Evidence map›Paper›PMID 38258667›Full record

ReviewJournal of the American Heart Association2024

Current Mouse Models of Intracranial Aneurysms: Analysis of Pharmacological Agents Used to Induce Aneurysms and Their Impact on Translational Research.

Dilaware Khan, Xuanchen Li, Tomoki Hashimoto, Rokuya Tanikawa, Mika Niemela, Michael Lawton, Sajjad Muhammad

Open access · goldAbstract readReview
In one paragraph

Review in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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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

7 authors at 4 institutions in 4 countries.

Dilaware KhanDepartment of Neurosurgery Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-Universität Düsseldorf Düsseldorf Germany.ORCID 0000-0001-8268-2671
Xuanchen LiDepartment of Neurosurgery Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-Universität Düsseldorf Düsseldorf Germany.ORCID 0000-0003-4922-0226
Tomoki HashimotoDepartment of Neurosurgery and Neurobiology Barrow Neurological Institute Phoenix AZ USA.ORCID 0000-0002-6046-9148
Rokuya TanikawaDepartment of Neurosurgery, Stroke Center Sapporo Teishinkai Hospital Sapporo Hokkaido Japan.
Mika NiemelaDepartment of Neurosurgery University of Helsinki and Helsinki University Hospital Helsinki Finland.
Michael LawtonDepartment of Neurological Surgery Barrow Neurological Institute, St. Joseph's Hospital and Medical Center Phoenix AZ USA.ORCID 0000-0002-1887-3980
Sajjad MuhammadDepartment of Neurosurgery Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-Universität Düsseldorf Düsseldorf Germany.ORCID 0000-0002-6734-7979
Barrow Neurological Institute · USDüsseldorf University Hospital · DEUniversity of Helsinki · FIKeiyukai Sapporo Hospital · JP

Funding

Roles of aging and cellular senescence in the development of intracranial aneurysm ruptureR01AG077780 · NIA · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI SATORU EGUCHI, TOMOKI HASHIMOTO · 2023 to 2026
$2.4M
EGF-ADAM17 axis in the pathophysiology of intracranial aneurysmR01NS109382 · NINDS · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI EGUCHI, SATORU, HASHIMOTO, TOMOKI · 2019 to 2023
$2.2M
Mechanisms for intracranial aneurysm ruptureR01NS109584 · NINDS · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI HASHIMOTO, TOMOKI · 2020 to 2024
$1.9M
NIA NIH HHS R01 AG077780NINDS NIH HHS R01 NS109382NINDS NIH HHS R01 NS109584
6 · The paper itself

Abstract

Intracranial aneurysms (IAs) are rare vascular lesions that are more frequently found in women. The pathophysiology behind the formation and growth of IAs is complex. Hence, to date, no single pharmacological option exists to treat them. Animal models, especially mouse models, represent a valuable tool to explore such complex scientific questions. Genetic modification in a mouse model of IAs, including deletion or overexpression of a particular gene, provides an excellent means for examining basic mechanisms behind disease pathophysiology and developing novel pharmacological approaches. All existing animal models need some pharmacological treatments, surgical interventions, or both to develop IAs, which is different from the spontaneous and natural development of aneurysms under the influence of the classical risk factors. The benefit of such animal models is the development of IAs in a limited time. However, clinical translation of the results is often challenging because of the artificial course of IA development and growth. Here, we summarize the continuous improvement in mouse models of IAs. Moreover, we discuss the pros and cons of existing mouse models of IAs and highlight the main translational roadblocks and how to improve them to increase the success of translational IA research.

Indexed as

Intracranial AneurysmAnimalsDisease Models, AnimalFemaleHumansMiceRisk FactorsTranslational Research, Biomedicalartery ligationhypertensionintracranial aneurysmmouse modelspharmacological treatments

Identifiers

PMID38258667
PMCPMC11056163
OpenAlexW4391139449

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.