Evidence map›Paper›PMID 28446191›Full record

Observational studyJournal of translational medicine2017

Longitudinal analysis of serum oxylipin profile as a novel descriptor of the inflammatory response to surgery.

Arnaud M Wolfer, Alasdair J Scott, Claudia Rueb, Mathieu Gaudin, Ara Darzi, Jeremy K Nicholson, Elaine Holmes, James M Kinross

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 16 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

8 authors at 2 institutions in 1 country.

Arnaud M WolferDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Alasdair J ScottDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Claudia RuebImperial College Healthcare NHS Trust, London, UK.
Mathieu GaudinDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Ara DarziDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Jeremy K NicholsonDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Elaine HolmesDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK. elaine.holmes@imperial.ac.uk.
James M KinrossDivision of Computational and Systems Medicine, Department of Surgery and Cancer, Imperial College London, London, UK.
Imperial College London · GBImperial College Healthcare NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOxylipins are potent lipid mediators demonstrated to initiate and regulate inflammation yet little is known regarding their involvement in the response to surgical trauma. As key modulators of the inflammatory response, oxylipins have the potential to provide novel insights into the physiological response to surgery and the pathophysiology of post-operative complications. We aimed to investigate the effects of major surgery on longitudinal oxylipin profile.

methodsAdults patients undergoing elective laparoscopic or open colorectal resections were included. Primary outcomes were serum oxylipin profile quantified by ultra high-performance liquid chromatography-mass spectrometry, serum white cell count and C-reactive protein concentration. Serum samples were taken at three time-points: pre-operative (day zero), early post-operative (day one) and late post-operative (day four/five).

resultsSome 55 patients were included, of which 33 (60%) underwent surgery that was completed laparoscopically. Pre-operative oxylipin profiles were characterised by marked heterogeneity but surgery induced a common shift resulting in more homogeneity at the early post-operative time-point. By the late post-operative phase, oxylipin profiles were again highly variable. This evolution was driven by time-dependent changes in specific oxylipins. Notably, the levels of several oxylipins with anti-inflammatory properties (15-HETE and four regioisomers of DHET) were reduced at the early post-operative point before returning to baseline by the late post-operative period. In addition, levels of the pro-inflammatory 11-HETE rose in the early post-operative phase while levels of anti-thrombotic mediators (9-HODE and 13-HODE) fell; concentrations of all three oxylipins then remained fairly static from early to late post-operative phases. Compared to those undergoing laparoscopic surgery, patients undergoing open surgery had lower levels of some anti-inflammatory oxylipins (8,9-DHET and 17-HDoHE) in addition to reduced concentrations of anti-thrombotic mediators (9-HODE and 13-HODE) with increased concentration of their pro-thrombotic counterpart (TxB2).

conclusionsSerum oxylipin profile is modified by surgical intervention and may even be sensitive to the degree of surgical trauma and therefore represents a novel descriptor of the surgical systemic inflammatory response.

Indexed as

LaparoscopyAgedC-Reactive ProteinDemographyFatty Acids, UnsaturatedFemaleHumansInflammationLeukocyte CountLongitudinal StudiesMaleMiddle AgedOxylipinsPrincipal Component AnalysisTime FactorsC-Reactive ProteinFatty Acids, UnsaturatedOxylipinsColorectal surgeryMass spectrometryMetabonomicsOxylipinSurgerySystemic inflammatory response syndrome

Identifiers

PMID28446191
PMCPMC5405545
OpenAlexW2608314123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.