Advancements and progress in juvenile idiopathic arthritis: A Review of pathophysiology and treatment

Author:

Huang Helen Ye Rim1,Wireko Andrew Awuah2ORCID,Miteu Goshen David34,Khan Adan5,Roy Sakshi6,Ferreira Tomas7,Garg Tulika8,Aji Narjiss9,Haroon Faaraea10,Zakariya Farida11,Alshareefy Yasir12,Pujari Anushka Gurunath113,Madani Djabir14,Papadakis Marios15

Affiliation:

1. Faculty of Medicine and Health Science, Royal College of Surgeons in Ireland, Dublin, Ireland

2. Sumy State University, Sumy, Ukraine

3. School of Biosciences, Biotechnology, University of Nottingham, Nottingham, UK

4. Department of Biochemistry, Caleb University Lagos, Lagos, Nigeria

5. Kent and Medway Medical School, Canterbury, Kent, UK

6. School of Medicine, Queen’s University Belfast, Belfast, Northern Ireland, UK

7. School of Clinical Medicine, University of Cambridge, Cambridge, UK

8. Government Medical College and Hospital Chandigarh, Chandigarh, India

9. Faculty of Medicine and Pharmacy of Rabat, Rabat, Morocco

10. Faculty of Public Health, Health Services Academy, Islamabad, Pakistan

11. Faculty of Pharmaceutical Sciences, Ahmadu Bello University Zaria, Zaria, Nigeria

12. School of Medicine, Trinity College Dublin, The University of Dublin, Dublin, Ireland

13. Department of Kinesiology, Faculty of Science, McMaster University, Hamilton, Ontario, Canada

14. UCD Lochlann Quinn School of Business and Sutherland School of Law, University College Dublin, Dublin, Ireland

15. Department of Surgery II, University Hospital Witten-Herdecke, University of Witten-Herdecke, Wuppertal, Germany.

Abstract

Juvenile idiopathic arthritis (JIA) is a chronic clinical condition characterized by arthritic features in children under the age of 16, with at least 6 weeks of active symptoms. The etiology of JIA remains unknown, and it is associated with prolonged synovial inflammation and structural joint damage influenced by environmental and genetic factors. This review aims to enhance the understanding of JIA by comprehensively analyzing relevant literature. The focus lies on current diagnostic and therapeutic approaches and investigations into the pathoaetiologies using diverse research modalities, including in vivo animal models and large-scale genome-wide studies. We aim to elucidate the multifactorial nature of JIA with a strong focus towards genetic predilection, while proposing potential strategies to improve therapeutic outcomes and enhance diagnostic risk stratification in light of recent advancements. This review underscores the need for further research due to the idiopathic nature of JIA, its heterogeneous phenotype, and the challenges associated with biomarkers and diagnostic criteria. Ultimately, this contribution seeks to advance the knowledge and promote effective management strategies in JIA.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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