Evidence map›Paper›PMID 35385497›Full record

ArticlePloS one2022

Plasma DNA and deoxyribonuclease are associated with glucose metabolism in healthy mice.

Katarína Kmeťová, Jozef Čonka, Jakub Janko, Júlia Illés, Oľga Uličná, Peter Celec

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Katarína KmeťováFaculty of Medicine, Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.ORCID 0000-0002-2730-4587
Jozef ČonkaFaculty of Medicine, Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.
Jakub JankoFaculty of Medicine, Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.
Júlia IllésFaculty of Medicine, Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.
Oľga UličnáFaculty of Medicine, Pharmacobiochemical Laboratory of Third Department of Internal Medicine, Comenius University, Bratislava, Slovakia.
Peter CelecFaculty of Medicine, Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.ORCID 0000-0001-5883-3580
Comenius University Bratislava · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is currently unknown why obesity leads in some patients to prediabetes and metabolic syndrome. Microinflammation potentially caused by extracellular DNA is supposed to be involved. The aim of this cross-sectional study in healthy mice was to analyze the association between plasma extracellular DNA and glucose metabolism. Fasting glycemia and insulin were measured in healthy adult female mice that subsequently underwent an oral glucose tolerance test. Indices of glucose metabolism and insulin sensitivity were calculated. DNA was isolated from plasma and quantified fluorometrically. Deoxyribonuclease (DNase) activity of plasma was measured using the single radial enzyme diffusion method. Fasting glycemia correlated negatively with both, extracellular DNA and DNase (r = -0.44 and r = -0.32, respectively). DNase was associated positively with the incremental area under curve (r = 0.35), while extracellular DNA correlated negatively with total area under curve of glycemia during oral glucose tolerance test (r = -0.34). Measures of insulin sensitivity were found to be associated with neither extracellular DNA, nor DNase. The hypothesis of an association of low DNase with increased fasting glucose was partially proved. Surprisingly, low extracellular DNA is associated with higher fasting glucose and lower glucose tolerance in mice. As novel therapeutic targets for prediabetes and metabolic syndrome are highly needed, this study provides novel unexpected associations within the limitations of the focus on physiological variability as it was conducted on healthy mice. The causality of these associations should be proved in further interventional experiments.

Indexed as

DeoxyribonucleasesDNAInsulin ResistanceMetabolic SyndromePrediabetic StateAnimalsBlood GlucoseCross-Sectional StudiesFemaleInsulinMiceBlood GlucoseDeoxyribonucleasesDNAInsulin

Identifiers

PMID35385497
PMCPMC8985945
OpenAlexW4225915917

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.