Evidence map›Paper›PMID 26921255›Full record

ArticleInnate immunity2016

Heat shock proteins and chronic fatigue in primary Sjögren's syndrome.

Kjetil Bårdsen, Mari Mæland Nilsen, Jan Terje Kvaløy, Katrine Brække Norheim, Grete Jonsson, Roald Omdal

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Innate immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05587777 (REsearch on BrEast Cancer Induced Chronic Conditions Supported by Causal Analysis of Multi-source Data), which is not on this map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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.

NCT05587777 recruitingnot on this mapstarted 2022, after this paper: background citation

REsearch on BrEast Cancer Induced Chronic Conditions Supported by Causal Analysis of Multi-source Data

TypeobservationalSponsorHelse Stavanger HFRan2022 to 2028Enrolled150ConditionsBreast Cancer, Chronic Fatigue Syndrome
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Genetic variants at theRMD open · 2021
    Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The Involvement of Alarmins in the Pathogenesis of Sjögren's Syndrome.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Genetic Variants of theFrontiers in immunology · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Heat-shock protein 90Innate immunity · 2020
    Article
  19. Article
  20. Article
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 4 institutions in 1 country.

Kjetil BårdsenResearch Department, Stavanger University Hospital, Stavanger, Norway.
Mari Mæland NilsenInternational Research Institute of Stavanger, Stavanger, Norway.
Jan Terje KvaløyResearch Department, Stavanger University Hospital, Stavanger, Norway Department of Mathematics and Natural Sciences, University of Stavanger, Stavanger, Norway.
Katrine Brække NorheimClinical Immunology Unit, Department of Internal Medicine, Stavanger University, Hospital, Stavanger, Norway.
Grete JonssonDepartment of Medical Biochemistry, Stavanger University Hospital, Stavanger, Norway.
Roald OmdalClinical Immunology Unit, Department of Internal Medicine, Stavanger University, Hospital, Stavanger, Norway Department of Medical Science, Faculty of Medicine and Dentistry, University of Bergen, Bergen, Norway roald.omdal@sus.no.
Stavanger University Hospital · NOInternational Research Institute of Stavanger · NOUniversity of Bergen · NOUniversity of Stavanger · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fatigue occurs frequently in patients with cancer, neurological diseases and chronic inflammatory diseases, but the biological mechanisms that lead to and regulate fatigue are largely unknown. When the innate immune system is activated, heat shock proteins (HSPs) are produced to protect cells. Some extracellular HSPs appear to recognize cellular targets in the brain, and we hypothesize that fatigue may be generated by specific HSPs signalling through neuronal or glial cells in the central nervous system. From a cohort of patients with primary Sjögren's syndrome, 20 patients with high and 20 patients with low fatigue were selected. Fatigue was evaluated with a fatigue visual analogue scale. Plasma concentrations of HSP32, HSP60, HSP72 and HSP90α were measured and analysed to determine if there were associations with the level of fatigue. Plasma concentrations of HSP90α were significantly higher in patients with high fatigue compared with those with low fatigue, and there was a tendency to higher concentrations of HSP72 in patients with high fatigue compared with patients with low fatigue. There were no differences in concentrations of HSP32 and HSP60 between the high- and low-fatigue groups. Thus, extracellular HSPs, particularly HSP90α, may signal fatigue in chronic inflammation. This supports the hypothesis that fatigue is generated by cellular defence mechanisms.

Indexed as

AdultAgedAged, 80 and overBrainChronic DiseaseFatigueFemaleHSP90 Heat-Shock ProteinsHumansMaleMiddle AgedNeuronsSjogren's SyndromeHSP90 Heat-Shock Proteinsautoimmune diseasescellular stressChronic fatigueheat shock proteinsinnate immunitySjögren’s syndrome

Identifiers

PMID26921255
PMCPMC4804286
OpenAlexW2329083176

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.