Juvenile idiopathic arthritis - from macrophage to mortality

Forskningsoutput: AvhandlingDoktorsavhandling (sammanläggning)

67 Nedladdningar (Pure)

Sammanfattning

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in children. Studies of the immunopathogenesis in JIA has mainly focused on the adaptive immune system, while less is known of the role of the monocytes. JIA is considered a chronic disease, although only about 50% of participants in long-term follow-up studies have active disease as adults. The treatment arsenal for JIA has expanded during the last three decades, but if this has improved the long-term outcome is not known.

When a diagnosis of JIA is confirmed almost all children and parents ask the same important questions: “Why did I/my child get this disease?”, “What will happen to me now?” and “Will I ever get well?”. The overall aim of this thesis has been to study different aspects of these questions – from the pathophysiological role of monocytes and their function in blood and the synovial environment, to incidence, outcome measures with short- and long-term perspectives, risk of depression and anxiety, and mortality.

Children with active oligoarticular JIA display monocytes of a mixed pro- and anti-inflammatory polarization pattern in the synovial environment, with reduced capacity to phagocytize, unique for this JIA subtype. This supports the hypothesis that oligoarticular JIA should not be considered as a pediatric version of adult rheumatic arthritides.
The mean annual incidence rate in Skåne (the southernmost region of Sweden) 1980 – 2010 was 9.9/100,000 children < 16 years, with significantly increasing numbers during the period. The mortality was interpreted as low, fewer patients were diagnosed with JIA-associated uveitis and the need of joint corrective surgery was decreased compared to previously published data. However, children with JIA diagnosed since the introduction of biologic immunomodulatory treatment still experienced disease activity more than 50% of the follow-up years. No increased risk for diagnosis with depression or anxiety was found in JIA patients and they were also not diagnosed at an earlier age than age- and sex-matched controls.

In conclusion, the long-term outcome of JIA has improved and the risk for depression and anxiety is not found to be increased in JIA. There are however still challenges with active disease more than half of the time in spite of state-of-the-art treatment. Follow-up in adulthood is needed to answer the question of how many JIA patients that still needs healthcare as adults.
Originalspråkengelska
KvalifikationDoktor
Tilldelande institution
  • Institutionen för kliniska vetenskaper, Lund
Handledare
  • Kahn, Robin, handledare
  • Månsson, Bengt, Biträdande handledare
  • Bengtsson, Anders, Biträdande handledare
Tilldelningsdatum2022 apr. 29
UtgivningsortLund
Förlag
ISBN (tryckt)978-91-8021-217-5
StatusPublished - 2022

Bibliografisk information

Defence details
Date: 2022-04-29
Time: 09:00
Place: Reumatologiska klinikens föreläsningssal, Lottasalen, Universitetssjukhuset i Lund. Join by Zoom: https://lu-se.zoom.us/j/67302589343
External reviewer(s)
Name: Rygg, Marite
Title: Professor
Affiliation: Norwegian University of Science and Technology, Trondheim, Norway

Ämnesklassifikation (UKÄ)

  • Reumatologi och inflammation

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