Evidence map›Paper›PMID 29735920›Full record

ArticleInternational journal of molecular sciences2018

Preanalytical Biases in the Measurement of Human Blood Sphingolipids.

Robert Brunkhorst, Waltraud Pfeilschifter, Sammy Patyna, Stefan Büttner, Timon Eckes, Sandra Trautmann, Dominique Thomas, Josef Pfeilschifter, Alexander Koch

Open access · goldAbstract read
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Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 22 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 1 institution in 1 country.

Robert BrunkhorstDepartment of Neurology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. robert.brunkhorst@kgu.de.
Waltraud PfeilschifterDepartment of Neurology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. waltraud.pfeilschifter@kgu.de.ORCID 0000-0001-6935-8842
Sammy PatynaDepartment of General Pharmacology and Toxicology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. sammy.patyna@googlemail.com.
Stefan BüttnerDepartment of Nephrology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. stefan.buettner@kgu.de.ORCID 0000-0002-9085-2455
Timon EckesDepartment of General Pharmacology and Toxicology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. eckes@em.uni-frankfurt.de.
Sandra TrautmannDepartment of Clinical Pharmacology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. labocha@med.uni-frankfurt.de.
Dominique ThomasDepartment of Clinical Pharmacology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. Thomas@med.uni-frankfurt.de.ORCID 0000-0002-4153-3669
Josef PfeilschifterDepartment of General Pharmacology and Toxicology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. pfeilschifter@em.uni-frankfurt.de.
Alexander KochDepartment of General Pharmacology and Toxicology, Goethe University Hospital Frankfurt, 60590 Frankfurt am Main, Germany. koch@med.uni-frankfurt.de.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of blood sphingolipids is an emerging topic in clinical science. The objective of this study was to determine preanalytical biases that typically occur in clinical and translational studies and that influence measured blood sphingolipid levels. Therefore, we collected blood samples from four healthy male volunteers to investigate the effect of storage conditions (time, temperature, long-term storage, freeze⁻thaw cycles), blood drawing (venous or arterial sampling, prolonged venous compression), and sample preparation (centrifugation, freezing) on sphingolipid levels measured by LC-MS/MS. Our data show that sphingosine 1-phosphate (S1P) and sphinganine 1-phosphate (SA1P) were upregulated in whole blood samples in a time- and temperature-dependent manner. Increased centrifugation at higher speeds led to lower amounts of S1P and SA1P. All other preanalytical biases did not significantly alter the amounts of S1P and SA1P. Further, in almost all settings, we did not detect differences in (dihydro)ceramide levels. In summary, besides time-, temperature-, and centrifugation-dependent changes in S1P and SA1P levels, sphingolipids in blood remained stable under practically relevant preanalytical conditions.

Indexed as

Blood PreservationBlood Specimen CollectionTandem Mass SpectrometryAdultCeramidesChromatography, LiquidHumansLysophospholipidsMaleSphingolipidsSphingosineYoung AdultCeramidesdihydrosphingosine 1-phosphateLysophospholipidsSphingolipidsSphingosinesphingosine 1-phosphatebloodceramidesdihydroceramidessphinganine 1-phosphatesphingolipidssphingosine 1-phosphate

Identifiers

PMID29735920
PMCPMC5983773
OpenAlexW2800502596

What OpenQuestion holds

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LicenceCC BY
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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.