Evidence map›Paper›PMID 30736351›Full record

ArticleInternational journal of molecular sciences2019

Evaluation of Storage Tubes for Combined Analysis of Circulating Nucleic Acids in Liquid Biopsies.

Aoife Ward Gahlawat, Judith Lenhardt, Tania Witte, Denise Keitel, Anna Kaufhold, Kendra K Maass, Kristian W Pajtler, Christof Sohn, Sarah Schott

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Explore the role of ctHPVDNA kinetics during diagnosis and follow-up of HPV OPSCC.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
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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.

Aoife Ward GahlawatDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. Aoife.Gahlawat@med.uni-heidelberg.de.
Judith LenhardtDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. J.Lenhardt@stud.uni-heidelberg.de.
Tania WitteDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. Tania.WitteTobar@med.uni-heidelberg.de.
Denise KeitelDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. Denise.Keitel@med.uni-heidelberg.de.
Anna KaufholdDivision of Pediatric Neuro-oncology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. a.kaufhold@kitz-heidelberg.de.
Kendra K MaassDivision of Pediatric Neuro-oncology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. k.maass@kitz-heidelberg.de.
Kristian W PajtlerDivision of Pediatric Neuro-oncology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany. k.pajtler@kitz-heidelberg.de.
Christof SohnDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. Christof.Sohn@med.uni-heidelberg.de.
Sarah SchottDepartment of Gynecology and Obstetrics, University Hospital of Heidelberg, 69120 Heidelberg, Germany. sarah.schott@med.uni-heidelberg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last decade, circulating nucleic acids such as microRNAs (miRNAs) and cell-free DNA (cfDNA) have become increasingly important in serving as potential novel biomarkers for a variety of human diseases. If cell-free nucleic acids are to become routinely used in diagnostics, the difference in plasma miRNA and cfDNA levels between healthy and diseased subjects must exceed pre-analytical and analytical variability. Until now, few studies have addressed the time limitations of pre-processing or explored the potential use of long-term blood storage tubes, which might need to be implemented in real-life diagnostics. In this study, we analyzed the stability of four breast cancer-associated miRNAs and two cancer-associated genes under various storage conditions, to test their limitations for potential application in clinical diagnostics. In two consecutive experiments, we tested the limits of conventional EDTA tubes, as well as long-term storage blood collection tubes (BCTs) from four different manufacturers. We found that circulating miRNAs are relatively stable when stored in EDTA monovettes for up to 12 h before processing. When stored in BCTs, circulating miRNAs and cfDNA are stable for up to 7 days, depending on the manufacturer. Norgen tubes were superior for cfDNA yield, while Streck tubes performed the worst in our study with hemolysis induction. In conclusion, plasma prepared from whole blood is suitable for the quantification of both cf-miRNAs and cfDNA simultaneously.

Indexed as

Blood Specimen CollectionCell-Free Nucleic AcidsLiquid BiopsyBiomarkersBlood PreservationCirculating MicroRNAFemaleHumansMalePolymerase Chain ReactionRNA StabilityTime FactorsBiomarkersCell-Free Nucleic AcidsCirculating MicroRNAblood collection tubesblood storagecell-free DNAcirculating miRNA

Identifiers

PMID30736351
PMCPMC6387045

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Registered trials

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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.