Evidence map›Paper›PMID 32730233›Full record

Trial reportThe Journal of clinical investigation2020

Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2.

Caroline Diorio, Sarah E Henrickson, Laura A Vella, Kevin O McNerney, Julie Chase, Chakkapong Burudpakdee, Jessica H Lee, Cristina Jasen, Fran Balamuth, David M Barrett and 27 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of clinical investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 252 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
252citing papers in PubMed, 10 pooled it
72.1field-weighted citation impact, top 1% 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

252 citing papers in PubMed, 10 syntheses or guidelines pooled it, 413 citations in OpenAlex.

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  4. Pediatric endocrinopathies related to COVID-19: an update.World journal of pediatrics : WJP · 2023
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192 more citing papers are in PubMed but not listed here.

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

37 authors at 5 institutions in 2 countries.

Caroline DiorioImmune Dysregulation Frontier Program.
Sarah E HenricksonImmune Dysregulation Frontier Program.
Laura A VellaImmune Dysregulation Frontier Program.
Kevin O McNerneyImmune Dysregulation Frontier Program.
Julie ChaseImmune Dysregulation Frontier Program.
Chakkapong BurudpakdeeImmune Dysregulation Frontier Program.
Jessica H LeeImmune Dysregulation Frontier Program.
Cristina JasenImmune Dysregulation Frontier Program.
Fran BalamuthDivision of Emergency Medicine, and.
David M BarrettImmune Dysregulation Frontier Program.
Brenda L BanwellImmune Dysregulation Frontier Program.
Kathrin M BerntDivision of Oncology.
Allison M BlatzDivision of Infectious Diseases.
Kathleen ChiotosDivision of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
Brian T FisherImmune Dysregulation Frontier Program.
Julie C FitzgeraldDivision of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
Jeffrey S GerberDivision of Infectious Diseases.
Kandace GollompImmune Dysregulation Frontier Program.
Christopher GrayImmune Dysregulation Frontier Program.
Stephan A GruppDivision of Oncology.
Rebecca M HarrisDivision of Infectious Diseases.
Todd J KilbaughDivision of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
Audrey R Odom JohnDivision of Infectious Diseases.
Michele LambertImmune Dysregulation Frontier Program.
Emily J LieblingDivision of Rheumatology.
Michele E PaesslerImmune Dysregulation Frontier Program.
Whitney PetrosaImmune Dysregulation Frontier Program.
Charles PhillipsDivision of Oncology.
Anne F ReillyImmune Dysregulation Frontier Program.
Neil D RombergImmune Dysregulation Frontier Program.
Alix SeifImmune Dysregulation Frontier Program.
Deborah A Sesok-PizziniPathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Kathleen E SullivanImmune Dysregulation Frontier Program.
Julie VardaroCenter for Healthcare Quality and Analytics (CHQA), Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Edward M BehrensImmune Dysregulation Frontier Program.
David T TeacheyImmune Dysregulation Frontier Program.
Hamid BassiriImmune Dysregulation Frontier Program.
Frontier Hospital · ZAOffice of Infectious Diseases · USChildren's Hospital of Philadelphia · USCenter for Rheumatology · USUniversity of Pennsylvania · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Improving risk allocation and developing novel therapies for children with T-ALL and T-LLR01CA193776 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI Terzah M Horton, ADAM B OLSHEN · 2015 to 2026
$6.2M
MEP pathway resistance in Plasmodium falciparumR01AI103280 · NIAID · WASHINGTON UNIVERSITY · PI Audrey Ragan Odom John · 2013 to 2026
$5.5M
COG NCTN Integrated Translational Science Center for Hematopoietic Malignancies in ChildrenUG1CA233249 · NCI · PUBLIC HEALTH INSTITUTE · PI MESHINCHI, SOHEIL · 2019 to 2025
$4.9M
IL-33 Blockade as a Novel Therapeutic for T-cell Mediated Hypercytokinemia SyndromesR01AI121250 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI BEHRENS, EDWARD M, KAMBAYASHI, TAKU · 2016 to 2020
$3.0M
Inhibition of MEP pathway Isoprenoid BiosynthesisR01AI123433 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI DOWD, CYNTHIA SCHIECK, MEYERS, MARVIN J · 2016 to 2020
$2.6M
Obesity dysregulates immune and metabolic status in asthma and alters infection susceptibility.K08AI135091 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI HENRICKSON, SARAH E · 2019 to 2023
$935k
Pediatric septic acute kidney injury: personalizing antibiotic dosing through understanding acute kidney injury risk factors and biomarker profilesK23DK119463 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI FITZGERALD, JULIE C. HOLLOWS · 2020 to 2024
$810k
Transcriptional and epigenetic regulation of Tfh dysfunction in HIVK08AI136660 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI VELLA, LAURA A · 2018 to 2022
$778k
Towards noninvasive diagnosis of malariaR21AI144472 · NIAID · WASHINGTON UNIVERSITY · PI ODOM JOHN, AUDREY RAGAN · 2019 to 2020
$485k
NCI NIH HHS R01 CA193776NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS UG1 CA233249NIAID NIH HHS K08 AI135091NIAID NIH HHS K08 AI136660NIAID NIH HHS R01 AI103280NIAID NIH HHS R01 AI121250NIAID NIH HHS R01 AI123433NIAID NIH HHS R21 AI144472NIDDK NIH HHS K23 DK119463
6 · The paper itself

Abstract

BACKGROUNDInitial reports from the severe acute respiratory coronavirus 2 (SARS-CoV-2) pandemic described children as being less susceptible to coronavirus disease 2019 (COVID-19) than adults. Subsequently, a severe and novel pediatric disorder termed multisystem inflammatory syndrome in children (MIS-C) emerged. We report on unique hematologic and immunologic parameters that distinguish between COVID-19 and MIS-C and provide insight into pathophysiology.METHODSWe prospectively enrolled hospitalized patients with evidence of SARS-CoV-2 infection and classified them as having MIS-C or COVID-19. Patients with COVID-19 were classified as having either minimal or severe disease. Cytokine profiles, viral cycle thresholds (Cts), blood smears, and soluble C5b-9 values were analyzed with clinical data.RESULTSTwenty patients were enrolled (9 severe COVID-19, 5 minimal COVID-19, and 6 MIS-C). Five cytokines (IFN-γ, IL-10, IL-6, IL-8, and TNF-α) contributed to the analysis. TNF-α and IL-10 discriminated between patients with MIS-C and severe COVID-19. The presence of burr cells on blood smears, as well as Cts, differentiated between patients with severe COVID-19 and those with MIS-C.CONCLUSIONPediatric patients with SARS-CoV-2 are at risk for critical illness with severe COVID-19 and MIS-C. Cytokine profiling and examination of peripheral blood smears may distinguish between patients with MIS-C and those with severe COVID-19.FUNDINGFinancial support for this project was provided by CHOP Frontiers Program Immune Dysregulation Team; National Institute of Allergy and Infectious Diseases; National Cancer Institute; the Leukemia and Lymphoma Society; Cookies for Kids Cancer; Alex's Lemonade Stand Foundation for Childhood Cancer; Children's Oncology Group; Stand UP 2 Cancer; Team Connor; the Kate Amato Foundations; Burroughs Wellcome Fund CAMS; the Clinical Immunology Society; the American Academy of Allergy, Asthma, and Immunology; and the Institute for Translational Medicine and Therapeutics.

Indexed as

Coronavirus InfectionsPandemicsPneumonia, ViralSystemic Inflammatory Response SyndromeAdolescentBetacoronavirusChildChild, PreschoolComplement Membrane Attack ComplexCOVID-19CytokinesFemaleHumansMaleProspective StudiesSARS-CoV-2Complement Membrane Attack ComplexCytokinesCOVID-19Cytokines

Identifiers

PMID32730233
PMCPMC7598044
OpenAlexW3046404304

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.