Evidence map›Paper›PMID 31550260›Full record

ArticlePloS one2019

Identification of inflammatory markers suitable for non-invasive, repeated measurement studies in biobehavioral research: A feasibility study.

H M Schenk, S L van Ockenburg, M C Nawijn, P De Jonge, J G M Rosmalen

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. 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
0.1field-weighted citation impact, top 58% 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. Article
  3. Biomarkers of Stress and Inflammation in Children.Biological research for nursing · 2023
    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

5 authors at 1 institution in 1 country.

H M SchenkInterdisciplinary Center Psychopathology and Emotion regulation (ICPE), University Center for Psychiatry, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0002-2799-0265
S L van OckenburgInterdisciplinary Center Psychopathology and Emotion regulation (ICPE), University Center for Psychiatry, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
M C NawijnDepartment of Pathology and Medical Biology, GRIAC Research Institute, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
P De JongeInterdisciplinary Center Psychopathology and Emotion regulation (ICPE), University Center for Psychiatry, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
J G M RosmalenInterdisciplinary Center Psychopathology and Emotion regulation (ICPE), University Center for Psychiatry, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
University Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionStudying the role of the immune system in the interaction between mental and physical health is challenging. To study individuals with an intensive, longitudinal study design that requires repetitive sampling in their daily life, non-invasive sampling techniques are a necessity. Urine can be collected in a non-invasive way, but this may be demanding for participants and little is known about fluctuation of inflammatory markers in urine over time. The aim of this study was to investigate the feasibility of non-invasive sampling, and to explore intra-individual differences in inflammatory markers in urine. MATERIALS &

methodsTen healthy individuals collected 24-hour urine for 63 consecutive days. In a pilot analysis, 39 inflammatory markers were examined for detectability in urine, stability over time and under storage conditions, and daily fluctuations. Multiplex analyses were used to quantify levels of eight selected markers: C-reactive protein (CRP), Fractalkine, Interleukin-1 receptor-antagonist (IL-1RA), interferon-α (IFNα), interferon-γ (IFNγ), Interferon gamma-induced protein 10 (IP10), Macrophage inflammatory protein-1β (MIP-1β), and Vascular Endothelial Growth Factor (VEGF). Cross-correlations were calculated between the overnight and 24-hour samples were calculated, to examine whether 24-hour urine could be replaced by the overnight portion for better feasibility. We examined intra- and interindividual differences in the levels of inflammatory markers in urine and the fluctuations thereof.

resultsThis study showed that levels of selected inflammatory markers can be detected in urine. Cross-correlation analyses showed that correlations between levels of inflammatory markers in the night portion and the 24-hour urine sample varied widely between individuals. In addition, analyses of time series revealed striking inter- and intra-individual variation in levels of inflammatory markers and their fluctuations.

conclusionWe show that the assessment of urinary inflammatory markers is feasible in an intensive day-to-day study in healthy individuals. However, 24-hour urine cannot be replaced by an overnight portion to alleviate the protocol burden. Levels of inflammatory markers show substantial variation between and within persons.

Indexed as

AdultBiobehavioral SciencesBiological Variation, IndividualBiomarkersChemokine CCL4Chemokine CX3CL1Chemokine CXCL10C-Reactive ProteinFeasibility StudiesFemaleHealthy VolunteersHumansInflammation MediatorsInterferon-alphaInterferon-gammaInterleukin 1 Receptor Antagonist ProteinBiomarkersCCL4 protein, humanChemokine CCL4Chemokine CX3CL1Chemokine CXCL10C-Reactive ProteinCX3CL1 protein, humanCXCL10 protein, humanInflammation MediatorsInterferon-alphaInterferon-gammaInterleukin 1 Receptor Antagonist ProteinVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID31550260
PMCPMC6759186
OpenAlexW2976506784

What OpenQuestion holds

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LicenceCC BY
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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.