Evidence map›Paper›PMID 36698932›Full record

ReviewFrontiers in cardiovascular medicine2022

Mechanosignals in abdominal aortic aneurysms.

Christiana Lowis, Aurellia Ramara Winaya, Puja Kumari, Cristobal F Rivera, John Vlahos, Rio Hermantara, Muhammad Yogi Pratama, Bhama Ramkhelawon

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cardiovascular medicine, 2022. 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
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Article
  7. Piezo1, the new actor in cell volume regulation.Pflugers Archiv : European journal of physiology · 2024
    Review
  8. Review
  9. Article
  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

8 authors at 2 institutions in 2 countries.

Christiana LowisDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
Aurellia Ramara WinayaDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
Puja KumariDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
Cristobal F RiveraDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
John VlahosDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
Rio HermantaraDepartment of Biomedicine, Indonesia International Institute for Life-Sciences, Jakarta, Indonesia.
Muhammad Yogi PratamaDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
Bhama RamkhelawonDivision of Vascular and Endovascular Surgery, Department of Surgery, New York University Langone Medical Center, New York, NY, United States.
NYU Langone Health · USIndonesia International Institute for Life Sciences · ID

Funding

Spatiotemporal checkpoints of macrophages in aortic aneurysms- RenewalR01HL146627 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Bhama Ramkhelawon · 2019 to 2026
$6.1M
NHLBI NIH HHS R01 HL146627
6 · The paper itself

Abstract

Cumulative evidence has shown that mechanical and frictional forces exert distinct effects in the multi-cellular aortic layers and play a significant role in the development of abdominal aortic aneurysms (AAA). These mechanical cues collectively trigger signaling cascades relying on mechanosensory cellular hubs that regulate vascular remodeling programs leading to the exaggerated degradation of the extracellular matrix (ECM), culminating in lethal aortic rupture. In this review, we provide an update and summarize the current understanding of the mechanotransduction networks in different cell types during AAA development. We focus on different mechanosensors and stressors that accumulate in the AAA sac and the mechanotransduction cascades that contribute to inflammation, oxidative stress, remodeling, and ECM degradation. We provide perspectives on manipulating this mechano-machinery as a new direction for future research in AAA.

Indexed as

abdominal aortic aneurysmmechanical stressmechanosignalsmechanotransductionshear stressvascular pathology

Identifiers

PMID36698932
PMCPMC9868277
OpenAlexW4313824624

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.