Evidence map›Paper›PMID 33912688›Full record

ArticleTrauma surgery & acute care open2021

Quantification of von Willebrand factor and ADAMTS-13 after traumatic injury: a pilot study.

Taleen A MacArthur, Julie Goswami, Laurie Moon Tasson, Alexander Tischer, Kent R Bailey, Grant M Spears, Jing-Fei Dong, Matthew Auton, Rosemary Kozar, Myung S Park

Open access · goldAbstract read
In one paragraph

Article in Trauma surgery & acute care open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

10 authors at 3 institutions in 1 country.

Taleen A MacArthurTrauma, Critical Care and General Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Julie GoswamiTrauma, Critical Care and General Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Laurie Moon TassonHematology, Mayo Clinic, Rochester, Minnesota, USA.
Alexander TischerHematology, Mayo Clinic, Rochester, Minnesota, USA.
Kent R BaileyDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Grant M SpearsDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.
Jing-Fei DongDepartment of Hematology, University of Washington School of Medicine, Seattle, Washington, USA.
Matthew AutonBiochemistry and Molecular Biology, Mayo Clinic, Rochester, New York, USA.
Rosemary KozarDepartment of Surgery, R Adams Cowley Shock Trauma Center, Baltimore, Maryland, USA.
Myung S ParkSurgery, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Clinic · USMayo Clinic in Florida · USUniversity of Washington · US

Funding

MAYO CLINIC CENTER FOR TRANSLATIONAL SCIENCE ACTIVITIESUL1RR024150 · NCRR · MAYO CLINIC ROCHESTER · PI RIZZA, ROBERT A. · 2006 to 2011
$66.4M
Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
Analysis and Characterization of Trauma-Induced CoagulopathyUM1HL120877 · NHLBI · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI MORRISSEY, JAMES H., WISNIEWSKI, STEPHEN R · 2013 to 2019
$26.6M
Predictors of Venous Thromboembolism: A Multicenter Prospective Cohort StudyR01GM126086 · NIGMS · MAYO CLINIC ROCHESTER · PI PARK, MYUNG SOO · 2018 to 2022
$3.4M
von Willebrand Factor in Traumatic Brain Injury and Associated CoagulopathyR01HL152200 · NHLBI · BLOODWORKS · PI DONG, JING-FEI · 2020 to 2023
$3.1M
Venous Thrombosis After Traumatic InjuryR01HL162729 · NHLBI · MAYO CLINIC ROCHESTER · PI Matthew Thomas Auton, MYUNG SOO PARK · 2023 to 2026
$2.6M
Mayo Clinic StARR ProgramR38HL150086 · NHLBI · MAYO CLINIC ROCHESTER · PI VESNA D GAROVIC, KARL A. NATH · 2020 to 2026
$2.5M
Structure-Resolved Mechanistic Phenotyping of Von Willebrand DiseaseR01HL146508 · NHLBI · MAYO CLINIC ROCHESTER · PI AUTON, MATTHEW · 2020 to 2023
$1.9M
Thermodynamics of the Conformational Activation of Von Willebrand FactorR01HL109109 · NHLBI · MAYO CLINIC ROCHESTER · PI AUTON, MATTHEW · 2011 to 2015
$1.7M
Postdoctoral Training Program for Research on AgingT32AG049672 · NIA · MAYO CLINIC ROCHESTER · PI PASSOS, JOAO · 2016 to 2022
$1.3M
NCATS NIH HHS UL1 TR000135NCRR NIH HHS UL1 RR024150NHLBI NIH HHS R01 HL109109NHLBI NIH HHS R01 HL146508NHLBI NIH HHS R01 HL152200NHLBI NIH HHS R01 HL162729NHLBI NIH HHS R38 HL150086NHLBI NIH HHS UM1 HL120877NIA NIH HHS T32 AG049672NIGMS NIH HHS R01 GM126086
6 · The paper itself

Abstract

backgroundVon Willebrand factor (VWF) is an acute phase reactant synthesized in the megakaryocytes and endothelial cells. VWF forms ultra-large multimers (ULVWF) which are cleaved by the metalloprotease ADAMTS-13, preventing spontaneous VWF-platelet interaction. After trauma, ULVWF is released into circulation as part of the acute phase reaction. We hypothesized that trauma patients would have increased levels of VWF and decreased levels of ADAMTS-13 and that these patients would have accelerated thrombin generation.

methodsWe assessed plasma concentrations of VWF antigen and ADAMTS-13 antigen, the Rapid Enzyme Assays for Autoimmune Diseases (REAADS) activity of VWF, which measure exposure of the platelet-binding A1 domain, and thrombin generation kinetics in 50 samples from 30 trauma patients and an additional 21 samples from volunteers. Samples were analyzed at 0 to 2 hours and at 6 hours from the time of injury. Data are presented as median (IQR) and Kruskal-Wallis test was performed between trauma patients and volunteers at both time points.

resultsREAADS activity was greater in trauma patients than volunteers both at 0 to 2 hours (190.0 (132.0-264.0) vs. 92.0 (71.0-114.0), p<0.002) and at 6 hours (167.5 (108.0-312.5.0) vs. 92.0 (71.0-114.0), p<0.001). ADAMTS-13 antigen levels were also decreased in trauma patients both at 0 to 2 hours (0.84 (0.51-0.94) vs. 1.00 (0.89-1.09), p=0.010) and at 6 hours (0.653 (0.531-0.821) vs. 1.00 (0.89-1.09), p<0.001). Trauma patients had accelerated thrombin generation kinetics, with greater peak height and shorter time to peak than healthy volunteers at both time points. DISCUSSION: Trauma patients have increased exposure of the VWF A1 domain and decreased levels of ADAMTS-13 compared with healthy volunteers. This suggests that the VWF burst after trauma may exceed the proteolytic capacity of ADAMTS-13, allowing circulating ULVWF multimers to bind platelets, potentially contributing to trauma-induced coagulopathy. LEVEL OF EVIDENCE: Prospective case cohort study.

Indexed as

coagulopathymultiple traumathromboembolismvenous thromboembolism

Identifiers

PMID33912688
PMCPMC8030476
OpenAlexW3141818283

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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.