Malmö University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Orofacial pain in juvenile idiopathic arthritis is associated with stress as well as psychosocial and functional limitations
Malmö University, Faculty of Odontology (OD). Linkoping Univ, Ctr Oral Rehabil Linkoping, Linkoping, Sweden.;Linkoping Univ, Dept Biomed & Clin Sci, Linkoping, Sweden.;Scandinavian Ctr Orofacial Neurosci, Malmo, Sweden..ORCID iD: 0000-0002-2260-8442
Kalmar Cty Hosp, Dept Stomatognath Physiol, Kalmar, Sweden..
Vasterv Hosp, Dept Pediat, Vastervik, Sweden.;Linkoping Univ, Dept Clin & Expt Med, Div Pediat, Linkoping, Sweden.;Skaraborg Hosp, Dept Pediat, Skovde, Sweden..
Linkoping Univ, Dept Clin & Expt Med, Div Neuro & Inflammat Sci, Linkoping, Sweden..
Show others and affiliations
2019 (English)In: Pediatric Rheumatology, E-ISSN 1546-0096, Vol. 17, no 1, article id 83Article in journal (Refereed) Published
Abstract [en]

Background The aim of this study was to investigate relations between psychosocial factors, signs and symptoms of orofacial pain and jaw dysfunction in patients with juvenile idiopathic arthritis (JIA). Methods Forty-five patients with JIA (median age 12 years) and 16 healthy matched controls (median age 13 years) were examined according to the diagnostic criteria for temporomandibular disorders (DC/TMD). The subjects answered the DC/TMD questionnaires regarding psychosocial factors (pain intensity, pain-related disability, depression, stress, catastrophizing, pain locations and jaw function). Results JIA patients with orofacial pain had higher degree of stress, depression, catastrophizing and jaw dysfunction compared to subjects without. In turn, these factors were associated with orofacial pain intensity. Also, patients with orofacial pain had higher systemic inflammatory activity. Conclusions Orofacial pain in patients with JIA is associated with stress, psychological distress, jaw dysfunction and loss of daily living activities. Pain intensity seems to be the major pain aspect related to these factors. In addition, systemic inflammatory activity appears to be an important factor contributing to orofacial pain in JIA.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2019. Vol. 17, no 1, article id 83
Keywords [en]
Adolescents, Children, Juvenile idiopathic arthritis, Orofacial pain, Psychosocial, Stress Temporomandibular joint disorders
National Category
Rheumatology and Autoimmunity
Identifiers
URN: urn:nbn:se:mau:diva-17239DOI: 10.1186/s12969-019-0385-7ISI: 000512605400001PubMedID: 31856854Scopus ID: 2-s2.0-85077044869OAI: oai:DiVA.org:mau-17239DiVA, id: diva2:1430025
Available from: 2020-05-13 Created: 2020-05-13 Last updated: 2024-03-21Bibliographically approved
In thesis
1. The Temporomandibular Joint in Juvenile Idiopathic Arthritis: Psychosocial, clinical, imaging and parotid saliva biomarkers
Open this publication in new window or tab >>The Temporomandibular Joint in Juvenile Idiopathic Arthritis: Psychosocial, clinical, imaging and parotid saliva biomarkers
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. The disease can affect the temporomandibular joint (TMJ) and cause orofacial growth disturbances, pain, and jaw dysfunction. TMJ arthritis is often asymptomatic and therefore a challenging joint to diagnose. Clinical assessment of the TMJ is hampered by the low sensitivity and specificity of joint pain and the absence of physical findings early in the disease process. More specific methods are therefore needed for diagnosing TMJ arthritis. Saliva and blood are promising as diagnostic fluids for various diseases. Also, adolescents with chronic pain report high rates of psychosocial stress. Psychosocial stress may also be involved in JIA as a trigger and maintaining factor of the disease. Aim: The main aim of this thesis research was to investigate the relation between clinical variables, psychosocial factors, MRI findings, and inflammatory biomarkers in saliva and blood in relation to TMJ involvement in JIA. The secondary aim was to investigate the relation between stress and change in stress over time in comparison with orofacial pain, psychosocial factors, and jaw function in JIA patients. Methods: This was a cross-sectional case-control study and a longitudinal cohort study. Forty-five patients (6-16 years old) with JIA and 16 healthy age- and sex-matched healthy individuals were examined according to the diagnostic criteria for temporomandibular disorders (DC/TMD). The study subjects completed questionnaires regarding psychosocial factors and underwent bilateral MRI of their TMJs. Unstimulated parotid saliva and venous blood samples were collected. Biochemical analyses were performed using a multiplex platform electrochemiluminescence assay from Meso Scale Discovery (MSD) for measuring cytokine concentrations in saliva and blood. A two-year prospective follow-up study was performed in 40 JIA patients from our original baseline study. The JIA patients underwent the same clinical examination and completed the same questionnaires regarding psychosocial factors as in the baseline studies. Results: The JIA patients with orofacial pain had higher degrees of stress, depression, catastrophizing, and jaw dysfunction than did those JIA patients without such pain. These factors were also associated with orofacial pain intensity. Additionally, patients with orofacial pain had higher systemic inflammatory activity. In the two-year follow-up study, we observed that change in stress was associated with changes in catastrophizing, psychological distress, as well as limitations in both general and jaw functions. Regarding TMJ MRI findings, there were no significant differences between JIA patients and healthy individuals in either the inflammatory or damage domain. Moderate/severe TMJ changes in the inflammatory and damage domains were, however, only found in the JIA patients. Among JIA patients, orofacial pain intensity was correlated to TMJ bone marrow edema, and pain in jaw muscles during jaw function was related to both TMJ bone marrow edema and erosion. JIA patients had lower concentrations of interleukin receptor 6 (IL-6R) and glycoprotein 130 (gp130) in parotid saliva than in plasma. Higher concentrations of IL-6 were found in parotid saliva than in plasma. The members of the interleukin-6 family (i.e., IL-6, IL-6R, and gp130) in parotid saliva were found to be explanatory factors for the presence of bone marrow edema and effusion in the JIA patients. Conclusions: Orofacial pain in patients with JIA is associated with stress, psychological distress, jaw dysfunction, and loss of daily living activities. Pain intensity seems to be the major aspect related to these factors. Increased disease activity with more joint involvement seems to be an important factor contributing to orofacial pain in JIA. Myalgia, in addition to arthritis, seems to be an important source of orofacial pain in these patients. Maintaining a low stress level in JIA patients seems to be crucial, as an increase in stress level over a two-year period appears to negatively impact both jaw function as well as psychosocial distress and catastrophizing. There was an overlap of TMJ MRI findings regarding signs of inflammatory and bone tissue changes between JIA patients and healthy individuals. Among, JIA patients, the presence of inflammatory MRI signs, and bone marrow edema seems to worsen orofacial pain intensity. The IL-6 family in parotid saliva is associated with TMJ bone marrow edema and effusion in patients with JIA, suggesting that IL-6 has promising properties as a parotid saliva biomarker of TMJ inflammatory activity. In addition there seems to be local production of the IL-6 family in the parotid gland in JIA patients and healthy individuals. However, parotid saliva does not seem to reflect the plasma content in terms of the investigated biomarkers in JIA.

Abstract [sv]

Juvenil idiopatisk artrit (JIA) är ett samlingsbegrepp för kroniska ledinflammatoriska sjukdomar hos barn. I Sverige insjuknar årligen ungefär 200 barn. För att få diagnosen JIA skall debuten ske före 16 års ålder. Vid JIA kan de flesta leder drabbas med olika problem som följd. Den här avhandlingen fokuserar på käkleden där inflammation (käkledsartrit) på grund av JIA kan orsaka smärta, brosk- och bennedbrytning och nedsatt käkfunktion. Inflammationen kan även påverka tillväxt så att patienterna kan få en liten haka och öppet bett. Samtidigt är det så att många barn med JIA i käkleden inte upplever några symtom, trots en pågående käkledsinflammation. Detta gör det mycket svårt att upptäcka sjukdomen i käkleden tidigt. Idag saknas etablerade och validerade kliniska diagnostiska kriterier för att identifiera patienter med käkledsartrit. Det betyder att metodik för att undersöka patienter och definition av käkledsartrit vid JIA varierar avsevärt, både i det kliniska arbetet och i vetenskapliga studier samt mellan olika kliniker och länder. Syftet med denna avhandling var att undersöka hur smärta och funktion i käksystemet relaterar till generell inflammatorisk aktivitet, biomarkörer i parotissaliv och blod, inflammatoriska förändringar i käkled och psykosociala faktorer, både vid första undersökningen och över en två-årsperiod. Avhandlingen visar bland annat att smärta i käksystemet har tydliga samband med stress och nedsatt käkfunktion där smärtintensiteten verkar vara den viktigaste faktorn. Ökad stress över en två-årsperiod är associerad med försämrad käkfunktion och mående. Det finns ett överlapp av fynd på magnetkamera vad gäller käkledsförändringar mellan patienter med JIA och friska kontroller. Hos patienterna med JIA förefaller benmärgsöden i käkledshuvudet vara relaterat till smärta i käksystemet. När det gäller de inflammationssubstanser vi undersökte i saliv visar denna avhandling att Interleukin-6-familjen möjligen kan ha egenskaper som biomarkör relaterat till benmärgsödem i käkledshuvudet. Sjukdomen JIA är en klinisk utmaning att identifiera, diagnostisera, följa och behandla vad gäller käkleden. Här behövs mycket mer forskning där ett viktigt steg är att etablera valida diagnostiska kriterier. De drabbade barnen kan idag få stora skador i käkleden, ibland med associerad smärta och nedsatt käkfunktion. Sammanfattningsvis visar avhandlingen att stress samt smärta och käkfunktion i hela käksystemet är viktiga faktorer att undersöka och ta med i den kliniska bedömningen och behandlingen. Det överlapp av fynd från käkleden vid undersökning med magnetkamera mellan barn med JIA och friska kontrollen innebär att man behöver tolka fynd från magnetkamera med försiktighet.

Place, publisher, year, edition, pages
Malmö: Malmö University Press, 2024. p. 90
Series
Malmö University Odontological Dissertations, ISSN 1650-6065
Keywords
Biomarkers, Juvenile Idiopathic Arthritis, Magnetic resonance imaging, Orofacial pain, Parotid gland, Plasma, Psychological distress, Psychosocial, Saliva, Stress, Temporomandibular joint, Biomarkörer, Juvenil idiopatisk artrit, Käkled, Magnetisk resonanstomografi, Orofacial smärta, Saliv, Spottkörtel, Stress
National Category
Dentistry
Identifiers
urn:nbn:se:mau:diva-66397 (URN)10.24834/isbn.9789178773763 (DOI)978-91-7877-375-6 (ISBN)978-91-7877-376-3 (ISBN)
Public defence
2024-04-19, Faculty of Odontology, Aulan (KL:2370), Smedjegatan 16, Malmö, 09:15 (Swedish)
Opponent
Supervisors
Funder
Region Östergötland, FOU 2-15-14Medical Research Council of Southeast Sweden (FORSS), FORSS-748481Swedish Dental Association
Note

Paper III is not included in the fulltext online

Paper III in dissertation as manuscript

Available from: 2024-03-22 Created: 2024-03-21 Last updated: 2024-03-22Bibliographically approved

Open Access in DiVA

fulltext(1196 kB)79 downloads
File information
File name FULLTEXT01.pdfFile size 1196 kBChecksum SHA-512
c36de18bc7f5e545a58597ba641a2d18196a8094131076243f1ada68b6cfd3ce2de736fe94680418b7a64e5ce2a32382b380ce3252e855140f97ef78f5019ca9
Type fulltextMimetype application/pdf

Other links

Publisher's full textPubMedScopus

Authority records

Carlsson, Alexandra DimitrijevicAlstergren, Per

Search in DiVA

By author/editor
Carlsson, Alexandra DimitrijevicAlstergren, Per
By organisation
Faculty of Odontology (OD)
In the same journal
Pediatric Rheumatology
Rheumatology and Autoimmunity

Search outside of DiVA

GoogleGoogle Scholar
Total: 79 downloads
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 98 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf