Evidence map›Paper›PMID 26360605›Full record

ArticlePloS one2015

Assessment of Novel Anti-thrombotic Fusion Proteins for Inhibition of Stenosis in a Porcine Model of Arteriovenous Graft.

Christi M Terry, Ilya Zhuplatov, Yuxia He, Tze-Chein Wun, Seong-Eun Kim, Alfred K Cheung

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 19% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Autologous fat transplants to deliver glitazone and adiponectin for vasculoprotection.Journal of controlled release : official journal of the Controlled Release Society · 2017
    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

6 authors at 2 institutions in 1 country.

Christi M TerryDivision of Nephrology & Hypertension, University of Utah, Salt Lake City, UT, United States of America.
Ilya ZhuplatovDivision of Nephrology & Hypertension, University of Utah, Salt Lake City, UT, United States of America.
Yuxia HeDivision of Nephrology & Hypertension, University of Utah, Salt Lake City, UT, United States of America.
Tze-Chein WunEVAS Therapeutics, LLC, Ballwin, MO, United States of America.
Seong-Eun KimDepartment of Radiology, Utah Center for Advanced Imaging Research, University of Utah, Salt Lake City, Utah, United States of America.
Alfred K CheungDivision of Nephrology & Hypertension, University of Utah, Salt Lake City, UT, United States of America; Veterans Affairs Salt Lake City Healthcare System, Salt Lake City, UT, United States of America.
University of Utah · USVA Salt Lake City Healthcare System · US

Funding

University of Utah Center for Clinical and Translational ScienceUL1TR001067 · NCATS · UNIVERSITY OF UTAH · PI DERE, WILLARD H., HESS, RACHEL · 2013 to 2017
$19.8M
UNIVERSITY OF UTAH CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCE-UL1: BPCAUL1RR025764 · NCRR · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2008 to 2011
$19.4M
University of Utah Center for Clinical and Translational Science-UL1UL1TR000105 · NCATS · UNIVERSITY OF UTAH · PI MCCLAIN, DONALD A. · 2012 to 2013
$5.1M
Novel antithrombotic agents to prevent hemodialysis vascular access failureR44HL093848 · NHLBI · EVAS THERAPEUTICS, LLC. · PI WUN, TZE-CHEIN · 2012 to 2013
$1.4M
NCATS NIH HHS 5UL1TR001067-02NCATS NIH HHS 8UL1TR000105NCATS NIH HHS UL1 TR000105NCATS NIH HHS UL1 TR001067NCRR NIH HHS UL1 RR025764NCRR NIH HHS UL1RR025764NHLBI NIH HHS R44 HL093848NHLBI NIH HHS R44HL093848
6 · The paper itself

Abstract

backgroundHemodialysis arteriovenous synthetic grafts (AVG) provide high volumetric blood flow rates shortly after surgical placement. However, stenosis often develops at the vein-graft anastomosis contributing to thrombosis and early graft failure. Two novel fusion proteins, ANV-6L15 and TAP-ANV, inhibit the tissue factor/factor VIIa coagulation complex and the factor Xa/factor Va complex, respectively. Each inhibitor domain is fused to an annexin V domain that targets the inhibitor activity to sites of vascular injury to locally inhibit thrombosis. This study's objective was to determine if these antithrombotic proteins are safe and effective in inhibiting AVG stenosis.

methodsA bolus of either TAP-ANV or ANV-6L15 fusion protein was administered intravenously immediately prior to surgical placement of a synthetic graft between the external jugular vein and common carotid artery in a porcine model. At surgery, the vein and artery were irrigated with the anti-thrombotic fusion protein. Control animals received intravenous heparin. At 4 weeks, MRI was performed to evaluate graft patency, the pigs were then euthanized and grafts and attached vessels were explanted for histomorphometric assessment of neointimal hyperplasia at the vein-graft anastomosis. Blood was collected at surgery, immediately after surgery and at euthanasia for serum metabolic panels and coagulation chemistries.

resultsNo acute thrombosis occurred in the control group or in either experimental group. No abnormal serum chemistries, activated clotting times or PT, PTT values were observed after treatment in experimental or control animals. However, at the vein-graft anastomosis, there was no difference between the control and experimental groups in cross-sectional lumen areas, as measured on MRI, and no difference in hyperplasia areas as determined by histomorphometry. These results suggest that local irrigation of TAP-ANV or ANV-6L15 intra-operatively was as effective in inhibiting acute graft thrombosis as intravenous administration of heparin, but failed to inhibit hyperplasia development and stenosis in AVG.

Indexed as

AnimalsArteriovenous Shunt, SurgicalBlood Coagulation TestsDisease Models, AnimalDrug Evaluation, PreclinicalFemaleFibrinolytic AgentsGraft Occlusion, VascularMagnetic Resonance ImagingRecombinant Fusion ProteinsSwineFibrinolytic AgentsRecombinant Fusion Proteins

Identifiers

PMID26360605
PMCPMC4567316
OpenAlexW2339987734

What OpenQuestion holds

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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.