Evidence map›Paper›PMID 23225307›Full record

ArticleAnnals of neurology2013

Role of reduced ADAMTS13 in arterial ischemic stroke: a pediatric cohort study.

Moritz Lambers, Neil A Goldenberg, Gili Kenet, Fenella J Kirkham, Daniela Manner, Timothy Bernard, Rolf M Mesters, Ralf Junker, Monika Stoll, Ulrike Nowak-Göttl

Abstract read
In one paragraph

Article in Annals of neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 55 citations in OpenAlex.

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  11. A Single Synonymous Variant (c.354G>A [p.P118P]) inInternational journal of molecular sciences · 2019
    Article
  12. Article
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  14. Role of CD40 and ADAMTS13 in von Willebrand factor-mediated endothelial cell-platelet-monocyte interaction.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. Von Willebrand Factor: Multimeric Structure and Functional Activity in Patients With Atrial Fibrillation With and Without Oral Anticoagulation.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis · 2018
    Article
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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 9 institutions in 4 countries.

Moritz LambersFaculty of Medicine, University of Münster, Germany.
Neil A Goldenberg
Gili Kenet
Fenella J Kirkham
Daniela Manner
Timothy Bernard
Rolf M Mesters
Ralf Junker
Monika Stoll
Ulrike Nowak-Göttl
University Hospital Schleswig-Holstein · DEChildren's Hospital Colorado · USFH Münster · DELeibniz Association · DESheba Medical Center · ILUniversity College London · GBUniversity Hospital Münster · DEUniversity of Colorado Denver · USUniversity of Lübeck · DE

Funding

Investigation of Prognostic Factors in Childhood-Onset AIS: Role of Stroke SubtypK23HL096895 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BERNARD, TIMOTHY J · 2010 to 2014
$690k
NHLBI NIH HHS K23 HL096895
6 · The paper itself

Abstract

objectivePrevious studies in adults and mice have implicated ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13), also known as von Willebrand factor (VWF)-cleaving protease, as a protective factor for stroke. Here we investigated ADAMTS13 in 208 pediatric patients with arterial ischemic stroke (AIS) and 125 population-based control children in a frequency-matched case-control study.

methodsThe proportion of patients/controls with ADAMTS13 activity levels below and above the 10th percentile was compared. Additionally, in a quintile comparison, the proportion of patients versus controls in the lowest ADAMTS13 quintile was compared to those in the 2nd to 5th quintiles. Adjustment was performed for VWF antigen (VWF:Ag), factor VIII activity (FVIII:C), blood group, and age.

resultsForty-six of 208 patients (22%) showed ADAMTS13 levels below the 10th percentile, compared with 5 of 125 controls (4%; p < 0.001). Odds ratios/95% confidence intervals were 7.30/2.73-19.50 for the lowest percentile and 2.44/1.15-5.16 in the quintile comparison after adjustment for VWF:Ag, FVIII:C, blood group, and age. Comparing the proportion of patients with ADAMTS13 activity below the 10th percentile within the different stroke subtypes (undetermined, cardioembolic, steno-occlusive arteriopathies), no statistically significant differences were found (undetermined, 16 of 89; cardioembolic, 6 of 40; steno-occlusive arteriopathies, 24 of 79; p = 0.08). ADAMTS13 levels did not significantly differ among stroke subtypes (p = 0.29).

interpretationOur findings implicate reduced ADAMTS13 activity as a risk factor for pediatric AIS, and support the concept that ADAMTS13 has a role in the pathogenesis of pediatric AIS.

Indexed as

ADAM ProteinsADAMTS13 ProteinAdolescentAge FactorsBrain IschemiaCase-Control StudiesChildChild, PreschoolCohort StudiesFemaleFollow-Up StudiesHumansInfantMalePopulation SurveillanceRisk FactorsADAM ProteinsADAMTS13 ProteinADAMTS13 protein, human

Identifiers

PMID23225307
PMCPMC3703929
OpenAlexW1986048680

What OpenQuestion holds

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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.