Evidence map›Paper›PMID 28569153›Full record

ArticleJournal of translational medicine2017

Aberrant monocyte responses predict and characterize dengue virus infection in individuals with severe disease.

Yean K Yong, Hong Y Tan, Soe Hui Jen, Esaki M Shankar, Santha K Natkunam, Jameela Sathar, Rishya Manikam, Shamala D Sekaran

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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  17. Inflammasome Fuels Dengue Severity.Frontiers in cellular and infection microbiology · 2020
    Review
  18. Increased serum ferritin and interleukin-18 levels in children with dengue.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2019
    Article
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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

8 authors at 5 institutions in 2 countries.

Yean K YongCentre of Excellence for Research in AIDS (CERiA), Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Hong Y TanDepartment of Medical Microbiology, Faculty of Medicine, University of Malaya, Lembah Pantai, 50603, Kuala Lumpur, Malaysia.
Soe Hui JenDepartment of Medical Microbiology, Faculty of Medicine, University of Malaya, Lembah Pantai, 50603, Kuala Lumpur, Malaysia.
Esaki M ShankarDivision of Infection Biology and Microbiology, Department of Life Sciences, School of Basic and Applied Sciences, Central University of Tamil Nadu (CUTN), Neelakudi Campus, Tiruvarur, India.
Santha K NatkunamHospital Tengku Ampuan Rahimah, Persiaran Tengku Ampuan Rahimah, Klang, Selangor, Malaysia.
Jameela SatharClinical Hematology Laboratory, Department of Hematology, Hospital Ampang, Ampang, Selangor, Malaysia.
Rishya ManikamDepartment of Trauma and Emergency Medicine, University Malaya Medical Centre, Kuala Lumpur, Malaysia.
Shamala D SekaranDepartment of Medical Microbiology, Faculty of Medicine, University of Malaya, Lembah Pantai, 50603, Kuala Lumpur, Malaysia. shamala@ummc.edu.my.ORCID 0000-0002-0478-0425
University of Malaya · MYUniversity Malaya Medical Centre · MYCentral University of Tamil Nadu · INKPJ Ampang Puteri Specialist Hospital · MYTengku Ampuan Rahimah Hospital · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently, several assays can diagnose acute dengue infection. However, none of these assays can predict the severity of the disease. Biomarkers that predicts the likelihood that a dengue patient will develop a severe form of the disease could permit more efficient patient triage and allows better supportive care for the individual in need, especially during dengue outbreaks.

methodsWe measured 20 plasma markers i.e. IFN-γ, IL-10, granzyme-B, CX3CL1, IP-10, RANTES, CXCL8, CXCL6, VCAM, ICAM, VEGF, HGF, sCD25, IL-18, LBP, sCD14, sCD163, MIF, MCP-1 and MIP-1β in 141 dengue patients in over 230 specimens and correlate the levels of these plasma markers with the development of dengue without warning signs (DWS-), dengue with warning signs (DWS+) and severe dengue (SD).

resultsOur results show that the elevation of plasma levels of IL-18 at both febrile and defervescence phase was significantly associated with DWS+ and SD; whilst increase of sCD14 and LBP at febrile phase were associated with severity of dengue disease. By using receiver operating characteristic (ROC) analysis, the IL-18, LBP and sCD14 were significantly predicted the development of more severe form of dengue disease (DWS+/SD) (AUC = 0.768, P < 0.0001; AUC = 0.819, P < 0.0001 and AUC = 0.647, P = 0.014 respectively). Furthermore, we also found that the levels of VEGF were directly correlated and sCD14 was inversely correlated with platelet count, suggesting that the endothelial activation and microbial translocation may played a role in pathogenesis of dengue disease.

conclusionsGiven that the elevation IL-18, LBP and sCD14 among patients with severe form of dengue disease, our findings suggest a pathogenic role for an aberrant inflammasome and monocyte activation in the development of severe form of dengue disease.

Indexed as

Acute-Phase ProteinsAdultArea Under CurveBiomarkersCarrier ProteinsCytokinesDengueDengue VirusDisease OutbreaksFemaleHumansInflammasomesInflammationInterleukin-18Lipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsAcute-Phase ProteinsBiomarkersCarrier ProteinsCytokinesInflammasomesInterleukin-18Lipopolysaccharide-Binding ProteinLipopolysaccharide ReceptorsMembrane GlycoproteinsDengueDengue with warning signsIL-18LBPMicrobial translocationMonocyte activationsCD14Severe dengue

Identifiers

PMID28569153
PMCPMC5452397
OpenAlexW2620503990

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.