Evidence map›Paper›PMID 29149303›Full record

ArticleThe Journal of infectious diseases2018

Changes in Cytokine, Filarial Antigen, and DNA Levels Associated With Adverse Events Following Treatment of Lymphatic Filariasis.

Britt J Andersen, Jessica Kumar, Kurt Curtis, Nelly Sanuku, Samson Satofan, Christopher L King, Peter U Fischer, Gary J Weil

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

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  10. Frontiers in tropical diseases · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Britt J AndersenInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
Jessica KumarCenter for Global Health and Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Kurt CurtisInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
Nelly SanukuPapua New Guinea Institute of Medical Research, Goroka.
Samson SatofanPapua New Guinea Institute of Medical Research, Goroka.
Christopher L KingCenter for Global Health and Diseases, Case Western Reserve University School of Medicine, Cleveland, Ohio.
Peter U FischerInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
Gary J WeilInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri.
Washington University in St. Louis · USPapua New Guinea Institute of Medical Research · PGCase Western Reserve University · USCenter for Global Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mild to moderate adverse events (AEs) are common after treatment of lymphatic filariasis (LF) and pose a major challenge for the global LF elimination program. We studied changes in cytokine levels and filarial worm components in plasma of subjects with and without AEs following treatment of LF. Methods: Participants (n = 24) were hospitalized and monitored for AEs following treatment. Cytokines (27), filarial DNA, circulating filarial antigen (CFA), and immune complexes were measured in plasma samples collected before and after treatment. Results: Levels for 16 cytokines increased after treatment in individuals with moderate AEs compared to individuals with no and/or mild AEs. These included 3 major proinflammatory cytokines (interleukin 6, tumor necrosis factor α, and interleukin 1β). Eotaxin-1 levels were elevated at baseline in individuals who developed moderate AEs after treatment; thus, eotaxin-1 is a potential biomarker for AE risk. CFA and filarial DNA levels increased more in individuals with moderate AEs after treatment than in people with no/mild AEs. Conclusions: Increases in cytokine, filarial DNA, and CFA levels were associated with development of AEs following treatment of LF. Improved understanding of the pathogenesis of AEs may lead to improved methods for their prevention or management that could increase compliance in elimination programs.

Indexed as

Antigen-Antibody ComplexAntigens, HelminthCytokinesDNA, HelminthDrug-Related Side Effects and Adverse ReactionsElephantiasis, FilarialFilaricidesHumansPlasmaAntigen-Antibody ComplexAntigens, HelminthCytokinesDNA, HelminthFilaricidesadverse eventscirculating filarial antigenemiacytokineslymphatic filariasistherapy

Identifiers

PMID29149303
PMCPMC5853815
OpenAlexW2770098259

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.