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dc.contributor.authorSchistad, Ellina Iordanova
dc.contributor.authorKong, Xiang Yi
dc.contributor.authorFurberg, Anne-Sofie
dc.contributor.authorBäckryd, Emmanuel
dc.contributor.authorGrimnes, Guri
dc.contributor.authorEmaus, Nina
dc.contributor.authorRosseland, Leiv Arne
dc.contributor.authorGordh, Torsten
dc.contributor.authorStubhaug, Audun
dc.contributor.authorEngdahl, Bo Lars
dc.contributor.authorHalvorsen, Bente Evy
dc.contributor.authorNielsen, Christopher Sivert
dc.date.accessioned2020-02-19T07:18:10Z
dc.date.available2020-02-19T07:18:10Z
dc.date.issued2019-10-21
dc.description.abstractTwo recent studies suggest that experimental pain sensitivity is associated with low-grade systemic inflammation. However, only 2 biomarkers have been identified, and the studies were conducted in adult individuals where confounding effects of comorbid diseases cannot be excluded. We therefore tested associations between pain sensitivity and 119 inflammation-related serum biomarkers in 827 healthy adolescents (15-19 years) in the population-based Tromsø Study: Fit Futures. The main outcome measure was cold-pressor pain tolerance (CPT), tested by placing the dominant hand in circulating cold (3°C) water for a maximum of 105 seconds. Secondary outcomes were heat and pressure pain threshold and tolerance. Twelve proteins and 6 fatty acids were significantly associated with CPT after adjustment for possible confounding factors and correction for multiple comparisons. Of these, all fatty acids and 10 proteins were protective, ie, higher biomarkers levels were associated with increased CPT, whereas 2 biomarkers were associated with lower tolerance. Taken together, these biomarkers predicted completion of the tolerance test with a C-statistic of 0.65. Results for heat and pressure pain tolerance were remarkably similar, strengthening the generalizability of our findings. In this cohort of young healthy individuals, we found a relationship between inflammation-related biomarkers and pain tolerance and thresholds. Biomarkers with anti-inflammatory and analgesic effects predominated, suggesting that the development of prophylactic dietary or pharmaceutical treatments may be possible.en_US
dc.descriptionThis is a non-final version of an article published in final form in Schistad, E. I., Kong, X. Y., Furberg, A.-S., Bäckryd, E., Grimnes, G., Emaus, N., ... Nielsen, C. S. (2019). A population-based study of inflammatory mechanisms and pain sensitivity. <i>Pain, 161</i>(2), 338-350. <a href=https://doi.org/10.1097/j.pain.0000000000001731>https://doi.org/10.1097/j.pain.0000000000001731</a>en_US
dc.identifier.citationSchistad E, Kong XY, Furberg, Bäckryd, Grimnes, Emaus N, Rosseland, Gordh, Stubhaug, Engdahl, Halvorsen, Nielsen. A population-based study of inflammatory mechanisms and pain sensitivity. Pain. 2019;161(2):338-350en_US
dc.identifier.cristinIDFRIDAID 1758360
dc.identifier.doi10.1097/j.pain.0000000000001731
dc.identifier.issn0304-3959
dc.identifier.issn1872-6623
dc.identifier.urihttps://hdl.handle.net/10037/17420
dc.language.isoengen_US
dc.publisherLippincott, Williams & Wilkinsen_US
dc.relation.journalPain
dc.rights.accessRightsopenAccessen_US
dc.rights.holder© 2019 International Association for the Study of Painen_US
dc.subjectVDP::Medical disciplines: 700en_US
dc.subjectVDP::Medisinske Fag: 700en_US
dc.titleA population-based study of inflammatory mechanisms and pain sensitivityen_US
dc.type.versionacceptedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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