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Visualization of painful inflammation in patients with pain after traumatic ankle sprain using [(11)C]-D-deprenyl PET/CT.

Aarnio, Mikko (författare)
Uppsala universitet,Anestesiologi och intensivvård
Appel, Lieuwe (författare)
Uppsala universitet,Radiologi
Fredriksson, Mats (författare)
Karolinska Institutet,Uppsala universitet,Institutionen för psykologi,Karolinska Inst, Dept Neurosci, Stockholm, Sweden
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Gordh, Torsten (författare)
Uppsala universitet,Anestesiologi och intensivvård
Wolf, Olof (författare)
Uppsala universitet,Ortopedi
Sörensen, Jens (författare)
Uppsala universitet,Radiologi
Eriksson, Måns, 1986- (författare)
Uppsala universitet,Statistiska institutionen
Peterson, Magnus, 1966- (författare)
Uppsala universitet,Allmänmedicin och preventivmedicin
Linnman, Clas (författare)
Harvard Med Sch, Boston Childrens Hosp, Dept Anesthesiol, Boston, MA USA
Thulin, M (författare)
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 (creator_code:org_t)
Walter de Gruyter, 2017
2017
Engelska.
Ingår i: Scandinavian Journal of Pain. - : Walter de Gruyter. - 1877-8860 .- 1877-8879. ; 17:1, s. 418-424
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND AND AIMS: Positron emission tomography (PET) with the radioligand [(11)C]-D-deprenyl has shown increased signal at location of pain in patients with rheumatoid arthritis and chronic whiplash injury. The binding site of [(11)C]-D-deprenyl in peripheral tissues is suggested to be mitochondrial monoamine oxidase in cells engaged in post-traumatic inflammation and tissue repair processes. The association between [(11)C]-D-deprenyl uptake and the transition from acute to chronic pain remain unknown. Further imaging studies of musculoskeletal pain at the molecular level would benefit from establishing a clinical model in a common and well-defined injury in otherwise healthy and drug-naïve subjects. The aim of this study was to investigate if [(11)C]-D-deprenyl uptake would be acutely elevated in unilateral ankle sprain and if tracer uptake would be reduced as a function of healing, and correlated with pain localizations and pain experience.METHODS: Eight otherwise healthy patients with unilateral ankle sprain were recruited at the emergency department. All underwent [(11)C]-D-deprenyl PET/CT in the acute phase, at one month and 6-14 months after injury.RESULTS: Acute [(11)C]-D-deprenyl uptake at the injury site was a factor of 10.7 (range 2.9-37.3) higher than the intact ankle. During healing, [(11)C]-D-deprenyl uptake decreased, but did not normalize until after 11 months. Patients experiencing persistent pain had prolonged [(11)C]-D-deprenyl uptake in painful locations.CONCLUSIONS AND IMPLICATIONS: The data provide further support that [(11)C]-D-deprenyl PET can visualize, quantify and follow processes in peripheral tissue that may relate to soft tissue injuries, inflammation and associated nociceptive signaling. Such an objective correlate would represent a progress in pain research, as well as in clinical pain diagnostics and management.

Nyckelord

Ankle injuries
Carbon-11
Deprenyl
Inflammation
PET
Pain

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