Evidence map›Paper›PMID 26352243›Full record

ReviewCurrent opinion in cardiology2015

Abdominal aortic aneurysm: novel mechanisms and therapies.

Frank M Davis, Debra L Rateri, Alan Daugherty

Registry-linked trialAbstract readReview
In one paragraph

Review in Current opinion in cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07473102 (PET Imaging of MMP Activation in AAA), which is not on this map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
9.8field-weighted citation impact, top 1% 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.

NCT07473102 early_phase1recruitingnot on this mapstarted 2025, after this paper: background citation

PET Imaging of MMP Activation in AAA: Clinical Component

TypeinterventionalSponsorWashington University School of MedicineRan2025 to 2027Enrolled28ConditionsAbdominal Aortic AneurysmArmsCu-64-RYM2, PET imaging using Cu-64
3 · Its place in the literature

Who cites it

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 166 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cancer Incidence After Diagnosis of Abdominal Aortic Aneurysm-Brief Report.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Role of Extracellular Matrix and Inflammation in Abdominal Aortic Aneurysm.International journal of molecular sciences · 2022
    Review

20 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Frank M DavisaSection of Vascular Surgery, Department of Surgery, University of Michigan, Ann Arbor, Michigan bSaha Cardiovascular Research Center cDepartment of Physiology, University of Kentucky, Lexington, Kentucky, USA.
Debra L Rateri
Alan Daugherty
Cardiovascular Research Center · BRUniversity of Michigan–Ann Arbor · US

Funding

Specific Secretory Phospholipase A2 Isozymes Promote Aneurysm FormationP01HL080100 · NHLBI · UNIVERSITY OF KENTUCKY · PI DAUGHERTY, ALAN · 2006 to 2010
$8.2M
Mechanisms of thoracic aortic aneurysmsR01HL107319 · NHLBI · UNIVERSITY OF KENTUCKY · PI DAUGHERTY, ALAN · 2012 to 2015
$2.1M
NHLBI NIH HHS HL107319NHLBI NIH HHS P01 HL080100NHLBI NIH HHS R01 HL107319
6 · The paper itself

Abstract

purpose of reviewAbdominal aortic aneurysm (AAA) is a pathological condition of permanent dilation that portends the potentially fatal consequence of aortic rupture. This review emphasizes recent advances in mechanistic insight into aneurysm pathogenesis and potential pharmacologic therapies that are on the horizon for AAAs. RECENT

findingsAn increasing body of evidence demonstrates that genetic factors, including 3p12.3, DAB2IP, LDLr, LRP1, matrix metalloproteinase (MMP)-3, TGFBR2, and SORT1 loci, are associated with AAA development. Current human studies and animal models have shown that many leukocytes and inflammatory mediators, such as IL-1, IL-17, TGF-β, and angiotensin II, are involved in the pathogenesis of AAAs. Leukocytic infiltration into aortic media leads to smooth muscle cell depletion, generation of reactive oxygen species, and extracellular matrix fragmentation. Preclinical investigations into pharmacological therapies for AAAs have provided intriguing insight into the roles of microRNAs in regulating many pathological pathways in AAA development. Several large clinical trials are ongoing, seeking to translate preclinical findings into therapeutic options. SUMMARY: Recent studies have identified many potential mechanisms involved in AAA pathogenesis that provide insight into the development of a medical treatment for this disease.

Indexed as

Aortic Aneurysm, AbdominalDiagnostic ImagingGenetic MarkersGenetic TherapyGenome-Wide Association StudyHumansGenetic Markers

Identifiers

PMID26352243
PMCPMC4624089
OpenAlexW2358688435

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.