6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Pain sensitivity in young adults with juvenile idiopathic arthritis: a quantitative sensory testing study

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          To study for the first-time, pain perception, pain sensitivity, and self-reported pain in young adults with long disease duration of juvenile idiopathic arthritis (JIA) compared with controls.

          Methods

          Children from Central Norway diagnosed with JIA between 1997 and 2004 were included consecutively in a population-based prospective study. Children with onset 1997–2000 were part of the Nordic JIA cohort. Controls were age- and sex-matched. In 2015–2017, study visits with investigator-blinded quantitative sensory testing (QST) comprising cold and warm detection thresholds (CDT/WDT), cold and heat pain thresholds (CPT/HPT), pressure pain threshold (PPT), and a suprathreshold heat pain test were performed. We constructed separate multilevel models for each variable of detection and pain thresholds with interaction between groups and site adjusted for the effect of age and sex.

          Results

          Among 96 young adults with JIA, 71% were female, median age was 22.7 years, disease duration was 16.1 years, and 47% had oligoarticular disease. Among 109 controls, 71% were female, and median age was 23.5 years. Participants with JIA had lower pressure pain thresholds (PPTs) (95% CI) compared to controls, upper limb 888 (846,930) versus 1029 (999,1059) kPa and lower limb 702 (670,734) versus 760 (726,794) kPa. Participants with inactive disease had the lowest PPTs and cold pain thresholds (CPTs), compared to those in remission off medication and those with active disease. Minor differences were found regarding CDT/WDT and CPT/HPT in JIA compared to controls. The median (IQR) temperature needed to evoke pain = 6 on a 0–10 numeric rating scale (NRS) in the suprathreshold heat pain tests were lower in JIA than in controls (46 °C (45–47 °C) versus 47 °C (46–48 °C)). We found no associations between self-reported pain and pain thresholds.

          Conclusions

          Our results indicate for the first time that young adults with long disease duration of JIA may have altered pain perception and sensitivity compared to controls. A clinical implication may be the importance of early treatment to quickly achieve pain-free remission and avoid long-term pain sensitization.

          Related collections

          Most cited references48

          • Record: found
          • Abstract: found
          • Article: not found

          Central sensitization: a generator of pain hypersensitivity by central neural plasticity.

          Central sensitization represents an enhancement in the function of neurons and circuits in nociceptive pathways caused by increases in membrane excitability and synaptic efficacy as well as to reduced inhibition and is a manifestation of the remarkable plasticity of the somatosensory nervous system in response to activity, inflammation, and neural injury. The net effect of central sensitization is to recruit previously subthreshold synaptic inputs to nociceptive neurons, generating an increased or augmented action potential output: a state of facilitation, potentiation, augmentation, or amplification. Central sensitization is responsible for many of the temporal, spatial, and threshold changes in pain sensibility in acute and chronic clinical pain settings and exemplifies the fundamental contribution of the central nervous system to the generation of pain hypersensitivity. Because central sensitization results from changes in the properties of neurons in the central nervous system, the pain is no longer coupled, as acute nociceptive pain is, to the presence, intensity, or duration of noxious peripheral stimuli. Instead, central sensitization produces pain hypersensitivity by changing the sensory response elicited by normal inputs, including those that usually evoke innocuous sensations. In this article, we review the major triggers that initiate and maintain central sensitization in healthy individuals in response to nociceptor input and in patients with inflammatory and neuropathic pain, emphasizing the fundamental contribution and multiple mechanisms of synaptic plasticity caused by changes in the density, nature, and properties of ionotropic and metabotropic glutamate receptors.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            International League of Associations for Rheumatology classification of juvenile idiopathic arthritis: second revision, Edmonton, 2001.

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              SF-36 Health Survey Update

                Bookmark

                Author and article information

                Contributors
                ellen.d.arnstad@ntnu.no
                Journal
                Arthritis Res Ther
                Arthritis Res Ther
                Arthritis Research & Therapy
                BioMed Central (London )
                1478-6354
                1478-6362
                5 November 2020
                5 November 2020
                2020
                : 22
                : 262
                Affiliations
                [1 ]GRID grid.414625.0, ISNI 0000 0004 0627 3093, Department of Pediatrics, Levanger Hospital, , Nord-Trøndelag Hospital Trust, ; Levanger, Norway
                [2 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Department of Clinical and Molecular Medicine, , NTNU—Norwegian University of Science and Technology, ; Trondheim, Norway
                [3 ]GRID grid.416371.6, ISNI 0000 0001 0558 0946, Department of Internal Medicine, , Nordland Hospital, ; Bodø, Norway
                [4 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Department of Neuromedicine and Movement Science, , NTNU—Norwegian University of Science and Technology, ; Trondheim, Norway
                [5 ]GRID grid.52522.32, ISNI 0000 0004 0627 3560, Department of Neurology and Clinical Neurophysiology, , St. Olavs Hospital, ; Trondheim, Norway
                [6 ]GRID grid.154185.c, ISNI 0000 0004 0512 597X, Department of Pediatrics, , Aarhus University Hospital, ; Aarhus, Denmark
                [7 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Department of Public Health and Nursing, , NTNU—Norwegian University of Science and Technology, ; Trondheim, Norway
                [8 ]GRID grid.52522.32, ISNI 0000 0004 0627 3560, Department of Pediatrics, , St. Olavs Hospital, ; Trondheim, Norway
                Author information
                http://orcid.org/0000-0003-0635-5198
                Article
                2345
                10.1186/s13075-020-02345-2
                7643261
                33153493
                3dcd767f-8612-496e-bba7-7902c5c99034
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 14 September 2020
                : 5 October 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100009123, Norges Teknisk-Naturvitenskapelige Universitet;
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                Orthopedics
                juvenile idiopathic arthritis (jia),young adults,long-term outcomes,quantitative sensory testing (qst) ,pain threshold,pain perception,pain sensitivity,pain sensitization,self-reported pain

                Comments

                Comment on this article