Evidence map›Paper›PMID 35082332›Full record

Trial reportScientific reports2022

Circulating Interleukin-6 and CD16 positive monocytes increase following angioplasty of an arteriovenous fistula.

Seran Hakki, Emily J Robinson, Michael G Robson

Erratum issuedAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Seran HakkiSchool of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, SE1 9RT, UK.
Emily J RobinsonSchool of Population Health and Environmental Sciences, Faculty of Life Sciences and Medicine, King's College London, London, UK.
Michael G RobsonSchool of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, King's College London, Guy's Hospital, London, SE1 9RT, UK. Michael.robson@kcl.ac.uk.ORCID http://orcid.org/0000-0002-1192-1353

Funding

Department of HealthMedical Research Council MC_PC_15109National Institute for Health Research 13/94/10
6 · The paper itself

Abstract

Arteriovenous fistulas are the ideal form of vascular access that allows provision of haemodialysis. Stenotic lesions caused by neointimal hyperplasia commonly occur resulting in patients requiring a fistuloplasty. This is effective but there is a high recurrence rate. We sought to investigate the effects of a fistuloplasty on monocyte populations. Blood samples were taken from patients before and after their fistuloplasty procedure. Samples were analysed using flow cytometry, ELISA and Luminex assays. Univariate cox regression was carried out to investigate associations with post fistuloplasty patency. At 1-2 days post fistuloplasty, the proportion of classical (CD14++CD16-) monocytes decreased (p < 0.001), whilst intermediate (CD14++CD16+) and non-classical (CD14+CD16+) monocytes increased (both p < 0.01) in a cohort of 20 patients. A time course study carried out in 5 patients showed that this was due to an increase in absolute numbers of non-classical and intermediate monocytes. Higher levels of non-classical monocytes pre-fistuloplasty were associated with an increased risk for patency loss (p < 0.05). We measured 41 soluble factors in plasma samples taken before a fistuloplasty in 54 patients, with paired post-fistuloplasty samples (1-2 days) available in 30 patients. After correcting for false discovery, the only factor with a significant change in level was IL-6 (P = 0.0003, q = 0.0124). In a further time-course study in 6 patients, peak level of IL-6 occurred 2-3 h post fistuloplasty. This study demonstrates that there is a systemic inflammatory response to the fistuloplasty procedure and that monocyte subsets and IL-6 may be important in the pathophysiology of restenosis.

Indexed as

AgedAngioplastyArteriovenous FistulaBiomarkersFemaleGene ExpressionGPI-Linked ProteinsHumansHyperplasiaInterleukin-6Lipopolysaccharide ReceptorsMaleMiddle AgedMonocytesNeointimaReceptors, IgGBiomarkersCD14 protein, humanFCGR3B protein, humanGPI-Linked ProteinsIL6 protein, humanInterleukin-6Lipopolysaccharide ReceptorsReceptors, IgG

Identifiers

PMID35082332
PMCPMC8792046

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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.