Evidence map›Paper›PMID 30744022›Full record

ReviewInternational journal of molecular sciences2019

Role of the Angiotensin Pathway and its Target Therapy in Epilepsy Management.

Shaip Krasniqi, Armond Daci

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.3field-weighted citation impact, top 4% of its field
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

20 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. The Development of Epilepsy Following CNS Viral Infections: Mechanisms.Current neurology and neuroscience reports · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Neurological complications and infection mechanism of SARS-COV-2.Signal transduction and targeted therapy · 2021
    Review
  12. Article
  13. Hearing Loss in SARS-CoV-2: What Do We Know?Ear, nose, & throat journal · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Comment on "Hearing loss and COVID-19: A note".American journal of otolaryngology
    Article
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Shaip KrasniqiInstitute of Pharmacology and Toxicology, Faculty of Medicine, University of Prishtina, 10000 Prishtina, Kosovo. shaip.krasniqi@uni-pr.edu.
Armond DaciDepartment of Pharmacy, Faculty of Medicine, University of Prishtina, 10000 Prishtina, Kosovo. armond.daci@uni-pr.edu.
University of Prishtina · XK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite extensive research on epileptogenesis, there is still a need to investigate new pathways and targeted therapeutic approaches in this complex process. Inflammation, oxidative stress, neurotoxicity, neural cell death, gliosis, and blood⁻brain barrier (BBB) dysfunction are the most common causes of epileptogenesis. Moreover, the renin⁻angiotensin system (RAS) affects the brain's physiological and pathological conditions, including epilepsy and its consequences. While there are a variety of available pharmacotherapeutic approaches, information on new pathways is in high demand and the achievement of treatment goals is greatly desired. Therefore, targeting the RAS presents an interesting opportunity to better understand this process. This has been supported by preclinical studies, primarily based on RAS enzyme, receptor-inhibition, and selective agonists, which are characterized by pleiotropic properties. Although there are some antiepileptic drugs (AEDs) that interfere with RAS, the main targeted therapy of this pathway contributes in synergy with AEDs. However, the RAS-targeted treatment alone, or in combination with AEDs, requires clinical studies to contribute to, and clarify, the evidence on epilepsy management. There is also a genetic association between RAS and epilepsy, and an involvement of pharmacogenetics in RAS, so there are possibilities for the development of new diagnostic and personalized treatments for epilepsy.

Indexed as

Molecular Targeted TherapyAngiotensin II Type 1 Receptor BlockersAngiotensinsAnimalsAnticonvulsantsAstrocytesBiomarkersBlood-Brain BarrierDrug DiscoveryEpilepsyHumansMicrogliaPharmacogeneticsPrecision Medicineras ProteinsReceptor, Angiotensin, Type 1Angiotensin II Type 1 Receptor BlockersAngiotensinsAnticonvulsantsBiomarkersras ProteinsReceptor, Angiotensin, Type 1antiepileptic drugsepileptogenesispersonalized treatmentrenin–angiotensin system

Identifiers

PMID30744022
PMCPMC6386974
OpenAlexW2911890416

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.