Evidence map›Paper›PMID 26694930›Full record

ArticlePloS one2015

A Transcriptional Signature of Fatigue Derived from Patients with Primary Sjögren's Syndrome.

Katherine James, Shereen Al-Ali, Jessica Tarn, Simon J Cockell, Colin S Gillespie, Victoria Hindmarsh, James Locke, Sheryl Mitchell, Dennis Lendrem, Simon Bowman and 30 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 177 citations in OpenAlex.

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  11. Review
  12. IRF9 and XAF1 as Diagnostic Markers of Primary Sjogren Syndrome.Computational and mathematical methods in medicine · 2022
    Article
  13. Genetic Variants of theFrontiers in immunology · 2022
    Article
  14. New developments in Sjogren's syndrome.Rheumatology (Oxford, England) · 2021
    Review
  15. Review
  16. Article
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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

40 authors at 20 institutions in 2 countries.

Katherine JamesInterdisciplinary Computing and Complex BioSystems Research Group, Newcastle University, Newcastle upon Tyne, United Kingdom.
Shereen Al-AliMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Jessica TarnMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Simon J CockellBioinformatics Support Unit, Newcastle University, Newcastle upon Tyne, United Kingdom.
Colin S GillespieSchool of Mathematics & Statistics, Newcastle University, Newcastle upon Tyne, United Kingdom.
Victoria HindmarshNewcastle-upon-Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
James LockeMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Sheryl MitchellNewcastle-upon-Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
Dennis LendremMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Simon BowmanRheumatology Department, University Hospital Birmingham, Birmingham, United Kingdom.
Elizabeth PriceGreat Western Hospitals NHS Foundation Trust, Swindon, United Kingdom.
Colin T PeaseSection of Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds & NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals Trust, Leeds, United Kingdom.
Paul EmerySection of Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds & NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals Trust, Leeds, United Kingdom.
Peter LanyonNottingham University Hospital, Nottingham, United Kingdom.
John A HunterGartnavel General Hospital, Glasgow, United Kingdom.
Monica GuptaGartnavel General Hospital, Glasgow, United Kingdom.
Michele BombardieriBarts and the London NHS Trust & Barts and the London School of Medicine and Dentistry, London, United Kingdom.
Nurhan SutcliffeBarts and the London NHS Trust & Barts and the London School of Medicine and Dentistry, London, United Kingdom.
Costantino PitzalisBarts and the London NHS Trust & Barts and the London School of Medicine and Dentistry, London, United Kingdom.
John McLarenNHS Fife, Whyteman's Brae Hospital, Kirkcaldy, United Kingdom.
Annie CooperRoyal Hampshire County Hospital, Winchester, United Kingdom.
Marian ReganRoyal Derby Hospital, Derby, United Kingdom.
Ian GilesUniversity College London Hospitals NHS Foundation Trust, London, United Kingdom.
David IsenbergUniversity College London Hospitals NHS Foundation Trust, London, United Kingdom.
Vadivelu SaravananQueen Elizabeth Hospital, Gateshead, United Kingdom.
David CoadySunderland Royal Hospital, Sunderland, United Kingdom.
Bhaskar DasguptaSouthend University Hospital, Southend, United Kingdom.
Neil McHughRoyal National Hospital for Rheumatic Diseases, Bath, United Kingdom.
Steven Young-MinPortsmouth Hospitals NHS Trust, Portsmouth, United Kingdom.
Robert MootsAintree University Hospitals, Liverpool, United Kingdom.
Nagui GendiBasildon Hospital, Basildon, United Kingdom.
Mohammed AkilRoyal Hallamshire Hospital, Sheffield, United Kingdom.
Bridget GriffithsNewcastle-upon-Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
UK Primary Sjögren’s Syndrome registry
Anil WipatInterdisciplinary Computing and Complex BioSystems Research Group, Newcastle University, Newcastle upon Tyne, United Kingdom.
Julia NewtonNewcastle-upon-Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom.
David E JonesMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
John IsaacsMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Jennifer HallinanInterdisciplinary Computing and Complex BioSystems Research Group, Newcastle University, Newcastle upon Tyne, United Kingdom.
Wan-Fai NgMusculoskeletal Research Group, Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Newcastle University · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBNational Institute for Health Research · GBBarts Health NHS Trust · GBGartnavel General Hospital · GBUniversity College London Hospitals NHS Foundation Trust · GBUniversity of Leeds · GBBasildon Hospital · GBGreat Western Hospitals NHS Foundation Trust · GBNHS Fife · GBNIHR Surgical Reconstruction and Microbiology Research Centre · GBPortsmouth Hospitals NHS Trust · GBQueen Elizabeth Hospital · GBRoyal Derby Hospital · GBRoyal Hallamshire Hospital · GBRoyal Hampshire County Hospital · GBRoyal National Hospital for Rheumatic Diseases · GBSouthend University Hospital NHS Foundation Trust · GBSunderland Royal Hospital · GBUniversity of Basrah · IQ

Funding

Arthritis Research UK 18475Medical Research Council G0800629Medical Research Council MR/J002720/1Medical Research Council MR/N003063/1
6 · The paper itself

Abstract

backgroundFatigue is a debilitating condition with a significant impact on patients' quality of life. Fatigue is frequently reported by patients suffering from primary Sjögren's Syndrome (pSS), a chronic autoimmune condition characterised by dryness of the eyes and the mouth. However, although fatigue is common in pSS, it does not manifest in all sufferers, providing an excellent model with which to explore the potential underpinning biological mechanisms.

methodsWhole blood samples from 133 fully-phenotyped pSS patients stratified for the presence of fatigue, collected by the UK primary Sjögren's Syndrome Registry, were used for whole genome microarray. The resulting data were analysed both on a gene by gene basis and using pre-defined groups of genes. Finally, gene set enrichment analysis (GSEA) was used as a feature selection technique for input into a support vector machine (SVM) classifier. Classification was assessed using area under curve (AUC) of receiver operator characteristic and standard error of Wilcoxon statistic, SE(W).

resultsAlthough no genes were individually found to be associated with fatigue, 19 metabolic pathways were enriched in the high fatigue patient group using GSEA. Analysis revealed that these enrichments arose from the presence of a subset of 55 genes. A radial kernel SVM classifier with this subset of genes as input displayed significantly improved performance over classifiers using all pathway genes as input. The classifiers had AUCs of 0.866 (SE(W) 0.002) and 0.525 (SE(W) 0.006), respectively.

conclusionsSystematic analysis of gene expression data from pSS patients discordant for fatigue identified 55 genes which are predictive of fatigue level using SVM classification. This list represents the first step in understanding the underlying pathophysiological mechanisms of fatigue in patients with pSS.

Indexed as

TranscriptomeAdultAgedArea Under CurveFatigueFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedOligonucleotide Array Sequence AnalysisSeverity of Illness IndexSjogren's Syndrome

Identifiers

PMID26694930
PMCPMC4687914
OpenAlexW638751764

What OpenQuestion holds

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LicenceCC BY
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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.