Evidence map›Paper›PMID 28542479›Full record

ArticlePloS one2017

Preliminary study of hypoxia-related cardiovascular mediator-markers in patients with end-stage renal disease with and without diabetes and the effects of haemodialysis.

A Treweeke, J Hall, S Lambie, S J Leslie, I L Megson, S M MacRury

Open access · goldAbstract read
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Article in PloS one, 2017. 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
0.5field-weighted citation impact, top 35% 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

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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, 4 citations in OpenAlex.

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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 1 country.

A TreweekeDivision of Health Research, University of the Highlands and Islands, Inverness, Scotland.
J HallDivision of Health Research, University of the Highlands and Islands, Inverness, Scotland.
S LambieDepartment of Medicine, Raigmore Hospital, Inverness, Scotland.
S J LeslieDivision of Health Research, University of the Highlands and Islands, Inverness, Scotland.
I L MegsonDivision of Health Research, University of the Highlands and Islands, Inverness, Scotland.
S M MacRuryDivision of Health Research, University of the Highlands and Islands, Inverness, Scotland.ORCID http://orcid.org/0000-0001-7599-1302
Raigmore Hospital · GBUniversity of the Highlands and Islands · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence points to activation of pro-inflammatory and pro-thrombotic stimuli during the haemodialysis process in end-stage renal disease (ESRD) with potential to predispose to cardiovascular events. Diabetes is associated with a higher incidence of cardiovascular disease in haemodialysis patients. We tested the hypothesis that a range of mediators and markers that modulate cardiovascular risk are elevated in haemodialysis patients with diabetes compared to those without.

methodsMen and women with diabetes (n = 6) and without diabetes (n = 6) aged 18-90 years receiving haemodialysis were recruited. Blood samples were collected and analysed pre- and post-haemodialysis sessions for (platelet-monocyte conjugates (PMC), oxidised LDL (Ox-LDL), endothelin 1 (ET-1) and vascular endothelial growth factor (VEGF-A).

resultsPMC levels significantly increased after haemodialysis in both groups (diabetes p = 0.047; non-diabetes p = 0.005). Baseline VEGF-A was significantly higher in people with diabetes (p = 0.009) and post-dialysis levels were significantly reduced in both groups (P = 0.002). Ox-LDL and CRP concentrations were not significantly different between groups nor affected in either group post-dialysis. Similarly, ET-1 concentrations were comparable in all patients at baseline, with no change post-dialysis in either group.

conclusionsIn this pilot study, we have confirmed that circulating PMCs are increased following dialysis irrespective of diabetes status. This is likely to be a mechanistic process and offers a potential explanation for high rates of vascular events associated with haemodialysis. The higher VEGF-A concentrations between patients with and without diabetes is a previously unreported finding in diabetic ESRD. Further research is merited to establish whether VEGF-A is a marker or mediator (or both) of cardiovascular risk in haemodialysis.

Indexed as

Renal DialysisAdolescentAdultAgedAged, 80 and overBiomarkersCardiovascular DiseasesCholesterol, LDLDiabetes ComplicationsEndothelin-1FemaleHumansHypoxiaKidney Failure, ChronicMaleMiddle AgedBiomarkersCholesterol, LDLEndothelin-1Vascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID28542479
PMCPMC5441650
OpenAlexW2617618426

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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.