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Sökning: id:"swepub:oai:DiVA.org:uu-319693" > Evidence of both sy...

Evidence of both systemic inflammation and neuroinflammation in fibromyalgia patients, as assessed by a multiplex protein panel applied to the cerebrospinal fluid and to plasma

Bäckryd, Emmanuel, 1974- (författare)
Linköpings universitet,Avdelningen för samhällsmedicin,Medicinska fakulteten,Region Östergötland, Smärt och rehabiliteringscentrum
Tanum, Lars (författare)
Akershus Univ Hosp, Dept R&D Mental Hlth, Lorenskog, Norway.,Akershus University Hospital, Norway
Lind, Anne-Li (författare)
Uppsala universitet,Anestesiologi och intensivvård,Uppsala University, Sweden
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Larsson, Anders (författare)
Uppsala universitet,Institutionen för medicinska vetenskaper,Uppsala University, Sweden
Gordh, Torsten (författare)
Uppsala universitet,Anestesiologi och intensivvård,Uppsala University, Sweden
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 (creator_code:org_t)
DOVE MEDICAL PRESS LTD, 2017
2017
Engelska.
Ingår i: Journal of Pain Research. - : DOVE MEDICAL PRESS LTD. - 1178-7090. ; 10
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • In addition to central hyperexcitability and impaired top-down modulation, chronic inflammation probably plays a role in the pathophysiology of fibromyalgia (FM). Indeed, on the basis of both animal experiments and human studies involving the analysis of cytokines and other inflammation-related proteins in different body fluids, neuroinflammatory mechanisms are considered to be central to the pathophysiology of many chronic pain conditions. However, concerning FM, previous human plasma/serum and/or cerebrospinal fluid (CSF) cytokine studies have looked only at a few predetermined cytokine candidates. Instead of analyzing only a few substances at a time, we used a new multiplex protein panel enabling simultaneous analysis of 92 inflammation-related proteins. Hence, we investigated the CSF and plasma inflammatory profiles of 40 FM patients compared with CSF from healthy controls (n= 10) and plasma from blood donor controls (n= 46). Using multivariate data analysis by projection, we found evidence of both neuroinflammation (as assessed in CSF) and chronic systemic inflammation (as assessed in plasma). Two groups of proteins (one for CSF and one for plasma) highly discriminating between patients and controls are presented. Notably, we found high levels of CSF chemokine CX3CL1 (also known as fractalkine). In addition, previous findings concerning IL-8 in FM were replicated, in both CSF and plasma. This is the first time that such an extensive inflammatory profile has been described for FM patients. Hence, FM seems to be characterized by objective biochemical alterations, and the lingering characterization of its mechanisms as essentially idiopathic or even psychogenic should be seen as definitively outdated.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

cerebrospinal fluid
chemokines
chronic pain
cytokines
fibromyalgia
inflammation

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