Evidence map›Paper›PMID 35268506›Full record

ArticleJournal of clinical medicine2022

CXCL10/IP10 as a Biomarker Linking Multisystem Inflammatory Syndrome and Left Ventricular Dysfunction in Children with SARS-CoV-2.

Eviç Zeynep Başar, Hafize Emine Sönmez, Hüseyin Uzuner, Aynur Karadenizli, Hüseyin Salih Güngör, Gökmen Akgün, Ayşe Filiz Yetimakman, Selim Öncel, Kadir Babaoğlu

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Eviç Zeynep BaşarDivision of Pediatric Cardiology, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.
Hafize Emine SönmezDivision of Pediatric Rheumatology, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.
Hüseyin UzunerMedical Laboratory Techniques Program, Section of Medical Services and Techniques, Kocaeli Vocational School of Health Services, Kocaeli University, Kocaeli 41001, Turkey.
Aynur KaradenizliAntibody Research and Production Laboratory, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.
Hüseyin Salih GüngörDivision of Pediatric Cardiology, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.
Gökmen AkgünPediatric Cardiology Unit, Darıca Farabi Training and Research Hospital, Kocaeli 41700, Turkey.
Ayşe Filiz YetimakmanDivision of Pediatric Intensive Care, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.ORCID 0000-0002-9334-4464
Selim ÖncelDivision of Pediatric Infectious Diseases, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.ORCID 0000-0002-5493-1818
Kadir BabaoğluDivision of Pediatric Cardiology, Department of Pediatrics and Child Health, Section of Internal Medical Sciences, Faculty of Medicine, Kocaeli University, Kocaeli 41001, Turkey.
Kocaeli Üniversitesi · TRFarabi Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo investigate the diagnostic accuracy of CXCL10/IP10 for left ventricular (LV) dysfunction in multisystemic inflammatory syndrome (MIS-C).

methodsThis cross-sectional, longitudinal study included 36 patients with MIS-C. Patients were classified as follows: (1) patients presenting with Kawasaki-like features (group I = 11); (2) patients presenting with LV systolic dysfunction (group II = 9); and (3) other presentations (group III = 3). CXCL10/IP10 levels were measured upon admission and on days 3 and 7 of treatment.

resultsTwenty patients were male and 16 were female. The median age of patients at diagnosis was 7.5 (1.5-17) years. All patients had a fever lasting for a median of 4 (2-7) days. Ten patients had LV systolic dysfunction. The duration of hospitalization was longer in group II. Lymphocyte and platelet counts were lower, whereas NT-pro-BNP, troponin-I, D-dimer, and CXCL10/IP10 levels were higher in group II. Baseline levels of CXCL10/IP10 were weakly negatively correlated with ejection fraction (r = -0.387,

conclusionHaving a good correlation with cardiac function, CXCL10/IP10 is a potential biomarker to predict LV dysfunction in MIS-C patients.

Indexed as

CXCL10/IP 10left ventricular dysfunctionmultisystem hyperinflammatory syndromeSARS-CoV-2

Identifiers

PMID35268506
PMCPMC8911504
OpenAlexW4220872722

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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.