Evidence map›Paper›PMID 33809042›Full record

ArticleInternational journal of molecular sciences2021

Cytokine Signature of Dengue Patients at Different Severity of the Disease.

Irwin Puc, Tzu-Chuan Ho, Ko-Lun Yen, Amrita Vats, Jih-Jin Tsai, Po-Lin Chen, Yu-Wen Chien, Yu-Chih Lo, Guey Chuen Perng

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 49 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 3 institutions in 1 country.

Irwin PucInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.ORCID 0000-0002-0182-3768
Tzu-Chuan HoInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
Ko-Lun YenInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
Amrita VatsInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
Jih-Jin TsaiTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung 807378, Taiwan.ORCID 0000-0003-2226-8916
Po-Lin ChenDepartment of Internal Medicine, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
Yu-Wen ChienDepartment of Public Health, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
Yu-Chih LoDepartment of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan 701401, Taiwan.
Guey Chuen PerngInstitute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan 701401, Taiwan.
National Cheng Kung University · TWKaohsiung Medical University · TWNational Cheng Kung University Hospital · TW

Funding

Ministry of Health and Welfare MOHW104-CDC-C-114-114901Ministry of Science and Technology MOST 103 - 2320 - B -006 - 030 - MY3Ministry of Science and Technology MOST-106-2321-B-006 -012Ministry of Science and Technology MOST 107-2314-B-006 -063 -MY3National Science Council Grant NSC 102-2320-B-006-049
6 · The paper itself

Abstract

Clinical presentations of dengue fever (DF) are diverse and non-specific, causing unpredictable progression and outcomes. Its progression and severity have been associated with cytokine levels alteration. In this study, dengue patients were classified into groups following the 2009 WHO dengue classification scheme to investigate the cytokine signature at different severity of the disease: dengue without warning sign symptoms (A); dengue with warning signs (B); severe dengue (C); other fever (OF) and healthy (Healthy). We analyzed 23 different cytokines simultaneously, namely IL-1b, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-17A, IL-33, CD14, CD54, CD62E, CD62L, CD62p, CD106, CD121b, CD154, CD178, GM-CSF, IFN-g, MIF, ST2 and TNF from patients admitted to National Cheng Kung University Hospital during the 2015 Taiwan dengue outbreak. Cytokines TNF, CD54, CD62E, CD62L, CD62P, GM-CSF, IL-1b, IL-2, IL-6, IL-8, IL-10, IL-12p70, IL-17A, INF-g and MIF were elevated while CD106, CD154, IL-4 and L-33 were decreased when compared to the control. IL-10 demonstrated to be a potential diagnostic marker for DF (H and A group; AUC = 0.944, H and OF group; AUC = 0.969). CD121b demonstrated to be predictive of the SD (A and B group; AUC = 0.744, B and C group; AUC = 0.775). Our results demonstrate the cytokine profile changes during the progression of dengue and highlight possible biomarkers for optimizing effective intervention strategies.

Indexed as

AdolescentAdultAgedAged, 80 and overBiomarkersCytokinesDengueDengue VirusFemaleHumansInterleukin-10MaleMiddle AgedReceptors, Interleukin-1 Type IISeverity of Illness IndexTranscriptomeBiomarkersCytokinesIL1R2 protein, humanInterleukin-10Receptors, Interleukin-1 Type IIbiomarker predictioncytokinesdengueflavivirusessevere dengue

Identifiers

PMID33809042
PMCPMC7999441
OpenAlexW3135948808

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.