRP and IL-6 present in the patient populations. The review suggests the role of astrocytic insulin signalling, adipokines, and toll-like receptors as key molecular links. Interventions such as caloric restriction, hydroxytyrosol (HT), and intranasal insulin have shown promising outcomes at preclinical and early clinical stages. Antidiabetic drugs like metformin, liraglutide, and GLP-1 receptor agonists have the potential to modulate neuroinflammation and improve cognition. Angiotensin receptor blockers like losartan and candesartan also exhibit neuroprotection via RAS pathway modulation. The review emphasizes the need for longitudinal studies and clinical trials to confirm these therapeutic agents and develop effective and cost-friendly interventions for the prevention and management of neurodegeneration in patients with metabolic syndrome.

Indexed as

Metabolic SyndromeNeurodegenerative DiseasesAnimalsHumansAstrocytesHealthImproved nutritionInflammationInsulin resistanceMetabolic syndromeMitochondrial damageNeurodegenerative diseasesObesity

Identifiers

What Socratic holds

Textmetadata
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.