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April 13, 2026Wiadomości Lekarskie0 citationsOpen Access

Characteristics of Adult Patients with Juvenile Idiopathic Arthritis

JBJózef BalickiMedical University of LublinPKPaweł KamińskiInstitute of Soil Science and Plant CultivationMRMarek RybakMedical University of Lublin

Key Points

  • Explore the impact of juvenile idiopathic arthritis (JIA) on quality of life and psychosocial outcomes in adulthood.
  • Analyzed health outcomes of adults diagnosed with juvenile idiopathic arthritis.
  • Evaluated quality of life, psychosocial well-being, and functional impairment.
  • Examined associations between disease activity and various health metrics.
  • Adults with JIA experience decreased quality of life and psychosocial well-being.
  • Active disease affects half of young adults with JIA, with many exhibiting disability and organ damage.
  • Emotional health outcomes showed no significant increase in depression or anxiety among patients.

Abstract

Conclusions: Results show that quality of life and psychosocial well-being, occupational and social functioning, and, sometimes, cognitive functioning are decreased, while pain and fatigue are increased. In contrast, analyses of emotional health outcomes did not show a higher prevalence of depression or anxiety in adults with JIA. Half of young adults with JIA have active disease, and more than one-third suffer detectable degrees of disability and organ damage. Frequent complaints and conditions are: abdominal pain, TMJ pain, uveitis, and juvenile fibromyalgia syndrome. JIA may also affect BMI, inflammation, and pain of the joints, Growth disorders, overall dysregulation of the immune system, and a negative correlation between disease activity and vitamin D levels. Nevertheless, patients with JIA exhibit lower functional impairment and better quality of life compared to other rheumatic diseases, such as rheumatoid arthritis and spondyloarthropathies. Understanding the lasting impact on health and life satisfaction among adult patients with JIA requires a comprehensive approach that accounts for the multifactorial aspects of the individual's experience with the disease.

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Cite This Study

Balicki et al. (2026) studied this question.

synapsesocial.com/papers/69dc874a3afacbeac03e9c3fhttps://doi.org/10.36740/wlek/217867
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