Evidence map›Paper›PMID 39891777›Full record

ReviewMetabolic brain disease2025

Brain interleukins and Alzheimer's disease.

Heba G Abdelhamed, Arwa A Hassan, Alaa A Sakraan, Radwa T Al-Deeb, Dalia M Mousa, Heba S Aboul Ezz, Neveen A Noor, Yasser A Khadrawy, Nasr M Radwan

Abstract readReview
In one paragraph

Review in Metabolic brain disease, 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. Article
  2. Article
  3. Review
  4. Review
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  7. Article
  8. Review
  9. Review
  10. Article
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.

Heba G AbdelhamedDepartment of Zoology and Chemistry, Faculty of Science, Cairo University, Giza, Egypt.
Arwa A HassanFaculty of Pharmacy & Pharmaceutical Industries, Sinai University, Sinai, Egypt.
Alaa A SakraanDepartment of Zoology, Faculty of Science, Cairo University, Giza, Egypt.
Radwa T Al-DeebNational Cancer Institute, Cairo, Egypt.
Dalia M MousaDepartment of Biotechnology, Faculty of Science, Cairo University, Giza, Egypt.
Heba S Aboul EzzDepartment of Zoology, Faculty of Science, Cairo University, Giza, Egypt. hebaezz@sci.cu.edu.eg.
Neveen A NoorDepartment of Zoology, Faculty of Science, Cairo University, Giza, Egypt.
Yasser A KhadrawyMedical Physiology Department, Medical Research and Clinical Studies Institute, National Research Center, Giza, Egypt.
Nasr M RadwanDepartment of Zoology, Faculty of Science, Cairo University, Giza, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The central nervous system (CNS) is immune-privileged by several immuno-modulators as interleukins (ILs). ILs are cytokines secreted by immune cells for cell-cell signaling communications and affect the functions of the CNS. ILs were reported to orchestrate different molecular and cellular mechanisms of both physiological and pathological events, through overproduction or over-expression of their receptors. They interact with numerous receptors mediating pro-inflammatory and/or anti-inflammatory actions. Interleukins have been implicated to participate in neurodegenerative diseases. They play a critical role in Alzheimer's disease (AD) pathology which is characterized by the over-production of pro-inflammatory ILs. These may aggravate neurodegeneration, in addition to their contribution to detrimental mechanisms as oxidative stress, and excitotoxicity. However, recent research on the relation between ILs and AD revealed major discrepancies. Most of the major ILs were shown to play both pro- and anti-inflammatory roles in different experimental settings and models. The interactions between different ILs through shared pathways also add to the difficulty of drawing solid conclusions. In addition, targeting the different ILs has not yielded consistent results. The repeated failures of therapeutic drugs in treating AD necessitate the search for novel agents targeting multiple mechanisms of the disease pathology. In this context, the understanding of interleukins and their roles throughout the disease progression and interaction with other systems in the brain may provide promising therapeutic targets for the prevention or treatment of AD.

Indexed as

Alzheimer DiseaseBrainInterleukinsAnimalsHumansInterleukinsAlzheimer’s diseaseExcitotoxicityInflammationInterleukinsOxidative stress

Identifiers

PMID39891777
PMCPMC11787210

What OpenQuestion holds

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Registered trials

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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.