Evidence map›Paper›PMID 32251424›Full record

ArticlePloS one2020

The art of obtaining a high yield of cell-free DNA from urine.

Elien Augustus, Kaat Van Casteren, Laure Sorber, Peter van Dam, Geert Roeyen, Marc Peeters, Alex Vorsters, An Wouters, Jo Raskin, Christian Rolfo and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.2field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 59 citations in OpenAlex.

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  20. Network approach in liquidomics landscape.Journal of experimental & clinical cancer research : CR · 2023
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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

12 authors at 3 institutions in 2 countries.

Elien AugustusCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.ORCID 0000-0002-2383-381X
Kaat Van CasterenCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.ORCID 0000-0002-6339-9771
Laure SorberCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.
Peter van DamCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.ORCID 0000-0002-9184-7703
Geert RoeyenDepartment of Hepato-Pancreato-Biliary and Transplant Surgery, Antwerp University Hospital (UZA), Edegem, Belgium.
Marc PeetersCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.ORCID 0000-0003-4969-2303
Alex VorstersCentre for the Evaluation of Vaccination, Vaccine & Infectious Disease Institute, University of Antwerp (UA), Wilrijk, Belgium.
An WoutersCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.
Jo RaskinDepartment of Pulmonology and Thoracic Oncology, Antwerp University Hospital (UZA), Edegem, Belgium.
Christian RolfoThoracic Medical Oncology and the Early Clinical Trials at the University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center (UMGCCC), Baltimore, Maryland, United States of America.ORCID 0000-0002-7860-8417
Karen ZwaenepoelCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.
Patrick PauwelsCenter for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.
University of Antwerp · BEAntwerp University Hospital · BEUniversity of Maryland, Baltimore · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although liquid biopsies offer many advantages over tissue biopsies, they are not yet standard practice. An important reason for the lack of implementation is the unavailability of well standardized techniques and guidelines, especially for pre-analytical conditions which are an important factor causing the current sensitivity issues. To overcome these limitations, we investigated the effect of several pre-analytical conditions on the concentration of cell-free DNA (cfDNA) and cellular genomic DNA (gDNA) contamination. Urine samples from healthy volunteers (HVs) and cancer patients were collected and processed according to specific pre-analytical conditions. Our results show that in samples with a relatively small volume more than 50% of the cfDNA can be found in the first 50 mL of the urine sample. The total DNA concentration increased again when samples were collected more than 3.5 hours apart. Adding preservative to urine samples is recommended to obtain high concentrations of cfDNA. To remove the cellular content, high speed centrifugation protocols as 4,000g 10min or 3,000g 15min are ideal for urine collected in cfDNA Urine Preserve (Streck). Although this study was a pilot study and needs to be confirmed in a larger study population, clear trends in the effect of several pre-analytical conditions were observed.

Indexed as

AdultAgedCell-Free Nucleic AcidsCentrifugationDiagnostic Tests, RoutineFemaleHealthy VolunteersHumansLiquid BiopsyMaleMiddle AgedNeoplasmsPilot ProjectsTemperatureTime FactorsUrinalysisCell-Free Nucleic Acids

Identifiers

PMID32251424
PMCPMC7135229
OpenAlexW3014712910

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.