Evidence map›Paper›PMID 40308204›Full record

ArticleStroke2025

Infection in Childhood Arterial Ischemic Stroke: Metagenomic Next-Generation Sequencing Results of the VIPS II Study.

Mary C Karalius, Prashanth S Ramachandran, Annie Wapniarski, Mary Wang, Maham Zia, Nancy K Hills, Max Wintermark, Charles Grose, Michael M Dowling, Jenny L Wilson and 8 more

Abstract readMulticenter Study
In one paragraph

Article in Stroke, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Mary C KaraliusDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0003-3570-5353
Prashanth S RamachandranDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0001-8464-1355
Annie WapniarskiDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0001-9937-2442
Mary WangDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.
Maham ZiaDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.
Nancy K HillsDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0002-1041-8182
Max WintermarkDepartment of Radiology, MD Anderson Cancer Center, Houston, TX (M. Wintermark).ORCID 0000-0002-6726-3951
Charles GroseDepartment of Pediatrics, University of Iowa (C.G.).ORCID 0000-0001-6884-6668
Michael M DowlingDepartments of Pediatrics and Neurology, University of Texas Southwestern Medical Center, Dallas (M.M.D.).ORCID 0000-0001-5058-6589
Jenny L WilsonDepartment of Biochemistry and Biophysics (J.L.D.), University of California San Francisco.ORCID 0000-0001-6677-869X
Sarah LeeDepartment of Neurology, Stanford University, Palo Alto, CA (S.L.).ORCID 0000-0002-8821-6636
Melissa ChungDepartment of Pediatrics, Nationwide Children's Hospital, Columbus, OH (M.C.).
Megan BarryDepartment of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL (M.B.).ORCID 0000-0002-5256-8269
Huichun XuDepartment of Medicine, University of Maryland School of Medicine, Baltimore (H.X.).ORCID 0000-0001-8118-9607
Joseph L DeRisiChan Zuckerberg Biohub SF, San Francisco, CA (J.L.D.).ORCID 0000-0002-4611-9205
Michael R WilsonDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0002-8705-5084
Heather J FullertonDepartment of Neurology, Weill Institute for Neurosciences (M.C.K., P.S.R., A.W., M. Wang, M.Z., N.K.H., M.R.W., H.J.F.), University of California San Francisco.ORCID 0000-0002-4828-1687
VIPS II Investigators

Funding

The Vascular effects of Infection in Pediatric Stroke (VIPS II) StudyR01NS104094 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FULLERTON, HEATHER J · 2017 to 2022
$3.5M
NINDS NIH HHS R01 NS104094
6 · The paper itself

Abstract

backgroundAcute respiratory infection transiently increases risk for childhood arterial ischemic stroke (AIS). We hypothesize that this paradox of a common exposure linked to a rare outcome could be explained by either (1) the infection hypothesis: unusual or multiple pathogens or (2) the host response hypothesis: heterogeneity in the inflammatory response to infection. We leverage metagenomic next-generation sequencing (mNGS), a comprehensive microbial detection tool, to test the first hypothesis.

methodsThe VIPS II study (Vascular Effects of Infection in Pediatric Stroke II) prospectively enrolled children with AIS at 22 international sites over 5 years (December 2016 to January 2022). Sites measured prestroke clinical infection via standardized parental interviews and chart abstraction. To assess more broadly the background spectrum of pathogens, a central research laboratory performed mNGS on plasma and oropharyngeal swabs collected within 72 hours of stroke. mNGS was also performed on biological samples from stroke-free children (June 2017 to January 2022), both without (well) and with (ill) documentation of clinical infection.

resultsVIPS II enrolled 205 patients with AIS, 95 stroke-free well children, and 47 stroke-free ill children. Clinical infection, most commonly upper respiratory tract infection, was detected in 81 of 205 (40%) of patients. Both plasma and oropharyngeal swab mNGS data were available for 190 of 205 patients with AIS, 91 of 95 stroke-free well children, and 27 of 47 stroke-free ill children. mNGS detected viruses in 27 of 190 (14%) patients with AIS, 9 of 91 stroke-free well children (10%), and 9 of 27 (33%) stroke-free ill children. Most were common upper respiratory viruses. Coinfections were rare. Similar viruses were found in patients with AIS and stroke-free children.

conclusionsmNGS detected a variety of common childhood viruses in both patients with AIS and stroke-free children, suggesting that the type of infection does not explain AIS susceptibility. Rather, the alternative hypothesis regarding an unusual host immune response to common infections in the pathogenicity of AIS should be further explored.

Indexed as

Ischemic StrokeMetagenomicsRespiratory Tract InfectionsStrokeAdolescentChildChild, PreschoolFemaleHigh-Throughput Nucleotide SequencingHumansInfantMaleProspective Studieschildischemic strokerespiratory tract infectionsriskviruses

Identifiers

PMID40308204
PMCPMC12303748

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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.