Evidence map›Paper›PMID 25857553›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

Quantifying progression and regression of thrombotic risk in experimental atherosclerosis.

Rohun U Palekar, Andrew P Jallouk, Matthew J Goette, Junjie Chen, Jacob W Myerson, John S Allen, Antonina Akk, Lihua Yang, Yizheng Tu, Mark J Miller and 3 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Fluorine (Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. The principles and applications of avidin-based nanoparticles in drug delivery and diagnosis.Journal of controlled release : official journal of the Controlled Release Society · 2017
    Review
  9. 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

13 authors at 1 institution in 1 country.

Rohun U Palekar*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Andrew P Jallouk*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Matthew J Goette*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Junjie Chen*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Jacob W Myerson*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
John S Allen*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Antonina Akk*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Lihua Yang*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Yizheng Tu*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Mark J Miller*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Christine T N Pham*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA.
Samuel A Wickline*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA wicklines@aol.com hpan@dom.wustl.edu.
Hua Pan*Department of Biomedical Engineering and Department of Medicine, Washington University, St. Louis, Missouri, USA wicklines@aol.com hpan@dom.wustl.edu.
Washington University in St. Louis · US

Funding

METHODS IN MOLECULAR IMAGING AND TARGETED THERAPEUTICSR01HL073646 · NHLBI · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2004 to 2016
$13.7M
Translational Research Skills Development CoreU54HL112303 · NHLBI · WASHINGTON UNIVERSITY · PI SADLER, J EVAN · 2012 to 2016
$8.8M
Prevention and Treatment of Acute Kidney InjuryR01DK102691 · NIDDK · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2015 to 2018
$2.0M
Inhibition of NF-kB with siRNA/Peptide Nanoparticles for Arthritis TreatmentR01AR067491 · NIAMS · WASHINGTON UNIVERSITY · PI PHAM, CHRISTINE T., WICKLINE, SAMUEL A · 2015 to 2019
$1.8M
THERAPY NANOPARTICLES FOR MODULATION OF INFLAMMATION IN NEUROMUSCULAR DISEASER01AR056223 · NIAMS · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2009 to 2013
$1.6M
QUANTIFYING KIDNEY INJURY AND INFLAMMATION WITH FLUORINE (19F) MRIR21DK095555 · NIDDK · WASHINGTON UNIVERSITY · PI WICKLINE, SAMUEL A · 2012 to 2013
$411k
NHLBI NIH HHS HL073646NHLBI NIH HHS HL112303NHLBI NIH HHS R01 HL073646NHLBI NIH HHS U54 HL112303NIAMS NIH HHS AR056223NIAMS NIH HHS R01 AR056223NIAMS NIH HHS R01 AR067491NIDDK NIH HHS DK095555NIDDK NIH HHS R01 DK102691NIDDK NIH HHS R21 DK095555
6 · The paper itself

Abstract

Currently, there are no generally applicable noninvasive methods for defining the relationship between atherosclerotic vascular damage and risk of focal thrombosis. Herein, we demonstrate methods to delineate the progression and regression of vascular damage in response to an atherogenic diet by quantifying the in vivo accumulation of semipermeable 200-300 nm perfluorocarbon core nanoparticles (PFC-NP) in ApoE null mouse plaques with [(19)F] magnetic resonance spectroscopy (MRS). Permeability to PFC-NP remained minimal until 12 weeks on diet, then increased rapidly following 12 weeks, but regressed to baseline within 8 weeks after diet normalization. Markedly accelerated clotting (53.3% decrease in clotting time) was observed in carotid artery preparations of fat-fed mice subjected to photochemical injury as defined by the time to flow cessation. For all mice on and off diet, an inverse linear relationship was observed between the permeability to PFC-NP and accelerated thrombosis (P = 0.02). Translational feasibility for quantifying plaque permeability and vascular damage in vivo was demonstrated with clinical 3 T MRI of PFC-NP accumulating in plaques of atherosclerotic rabbits. These observations suggest that excessive permeability to PFC-NP may indicate prothrombotic risk in damaged atherosclerotic vasculature, which resolves within weeks after dietary therapy.

Indexed as

AnimalsApolipoproteins EAtherosclerosisCapillary PermeabilityCholesterolCrystallizationDiet, AtherogenicDiet, WesternDisease Models, AnimalDisease ProgressionEndothelium, VascularFluorocarbonsMagnetic Resonance ImagingMaleMiceMice, KnockoutApolipoproteins ECholesterolFluorocarbonsendotheliumMRInanoparticlesthrombosis

Identifiers

PMID25857553
PMCPMC4478795
OpenAlexW2063706136

What OpenQuestion holds

Textmetadata
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.