Evidence map›Paper›PMID 36568280›Full record

ArticleJVS-vascular science2022

Circulating fibrillin fragment concentrations in patients with and without aortic pathology.

Eric J Carlson, Megan Rushkin, Derek Darby, Trisha Chau, Renee L Shirley, Jeff S King, Khanh Nguyen, Gregory J Landry, Gregory L Moneta, Cherrie Abraham and 2 more

Open access · goldAbstract read
In one paragraph

Article in JVS-vascular science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Physiology (Bethesda, Md.) · 2026
    Review
  2. Review
  3. 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

12 authors at 2 institutions in 1 country.

Eric J CarlsonDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR.
Megan RushkinDepartment of Orthopedics, Oregon Health & Science University, Portland, OR.
Derek DarbyDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Trisha ChauDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Renee L ShirleyVirogenomics BioDevelopment, Inc, Portland, OR.
Jeff S KingVirogenomics BioDevelopment, Inc, Portland, OR.
Khanh NguyenDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Gregory J LandryDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Gregory L MonetaDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Cherrie AbrahamDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Lynn Y SakaiDepartment of Molecular and Medical Genetics, Oregon Health & Science University, Portland, OR.
Amir F AzarbalDivision of Vascular Surgery, Department of Surgery, Oregon Health & Science University, Portland, OR.
Oregon Health & Science University · USVirogenomics BioDevelopment (United States) · US

Funding

Developing novel fibrillin biomarkers for aortic diseaseR43HL147757 · NHLBI · VIROGENOMICS BIODEVELOPMENT, INC. · PI KING, JEFFREY S · 2019 to 2019
$269k
NHLBI NIH HHS R43 HL147757
6 · The paper itself

Abstract

Objective: Fragments of fibrillin-1 and fibrillin-2 will be detectable in the plasma of patients with aortic dissections and aneurysms. We sought to determine whether the plasma fibrillin fragment levels (PFFLs) differ between patients with thoracic aortic pathology and those presenting with nonaortic chest pain. Methods: PFFLs were measured in patients with thoracic aortic aneurysm (n = 27) or dissection (n = 28). For comparison, patients without aortic pathology who had presented to the emergency department with acute chest pain (n = 281) were categorized into three groups according to the cause of the chest pain: ischemic cardiac chest pain; nonischemic cardiac chest pain; and noncardiac chest pain. The PFFLs were measured using a sandwich enzyme-linked immunosorbent assay. Results: Fibrillin-1 fragments were detectable in all patients and were lowest in the ischemic cardiac chest pain group. Age, sex, and the presence of hypertension were associated with differences in fibrillin-1 fragment levels. Fibrillin-2 fragments were detected more often in the thoracic aneurysm and dissection groups than in the emergency department chest pain group ( Conclusions: Patients with thoracic aortic dissections demonstrated elevated plasma fibrillin-2 fragment levels (B205-HRP143) compared with patients presenting with ischemic or nonischemic cardiac chest pain and increased fibrillin-1 levels (B15-HRP26) compared with patients with ischemic cardiac chest pain. Investigation of fibrillin-1 and fibrillin-2 fragment generation might lead to diagnostic, therapeutic, and prognostic advances for patients with thoracic aortic dissection.

Indexed as

Aortic dissectionBiomarkersChest painFibrillin

Identifiers

PMID36568280
PMCPMC9772837
OpenAlexW4304893329

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.