Evidence map›Paper›PMID 30439997›Full record

Trial reportPloS one2018

Serum sphingolipid levels associate with upcoming virologic events and HBV genotype D in a cohort of patients with HBeAg-negative HBV infection.

Victoria Therese Mücke, Katja Jakobi, Viola Knop, Dominique Thomas, Marcus Maximilian Mücke, Kai-Henrik Peiffer, Stefan Zeuzem, Christoph Sarrazin, Josef Pfeilschifter, Georgios Grammatikos

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Altered Serum Phospholipids in Atopic Dermatitis and Association with Clinical Status.JID innovations : skin science from molecules to population health · 2022
    Article
  3. Article
  4. Article
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

10 authors at 2 institutions in 1 country.

Victoria Therese MückeUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.ORCID 0000-0002-1653-7246
Katja JakobiPharmazentrum Frankfurt, Institut für Allgemeine Pharmakologie, Frankfurt am Main, Germany.
Viola KnopUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.
Dominique ThomasInstitut für Klinische Pharmakologie und Toxikologie, Frankfurt am Main, Deutschland.
Marcus Maximilian MückeUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.ORCID 0000-0001-8475-8369
Kai-Henrik PeifferUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.
Stefan ZeuzemUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.
Christoph SarrazinSt. Josefs-Hospital, Wiesbaden, Germany.
Josef PfeilschifterPharmazentrum Frankfurt, Institut für Allgemeine Pharmakologie, Frankfurt am Main, Germany.
Georgios GrammatikosUniversitätsklinikum Frankfurt, Frankfurt am Main, Germany.
Goethe University Frankfurt · DESt. Josefs Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesSphingolipids (SLs) have been implicated as potent regulators of the hepatitis B virus (HBV) life cycle. We investigated the SL biomarker potential regarding virologic endpoints in a prospective subgroup of patients with HBeAg-negative chronic HBV infection.

methodsFrom 2009-2016 98 patients with HBeAg-negative HBV infection were prospectively followed over four years. Clinical, laboratory and imaging data were evaluated annually. SLs were assessed in available serum probes via liquid chromatography coupled to tandem mass spectrometry.

resultsOf those 98 patients, 10 (10.2%) showed HBV reactivation, 13 (13.2%) lost HBsAg and 9 (9.1%) gained status of HBsAg-/HBsAb-coexistence, whereas 66 (67.3%) had no events. Within the four-year analysis sphingosine (p = 0.020), sphinganine (p<0.001), dhS1P (p<0.001), C16DHC (p<0.01) and C20Cer (p<0.001) showed a significant upregulation in patients without virologic events, C18Cer significantly decreased (p<0.001). At baseline decreased S1P-, dhS1P- and C16Cer-levels were observed in patients with upcoming status of HBsAg-/HBsAb-coexistence. S1P and dhS1P levels were elevated HBV genotype D infected patients.

conclusionsIn a prospective cohort of patients with a HBeAg-negative HBV infection, serum SLs associated with the virologic course and HBV genotype D. Further studies are required to elucidate SLs as potential novel predictors of the course of HBeAg-negative HBV infection.

Indexed as

GenotypeHepatitis B virusAdolescentAdultAgedChromatography, LiquidFemaleHepatitis B, ChronicHepatitis B e AntigensHumansMaleMiddle AgedProspective StudiesSphingolipidsTandem Mass SpectrometryHepatitis B e AntigensSphingolipids

Identifiers

PMID30439997
PMCPMC6237377
OpenAlexW2901880389

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.