Evidence map›Paper›PMID 27090392›Full record

Trial reportRedox report : communications in free radical research2017

Oxidative stress is associated with decreased heart rate variability in patients with chronic kidney disease.

Shannon B Fadaee, Kassia S Beetham, Erin J Howden, Tony Stanton, Nicole M Isbel, Jeff S Coombes

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Redox report : communications in free radical research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

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  15. A Cross Sectional Study Evaluating Psychosocial Job Stress and Health Risk in Emergency Department Nurses.International journal of environmental research and public health · 2019
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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

6 authors at 2 institutions in 2 countries.

Shannon B Fadaeea School of Human Movement and Nutrition Sciences, The University of Queensland , Brisbane , Australia.
Kassia S Beethama School of Human Movement and Nutrition Sciences, The University of Queensland , Brisbane , Australia.
Erin J Howdenb Institute for Exercise and Environmental Medicine, University of Texas Southwestern Medical Centre , Dallas , USA.
Tony Stantonc School of Medicine, The University of Queensland , Brisbane , Australia.
Nicole M Isbelc School of Medicine, The University of Queensland , Brisbane , Australia.
Jeff S Coombesa School of Human Movement and Nutrition Sciences, The University of Queensland , Brisbane , Australia.
The University of Queensland · AUInstitute for Exercise and Environmental Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesElevated oxidative stress and reduced heart rate variability (HRV) is prevalent in patients with chronic kidney disease (CKD) and is associated with increased morbidity and mortality. Previous studies have identified a positive association between elevated oxidative stress and autonomic dysfunction, however this relationship has not yet been investigated in the CKD population.

methodsPlasma was collected from 78 patients with stage 3-4 CKD (estimated glomerular filtration rate 25-60 ml/min/1.73 m

resultsParticipants with elevated F2-isoprostanes had reduced HRV compared to patients with normal levels of F2-isoprostanes. A number of HRV parameters were found to be inversely correlated with F2-isoprostanes in all CKD patients, including SDNN (r = -0.337; P < 0.01), VLF (r = -0.281, P = 0.01), LF (r = -0.315, P < 0.01) and total power (r = -0.288, P = 0.01). Multiple linear regression found F2-isoprostanes to be an independent predictor of SDNN (r DISCUSSION: Oxidative stress is significantly and independently associated with HRV in patients with CKD. Identifying oxidative stress in the pathogenesis of autonomic dysfunction may help target therapeutic strategies.

Indexed as

Oxidative StressAgedAntioxidantsCross-Sectional StudiesF2-IsoprostanesFemaleGlutathione PeroxidaseHeart RateHumansMaleMiddle AgedRegression AnalysisRenal Insufficiency, ChronicAntioxidantsF2-IsoprostanesGlutathione PeroxidaseAutonomic dysfunctionChronic kidney diseaseHeart rate variabilityOxidative stress

Identifiers

PMID27090392
PMCPMC6837656
OpenAlexW2341642068

What OpenQuestion holds

Textmetadata
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.