Evidence map›Paper›PMID 37610270›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2024

Elevation of IL-17 Cytokines Distinguishes Kawasaki Disease From Other Pediatric Inflammatory Disorders.

Kailey E Brodeur, Meng Liu, Daniel Ibanez, Mareike J de Groot, Liang Chen, Yan Du, Eman Seyal, Raquel Laza-Briviesca, Annette Baker, Joyce C Chang and 15 more

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
11.7field-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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  8. Biomarkers in Primary Systemic Vasculitides: Narrative Review.International journal of molecular sciences · 2026
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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

25 authors at 2 institutions in 3 countries.

Kailey E BrodeurBoston Children's Hospital, Boston, Massachusetts.
Meng LiuBoston Children's Hospital, Boston, Massachusetts, and Guangdong Second Provincial General Hospital, Guangzhou, China.
Daniel IbanezBoston Children's Hospital, Boston, Massachusetts.
Mareike J de GrootBoston Children's Hospital, Boston, Massachusetts, and Heidelberg University Hospital, Heidelberg, Germany.
Liang ChenBoston Children's Hospital, Boston, Massachusetts.
Yan DuBoston Children's Hospital, Boston, Massachusetts, and The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Eman SeyalBoston Children's Hospital, Boston, Massachusetts.
Raquel Laza-BriviescaBoston Children's Hospital, Boston, Massachusetts.
Annette BakerBoston Children's Hospital, Boston, Massachusetts.
Joyce C ChangBoston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-1691-4814
Margaret H ChangBoston Children's Hospital, Boston, Massachusetts.
Megan Day-LewisBoston Children's Hospital, Boston, Massachusetts.
Fatma DedeogluBoston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-7516-0848
Audrey DionneBoston Children's Hospital, Boston, Massachusetts.
Sarah D de FerrantiBoston Children's Hospital, Boston, Massachusetts.
Kevin G FriedmanBoston Children's Hospital, Boston, Massachusetts.
Olha HalyabarBoston Children's Hospital, Boston, Massachusetts.
Mindy S LoBoston Children's Hospital, Boston, Massachusetts.ORCID 0000-0003-2328-3536
Esra MeidanBoston Children's Hospital, Boston, Massachusetts.
Robert P SundelBoston Children's Hospital, Boston, Massachusetts.
Lauren A HendersonBoston Children's Hospital, Boston, Massachusetts.ORCID 0000-0003-0242-4029
Peter A NigrovicBoston Children's Hospital and Brigham and Women's Hospital, Boston, Massachusetts.ORCID 0000-0002-2126-3702
Jane W NewburgerBoston Children's Hospital, Boston, Massachusetts.
Mary Beth SonBoston Children's Hospital, Boston, Massachusetts.
Pui Y LeeBoston Children's Hospital, Boston, Massachusetts.ORCID 0000-0002-5779-4193
Boston Children's Hospital · USBrigham and Women's Hospital · US

Funding

Joint Biology Consortium Resource-based CenterP30AR070253 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter A Nigrovic, Jeffrey Andrew Sparks · 2016 to 2026
$9.4M
Ly6 family members in neutrophil biologyR01AR065538 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NIGROVIC, PETER A · 2014 to 2024
$4.0M
Bridging the gap between GWAS and mechanism in JIAR01AR073201 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter A Nigrovic · 2019 to 2026
$3.2M
T resident memory cells in arthritisR01AR075906 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NIGROVIC, PETER A · 2019 to 2023
$2.1M
Cardiovascular health assessment & outcomes of systemic lupus erythematosus: bridging pediatric and adult-onset diseaseK23HL148539 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI CHANG, JOYCE CHUN-LING · 2020 to 2024
$973k
Metabolic control of monocyte development and function by amino acidsK08AR074562 · NIAMS · BOSTON CHILDREN'S HOSPITAL · PI LEE, PUI YUEN · 2019 to 2023
$868k
NHLBI NIH HHS K23 HL148539NIAMS NIH HHS K08 AR074562NIAMS NIH HHS P30 AR070253NIAMS NIH HHS P30-AR070253NIAMS NIH HHS R01 AR065538NIAMS NIH HHS R01-AR065538NIAMS NIH HHS R01 AR073201NIAMS NIH HHS R01-AR073201NIAMS NIH HHS R01 AR075906NIAMS NIH HHS R01-AR075906
6 · The paper itself

Abstract

objectiveKawasaki disease (KD) is a systemic vasculitis of young children that can lead to development of coronary artery aneurysms. We aimed to identify diagnostic markers to distinguish KD from other pediatric inflammatory diseases.

methodsWe used the proximity extension assay to profile proinflammatory mediators in plasma samples from healthy pediatric controls (n = 30), febrile controls (n = 26), and patients with KD (n = 23), multisystem inflammatory syndrome in children (MIS-C; n = 25), macrophage activation syndrome (n = 13), systemic and nonsystemic juvenile idiopathic arthritis (n = 14 and n = 10, respectively), and juvenile dermatomyositis (n = 9). We validated the key findings using serum samples from additional patients with KD (n = 37) and febrile controls (n = 28).

resultsHigh-fidelity proteomic profiling revealed distinct patterns of cytokine and chemokine expression across pediatric inflammatory diseases. Although KD and MIS-C exhibited many similarities, KD differed from MIS-C and other febrile diseases in that most patients exhibited elevation in one or more members of the interleukin-17 (IL-17) cytokine family, IL-17A, IL-17C, and IL-17F. IL-17A was particularly sensitive and specific, discriminating KD from febrile controls with an area under the receiver operator characteristic curve of 0.95 (95% confidence interval 0.89-1.00) in the derivation set and 0.91 (0.85-0.98) in the validation set. Elevation of all three IL-17-family cytokines was observed in over 50% of KD patients, including 19 of 20 with coronary artery aneurysms, but was rare in all other comparator groups.

conclusionElevation of IL-17 family cytokines is a hallmark of KD and may help distinguish KD from its clinical mimics.

Indexed as

Coronary AneurysmMucocutaneous Lymph Node SyndromeSystemic Inflammatory Response SyndromeChildChild, PreschoolCOVID-19CytokinesFeverHumansInterleukin-17ProteomicsCytokinesInterleukin-17

Identifiers

PMID37610270
PMCPMC10842426
OpenAlexW4386084796

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Registered trials

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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.